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Chemical & Biological Weapons. Fluorine chemicals. 1995 UN Monitoring and Verification of Iraq's Compliance.
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Online at http://www.fas.org/news/un/iraq/s/s1995-0208.htmUnited Nations
Security Council
Distr.
GENERAL
S/1995/208
17 March 1995
ORIGINAL: ENGLISHPLAN FOR FUTURE ONGOING MONITORING AND VERIFICATION OF IRAQ'S COMPLIANCE WITH RELEVANT PARTS OF SECTION C OF SECURITY COUNCIL RESOLUTION 687 (1991) REPORT OF THE SECRETARY-GENERAL (S/22871/Rev.1) REVISED ANNEXES II, III AND IV Note by the Executive Chairman of the Special Commission established pursuant to paragraph 9 (b) (i) of Security Council resolution 687 (1991) 1. On 2 October 1991, the Secretary-General submitted to the Security Council a report containing the Special Commission's plan for ongoing monitoring and verification of Iraq's compliance with relevant parts of section C of Security Council resolution 687 (1991). That plan (S/22871/Rev.1) was approved by the Security Council in its resolution 715 (1991) of 11 October 1991. 2. The plan contained annexes with lists of items relevant to the implementation in Iraq of monitoring and verification. As indicated in the report, these lists "should be taken into account in the development of a mechanism related to the sale or supply of items to Iraq by other countries". Paragraph 7 of resolution 715 (1991) calls for that mechanism to be developed in cooperation by the Committee established under resolution 661 (1990) (i.e. the Sanctions Committee), the Special Commission and the Director-General of the International Atomic Energy Agency (IAEA). The mechanism, as developed by the Sanctions Committee, the Special Commission and IAEA, will be transmitted shortly to the Council for its approval. 3. In the course of developing the mechanism, it became clear that, for the annexes to the plan to serve, as intended, as the lists of items to be reported by the exporting countries to the Special Commission and IAEA, it was necessary to elaborate upon generic descriptions in those annexes so that customs and control authorities would know precisely what items would be subject to notification. Consequently, with international expert assistance, the Special Commission has prepared a revision of the annexes to its plan in the chemical, biological and missile areas. These revised annexes do not materially differ 95-07628 (E) 220395/... *9507628* from the original annexes, elaborating instead on those annexes to produce a precise listing of items to be notified under the export/import mechanism. 4. The Special Commission's plan, as approved by the Security Council resolution 715 (1991), lays down in its paragraph 26 the following procedure for revising the annexes: "The Special Commission may, however, after informing the Security Council, update and revise the annexes in the light of information and experience gained in the course of implementation of resolutions 687 (1991) and 707 (1991) and of the Plan. The Special Commission shall inform Iraq of any such change." 5. In compliance with the foregoing procedure requiring it to inform the Council of revisions to the annexes, the Special Commission is transmitting herewith to the Council the text of the revised annexes. The Commission intends to proceed to notify Iraq of the revised annexes 30 days after the date of the submission of the present note to the Security Council, thus completing the procedure for revision, unless the Council instructs it otherwise. Revised annex II to the Special Commission's Plan* Provisions related to chemical items 1. The following list contains chemicals * T h e present annexes are being published as received, without formal editing. For the purposes of this annex the chemicals listed include their chemical forms and mixtures. It is understood that, if and when other processes are developed for the production of such chemicals, chemicals used in those processes which are not included in the present list shall be added through a revision of this list in accordance with the procedures detailed in paragraph 26 of the Plan. capable of being used for the development, production or acquisition of chemical weapons, but which also are usable for purposes not prohibited by resolution 687 (1991) and, therefore, are subject to monitoring and verification in accordance with paragraphs 29, 30 and 31 of the Plan. List A Chemical Abstracts Service (CAS) Chemical Registry No. 1.1Chemicals, except for those chemicals specified in list B of this annex, containing a phosphorus atom to which is bonded one H, alkyl or alkyl substitute group but no further carbon atoms e.g. Methyl thiophosphonyl dichloride (676-98-2) 1.2 Dialkyl or dialkyl-substituted (Me, monochloro-M, Et, n-Pr or i-Pr) N,N-dialkyl or N,N-dialkyl substitutes (Me, Et, n-Pr or i-Pr)-phosphoramidates e.g. Diethyl N,N-dimethylphosphoramidate (2404-03-7) 1.3 Arsenic trichloride (7784-34-1) 1.4 2,2-Diphenyl-2-hydroxyacetic acid (benzilic acid) (76-93-7) 1.5 Quinuclidin-3-ol (1619-34-7) Quinuclidin-3-ol hydrochloride (6238-13-7) Chemical Abstracts Service (CAS) Chemical Registry No. 1.6 N,N-Dialkyl (Me, Et, n-Pr or i-Pr) aminoethyl-2-chloride and corresponding protonated salts e.g. N,N-diisopropyl-2-aminoethyl chloride hydrochloride (4261-68-1) 1.7 N,N-Dialkyl (Me, Et, n-Pr or i-Pr) aminoethane-2-ol and corresponding protonated salts e.g. N,N-Diisopropyl-2-aminoethanol (96-80-0) 1.8 N,N-Dialkyl (Me, Et, n-Pr or i-Pr) aminoethane-2-thiol and corresponding protonated salts e.g. N,N-Diisopropyl-2-aminoethanethiol (5842-07-9) 1.9 Phosgene (75-44-5) 1.10 Cyanogen chloride (506-77-4) 1.11 Hydrogen cyanide (74-90-8) 1.12 Trichloronitromethane (chloropicrin) (76-06-2) 1.13 Phosphorus oxychloride (10025-87-3) 1.14 Phosphorus trichloride (7719-12-2) 1.15 Phosphorus pentachloride (10026-13-8) 1.16 Trimethyl phosphite (TMP) (121-45-9) 1.17 Triethyl phosphite (122-52-1) 1.18 Dimethyl phosphite (DMP) (868-85-9) 1.19 Diethyl phosphite (762-04-9) 1.20 Diisopropylphosphite (1809-20-7) 1.21 Triisopropylphosphite (116-17-6) 1.22 Sulphur monochloride (10025-67-9) 1.23 Sulphur dichloride (10545-99-0) 1.24 Thionyl chloride (7719-09-7) Chemical Abstracts Service (CAS) Chemical Registry No. 1.25 Cyclohexanol (108-93-0) 1.26 Hydrogen fluoride (7664-39-3) 1.27 Ortho-chlorobenzylidenemalononitri1e (CS) (2698-41-1) 1.28 Potassium fluoride (7789-23-3) 1.29 Ammonium bif1uoride (1341-49-7) 1.30 Sodium bifluoride (1333-83-1) 1.31 Sodium fluoride (7681-49-4) 1.32 Potassium bifluoride (7789-29-9) 1.33 Sodium sulphide (1313-82-2) 1.34 Hydrogen sulphide (7783-06-4) 1.35 Carbon disulphide (75-15-0) 1.36 Phosphorus pentasulphide (1314-80-3) 1.37 Chloroethanol (107-07-3) 1.38 Isopropanol (67-63-0) 1.39 Dimethylamine (124-40-3) 1.40 Dimethylamine hydrochloride (506-59-2) 1.41 Potassium cyanide (151-50-8) 1.42 Sodium cyanide (143-33-9) 1.43 Triethanolamine (102-71-6) 1.44 Triethanolamine hydrochloride (637-39-8) 1.45 Diisopropylamine (108-18-9) 1.46 Diisopropylamine hydrochloride (819-79-4) 1.47 Methyl diethanolamine (105-59-9) 1.48 Methyl diethanolamine hydrochloride (54060-15-0) Chemical Abstracts Service (CAS) Chemical Registry No. 1.49 Ethyl diethanolamine (139-87-7) 1.50 Ethyl diethanolamine hydrochloride (58901-15-8) 1.51 Methyl benzilate (76-89-1) 1.52 O,O-Diethyl phosphorothioate (2465-65-8) 1.53 O,O-Diethyl phosphorodithioate (298-06-6) 1.54 Ethylene oxide (75-21-8) 1.55 Propylene oxide (75-56-9) 1.56 Hydroxy-1-methylpiperidine (3554-74-3) 1.57 Hydroxy-1-methylpiperidine hydrochloride (164-45-6) 1.58 Quinuclidone (3731-38-2) 1.59 Quinuclidone hydrochloride (1193-65-3) 1.60 Phosphorus (7723-14-0) 1.61 Sulphur (7704-34-9) 1.62 Chlorine (7782-50-5) 1.63 Fluorine (7782-41-4) 2. The following list contains chemicals It is understood that, if and when new chemical warfare agents are developed or other processes are used for their production, those chemical warfare agents and the chemicals used in those processes which are not included in the present list shall be added through a revision to this list in accordance with the procedures detailed in paragraph 26 of the Plan. that have little or no use except as chemical warfare agents or for the development, production or acquisition of chemical weapons, or which have been used by Iraq as essential precursors for chemical weapons and are, therefore, prohibited to Iraq save under the procedure for special exceptions provided for in paragraph 32 of the Plan. List B Chemical Abstracts Service (CAS) Chemical Registry No. 2.1 O-Alkyl (<=C10, including cycloalkyl) alkyl (Me, Et, n-Pr or i-Pr)-phosphonofluoridates e.g. O-Isopropyl methylphosphono- fluoridate (Sarin) (107-44-8) O-Pinacolyl methylphosphono- fluoridate (Soman) (96-64-0) 2.2 O-Alkyl (<=C10- including cycloalkyl) N,N-dialkyl (Me, Et, n-Pr or i-Pr) phosphoramidocyanidates e.g. O-ethyl N,N-dimethylphosphoramido cyanidate (Tabun) (77-81-6) 2.3 O-Alkyl (H or <=C10, including cycloalkyl) S-2- dialkyl (Me, Et, n-Pr or i-Pr)-aminoethyl alkyl (Me, Et, n-Pr or i-Pr) phosphonothiolates or corresponding alkylated and protonated salts e.g. O-Ethyl S-2{-(N,N-diisopropylamino)ethyl} methylphosphonothiolate (VX) (50782-69-9) 2.4 Sulphur mustards: 2-Chloroethylchloromethylsulphide (2625-76-5) Bis (2-chloroethyl) sulphide (505-60-2) (Mustard gas, H) Bis(2-chloroethylthio)methane (63869-13-6) 1, 2-Bis(2-chloroethylthio)ethane (3563-36-8) (Sesquimustard, Q) 1,3-Bis(2-chloroethylthio)-n-propane (63905-10-2) 1,4-Bis(2-chloroethylthio)-n-butane (142868-93-7) l,5-Bis(2-chloroethylthio)-n-pentane (142868-94-8) Bis(2-chloroethylthiomethyl)ether (63918-90-1) Bis(2-chloroethylthioethyl)ether (63918-89-8) (O-Mustard, T) 2.5 Lewisites: 2-Chlorovinyldichlorarsine (541-25-3) (Lewisite l) Bis(2-chlorovinyl)chloroarsine (40334-69-8) (Lewisite 2) Tris(2-chlorovinyl)arsine (40334-70-1) (Lewisite 