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Ethalfluralin
CAS No. 55283-68-6
 
 

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Adverse Effects

ACTIVITY: Herbicide (2,6-Dinitroaniline)

CAS NAME: N-ethyl-N-(2-methyl-2-propenyl)-2,6-dinitro-4-(trifluoromethyl)benzenamine

Structure:

Reports available from
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Order No. Date/Title Keywords/Abstract

NTIS/OTS0545185

EPA/OTS; Doc #88-920006586

1992. INITIAL SUBMISSION: A TERATOLOGY STUDY WITH ETHALFLURALIN IN DUTCH-BELTED RABBITS WITH COVER LETTER DATED 08-21-92

ELI LILLY & CO

Ethalfluralin (CAS# 55283-68-6) was evaluated for developmental toxicity. The test material was administered orally to 14, 13, 15, and 13 inseminated Dutch-Belted rabbits in doses of 0, 250, 500, and 750 mg/kg/day, respectively, on days 6-18 of gestation. Four, 9, and 7 rabbits of the 250, 500, and 750 mg/kg/day groups, respectively, aborted and were killed. Abortions were preceded by extended periods of anorexia and weight loss. Anorexia and substantial weight loss were observed during dosing at 250 mg/kg/day and above. Decreased live litter size and an increase in resorption incidence occurred at 500 and 750 mg/kg/day. No live fetuses were recovered at 750 mg/kg/day. No effects on sex distribution or weight were observed. No treatment related skeletal or visceral defects were observed. The authors concluded that maternal toxicity was observed at all dose levels. No teratogenicity was observed at any dose level.

NTIS/OTS0545147

EPA/OTS; Doc #88-920006548

1992. INITIAL SUBMISSION: A TERATOLOGY STUDY WITH ETHALFLURALIN ADMINISTERED ORALLY TO DUTCH-BELTED RABBITS WITH COVER LETTER DATED 08-21-92

ELI LILLY & CO

Ethalfluralin (CAS# 55283-68-6) was evaluated for developmental toxicity. The test material was administered orally to 20 inseminated Dutch-Belted rabbits in doses of 0, 25, 75, 150, or 300 mg/kg/day on days 6-18 of gestation. At 150 and 300 mg/kg/day, maternal toxicity was indicated by abortions which followed anorexia and marked body weight loss. Absolute and relative liver weight were elevated at 300 mg/kg/day. Prenatal reproduction parameters, fetal body weights, and developmental variations or abnormalities were not treatment-related. The no-effect level for maternal toxicity was 75 mg/kg/day.

NTIS/OTS0545074

EPA/OTS; Doc #88-920006475

1992. INITIAL SUBMISSION: A PILOT TERATOLOGY STUDY WITH ETHALFLURALIN IN DUTCH-BELTED RABBITS WITH COVER LETTER DATED 08-21-92

ELI LILLY & CO

Ethalfluralin (CAS# 55283-68-6) was evaluated for developmental toxicity. Two, 4, 3, and 3 Dutch-Belted rabbits were dosed with 0, 250, 500, and 1000mg/kg/day, respectively, on days 6-18 of gestation. At 1000 mg/kg/day, all rabbits aborted and were killed. At 500 mg/kg/day, one rabbit aborted and was also killed. Markedly reduced food consumption was observed in all rabbits at 1000 mg/kg/day and in 1/3 at 500 mg/kg/day. Body weight was also reduced in these rabbits. Reproduction data (implantations, corpora lutea) in all groups were similar to controls. No resorptions were observed at any dose level. All fetuses were normal grossly. This study was briefly summarized.

NTIS/OTS0545085

EPA/OTS; Doc #88-920006486

1992. INITIAL SUBMISSION: A TERATOLOGY STUDY WITH ETHALFLURALIN IN DUTCH-BELTED RABBITS WITH COVER LETTER DATED 08-21-92

ELI LILLY & CO

Ethalfluralin (CAS# 55283-68-6) was evaluated for developmental toxicity. Fourteen, 11, and 14 pregnant Dutch-Belted rabbits were administered 0, 75, and 250 mg/kg/day of the test substance respectively, on days 6-18 of gestation. An increase in the number of anorectic rabbits occurred at 250 mg/kg/day. Four and 3 rabbits of the 75 and 250 mg/kg/day dose group, respectively, died or aborted. The abortions were preceded by anorexia and weight loss. Nine, 9, and 12 rabbits of the 0, 75, and 250 mg/kg/day dose groups were available for evaluation. Live litter size, resorption occurrence, fetal viability, and sex distribution were unaffected by treatment. Mean fetal weights of the treatment groups were lower than controls but the differences were not statistically significant. An increase in the incidence of skeletal abnormalities, including cleft palate and crooked ribs, was observed at 250 mg/kg/day. No treatment related visceral abnormalities were observed. The 250 mg/kg/day dose was maternally toxic but not teratogenic since the increased incidence of fetal defects was associated with anorexic dams. The 75 mg/kg/day dose was a no-effect level.