3) Chemical Abstracts Service (CAS) Chemical Registry No. 2.6 Nitrogen mustards: Bis(2-chloroethyl)ethylamine (538-07-8) (HN 1) Bis(2-chloroethyl)methylamine (51-75-2) (HN 2) Tris(2-chloroethyl)amine (555-77-1) (HN 3) and their protonated salts 2.7 3-Quinuclidinyl benzilate (BZ) (6581-06-2) 2.8 Saxitoxin (35523-89-8) 2.9 Ricin (9009-86-3) 2.10 Alkyl (Me, Et, n-Pr or i-Pr) phosphonyldihalides e.g. Methylphosphonyldifluoride (DF) (676-99-3) Methylphosphonyldichloride (DC, MPC) (676-97-1) 2.11 Dimethylmethylphosphonate (DMMP) (756-79-6) 2.12 O-Alkyl (H or <=C10, including cycloalkyl) O-2-Dialkyl (Me, Et, n-Pr or i-Pr)- aminoethyl alkyl (Me, Et, n-Pr or i-Pr) phosphonites and corresponding alkylated salts and protonated salts e.g. O-Ethyl 2-diisopropylaminoethyl methylphosphonite (QL) (57856-11-8) 2.13 O-Alkyl (<=C10, including cycloalkyl) alkyl (Me, Et, n-Pr or i-Pr)- phosphonochloridates e.g. O-Isopropyl methylphosphono- chloridate (1445-76-7) (Chlorosarin) O-Pinacolyl methylphosphono- chloridate (7040-57-5) (Chlorosoman) 2.14 N,N-Dialkyl (Me, Et, n-Pr or i-Pr) phosphoramidic dihalides e.g. N,N-dimethylphosphoramidic dichloride (677-43-0) Chemical Abstracts Service (CAS) Chemical Registry No. 2.15 Bis(2-hydroxyethyl)sulphide (Thiodiglycol) (111-48-8) Bis(2-hydroxyethyl)disulphide (Dithiodiglycol) (1892-29-1) 2.16 3,3-Dimethylbutan-2-ol (Pinacolyl alcohol) (464-07-3) 2.17 3,3-Dimethylbutanone (Pinacolone) (75-97-8) 2.18 Amiton: O,O-Diethyl S-(2-(diethylamino)ethyl)) phosphorothiolate and corresponding (78-53-5) alkylated and protonated salts 2.19 PFIB: 1,1,3,3,3-pentafluoro-2- (trifluoromethyl)-1-propene (382-21-8) 3. The initial information under paragraph 30 of the Plan, to be provided not later than 30 days after the adoption of the Plan by the Security Council, shall cover the period from 1 January 1988. Subsequent information shall be provided each 15 January and 15 July and shall cover the six-month period prior to the provision of the information. The advance notifications under paragraph 30 (d) of the Plan shall cover the subsequent six months. The special notifications under paragraph 31 of the Plan shall be provided not later than 30 days in advance. 4. Whenever the information that Iraq is required to provide under section C of the Plan and this annex is equal to nil, Iraq shall provide nil returns. 5. The information on chemicals to be provided under section C of the Plan shall, for each chemical, include: 5.1the chemical name, common or trade name used by the site or the facility, structural formula and Chemical Abstracts Service registry number (if assigned); 5.2the purposes for which the chemical is produced, processed, consumed, stored, imported or exported; and 5.3the total amount produced, processed, consumed, stored, imported or exported. 6. The information on sites or facilities to be provided under section C of the Plan shall, for each site or facility, include: 6.1the name of the site or facility and of the owner, company or enterprise operating the site or facility; 6.2the location of the site or facility; 6.3a general description of all types of activities at the site or facility; and 6.4the sources and amounts of the financing of the site or facility, and of its activities. 7. The location of a site or facility shall be specified by means of the address and a site diagram. Each diagram shall be drawn to scale and shall indicate the boundaries of the site or facility, all road and rail entrances and exits and all structures on the site or facility, indicating their purpose. If the site or facility is located within a larger complex, the diagram shall specify the exact location of the site or facility within the complex. On each diagram, the geographic coordinates of a point within the site or facility shall be specified to the nearest second. 8. In addition to information specified in paragraph 6 of this annex, the following information shall be provided for each site or facility that is or will be involved in production, processing, consumption, storage, import or export of chemicals specified in list A of this annex: 8.1a detailed description of activities related to these chemicals including, as applicable, material-flow and process-flow diagrams, chemical reactions and end-use; 8.2a list of equipment used in activities related to these chemicals; and 8.3the production capacity for these chemicals. 9. In addition to information specified in paragraph 6 of this annex, the following information shall be provided for each site or facility that is or will be involved in production or processing of organophosphorus chemicals or in production of organic chemicals by halogenation: 9.1a detailed description of activities related to the relevant chemicals, and the end-uses for which the chemicals are produced or processed; and 9.2a detailed description of the processes used in the production or processing of organophosphorus chemicals or in the production of organic chemicals by halogenation, including material-flow and process-flow diagrams, chemical reactions and list of equipment involved. 10. For equipment capable of being used in the activities described in paragraphs 8 and 9 above, Iraq shall, for each item, declare: 10.1the name of the site or facility at which it is located together with the names of the owner, company or enterprise operating the site or facility; 10.2 the location of the site or facility; 10.3the technical specifications of the equipment that make it capable of dual-use, including, where relevant, the material of construction, capacity, specifications of control mechanisms, temperature and pressure tolerances and flow-rates; and 10.4 any import or any other acquisition of such equipment. Such equipment shall include: 10.4.1corrosion resistant For the purposes of this annex, "corrosion resistant" means where all surfaces that come in direct contact with the chemical(s) being processed are made from the following: (a) glass (including vitrified or enamelled coatings or glass lining); (b) ceramics; (c) ferrosilicates; (d) titanium or titanium alloys (e.g. Monel 10 or 11, titanium 20, titanium nitride 70 or 90); (e) tantalum or tantalum alloys; (f) zirconium or zirconium alloys; (g) nickel or alloys with more than 40 per cent nickel by weight (e.g. Alloy 400, AMS 4675, ASME SB164-B, ASTM B127, DIN2.4375, EN60, FM60, IN60, Hastalloy, Monel, K500, UNS NO4400); (h) alloys with more than 25 per cent nickel and 20 per cent chromium and/or copper by weight (e.g. Cunifer 30Cr, ENiCu-7, IN 732 X, Monel 67, Monel WE 187, UNS C71900); (i) graphite; (j) fluoropolymers (e.g. Aflex COP, Aflon COP 88, F 40, Ftorlon, Ftoroplast, Neoflon, ETFE, Teflon, PVDF, Tefzel, PTFE, PE TFE 500 LZ, Haller); (k) natural or synthetic rubber coatings; (l) fibre reinforced polymers including glass or graphite; and (m) silver. chemical production equipment as follows: 10.4.1.1reactor vessels with a capacity of 0.050 m3 or more; 10.4.1.2 condensers and heat exchangers; 10.4.1.3 distillation columns; 10.4.1.4 scrubbers; 10.4.1.5tanks and other storage vessels Including halogen transport containers. with a volume of 0.05 m3 or more; and 10.4.1.6sheets made of corrosion resistant metal or alloy with a surface of more than 1 m2 and a thickness of 4 mm or more; 10.4.2corrosion resistant pumps with a maximum flow-rate of 0.01 m3 per minute or more (under standard temperature of 293 K, i.e. 20f C, and standard pressure conditions of 101.30 kPa, i.e. 101.30 kilonewton per square metre), including magnetic pumps and those using squeezers or progressive cavity tubing pumps (including peristaltic or roller pumps in which only the elastometric tubing is corrosion resistant), and corrosion resistant vacuum pumps with a maximum flow-rate of 0.08 m3 per minute or more under the same standard conditions; 10.4.3corrosion resistant pipes with an inner diameter of 12.5 mm or more and double-walled pipes with an inner diameter of 12.5 mm or more; 10.4.4corrosion resistant valves with a smallest inner diameter of 12.5 mm or more; 10.4.5corrosion resistant remote-controlled filling equipment; 10.4.6incineration equipment designed for the disposal of toxic chemicals with an average combustion chamber temperature of over 1273 K (1000f C) or with catalytic incineration over 623 K (350f C); 10.4.7equipment and instruments Including equipment for the detection or identification of chemical warfare agents, but excluding smoke detectors or stack emission monitor systems designed for use in household protection. capable of detecting, measuring or recording the air concentration of toxic organic substances or organic compounds containing the elements chlorine, fluorine, phosphorus or sulphur with a detection threshold from 0.3 mg/m3 or suitable for detection or measuring levels of cholinesterase-inhibitors in the air; and 10.4.8protective equipment designed for protection against toxic chemicals in lists A and B, as follows: 10.4.8.1external ventilated semi- or full-protection personal suits; 10.4.8.2 autonomous respirators; and 10.4.8.3air filtration equipment with liquid or solid adsorption agent. 11. For equipment identified in paragraph 10.4.1.5 of this annex capable of storing chemicals in lists A and B, Iraq shall, for each item, declare: 11.1the name of the site or facility at which it is located together with the names of the owner, company or enterprise operating the site or facility; 11.2the location of the site or facility; 11.3the net storage capacity of each piece of equipment and the aggregate storage capacity at the site; and 11.4any import or any other acquisition of such equipment. 12. For the purposes of information to be provided in accordance with paragraph 30 (e) of the Plan concerning technologies, Iraq shall report the import or other acquisition of any technologies or services for planning, construction, commissioning, start up or normal operation of a chemical production plant capable of producing any chemical in list A or to operate and maintain the equipment identified in paragraphs 10 and 11 above. 13. For munitions, rockets and missile warheads capable of dispersing chemical warfare agents, Iraq shall, for each item, declare: 13.1the name of the site or facility at which it is located together with the names of the owner, company or enterprise operating the site or facility; 13.2the location of the site or facility; 13.3the quantity of such items by type; and 13.4any import or any other acquisition of such items. 14. The information on each import to be provided under section C of the Plan and paragraphs 10, 11 and 13 of this annex shall include: 14.1specification of each item and the quantity imported and the purpose of its use in Iraq; 14.2country from which the item is imported and the specific exporter; 14.3point or port and time of entry of the item into Iraq; 14.4 site or facility where it is to be used; and 14.5 name of the specific importing organization in Iraq. Revised annex III to the Special Commission's Plan Provisions related to biological items 1. The following list contains equipment, "Equipment" means complete systems and any components or reagents thereof. biological material and other items capable of being used for the development, production or acquisition of biological and toxin weapons or of a biological and toxin weapons capability and, therefore, subject to monitoring and verification in accordance with paragraphs 34 to 38 of the Plan: 1.1microorganisms, For the purposes of the Plan, full lists of the microorganisms, other organisms and toxins concerned have been enumerated in two lists, one covering risk groups IV and III (List 1), the other covering risk group II (List 2). These lists are contained in an Explanatory Note which follows on the appendix to this annex. other organisms and toxins Including purified or crude material. meeting the criteria for risk groups IV, III and II according to the classification in the World Health Organization (WHO) Laboratory Biosafety Manual (Geneva 1993, second edition), and genetic material for such toxins; 1.2detection and assay systems for risk groups IV, III, and II microorganisms and toxins, or for genetic material, including immunological assays, gene probe assays and other specific detection systems; 1.3equipment designed or accepted for use for processing, handling, transporting or storing microorganisms, their products or components, including toxins, or other biological material including foodstuffs, including: 1.3.1centrifugal separators or decanters for continuous or semi-continuous operation; 1.3.2 continuous flow centrifuge rotors; 1.3.3 plate press filter separators; 1.3.4cross-flow or tangential filtration equipment with a filter area of 0.5 square metres or greater; 1.3.5 spray drying equipment; 1.3.6freeze-drying (lyophilisation) equipment with a condenser capacity greater than 1 kg of ice per 24 hours; 1.3.7pressure cell disruption equipment or continuous flow ultrasonic cell disruption equipment; 1.3.8chromatography equipment for preparative separations; 1.3.9pharmaceutical milling equipment; 1.3.10drum drying equipment; 1.3.11 jacketed vessels; and 1.3.12control units, valves and filters for the above types of equipment; 1.4biohazard containment equipment and decontamination equipment, including: 1.4.1facilities, rooms or other enclosures meeting the physical containment criteria for P3 or P4 (BL3, BL4, L3, L4) biological containment as defined in the WHO Laboratory Biosafety Manual and using laminar or turbulent air flow clean air conditions as specified for pharmaceutical, biotechnology, vaccine or other applications; 1.4.2biological safety cabinets meeting Class I, II and III containment standards, as defined in the WHO Laboratory Biosafety Manual; 1.4.3safety cabinets allowing manual or remote operations to be performed within at Class I, II or III biological containment levels, including flexible film isolators, rigid isolators, dry boxes, glove boxes, anaerobic chambers, interconnected cabinet lines, isolator lines and secondary containment systems designed to enclose fermenters or downstream processing equipment; 1.4.4rubber gloves specifically designed for use with safety cabinets and biological safety cabinets; 1.4.5autoclaves, with an internal volume of 0.3 m3 or more, designed to sterilise infectious material; 1.4.6other waste disposal systems for infectious material, such as liquid waste treatment systems, solid waste treatment systems, liquid waste disposal systems, solid waste disposal systems and incinerators; and 1.4.7positive pressure air-fed suits, half suits, helmets and respirators; 1.5equipment designed or accepted for use for the microencapsulation of living microorganisms, their products or components including toxins, or other biological material; 1.6complex media for the growth of risk groups IV, III and II microorganisms; 1.7fermentation vessels (including bioreactors, chemostats and continuous flow systems), orbital or reciprocal shakers and shaking incubators designed or accepted for use for the cultivation of microorganisms or eukaryotic cells or for the production of toxins, and components therefor, including control units for fermenters and other vessels; 1.8recombinant nucleic acids (DNA and RNA), equipment and reagents Including dimethoxytrityl (DMT)-ribonucleosides and dimethoxytrityl (DMT)-deoxyribonucleosides. for their isolation, characterization or production and equipment and reagents for the construction of synthetic genes, including nucleic acid sequencing equipment, nucleic acid synthesizers, electroporation or biolistics equipment, thermal cyclers, electrophoresis equipment, transilluminators, automatic work stations and automatic data collection systems, and components therefor, including derivatized solid supports for solid phase nucleotide synthesis; 1.9equipment for the release and/or dispersal into the environment or into cabinets, chambers, rooms or other enclosures of biological material and equipment capable of being modified for such use, excluding devices designed for personal use in self-administered prophylactic or therapeutic preparations by inhalation, but including crop sprayers, aircraft sprayers and tanks, other sprayers capable of chassis mounting and tanks, jet engine disseminators, aerosol disseminators, droplet disseminators, dry powder disseminators (including dry aerosol disseminators, venturi air movers and nebulisers), mist generators and foggers, including pulse jet disseminators; 1.10equipment designed or accepted for use for studying the aerobiological characteristics or aerosols of microorganisms, their components including toxins, or other biological material and equipment capable of being modified for such use, including aerosolization containers (drums, cabinets, chambers, rooms or other enclosures), nose-only aerosolization equipment and aerodynamic particle-sizing equipment; 1.11equipment for breeding of vectors of human, animal or plant diseases; 1.12vaccines for risk groups IV, III, and II microorganisms, whether for use with humans or animals and whether licensed, unlicensed or experimental; 1.13documents, "Documents" means blueprints, plans, diagrams, models, formulae, tables, engineering designs or specifications, manuals or instructions, and any database or software concerning risk groups IV, III and II microorganisms, toxins and genetic material, except those generally available to the public. information, software or technology for the design, development, use, storage, manufacture, maintenance or support of items listed in the preceding subparagraphs of this paragraph, or of biological weapons or any component thereof, or of biological and training activities or defence; and 1.14munitions, rockets or missile warheads Delivery systems are addressed in annex IV. capable of disseminating biological weapons agents. 2. The initial information under paragraphs 35 and 36 of the Plan to be provided not later than 30 days after the adoption of the Plan by the Security Council shall cover the period from 1 January 1986. Subsequent information shall be provided each 15 January and 15 July and shall cover the six-month period prior to the provision of the information. Notifications under paragraph 38 (a) of the Plan shall be provided not later than 60 days in advance. 3. Whenever the information that Iraq is required to provide under section D of the Plan and this annex is equal to nil, Iraq shall provide nil returns. 4. The information on each site or facility Including sites or facilities involved in the import, export or storage of the equipment, biological material and other items specified in paragraph 1 of this annex. to be provided under section D of the Plan shall include the following: 4.1the name of the site or facility and of the owner, company, or enterprise operating the facility; 4.2the location of the site or facility (including the address, geographic coordinates to the nearest second, and a site diagram. Each diagram shall be drawn to scale and shall indicate the boundaries of the site or facility, all road and rail entrances and all structures, indicating their purpose and any structure number. If the site or facility is located within a larger complex, the diagram shall specify the exact location of the site or facility within the larger complex); 4.3the sources and amounts of financing of the site or facility and of its activities; 4.4the main purpose of the site or facility, including research, development, use, production, storage, testing, import and export; 4.5the level of protection, including, as applicable, the number and size of maximum containment or containment laboratories (units); 4.6scope and description of activities, including, as applicable, a list of types and quantities of microorganisms, toxins or vaccines and equipment and other items specified in paragraph 1 of this annex; 4.7a list of microorganisms and toxins, equipment and vaccines imported or isolated for the use of the site or facility, or exported, indicating the supplier or recipient countries involved; 4.8the date when the planned activities, as described in paragraphs 35 (a) to 35 (g) of the Plan, are to begin at the site or facility; and 4.9the number of scientifically trained personnel and their main areas of responsibility. 