NTIS/OTS0545118

EPA/OTS; Doc #88-920006519

1992. INITIAL SUBMISSION: A TWO-YEAR DIETARY EVALUATION WITH ETHALFLURALIN IN FISCHER 344 RATS WITH COVER LETTER DATED 08-21-92

ELI LILLY & CO

ETHALFLURALIN
HEALTH EFFECTS
CHRONIC TOXICITY
COMBINED CHRONIC TOXICITY/CARCINOGENICITY
MAMMALS
RATS
ORAL
DIET
CAS No. 55283-68-6

NTIS/OTS0545090

EPA/OTS; Doc #88-920006491

1992. INITIAL SUBMISSION: A ONE-YEAR DIETARY TOXICITY STUDY WITH ETHALFLURALIN IN RATS WITH COVER LETTER DATED 08-21-92

ELI LILLY & CO

ETHALFLURALIN
HEALTH EFFECTS
CHRONIC TOXICITY
COMBINED CHRONIC TOXICITY/CARCINOGENICITY
MAMMALS
RATS
ORAL
DIET
CAS No. 55283-68-6

NTIS/OTS0555145

EPA/OTS; Doc #88-920008647

1992.
INITIAL SUBMISSION: DERMAL SENSITIZATION OF ETHALFLURALIN IN THE GUINEA PIG WITH COVER LETTER DATED 08/18/92

ELI LILLY & CO

ETHALFLURALIN
HEALTH EFFECTS
PRIMARY DERMAL SENSITIZATION
MAMMALS
GUINEA PIGS
DERMAL
CAS No. 55283-68-6

NTIS/OTS0544604

EPA/OTS; Doc #88-920005947

1992. INITIAL SUBMISSION: ACUTE RAT ORAL STUDY WITH ETHALFLURALIN AND LINURON WITH COVER LETTER DATED 08-03-92

ELI LILLY & CO

ETHALFLURALIN AND LINURON
HEALTH EFFECTS
ACUTE TOXICITY
MAMMALS
RATS
ORAL
GAVAGE
CAS No. 55283-68-6

NTIS/OTS0543399

EPA/OTS; Doc #88-920005936

1992. INITIAL SUBMISSION: LETTER FROM ELI LILLY & CO TO USEPA SUBMITTING RESULTS ON AN ACUTE INHALATION STUDY WITH ETHALFLURALIN AND FLURIDONE IN RATS WITH ATTACHMENTS

ELI LILLY & CO

ETHALFLURALIN
HEALTH EFFECTS
ACUTE TOXICITY
MAMMALS
RATS
INHALATION
CAS Nos.
55283-68-6
59756-60-4

NTIS/OTS0544603

EPA/OTS; Doc #88-920005946

1992. INITIAL SUBMISSION: ACUTE RAT ORAL STUDY WITH ETHALFLURALIN WITH COVER LETTER DATED 08-03-92

ELI LILLY & CO

ETHALFLURALIN
HEALTH EFFECTS
ACUTE TOXICITY
MAMMALS
RATS
ORAL
GAVAGE
CAS Registry Numbers:
330-55-2
55283-68-6

NTIS/OTS0544933

EPA/OTS; Doc #88-920006096


1992. INITIAL SUBMISSION: ACUTE RAT INHALATION STUDY WITH FLURIDONE & ETHALFLURALIN WITH COVER LETTER DATED 08-03-92

ELI LILLY & CO

FLURIDONE & ETHALFLURALIN
HEALTH EFFECTS
ACUTE TOXICITY
MAMMALS
RATS
INHALATION
CAS Registry Numbers:
55283-68-6
59756-60-4