5. Information on imports to be provided under paragraphs 35 (g) and 38 (a) of the Plan shall cover the items listed in the appendix to this annex and shall, for each import into Iraq, specify: 5.1types and quantities of microorganisms, other organisms, toxins, genetic material or vaccines; 5.2quantities of any equipment, facilities, information, software, technology or other items specified in the appendix to this annex; 5.3country of export and the specific exporter; 5.4point or port and time of entry into Iraq; 5.5site or facility where it is to be used and purpose of its use; and 5.6 name of the specific importing organization in Iraq. 6. The information under paragraph 37 of the Plan shall be provided within seven days of the occurrence and the standardized form contained in section III of the annex on confidence-building measures in document BWC/CONF.III/23/II shall be utilized as appropriate. 7. Iraq shall, not later than each 15 April, provide to the Special Commission the copies of the declarations, information and data that Iraq has sent to the Centre for Disarmament Affairs of the United Nations Secretariat pursuant to the agreements on confidence-building measures, including the exchange of information and data, reached at the Third Review Conference of the Parties to the Convention on the Prohibition of the Development, Production and Stockpiling of Bacteriological (Biological) and Toxin Weapons and on Their Destruction (document BWC/CONF.III/23/II and its annex on confidence-building measures). APPENDIX Items to be reported under paragraphs 35 (g) and 38 (a) of the Plan and paragraph 5 of its annex III 1. Risk groups IV and III For the purposes of the Plan, full lists of the microorganisms, other organisms and toxins concerned have been enumerated in two lists, one covering risk groups IV and III (List 1), the other covering risk group II (List 2). These lists are contained in an Explanatory Note which follows on the appendix to this annex. microorganisms, "Microorganisms" means bacteria, viruses, mycoplasmas, rickettsiae or fungi, whether natural, enhanced or modified, either in the form of isolated live cultures, including live cultures in dormant form or in dried preparations, or as material including living material which has been deliberately inoculated or contaminated with such cultures. other organisms, toxins, Including purified or crude material. or genetic material. 2. Biohazard containment and decontamination items as follows: 2.1 facilities, rooms or other enclosures: (a)meeting the physical containment criteria for P3 or P4 (BL3, BL4, L3, L4) biological containment as specified in the WHO Laboratory Biosafety Manual (Geneva, 1993); and (b)constructed such that the number of particles of 0.5 microns in diameter in the contained air does not exceed 35,000 particles per cubic metre; 2.2biological safety cabinets meeting Class I, II, or III standards The specifications for Class I, II and III biological safety cabinets in the WHO Laboratory Biosafety manual are: Class I cabinet: an open-fronted, ventilated cabinet for personal protection with an unrecirculated inward air flow away from the operator. It is fitted with a HEPA filter to protect the environment from discharge of microorganisms; Class II cabinet: an open-fronted, ventilated cabinet for personal, product and environmental protection, which provides an inward air flow and HEPA-filtered supply and exhaust air. There are two main variations: the Class IIA type recirculates 70 per cent of the air; the Class IIB type recirculates 30 per cent of the air; and Class III cabinet: a totally enclosed, ventilated cabinet which is gastight and is maintained under negative air pressure. The supply air is HEPA-filtered and the exhaust air is passed through two HEPA filters in series. Work is performed with attached long-sleeved gloves.as specified in the WHO Laboratory Biosafety Manual, including flexible film isolators, dry boxes, glove boxes, anaerobic chambers, interconnected cabinet lines, isolator lines and secondary containment systems designed to enclose fermenters or downstream processing equipment, and specially designed components therefor; 2.3 HEPA filters; The WHO Laboratory Biosafety Manual defines HEPA filters as high efficiency particulate air filters. They should conform to national standards and not more than three particles should be recovered when the filter is challenged with a dose of 100,000 particles. 2.4rubber gloves specially designed for use with safety cabinets and biological safety cabinets; 2.5autoclaves designed to sterilise infectious material, with an internal volume equal to or greater than 0.3 cubic metres, and specially designed components therefor; and 2.6positive pressure air-fed suits, half suits, helmets and respirators, and specially designed components therefor. 3. Fermentation equipment, as follows: 3.1fermenters, bioreactors, chemostats, and continuous flow fermentation systems and specially designed components therefor; 3.2other vessels suitable for use for the cultivation of microorganisms or eukaryotic cells or for toxin production, capable of operating without the propagation of aerosols, and capable of in situ steam sterilisation in the closed state, and specially designed components therefor; 3.3orbital or reciprocal shakers with a total flask capacity greater than 5 litres, and specially designed components therefor; and 3.4shaking incubators with a total flask capacity greater than 5 litres, and specially designed components therefor. 4. Equipment usable for processing, handling, transporting or storing microorganisms, their products or components excluding personal and household equipment, but including toxins, or other biological material (including foodstuffs), as follows, and specially designed components therefor: 4.1centrifugal separators or decanters for continuous or semi-continuous operation; 4.2continuous flow centrifuge rotors; 4.3plate press filter separators; 4.4 cross-flow and tangential filtration equipment with a filter area equal to or greater than 0.5 m2; 4.5spray drying equipment; 4.6 freeze-drying (lyophilisation) equipment with a condenser capacity greater than 1 kg of ice in 24 hours; 4.7pressure cell disruption and continuous flow ultrasonic cell disruption equipment; 4.8chromatography columns with internal volumes greater than 2 litres, and specially designed end pieces and flow adaptors for such columns; 4.9milling equipment capable of producing particle sizes of 10 microns or less; 4.10drum drying equipment; and 4.11jacketed vessels. 5. Formulated powdered complex media or concentrated liquid complex media for growth of microorganisms. 6. Detection and assay systems for microorganisms, toxins, or genetic material in List 1 and specially designed reagents therefor, as follows: 6.1immunological assay systems; 6.2gene probe assay systems; and 6.3biological agent detection systems designed for biological defence or civil defence applications. 7. Equipment and reagents for use in molecular biology research, as follows, and specially designed components therefor: 7.1nucleic acid sequencing equipment; 7.2nucleic acid synthesizers; 7.3 electroporation or biolistics equipment; 7.4 thermal cyclers; 7.5 specially designed automatic data collection systems; 7.6transilluminators; 7.7electrophoresis equipment; 7.8derivatized solid supports for solid phase nucleotide synthesis; 7.9dimethoxytrityl (DMT)-ribonucleosides; and 7.10dimethoxytrityl (DMT)-deoxyribonucleosides. 8. Equipment capable of dispersing aerosols at a flow rate exceeding 1 litre of liquid suspension per minute or 10 g of dry material per minute, as follows, and specially designed components therefor: 8.1crop sprayers; 8.2 aircraft sprayers and associated spray tanks; 8.3other sprayers, capable of chassis mounting, and associated spray tanks; 8.4 jet engine disseminators; 8.5 aerosol disseminators; 8.6 droplet disseminators; 8.7 dry powder disseminators; Including dry aerosol disseminators, venturi air movers and nebulisers. 8.8mist generators; and 8.9foggers. Including pulse jet disseminators. 9. Equipment usable in the study of aerosols, as follows, and specially designed components therefor: 9.1aerosolization drums, cabinets, chambers, rooms or other enclosures; 9.2nose-only aerosolization equipment but not devices for personal prophylaxis or therapy for medical conditions; and 9.3aerodynamic particle-sizing equipment. 10. Equipment designed for the microencapsulation of living organisms, their products or components including toxins, or other biological material. 11. Vaccines for microorganisms or toxins in List 1, whether for use with humans or animals and whether licensed, unlicensed or experimental. 12. Documents, "Document" means blueprints, plans, diagrams, models, formulae, tables, engineering designs or specifications, manuals or instructions, and any database or software pertaining to microorganisms, toxins and genetic material of List 1 items except those containing information generally available to the public. information, software or technology for the design, development, use, storage, manufacture, maintenance or support of entries 1 to 11 above, or of biological weapons or any component thereof, or of biological defence and training activities or defence. 13. Munitions, rockets and missile warheads Delivery systems are addressed in annex IV. capable of disseminating biological weapons agents. /... S/1995/208 English Page S/1995/208 English Page EXPLANATORY NOTE UNSCOM Biological Lists based on the classification in the World Health Organization (WHO) Laboratory Biosafety Manual LIST 1 - Risk Groups IV and III Microorganisms, The items in this list do not conform fully with the criteria for risk groups IV and III according to the classification in the 1983 World Health Organization (WHO) Laboratory Biosafety Manual but should be considered as doing so for the purposes of ongoing monitoring and verification activities in Iraq. other Organisms and Toxins 1.1 Bacteria 1.1.1 Bacillus anthracis 1.1.2 Bacillus cereus 1.1.3 Bacillus subtilis 1.1.4 Bacillus megaterium 1.1.5 Bacillus thuringensis 1.1.6 Brucella abortus 1.1.7 Brucella melitensis 1.1.8 Brucella suis 1.1.9 Chlamydia psittaci 1.1.10 Clostridium botulinum 1.1.11 Clostridium perfringens 1.1.12 Francisella tularensis 1.1.13 Pseudomonas mallei 1.1.14 Pseudomonas pseudomallei 1.1.15 Salmonella typhi (Salmonella enterica var typhi) 1.1.16 Serratia marcescens 1.1.17 Shigella dysenteriae 1.1.18 Vibrio cholera 1.1.19 Yersinia pestis (Yersinia pseudotuberculosis var pestis) 1.1.20 Xanthomonas albilineans 1.1.21Xanthomonas campestris pv. citri including strains referred to as Xanthomonas campestris pv. citri types A,B,C,D,E or otherwise classified as Xanthomonas citri, Xanthomonas campestris pv. aurantifolia or Xanthomonas campestris pv. citrumelo 1.2 Mycoplasma 1.2.1 Mycoplasma mycoides 1.3 Rickettsiae 1.3.1 Coxiella burnetii 1.3.2 Rickettsia prowasecki 1.3.3 Rickettsia quintana 1.3.4 Rickettsia rickettsii 1.4 Viruses 1.4.1 African swine fever virus 1.4.2 Avian influenza virus 1.4.3 Bluetongue virus 1.4.4 Chikungunya virus 1.4.5 Congo-Crimean haemorrhagic fever virus 1.4.6 Dengue fever virus 1.4.7 Eastern equine encephalitis virus 1.4.8 Ebola virus 1.4.9 Foot and mouth disease virus 1.4.10 Goat pox virus 1.4.11 Hantaan virus 1.4.12 Human influenza 1.4.13 Japanese encephalitis virus 1.4.14 Junin virus 1.4.15 Lassa fever virus 1.4.16 Lymphocytic choriomeningitis virus 1.4.17 Lyssa virus 1.4.18 Machupo virus 1.4.19 Marburg virus 1.4.20 Monkey pox virus 1.4.21 Newcastle disease virus 1.4.22 Peste des petits ruminants virus 1.4.23 Porcine herpes virus (Aujeszky's disease) 1.4.24 Rift Valley fever virus 1.4.25 Rinderpest virus 1.4.26 Sheep pox virus 1.4.27 Swine fever virus (Hog cholera virus) 1.4.28 Swine vesicular disease (Porcine enterovirus type 9) 1.4.29 Teschen disease virus 1.4.30Tick-borne encephalitis virus (Russian Spring-Summer encephalitis virus) 1.4.31 Variola virus 1.4.32 Venezuelan equine encephalitis virus 1.4.33 Vesicular stomatitis virus 1.4.34 Western equine encephalitis virus 1.4.35 White pox virus 1.4.36 Yellow fever virus 1.5 Toxins 1.5.1 Abrin 1.5.2 Botulinum toxins 1.5.3 Clostridium perfringens toxins 1.5.4 Conotoxin 1.5.5 Diphtheria exotoxin 1.5.6 Microcystins (Cyanginosins) 1.5.7 Modeccin 1.5.8 Pseudomonas exotoxin 1.5.9 Ricin Items 1.5.9 and 1.5.10 are prohibited to Iraq save under the procedure of special exceptions provided for in paragraph 32 of the Plan. 1.5.10 Saxitoxin 2/ 1.5.11 Shiga toxin 1.5.12 Staphylococcus aureus toxins 1.5.13 Tetrodotoxin 1.5.14 Verotoxin 1.5.15 Volkensin 1.6 Fungi 1.6.1 Colletotrichum cof feanum var. virulans 1.6.2 Cochliobolus miyabeanus (Helminthosporium oryzae) 1.6.3Magnaporthe grisea (Pyricularia grisea/Pyricularia oryzae) 1.6.4 Microcyclus ulei (syn. Dothidella ulei) 1.6.5 Puccinia graminis (syn. Puccinia graminis f. sp. tritici) 1.6.6 Pucciniastriiformis (syn.Puccinia glumarum) 1.7 Other organisms 1.7.1 Eukaryotic (non-microbial) organism which produce any listed toxin. 1.8 Genetically modified microorganisms, other organisms and genetic material 1.8.1The above listed microorganisms when they have been genetically modified. 1.8.2Other genetically modified microorganisms or genetic material that contain nucleic acid sequences derived from any of the listed microorganisms, or that contain nucleic acid sequences associated with pathogenicity determinants of any listed microorganism; or that contain nucleic acid sequences associated with any listed toxin. 1.8.3Genetically modified variants of eukaryotic (non-microbial) organisms which produce any listed toxin. LIST 2 - RISK GROUP II MICROORGANISMS, The items in this list do not conform fully with the criteria for risk group II according to the classification in the 1983 World Health Organization (WHO) Laboratory Biosafety Manual but should be considered as doing so for the purposes of ongoing monitoring and verification activities in Iraq. OTHER ORGANISMS AND TOXINS (A) HUMAN AND ANIMAL PATHOGENS Bacteria Actinobacillus actinomycetemcomitans Actinomadura madurae Actinomadura pelletieri Actinomyces gerencseriae Actinomyces israelii Actinomyces pyogenes Actinomyces spp Arcanobacterium haemolyticum (Corynebacterium haemolyticum) Bacteriodes fragilis Bartonella bacilliformis Bordetella bronchiseptica Bordetella parapertussis Bordetella pertussis Borrelia burgdorferi Borrelia duttonii Borrelia recurrentis Borrelia spp Brucella canis Campylobacter jejuni Campylobacter spp Cardiobacterium hominis Chlamydia pneumoniae Chlamydia trachomatis Clostridium tetani Corynebacterium diphtheriae Corynebacterium minutissimum Corynebacterium spp Edwardsiella tarda Ehrlichia sennetsu (Rickettsia sennetsu) Ehrlichia spp Elkenella corrodens Enterobacter aerogenes/cloacae Enterobacter spp Enterococcus spp Erysipelothrix rhusiopathiae Escherichia coli (except non-pathogenic strains) Flavobacterium meningosepticum Fluoribacter bozemanae (Legionella) Fusobacterium necrophorum Gardnerella vaginalis Haemophilus ducreyi Haemophilus influenzae Haemophilus spp Helicobacter pylori Klebsiella oxytoca Klebsiella pneumoniae Klebsiella spp Legionella pneumophila Legionella spp Listeria ivanovii Morganella morganii Mycobacterium africanum Mycobacterium chelonae Mycobacterium fortuitum Mycobacterium kansasii Mycobacterium leprae Mycobacterium malmoense Mycobacterium marinum Mycobacterium microti Mycobacterium scrofulaceum Mycobacterium simiae Mycobacterium szulgai Mycobacterium tuberculosis Mycobacterium ulcerans Mycobacterium xenopl Mycoplasma pneumoniae Neisseria gonorrhoeae Neisseria meningitidis Nocardia asteroides Nocardia brasiliensis Nocardia farcinica Nocardia nova Nocardia otitidiscaviarum Pasteurella multocida Peptostreptococcus anaerobius Plesiomonas shigelloides Porphyromonas spp Proteus mirabilis Proteus penneri Proteus vulgaris Providencia alcalifaciens Providencia rettgeri Providencia spp Pseudomonas aeruginosa Rhodococcus egui Salmonella arizonae Salmonella enteritidis Salmonella typhimurium Salmonella paratyphi A,B,C Salmonella (other serovars) Serpulina spp Shigella boydii Shigella flexneri Shigella sonnel Staphylococcus aureus Streptobacillus moniliformis Streptococcus pneumoniae Streptococcus pyogenes Streptococcus spp Treponema carateum Treponema pallidum Treponema pertenue Treponema spp Vibrio parahaemolyticus Vibrio spp Yersinia pseudotuberculosis Yersinia spp Rickettsia Rickettsia akari Rickettsia canada Rickettsia conorii Rickettsia montana Rickettsia spp Rickettsia typhi (Rickettsia mooseri) Rickettsia tsutsugamushi Viruses Absettarov Acute haemorrhagic conjunctivitis virus Adenoviridae Astroviridae Australia encephalitis (Murray Valley encephalitis) BK and JC viruses Buffalo pox virus Bunyamwera virus California encephalitis virus Central European tick-borne encephalitis virus Coltiviruses Coronaviridae Cow pox virus Coxsackie viruses Cytomega lovirus Echo viruses Elephant pox virus Epstein-Barr virus Hantaviruses Hanzalova Hazara virus Hepatitis A virus (human enterovirus type 72) Hepatitis B virus Hepatitis C virus Hepatitis D virus (Delta) Herpes virus simiae (b virus) Herpes simplex viruses types l and 2 Herpesvirus varicella-zoster Human B-lymphotropic virus Human Papillomaviruses Human Parvovirus (B19) Human Rotaviruses Hypr Influenza viruses types A,B and C Kumlinge Kyasanur Forest Louping Ill Measles virus Milkers' node virus Mopeia virus and other Tacaribe viruses Mumps virus Norwalk virus Omsk Orbiviruses Orf virus Oropouche virus Other Bunvaviridae known to be pathogenic Other Caliciviridae Other Flaviviruses known to be pathogenic Other Hantaviruses Parainfluenza viruses types 1 to 4 Polioviruses Powassan Prospect Hill virus Puumala virus Rabbit pox virus Reoviruses Respiratory syncytial virus Rhinoviruses Rocio Sandfly fever Seoul virus St. Louis Encephalitis Tick-borneOrthomyxoviridae: Dhoriand Thogoto viruses Toscana virus Vaccinia virus Wesselsbron virus West Mile fever virus Yatapox virus (Tana & Yaba) (B) OTHER ANIMAL PATHOGENS Actinomyces spp African horse sickness virus Anaplasma marginale Avian encephalomyelitis virus Avian infectious bronchitis virus Avian infectious laryngotracheitis virus Avian leucosis virus Babesia spp Bacteroides nodosus Bordetella bronchiseptica Borrelia anserina Bovine malignant catarrhal fever virus Bovine virus diarrhoea virus Campylobacter fetus Canine distemper virus Caprine arthritis/encephalitis virus Clostridium chauvoei Clostridium spp Coccidia spp Cochliomyia hominivorax Corynebacterium pseudotuberculosis Cowdria ruminantum Cysticercus bovis Cysticercus cellulosae Dermatophilus congolensiae Duck hepatitis virus Duck virus enteritis virus Echinococcus spp Enzootic bovine leucosis virus Equine herpesvirus 3 Equine infectious anaemia virus Equine influenza virus type A Equine rhinopneumonitis virus Erynipelou rhosiopathiae Fowl pox virus Haemophilus equigenitaliom Haemophilus paragallinarum Histoplasma jaraiminosom Horse pox virus Hypoderma spp Infectious arteritis virus Infectious bovine rhinotracheitis virus Infectious bursal disease virus Leishmania spp Leptospira spp Listeria monocytogenes Lumpy skin disease virus Maedi-visna virus Mareks disease virus Mycobacterium