NTIS/OTS0543304

EPA/OTS; Doc #88-920005843

1992. INITIAL SUBMISSION: LETTER FROM ELI LILLY & CO TO USEPA SUBMITTING RESULTS ON AN ACUTE INHALATION STUDY WITH ETHALFLURALIN IN RATS WITH ATTACHMENTS

ELI LILLY & CO

ETHALFLURALIN
HEALTH EFFECTS
ACUTE TOXICITY
MAMMALS
RATS
INHALATION
CAS Registry Numbers:
55283-68-6

NTIS/OTS0545116

EPA/OTS; Doc #88-920006517

1992. INITIAL SUBMISSION: A TWO-YEAR DIETARY EVALUATION WITH ETHALFLURALIN IN B6C3F1 MICE WITH COVER LETTER DATED 08-21-92

ELI LILLY & CO

ETHALFLURALIN
HEALTH EFFECTS
CHRONIC TOXICITY
COMBINED CHRONIC TOXICITY/CARCINOGENICITY
MAMMALS
MICE
ORAL
DIET
CAS Registry Numbers:
55283-68-6

NTIS/OTS0545236

EPA/OTS; Doc #88-920006698

1992. INITIAL SUBMISSION: A ONE-YEAR DIETARY TOXICITY STUDY WITH ETHALFLURALIN IN B6C3F1 MICE WITH COVER LETTER DATED 08-21-92

ELI LILLY & CO

ETHALFLURALIN
HEALTH EFFECTS
CHRONIC TOXICITY
MAMMALS
MICE
ORAL
DIET
CAS Registry Numbers:
55283-68-6

NTIS/OTS0543330

EPA/OTS; Doc #88-920005868

1992. INITIAL SUBMISSION: LETTER FROM ELI LILLY & CO TO USEPA SUBMITTING RESULTS ON AN ACUTE ORAL STUDY WITH R-O-66-83 IN RATS WITH ATTACHMENTS

ELI LILLY & CO

R-O-66-83
HEALTH EFFECTS
ACUTE TOXICITY
MAMMALS
RATS
ORAL
GAVAGE
CAS Registry Numbers:
55283-68-6

NTIS/OTS0570719

EPA/OTS; Doc #88-920008437

1992. INITIAL SUBMISSION: DERMAL SENSITIZATION OF BENZENAMINE, N-ETHYL-N-(2-METHYL-2-PROPENYL)-2,6-DINITRO-4-(TRIFLUOROMETHYL)- IN GUINEA PIGS WITH COVER LETTER DATED 08-18-92

ELI LILLY & CO

BENZENEAMINE, N-ETHYL-N-(2-METHYL-2-PROPENYL)-2,6-DINITRO-4-
HEALTH EFFECTS
PRIMARY DERMAL SENSITIZATION
MAMMALS
GUINEA PIGS
DERMAL
CAS Registry Numbers:
55283-68-6

NTIS/OTS0570822

EPA/OTS; Doc #88-920008537

1992. INITIAL SUBMISSION: ORAL PILOT TERATOLOGY STUDY OF BENZENAMINE, N-ETHYL-N-(2-METHYL-2-PROPENYL)-2,6-DINITRO-4-(TRIFLUOROMETHYL)- IN RABBITS WITH COVER LETTER DATED 08-18-92

ELI LILLY & CO

BENZENAMINE, N-ETHYL-N-(2-METHYL-2-PROPENYL)-2,6-DINITRO-4-*
HEALTH EFFECTS
REPRODUCTION/FERTILITY EFFECTS
TERATOGENICITY
MAMMALS
RABBITS
ORAL
GAVAGE
CAS Registry Numbers:
55283-68-6

NTIS/OTS0516618

EPA/OTS; Doc #88-890000001

1988. LETTER FROM ELI LILLY AND COMPANY TO USEPA REGARDING CASE STUDIES OF MONOLINURON EXPOSURE WITH ATTACHMENTS.

ELI LILLY & CO

MONOLINURON & ETHAFLURALIN
HEALTH EFFECTS
CASE REPORT
MAMMALS
HUMANS
CAS Registry Numbers:
1746-81-2
55283-68-6

NTIS/PB82-156035

21p

1982. The Determination of Dinitroaniline Pesticides in Industrial and Municipal Wastewater: Method 627

Pressley T, Longbottom JE

Environmental Monitoring and Support Lab.-Cincinnati, OH.

This is a gas chromatographic (GC) method applicable to the determination of selected pesticides in municipal and industrial discharges as provided under 40CFR 136.1. A sample is solvent extracted with methylene chloride using a separatory funnel. The extract is exchanged to hexane during concentration. GC conditions are described which permit measurement with an electron capture detector. The compounds included in the method scope are: benfluralin; ethalfluralin; isopropalin; profluralin; and trifluralin. Final rept.

 

http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15621183&query_hl=2

Chemosphere. 2005 Feb;58(6):693-703.
 
Atmospheric concentrations and dry and wet deposits of some herbicides currently used on the Canadian Prairies.

Waite DT, Bailey P, Sproull JF, Quiring DV, Chau DF, Bailey J, Cessna AJ.

Environment Canada, 300-2365 Albert Street, Regina, Sask., Canada S4P 4K1. don.waite@ec.gc.ca

High volume air sampling in the Canadian Prairies was used to characterize atmospheric concentrations for 10 herbicides (alachlor, atrazine, ethalfluralin, metolachlor, 2,4-D, dicamba, bromoxynil, MCPA, trifluralin, and triallate) along a 500-km north-south transect. Atmospheric concentration measurements at various altitudes identified that of the six herbicides present in the highest concentrations, triallate was strongly influenced by local sources, while 2,4-D, dicamba, bromoxynil, MCPA and trifluralin were dominated by regional atmospheric transport. Concentrations of the herbicides measured at various altitudes were compared with dry deposition rates measured using a dry/wet deposition sampler and used to calculate deposition velocities V(d). The primary atmospheric transport mechanism for MCPA and bromoxynil was shown to be adsorption to particles dispersed in the atmosphere, with the same mechanism also confirmed for 2,4-D and dicamba, while trifluralin was shown to be transported mainly in the gas phase. This method of calculation indicated that transportation of triallate was influenced by particle adsorption. Weekly maximum atmospheric loadings of the major herbicides present in the Prairies were estimated to range from 73 kg for trifluralin to 541 kg for 2,4-D.

PMID: 15621183 [PubMed - indexed for MEDLINE]


http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15366828&query_hl=2

J Agric Food Chem. 2004 Sep 22;52(19):5828-35.
 
Analysis of pesticides in honey by solid-phase extraction and gas chromatography-mass spectrometry.

Albero B, Sanchez-Brunete C, Tadeo JL.

Departamento de Medio Ambiente, INIA, Ctra de la Coruna Km 7, 28040 Madrid, Spain.

An analytical method for the simultaneous determination of 51 pesticides in commercial honeys was developed. Honey (10 g) was dissolved in water/methanol (70:30; 10 mL) and transferred to a C(18) column (1 g) preconditioned with acetonitrile and water. Pesticides were subsequently eluted with a hexane/ethyl acetate mixture (50:50) and determined by gas chromatography with electron impact mass spectrometric detection in the selected ion monitoring mode (GC-MS-SIM). Spiked blank samples were used as standards to counteract the matrix effect observed in the chromatographic determination. Pesticides were confirmed by their retention times, their qualifier and target ions, and their qualifier/target abundance ratios. Recovery studies were performed at 0.1, 0.05, and 0.025 microg/g fortification levels for each pesticide, and the recoveries obtained were >86% with relative standard deviations of <10%. Good resolution of the pesticide mixture was achieved in approximately 41 min. The detection limits of the method ranged from 0.1 to 6.1 microg/kg for the different pesticides studied. The developed method is linear over the range assayed, 25-200 microg/L, with determination coefficients of >0.996. The proposed method was applied to the analysis of pesticides in honey samples, and low levels of a few pesticides (dichlofluanid, ethalfluralin, and triallate) were detected in some samples.

PMID: 15366828 [PubMed - indexed for MEDLINE]


JOURNAL OF CHROMATOGRAPHY B; 714 (2). 1998. 205-213.

Headspace solid-phase microextraction and gas chromatographic determination of dinitroaniline herbicides in human blood, urine and environmental water.

GUAN F, WATANABE K, ISHII A, SENO H. KUMAZAWA T, HATTORI H, SUZUKI O

Dep. Legal Med., Hamamatsu Univ. Sch. Med., 3600 Handa-cho, Hamamatsu 431-3192, Japan.