avium Mycobacterium bovis Mycobacterium paratuberculosis Mycoplasma agalactiae Mycoplasma capricolum var capripneumoniae Mycoplasma gallisepticum Myxomatosis virus Nairobi sheep disease virus Pasteurella haemolytica Pasteurella multocida Pasteurella tularensis Porcine enteroviruses Psoroptes ovis Rabies and rabies related viruses Salmonella abortus equi Salmonella abortus ovis Salmonella gallinarum Salmonella pullorum Salmonella spp Sheep pulmonary adenomatosis virus Streptococcus equi The agent of Bovine Spongiforme encephalopathy The agent of porcine reproductive respiratory syndrome The agent of scrapie The agents of horse mange Theileria spp Toxoplasma gondii Transmissible gastroenteritis virus Trichinella spiralis Trichomonas fetus Trypanoroma evansi Trypanosoma spp Viral haemarrhagic disease of rabbits virus (C) PLANT PATHOGENS Citrus greening bacterium Citrus tristeza closterovirus Fusarium oxysporum f.sp. albedinis Glomerella gossypii Phymatotrichopsis omnivora Pseudomonas solanacearum Race 2 Thecaphora solani Tilletia indica Xanthomonas oryzae pvs oryzae & oryzicola Tricothecene-producing fungi including: Fusarium poae Fusarium sporotrichioides Fusarium tricinctum Micronectriella nivalis, anamorph Microdochium nivale (Syn. Fusarium nivale) (D) TOXINS Toxins other than specified on List 1 with a molecular weight of more than 250 daltons. (E) OTHER ORGANISMS Eukaryotic (non-microbial) organisms which produce any toxin. (F) GENETICALLY MODIFIED MICROORGANISMS, OTHER ORGANISMS AND GENETIC MATERIAL 1.The above listed microorganisms when they have been genetically modified. 2.Other genetically modified microorganisms or genetic material that contain nucleic acid sequences derived from any of the listed microorganisms, or that contain nucleic acid sequences associated with pathogenicity determinants of any listed microorganism; or that contain nucleic acid sequences associated with any listed toxin. 3.Genetically modified variants of eukaryotic (non-microbial) organisms which produce any toxin as above. Revised annex IV to the Special Commission's Plan Provisions related to missiles 1. The prohibitions under the Plan apply to any ballistic missiles or missile delivery systems (referred as "missile systems") capable of a range greater than 150 kilometres regardless of payload, and to any related major parts, including surface-to-surface missiles, space launch vehicles, sounding rockets, cruise missiles, target drones, reconnaissance drones, and other unmanned air vehicle systems and such other items as are identified below as being prohibited. 2. The following list contains equipment, other items and technologies capable of being used in the development, production, construction, modification or acquisition of missile systems capable of a range greater than 150 kilometres and shall therefore, in accordance with paragraph 40 of the Plan, be subject to ongoing monitoring and verification: 2.1Complete subsystems usable in missile systems, Re-entry vehicles and equipment designed or modified therefor, are prohibited. as follows, and technologies, production facilities, and production equipment therefor: 2.1.1 Individual rocket stages; 2.1.2 Solid- or liquid-fuel rocket engines; 2.1.3 Guidance sets; 2.1.4 Thrust vector controls, including, 2.1.4.1 Flexible nozzles; 2.1.4.2 Fluid or secondary gas injection systems; 2.1.4.3 Movable engines or nozzles; 2.1.4.4Deflection systems of the exhaust gas stream (e.g. jet vanes or probes); and 2.1.4.5 Thrust tabs. 2.1.5 Warhead or weapon safing, arming, fuzing and firing mechanisms. 2.2Propulsion components and equipment, including components, equipment, Such components and equipment cover the following, and production facilities and production equipment therefor: 1.Ramjet/scramjet/pulse jet/combined cycle engines, including devices to regulate combustion, and components therefor; 2.Hybrid rocket motors and components therefor. 3.Lightweight turbojet, turbofan and turbocompound engines that are small and fuel efficient, as follows: a.Engines with both of the following characteristics: i.Maximum thrust greater than 1000N (achieved un-installed) excluding civil certified engines with a maximum thrust greater than 8,890N (achieved un-installed), and ii.Specific fuel consumption of 0.13kg/N/hr or less (at sea level static and standard conditions); or b.Engines designed or modified for missile systems, regardless of thrust or specific fuel consumption. propellant and constituent chemicals for propellantsusable in missile systems, and technology, production facilities and production equipment, Production equipment also covers flow-forming machines, including machines combining the function of spin-forming and flow-forming, components and software therefor: 1.which, according to the manufacturer's technical specification, are capable of being equipped with numerical control units or a computer control, even when not equipped with such units at delivery, and 2.with more than two axes which are capable of being coordinated simultaneously for contouring control. as follows: 2.2.1Rocket-motor cases and production equipment therefor including interior lining, insulation and nozzles, and the technology, the production facilities and production equipment therefor; 2.2.2Staging mechanisms and production equipment therefor including separation mechanisms and interstages therefor, and clustering mechanisms, and the technology, production facilities and production equipment therefor; 2.2.3Liquid-fuel control systems and components therefor including liquid and slurry propellant (including oxidizers) control systems, and components therefor, designed or modified to operate in vibration environments of more than 5 g RMS between 20 Hz and 2,000 Hz, and the technology, the production facilities and production equipment therefor and also including: 2.2.3.1Servo valves designed for flow rates of 5 litres per minute or greater, at an absolute pressure of4,000 kPa (600 psi) or greater, with an actuator response time of less than 100 msec; Servo valves designed for flow rates of 24 litres per minute or greater, at an absolute pressure of 7,000 kPa (1,000 psi) or greater, with an actuator response time of less than 100 msec are prohibited. 2.2.3.2Pumps, for liquid propellants, with shaft speeds equal to or greater than 6,000 RPM or with discharge pressures equal to or greater than 4,000 kPa (600 psi) or with a flow rate of 200 litres per minute or greater at atmospheric pressure. Pumps, for liquid propellants, with shaft speeds equal to or greater than 8,000 RPM or with discharge pressures equal to or greater than 7,000 kPa (1,000 psi) or 450 litres per minute or greater at standard atmospheric pressure are prohibited. 2.2.4Propellants and constituent chemicals for propellants, including: 2.2.4.1 Propulsive substances: 2.2.4.1.1Hydrazine with a concentration of more than 70 per cent and its derivatives including monomethylhydrazine (MMH); 2.2.4.1.2 U n s y m m e t r i c dimethylhydrazine (UDMH); 2.2.4.1.3Ammonium perchlorate, and other solid oxidizers including salts of Nitroformic acid, Dinitroamines, Nitramines and Nitrocubanes; 2.2.4.1.4Spherical aluminium powder with particles of uniform diameter of less than 500 x 1O-6m (500 micrometer) and an aluminium content of 97 per cent by weight or greater; 2.2.4.1.5Metal fuels in particle sizes less than 500 x 10-6m (500 microns), whether spherical, atomized, spheroidal, flaked or ground, consisting of 97 per cent by weight or more of any of the following: zirconium, beryllium, boron, magnesium, zinc, and alloys of these; Misch metal; 2.2.4.1.6Nitro-amines cyclotetramethylenetetranitramine (HMX), cyclotrimethylenetrinitramine (RDX); 2.2.4.1.7Perchlorates, chlorates or chromates mixed with powdered metals or other high energy fuel components; 2.2.4.1.8Carboranes, decaboranes, pentaboranes and derivatives thereof; 2.2.4.1.9 Liquid oxidizers, as follows: 2.2.4.1.9.1 Dinitrogen trioxide; 2.2.4.1.9.2Nitrogen dioxide/dinitrogen tetroxide; 2.2.4.1.9.3 Dinitrogen pentoxide; 2.2.4.1.9.4Inhibited Red Fuming Nitric Acid (IRFNA); 2.2.4.1.9.5Compounds composed of fluorine and one or more of other halogens, oxygen or nitrogen; 2.2.4.1.9.6Hydrogen peroxide with a concentration greater than 70 per cent. 2.2.4.2 Polymeric substances: 2.2.4.2.1 Carboxyl-terminated polybutadiene (CTPB); 2.2.4.2.2 Hydroxyl-terminated polybutadiene (HTPB); 2.2.4.2.3 Glycidyl azide polymer (GAP); 2.2.4.2.4 Polybutadiene-acrylic acid (PBAA); 2.2.4.2.5Polybutadiene-acrylic acid-acrylonitrile (PBAN); 2.2.4.2.6Oxetanes including polymers of nitro methyl oxetane (NIMMO), and 3,3 Bis (azidomethyl oxetane)(BAMO). 2.2.4.3 Propellants: 2.2.4.3.1Composite propellants including case bonded propellants and propellants with nitrated binders; 2.2.4.3.2Noncomposite propellants including double base propellants. 2.2.4.4Other high energy density propellants, with an energy density of 40 x 106 joules/kg or greater, e.g. boron slurry. 2.2.4.5 Other propellant additives and agents: 2.2.4.5.1 Bonding agents as follows: 2.2.4.5.1.1Tris(1-(2-methyl)aziridinyl) phosphine oxide (MAPO); 2.2.4.5.1.2Trimesol-1(2-ethyl)aziridine (HX-868, BITA); 2.2.4.5.1.3 "Tepanol" (HX-878), reaction product of teraethylenepentamine, acrylonitrile and glycidol; 2.2.4.5.1.4 "Tepan" (HX-879), reaction production of tetlenepentamine and acrylonitrile; 2.2.4.5.1.5 Polyfunctional aziridene amides with isophthalic, trimesic, isocyanuric, or trimethyladipic backbone with a 2-methyl or 2-ethyl aziridine group (HX-752, H-874 and HX-877). 2.2.4.5.2 Curing agents and catalysts as follows: 2.2.4.5.2.1 Triphenyl bismuth (TPB); 2.2.4.5.3 Burning rate modifiers as follows: 2.2.4.5.3.1 Catocene; 2.2.4.5.3.2 N-butyl-ferrocene; 2.2.4.5.3.3 Butacene; 2.2.4.5.3.4 Other ferrocene derivatives. 