BIOSIS COPYRIGHT: BIOL ABS. Solid-phase microextraction (SPME) is a unique extraction and sampling technique, and it has been used for separation of volatile organics from water or other simple matrices. In this study, we have used SPME to separate dinitroaniline herbicides from complicated matrices of human urine and blood in order to broaden its application to biomedical analysis. The SPME conditions were optimized for water, urine and blood samples, in terms of pH, salt additives, extraction temperature, and fiber exposure time. Urine or water (1.0 ml) spiked with herbicides and 0.28 g of anhydrous sodium sulfate was preheated at 70C for 10 min, and a polydimethylsiloxane-coated fiber for SPME was exposed to the headspace at 70C for another 30 min; while spiked blood (0.5 ml) diluted with water (0.5 ml) was treated at 90C in the same way. The herbicides were extractable under these conditions, and could be determined by gas chromatography-electron capture detector (GC-ECD). The recoveries of [abstract truncated]

CAS Registry Numbers: (fluorinated pesticides in red)
55283-68-6 - Ethalfluralin
40487-42-1 - Pendimethalin
33820-53-0 - Isopropalin
33245-39-5 - Fluchloralin
29091-21-2 - Prodiamine
26399-36-0 - Profluralin
1861-40-1 - Benefin (Benfluralin)


J ENVIRON SCI HEALTH PART B PESTIC FOOD CONTAM AGRIC WASTES; 27 (6). 1992. 695-709.

Effect of some herbicides on activities of microorganisms and enzymes in soil.

TU CM

London Res. Centre, Agric. Canada, 1400 Western Rd., London, Ontario, Canada N6G 2V4.

BIOSIS COPYRIGHT: BIOL ABS. Laboratory tests were conducted with eight herbicides, atrazine, butylate, ethalfluralin, imazethapyr, linuron, metolachlor, metribuzin and trifluralin, applied to a loamy sand at rate of 10 mug/g to determine if these materials caused any serious effects on microbial and enzymatic activities related to soil fertility. Some herbicides showed an effect on bacteria and fungi for the first week of incubation, but, subsequently, the populations returned to levels similar to those obtained in the controls. After several herbicide treatments there appeared to cause a slight depression of nitrification. Sulfur oxidation was better than that obtained with untreated soil in all treatments. Oxygen consumption was increased significantly after 96 hr incubation with atrazine. The soil dehydrogenase and amylase activities were inhibited by ethalfluralin treatment respectively for 1 wk and 1 day, and p-nitrophenol liberation was inhibited for 2 hrs by all herbicide treatments. Result


CAN J SOIL SCI; 72 (3). 1992. 255-262.

The relative persistence of trifluralin (545 EC and 5 G) and ethalfluralin in prairie soils.

GERWING PD , MCKERCHER RB

Gulf Canada Resources Ltd., Calgary, Alberta T2P 2H7, Can.

BIOSIS COPYRIGHT: BIOL ABS. The persistence in soil of trifluralin 545 EC, trifluralin 5 G, and ethalfluralin 360 EC was studied over a 2-yr period at three different sites in Saskatchewan (Canada). At two of the three sites both formulations of trifluralin were more persistent than ethalfluralin when a canola crop was grown in the treated soil. In the high organic matter soil at the third site the persistance of trifluralin and ethalfluralin was similar under both fallow and cropped conditions. Crop response data gathered from wheat, oat and millet stands plus gas chromatographic analysis of soil extracts indicated that trifluralin 545 EC and trifluralin 5 G persisted in soil for comparable lengths of time when applied at rates between 0.85 and 1.40 kg a.i. ha-1. At recommended application rates to summerfallowed fields, the amount of herbicide remaining in the different soils at seeding time the following season was least for ethalfluralin 360 EC. The average amount of trifluralin 545 EC, triflur [abstract truncated]


J AGRIC FOOD CHEM; 39 (4). 1991. 700-704.

GC and LC/MS determination of 20 pesticides for which dietary oncogenic risk has been estimated./DIAGNOSIS

MATTERN GC, LIU C-H, LOUIS JB, ROSEN JD

Dep. Food Sci., Cook College, Rutgers Univ., New Brunswick, N.J. 08903.

BIOSIS COPYRIGHT: BIOL ABS. The National Research Council has estimated dietary oncogenic risk for 28 pesticides registered for use in the United States. We report a rapid analytical procedure for 20 of these pesticides in a variety of crops based on a single extraction step and the use of mass spectrometry for detection and quantification. Recovery and sensitivity studies were performed in various commodities (apples, peaches, potatoes, tomatoes, peppers, spinach, lettuce, snap beans, and sweet corn) for the suspected oncogenes acephate, alachlor, azinphos-methyl, captafol, captan, chlordimeform, chlorothalonil, cypermethrin, diclofopmethyl, ethanfluralin, metolachlor, oxadiazon, parathion, permethrin, pronamide, o-phenylphenol terbutryne, folpet, linuron, and oryzalin. All pesticides were determined by gas chromatography/chemical ionization mass spectrometry (GC) except the last three, for which high-performance liquid chromatography/mass spectrometry (HPLC/MS) was used. Average recoveries at th [abstract truncated]

CAS Registry Numbers:
55283-68-6
55283-68-6

52645-53-1
52315-07-8
51338-27-3
51218-45-2
30560-19-1
23950-58-5
19666-30-9
19044-88-3
15972-60-8
6164-98-3
2425-06-1
1897-45-6
886-50-0
330-55-2
133-07-3
133-06-2
90-43-7
86-50-0
56-38-2


J AGRIC FOOD CHEM; 39 (10). 1991. 1781-1785.

Using fluorine-19 NMR for trace analysis of fluorinated pesticides in food products.

MORTIMER RD, DAWSON BA

Food Res. Div., Bureau Chemical Safety, Food Directorate, Health Protection Branch, Health Welfare Canada, Ottawa, Ontario, Canada K1A 0L2.

BIOSIS COPYRIGHT: BIOL ABS. Fluorine nuclear magnetic resonance spectroscopy is sufficiently sensitive for the analysis of fluorinated pesticides in food sample extracts at the low parts per billion level without manipulation of large samples and lengthy instrument time. This sensitivity also permits the direct analysis of fluorine-containing compounds in liquid food products such as vegetable oil and wine at \ 1.0 mg with a 5 mm diameter probe.

CAS Registry Numbers:
82657-04-3 - Bifenthrin
69806-50-4 - Fluazifop-butyl
69409-94-5 - Fluvalinate
55283-68-6 - Ethalfluralin
53780-34-0 - Mefluidide
52756-25-9 - Flamprop-methyl
42874-03-3 - Oxyfluorofen
35367-38-5 - Diflubenzuron
27314-13-2 - Norflurazon
1582-09-8 - Trifluralin
1085-98-9 - Dichlofluanid


Teratology 1990 May;41(5):542

Developmental toxicity of dinitroanilines. II. Ethalfluralin.

Byrd RA, Adams ER, Robinson K, Markham JK

Lilly Research Laboratories, Eli Lilly and Co., Greenfield, Indiana.

Ethalfuralin [N-ethyl-N-(-methyl-2-propenyl)-2,6-dinitro-4-(trifluoromethyl) benzenamine] is the active ingredient in the herbicides SONALAN and EDGE. The potential developmental toxicity of ethalfluralin was evaluated in rats and rabbits. Pregnant rats and rabbits were dosed once daily by gavage on gestation days 6-15 and 6-18, respectively. Doses for rats were 0, 50, 250, and 1000 mg/kg; doses for rabbits were 0, 25, 75, 150, and 300 mg/kg. Cesarean sections were performed on rats and rabbits on gestation days 20 and 28, respectively. In rats, maternal toxicity was indicated at the 1000-mg/kg dose level by depression of body weight gain and food consumption. Fetal viability, weight, and morphology were not adversely affected at any dose level. The NOELs for maternal and developmental toxicity in the rat were 250 and 1000 mg/kg, respectively. The A/D ratio in rats was less than 1. In rabbits, maternal toxicity was indicated at the 150- and 300-mg/kg dose levels by abortions in conjunction with depression of food consumption. Fetal viability, weight, and morphology were not adversely affected by ethalfluralin. The NOELs for maternal and developmental toxicity in the rabbit were 75 and 300 mg/kg, respectively. The A/D ratio in rabbits was less than 1. Based on these data, ethalfluralin did not exhibit selective toxicity toward the developing conceptus.


CAN J SOIL SCI; 65 (3). 1985. 587-592.