2.2.4.5.4Nitrate esters and nitratoplasticizers as follows: 2.2.4.5.4.1Triethylene glycol dinitrate (TEGDN); 2.2.4.5.4.2Trimethylolethane trinitrate (TMETN); 2.2.4.5.4.31, 2, 4-butanetriol trinitrate(BTTN); 2.2.4.5.4.4Diethylene glycol dinitrate (DEGDN). 2.2.4.5.5 Stabilizers as follows: 2.2.4.5.5.1 2-nitrodiphenylamine; 2.2.4.5.5.2 N-methyl-p-nitroaniline. 2.2.5Production technology or production equipment for missile propellants and propellant constituents and specially designed components therefor, including: 2.2.5.1Production, handling or acceptance testing of liquid propellants or propellant constituents described in para. 2.2.4. 2.2.5.2Production, handling, mixing, curing, casting, pressing, machining, extruding or acceptance testing of solid propellants or propellant constituents described in para. 2.2.4, including: 2.2.5.2.1Batch mixers, capable of mixing under vacuum in the range of zero to 13.326 kPa and of controlling the temperature of the mixing chamber, and with a total volumetric capacity of 110 litre or more and at least one mixing/kneading shaft mounted off centre. Such batch mixers with a total volumetric capacity of more than 210 litres are prohibited. Continuous mixers with the same pressure and temperature characteristic and with two or more mixing/kneading shafts and capacity to open the mixing chamber are also prohibited. 2.2.5.2.2Equipment for the production of atomized or spherical metallic powder in a controlled environment; 2.2.5.2.3Fluid energy mills for grinding or milling ammonium perchlorate, RDX or HMX. 2.3Guidance and control equipment, flight control systems, and avionics equipment. 2.3.1Gyroscopes, accelerometers and inertial equipment, Continuous output accelerometers or gyros of any type, designed to function at acceleration levels greater than 100 g, are prohibited. including instrumentation, navigation and direction finding equipment and systems, and production and test equipment therefor, as follows, and components and software therefor: 2.3.1.1Integrated flight instrument systems, including gyrostabilizers or automatic pilots and integration software therefor, usable in missile systems; 2.3.1.2Gyro-astro compasses and other devices which derive position or orientation by means of automatically tracking celestial bodies or satellites; 2.3.1.3Accelerometers with a threshold of 0.5 g or less, or a linearity error of less than 0.25 per cent of full scale output, or both, designed for use in inertial navigation systems or in guidance systems of all types except those specially designed and developed as MWD (Measurement While Drilling) Sensors for use in downhole well service operations; 2.3.1.4All types of gyros usable in missile systems, with a rated drift rate stability of less than 5 degrees (1 sigma or rms) per hour in a 1 g environment; 2.3.1.5Inertial or other equipment using accelerometers described by para 2.3.1.3 or gyros described by para 2.3.1.4, and systems incorporating such equipment, and integration software therefor; 2.3.1.6Test, calibration, and alignment equipment, and production equipment for items specified in 2.3.1.1 to 2.3.1.5 above, including: 2.3.1.6.1For laser gyro equipment, the following equipment used to characterize mirrors, with the threshold accuracy shown or better: 2.3.1.6.1.1 Scatterometer (10 ppm); 2.3.1.6.1.2 Reflectometer (50 ppm); 2.3.1.6.1.3 Profilometer (5 Angstroms). 2.3.1.6.2 For other inertial equipment: 2.3.1.6.2.1Inertial Measurement Unit (IMU Module) Tester; 2.3.1.6.2.2 IMU Platform Tester; 2.3.1.6.2.3IMU Stable Element Handling Fixture; 2.3.1.6.2.4IMU Platform Balance fixture; 2.3.1.6.2.5 Gyro Tuning Test Station; 2.3.1.6.2.6 Gyro Dynamic Balance Station; 2.3.1.6.2.7Gyro Run-In/Motor Test Station; 2.3.1.6.2.8Gyro Evacuation and Filling Station; 2.3.1.6.2.9Centrifuge Fixture for Gyro Bearings; 2.3.1.6.2.10Accelerometer Axis Align Station; 2.3.1.6.2.11Accelerometer Test Station. 2.3.2Flight control systems and technology, as follows, designed or modified for use in missile systems and the test, calibration, and alignment equipment therefor: 2.3.2.1Hydraulic, mechanical, electro-optical, or electro-mechanical flight control systems (including fly-by-wire systems); 2.3.2.2 Attitude control equipment; 2.3.2.3Design technology for integration of air vehicle fuselage, propulsion system and lifting control surfaces to optimize aerodynamic performance throughout the flight regime of an unmanned air vehicle; 2.3.2.4Design technology for integration of the flight control, guidance, and propulsion data into a flight management system for optimization of rocket system trajectory. 2.3.3Avionics equipment, Including: 1. Terrain contour mapping equipment; 2.Scene mapping and correlation (both digital and analog) equipment; 3.Doppler navigation radar equipment; 4.Passive interferometer equipment; 5.Imaging sensor equipment (both active and passive). technology and components, as follows, designed or modified for use in missile systems, and software therefor: 2.3.3.1Radar and laser radar systems, including altimeters; 2.3.3.2Passive sensors for determining bearings to specific electromagnetic sources (direction finding equipment) or terrain characteristics; 2.3.3.3Global Positioning System (GPS) or similar satellite receivers; 2.3.3.3.1Capable of providing navigation information at speeds in excess of 515 m/sec (1,000 nautical miles/hour) and at altitudes in excess of 18 km (60,000 feet); or 2.3.3.3.2Designed or modified for use with missile systems. 2.3.3.4Electronic assemblies and components designed, modified, tested, certified, or screened for military use and operation at temperatures in excess of 125f C. 2.3.3.5Design technology for protection of avionics and electrical subsystems against electromagnetic pulse (EMP) and electromagnetic interference (EMI) hazards from external sources, as follows: 2.3.3.5.1 Design technology for shielding systems; 2.3.3.5.2Design technology for the configuration of hardened electrical circuits and subsystems; 2.3.3.5.3Determination of hardening criteria for the above. 2.4Equipment and technology for the production of structural composites usable in missile systems, as follows, and components, accessories andsoftware therefor, and structural materials usable in missile systems as follows: 2.4.1Filament winding machines for which the motions for positioning, wrapping and winding fibres are capable of being coordinated and programmed in three or more axes, designed to fabricate composite structures or laminates from fibrous or filamentary materials, and coordinating and programming controls; 2.4.2Tape-laying machines for which the motions for positioning and laying tape and sheets are capable of being coordinated and programmed in two or more axes, designed for the manufacture of composite airframes and missile structures; 2.4.3Multi-directional, multi-dimensional weaving machines or interlacing machines, including adapters and modification kits for weaving, interlacing or braiding fibres to manufacture composite structures, except textile machinery not modified for the above end uses; 2.4.4Equipment designed or modified for the production of fibrous or filamentary materials as follows: 2.4.4.1Equipment for converting polymeric fibres (e.g. polyacrylonitrile, rayon or polycarbosilane) including special provision to strain the fibre during heating; 2.4.4.2Equipment for the vapour deposition of elements or compounds on heated filament substrates; and 2.4.4.3Equipment for the wet-spinning of refractory ceramics (such as aluminium oxide); 2.4.5Equipment designed or modified for special fibre surface treatment and equipment designed or modified for producing prepregs and preforms, including: 2.4.5.1 Rollers; 2.4.5.2 Tension stretchers; 2.4.5.3 Coating equipment; 2.4.5.4 Cutting equipment; and 2.4.5.5 Clicker dies. 2.4.6Technical data (including processing conditions) and procedures for the regulation of temperature, pressures or atmosphere in autoclaves or hydroclaves in the production of composites or partially processed composites. 2.4.7Components and accessories for the machines, including moulds, mandrels, dies, fixtures and tooling for the preform pressing, curing, casting, sintering or bonding of composite structures, laminates and manufactures thereof. 2.4.8 Structural materials usable in missile systems, as follows: 2.4.8.1Composite structures, laminates, and manufactures thereof, designed or modified for missile systems or the subsystems in para 2.1, and resin impregnated fibre prepregs using resins with a glass transition temperature (Tg), after cure, exceeding 145f C as determined by ASTM D4065 or national equivalents, and metal-coated fibre preforms therefor, made either with organic matrix or metal matrix utilizing fibrous or filamentary reinforcements with a specific tensile strength greater than 7.62 x 104 m (3 x 106 inches) and a specific modulus greater than 3.18 x 106 m (1.25 x 108 inches); 2.4.8.2Resaturated pyrolized (i.e., carbon-carbon) materials designed for missile systems; 2.4.8.3Fine grain recrystallized bulk graphites (with a bulk density of at least 1.72 g/cc measured at 15f C and having a particle size of 100 x 10-6m (100 microns) or less), pyrolytic, or fibrous reinforced graphites usable for rocket nozzles and reentry vehicle nose tips; 2.4.8.4Ceramic composite materials (dielectric constant less than 6 at frequencies from 100 Hz to 10,000 MHz) for use in missile radomes, and bulk machinable silicon carbide reinforced unfired ceramic usable for nose tips; 2.4.8.5Tungsten, molybdenum and alloys of these metals in the form of uniform spherical or atomized particles of 500 micrometer diameter or less with a purity of 97 per cent or higher for fabrication of rocket motor components, including heat shields, nozzle substrates, nozzle throats and thrust vector control surfaces; 2.4.8.6Maraging steels (steels generally with high nickel, very low carbon content and using substitutional elements or precipitates to produce age-hardening) with an ultimate tensile strength of 1.5 x 109 Pa or greater, measured at 20f C in the form of sheet, plate or tubing with a wall or plate thickness equal to or less than 5.0 mm (0.2 inch). 2.5Pyrolytic deposition and densification equipment and technology as follows: 2.5.1Technology for producing pyrolytically derived materials formed on a mould, mandrel or other substrate from precursor gases which decompose in the 1,300f C to 2,900f C temperature range at pressures of 130 Pa (1 mm Hg) to 20 kPa (150 mm Hg) including technology for the composition of precursor gases, flow-rates and process control schedules and parameters; 2.5.2 Nozzles for the above processes; 2.5.3Equipment and process controls, and software therefor, designed or modified for densification and pyrolysis of structural composites, including: 2.5.3.1Isostatic presses with a maximum working pressure of 69 MPa (10,000 psi) or greater and designed to achieve and maintain a controlled thermal environment of 600f C or greater, and possessing a chamber cavity with an inside diameter of 254 mm (10 inches) or greater; 2.5.3.2Chemical vapour deposition furnaces designed or modified for the densification of carbon-carbon composites. 2.6Launch and ground support equipment, facilities and software usable for missile systems, as follows: 2.6.1Apparatus and devices designed or modified for the handling, control, activation and launching of missile systems; 2.6.2Vehicles designed or modified for the transport, handling, control, activation and launching of missile systems; 2.6.3Gravity meters (gravimeters), gravity gradiometers, and specially designed components therefor, designed or modified for airborne or marine use, and with a static or operational accuracy of 7 x 10-6 m/sec2 (0.7 milligal) or better, and a time to steady-state registration of two minutes or less; 2.6.4Telemetering and telecontrol equipment usable for missile systems; 2.6.5 Precision tracking systems, including: 2.6.5.1Tracking systems Tracking systems specified in para. 2.6.5.1 with a range greater than 150km are prohibited. using a code translator or transponder installed on the missile systems and either surface or airborne references or navigation satellite systems to provide real time measurements of in-flight position and velocity; 2.6.5.2Range instrumentation radars Range instrumentation radars specified in para. 2.6.5.2 with a range greater than 150km are prohibited. including associated optical/infrared trackers and the software therefor with an angular resolution better than 3 milli-radians (0.5 mils), and a range of 30 km or greater with a range resolution better than 10 metres RMS, and a velocity resolution better than 3 metres per second; and 2.6.5.3Software with post-flight, recorded data, for the determination of vehicle position throughout its flight path. 2.7Analog computers, digital computers or digital differential analyzers and analog-to-digital converters, including: 2.7.1Analog computers, digital computers, or digital differential analyzers usable in missile systems, having either of the following characteristics: 2.7.1.1Rated for continuous operation at temperatures from below minus 45f C to above plus 55f C; or 2.7.1.2Designed as ruggedized or radiation hardened; and 2.7.2Analog-to-digital converters, usable in missile systems, with either of the following characteristics: 2.7.2.1Designed to meet military specifications for ruggedized equipment; or, 2.7.2.2Designed, modified, tested, certified or screened for military use, and being one of the following types: 2.7.2.2.1Analog-to-digital converter microcircuits, with a resolution of 8 bits or more or which are radiation-hardened; and are rated for operation in the temperature range from below minus 45f C to above plus 125f C; and are hermetically sealed; and 2.7.2.2.2Electrical input type analog-to-digital converter printed circuit boards or modules, with having a resolution of 8 bits or more, which are rated for operation in the temperature range from below minus 45f C to above plus 55f C, and which incorporate microcircuits listed in paragraph 2.7.2.2.1. 2.8Test facilities and equipment usable for missile systems or sub-systems, as follows, and software therefor: 2.8.1Vibration test systems and components therefor, as follows: 2.8.1.1Vibration test systems using feedback or closed loop techniques and a digital controller, capable of vibrating a system at 10g RMS or more over the entire range 20 Hz to 2000 Hz and imparting forces of 25 kN (5,625 lbs), measured "bare table", or greater; 2.8.1.2Digital controllers, which use specially designed vibration test software, with a real-time bandwidth greater than 5 kHz and designed for use with vibration test systems in paragraph 2.8.1.1; 2.8.1.3Vibration thrusters (shaker units), with or without associated amplifiers, capable of imparting a force of 25 kN (5,625 lbs), measured "bare table", or greater, and usable in vibration test systems in paragraph 2.8.1.1; 2.8.1.4Test piece support structures and electronic units designed to combine multiple shaker units into a complete shaker system capable of providing an effective total force of 25kN, measured "bare table", or greater, and usable in vibration test systems in paragraph 2.8.1.1. 2.8.2 Wind-tunnels; 2.8.3Test benches/stands capable of handling solid or liquid propellant rockets or rocket motors of more than 10 kN of thrust, or capable of simultaneously measuring the three axial thrust components; 2.8.4Environmental chambers and anechoic chambers capable of simulating the following flight conditions at altitudes of 15,000 meters or greater, or at temperatures of at least minus 50f C to plus 125f C, and either vibration environments of 10 g RMS or greater between 20 Hz and 2,000 Hz imparting forces of 5 kN or greater, for environmental chambers, or acoustic environments at an overall sound pressure level of 140 dB orgreater (referenced to 2 x 10-5 N per square metre) or with a rated power output of 4 kiloWatts or greater, for anechoic chambers. 2.8.5Accelerators except those specially designed for medical purposes, capable of delivering electromagnetic radiation produced by "Bremsstrahlung" from accelerated electrons of 2 MeV or greater, and systems containing those accelerators. 2.9Software, or software with related specially designed hybrid (combined analogue/digital) computers, for modelling (including in particular the aerodynamic and thermodynamic analysis of the systems), simulation, or design integration of missile systems or subsystems. 2.10Materials, devices, and software for reduced observables (e.g. radar reflectivity, ultraviolet/infrared signatures and acoustic signatures, i.e. stealth technology), for applications usable for missile systems or subsystems including: 2.10.1Structural materials and coatings specially designed for reduced radar reflectivity; 2.10.2Coatings, including paints, specially designed for reduced or tailored reflectivity or emissivity in the microwave, infrared or ultraviolet spectra; 2.10.3Software or databases for analysis of signature reduction; 2.10.4 Radar cross section measurement systems. 2.11Material and devices for protecting missile systems against nuclear effects (e.g. Electromagnetic Pulse (EMP), X-rays, combined blast and thermal effects), as follows: 2.11.1 Radiation Hardened microcircuits and detectors; 2.11.2Radomes designed to withstand a combined thermal shock greater than 100 cal/sq cm accompanied by a peak over pressure of greater than 50 kPa. 3. The initial information under paragraph 43 of the Plan to be provided not later than 30 days after the adoption of the Plan by the Security Council shall cover the period from 1 January 1988. Subsequent information shall be provided each 15 January and 15 July and shall cover the six-month period prior to the provision of the information. Notifications under paragraph 44 of the Plan shall be provided not later than 14 days prior to the date of launch. 4. Whenever the information which Iraq is required to provide under section E of the Plan and this annex is equal to nil, Iraq shall provide nil returns. 5. The information on sites or facilities to be provided under section E of the Plan shall for each site or facility include: 5.1 The name of the site or facility and of the owner, company or enterprise operating the site or facility; 5.2 The location of the site or facility; 5.3The sources and amounts of the financing of the site or facility, and of its activities; 5.4A general description of all types of activities at the site or facility; 5.5List of equipment, other items and technologies specified in paragraph 1 of this annex used or present at the site or facility and their quantities; 5.6A detailed description of activities related to the equipment, other items and technologies specified in paragraph 1 of this annex. 6. The location of a site or facility shall be specified by means of the address and site diagram. Each diagram shall be drawn to scale and shall indicate the boundaries of the site or facility, all road and rail entrances and exits and all structures on the site or facility, indicating their purpose. If the site or facility is located within a larger complex, the diagram shall specify the exact location of the site or facility within the complex. On each diagram, the geographic coordinates of a point within the site or facility shall be specified to the nearest second. 7. The information on each import to be provided under section E of the Plan shall include: 7.1Specification of each item and the quantity imported and the purpose of its use in Iraq; 7.2Country of origin of each item and the quantity imported and the purpose of its use in Iraq; 7.3 Point or port and time of entry of the item in Iraq; 7.4 Project and site or facility where it is to be used; 7.5 Name of the specific importing organization in Iraq. ----- n .