DINITROANILINE HERBICIDE PERSISTENCE IN SOIL IN SOUTHWESTERN ONTARIO CANADA

GAYNOR JD

No absract available


SZEGI, J. (ED.). SOIL BIOLOGY AND CONSERVATION OF THE BIOSPHERE, VOLS. 1. AND 2; 8TH MEETING OF THE SOIL BIOLOGY SECTION OF THE HUNGARIAN SOCIETY FOR SOIL SCIENCE, GODOLLO, HUNGARY, AUG. 26-28, 1981. XV+460P.(VOL. 1); XII+439P.(VOL. 2). AKADEMIAI KIADO: BUDAPEST, HUNGARY. ILLUS. ISBN 963-05-3700-1(VOLS. 1 AND 2).; 0 (0). 1984. 239-250.

EFFECT OF HERBICIDE COMBINATIONS CONTAINING ETHALFLURALIN ON THE SOIL MICROFLORA AND THE NITROGEN-FIXING CAPACITY OF AZOTOBACTER-CHROOCOCCUM

HELMECZI B, NAGY M, KATAI J, BESSENYEI M


http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=7426803&query_hl=2

Bull Environ Contam Toxicol. 1980 Sep;25(3):508-11.

Comparison of the persistence of ethalfluralin and trifluralin in Saskatchewan field soils.

Hayden BJ, Smith AE.

No abstract available

PMID: 7426803 [PubMed - indexed for MEDLINE]


Toxicol. Appl. Pharmacol. 48(1): A7 1979

The biotransformation and biliary excretion of ethalfluralin in male rats.

Hanasono GK, Moss CL

Toxicol. Div., Lilly Res. Lab., Greenfield, IN

PESTAB. Ethalfluralin (E), N-ethyl- N-(2-methyl- 2-propenyl)- 2,6-dinitro- 4-(tri fluoromethyl) benzenamine, a dinitroaniline herbicide, is rapidly metabolized by rats. The peak plasma concentration of E (150 ng/ml) 2 hr after a single 100-mg/kg oral dose of ring-labeled [14C]E represented less than 2% of the total plasma radiocarbon content. Peak tissue concentrations of radioactivity at 8 hr in liver > fat > kidney were all 2- to 3-fold higher than in plasma. Bile-fistula rats excreted about one-third of the radiolabeled dose of E in the bile as metabolites during a 24-hr period. Almost half of the biliary radioactivity collected was characterized as glucuronide conjugates. GC-MS and NMR analyses showed that a diol metabolie of E, N-ethyl- N-(2-methyl- 2,3-dihydroxy propyl)- 2,6-dinitro- 4-(tri fluoromethyl) benzenamine, was a major glucuronide metabolite in bile. Approximately half of the biliary radioactivity infused into the duodena of bile-fistula rats underwent enterohepatic circulation and reappeared in the 24-hr bile collection. [Abstract #14 of the 1979 annual meeting of the Society of Toxicology.] (Author abstract by permission)


Toxicol. Appl. Pharmacol. 45(1): 321 1978

The metabolism and disposition of ethalfluralin, a dinitroaniline herbicide, in male rats.

Hanasono GK , Occolowitz JL, Wollen RL

Toxicol. Div., Lilly Res. Lab., Greenfield, IN

PESTAB. The excretion, biotransformation, and enterohepatic circulation of ring-labeled [14C] ethalfuralin [N-ethyl- N- (2-methyl- 2-propenyl)- 2,6-dinitro- 4(trifluro methyl) benzeamine] was investigated in male rats given single oral doses (100 mg/kg). The 7-day urinary and fecal excretion of radiolabeled materials by intact animals accounted for 24 and 71%, respectively, of the administered radioactivity. Three urinary metabolites of ethalfluralin were identified by GC-MS and by high-resolution mass spectrometry. A major urinary metabolite (ca. 25% of urinary 14C) was identified as 2-(hydroxymethyl)- 3-[2,6-dinitro- 4-(trifluoro- methyl) phenylamine] propanoic acid. Animals with biliary fistulas excreted 32% of the radiocarbon dose into the bile by 24 hr and 41% by 48 hr. When bile containing 14C-labeled metabolites of ethalfluralin was infused into the duodenum of other bile duct-cannulated rats, 45% of the administered radioactivity reappeared in the 24-hr bile collection. This indicated that an appreciable portion of the labeled materials excreted into the bile undergoes enterohepatic circulation. [Presented at the 17th Annu. Mtg. of the Soc. of Toxicol.] (Author abstract by permission)


PHYTOPARASITICA; 4 (2). 1976; 149

ETHALFLURALIN A NEW RESIDUAL HERBICIDE IN COTTON

KOREN E, DAHAN C, MARMELSTEIN M


 
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