Endosulfan

HCID 3224CAS 115-29-7

Basic information

Standard SMILES
O=S1OCC2C(CO1)C1(Cl)C(Cl)=C(Cl)C2(Cl)C1(Cl)Cl
InChIKey
RDYMFSUJUZBWLH-UHFFFAOYSA-N
Molecular formula
C9H6Cl6O3S
Average molar mass
406.9 g/mol
Monoisotopic mass
403.816881

Names & identifiers

Preferred name
Endosulfan
IUPAC
1,9,10,11,12,12-hexachloro-4,6-dioxa-5lambda4-thiatricyclo[7.2.1.02,8]dodec-10-ene 5-oxide
English name
Thiosulfan
Molecular formula
C9H6Cl6O3S
Molecular weight
406.93

Names & synonyms

endosulfanBenzoepin115-29-7ThiodanThionexChlorthiepinThiosulfanMalixDevisulphanEndosulphanInsectopheneRasayansulfan
Show more names
FANthionateENDOSULFANE3-oxide6,7,8,9,10,10-Hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzo[e]-dioxathiepin-3-oxideHilda
EndocelEndotafBeositHildanSialanThiforThimulTionex

Database identifiers

CAS
115-29-7
PubChem CID
3224
DTXSID
DTXSID1020560
ChEMBL
CHEMBL194399
ChEBI
CHEBI:4791
EC Number
204-079-4
Nikkaji
J2.897E

Properties

Computed structural properties

XLogP
3.8
Topological polar surface area
54.7 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
4
Rotatable bonds
0
Heavy atoms
19

Experimental & physicochemical properties

pHpH 7.2 in tap water
LogP · 2 items

log Kow = 3.83 (alpha); log Kow = 3.62 (beta)

3.55/3.62

Odor · 2 items

Similar to terpene.

... Slight, sulfur dioxide odor ...

Density · 6 items

1.745 at 68 °F (EPA, 1998) - Denser than water; will sink

1.745 at 20 °C

1.7 g/cm³

1.74

1.745 @ 20°C

1.74

Color/FormBrown crystals ... [Note: Technical product is a tan, waxy, isomer mixture].
Solubility · 6 items

less than 1 mg/mL at 73 °F (NTP, 1992)

Solubility at 22 °C and a pH 7.2 in tap water; alpha-Endosulfan: 0.15 mg/l.

Solubility at 22 °C and a pH 7.2 in tap water; beta-Endosulfan: 0.06 mg/l.

Sol in xylene, kerosene, chloroform, acetone, and alcohol

In ethyl acetate 200, dichloromethane 200, toluene 200, ethanol 65, hexane 24 (all in g/L, 20 °C)

In water, alpha-form = 0.32:, beta-form = 0.33 mg/L at 22 °C

Physicochemical properties

Melting point
106 °C · 106°C
Boiling point
106 °C · 106 °C(Press: 0.70 Torr)
Density
1.745 · 1.7450
vapor pressure
8.3 x · 8.3 x 10-4 Pa (25 °C) for 2:l mixture of α- and β-isomers
Flash point
-26 °C · -26 °C
storage temp.
4 °C · APPROX 4°C

Safety & regulation

GHS classification

GHS Classification · 6 items

Danger

H300: Fatal if swallowed [Danger Acute toxicity, oral];H312: Harmful in contact with skin [Warning Acute toxicity, dermal];H330: Fatal if inhaled [Danger Acute toxicity, inhalation];H400: Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard];H410: Very toxic to aquatic life with long lasting effects [Warning Hazardous to the aquatic environment, long-term hazard]

P260, P264, P270, P271, P273, P280, P284, P301+P316, P302+P352, P304+P340, P316, P317, P320, P321, P330, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)

Danger

Hazard information

Regulatory Information · 6 items

Hazard Traits - Bioaccumulation; Environmental Persistence; Environmental tox; Neurotoxicity;Authoritative List - ATSDR Neurotoxicants; CWA 303(d); EC PBTs; OSPAR Priority Action Part A;Report - if used as a fragrance or flavor ingredient

Regulation (EC) No 1107/2009 (amended)

Endosulfan is listed in the dataset of EPA Human Health Benchmarks for Pesticides under the Safe Drinking Water Act (40 eCFR 141)

05/864/EC

Substance: Endosulfan;EC: 204-079-4;Date of inclusion in the POPs Regulation: 19-Jun-2012;POPs Regulation Annex: Annex I, part A; Annex IV

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety Information · 1 item

IMAP assessments - 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide: Environment tier I assessment;IMAP assessments - 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide: Human health tier I assessment

DOT LabelPoison
Fire Hazards · 2 items

Container may explode in heat of fire. Fire or run off from fire control water may release irritating or poisonous gases. Slowly oxidizes in air. Do not store at temperature below 20F. (EPA, 1998)

Not combustible. Liquid formulations containing organic solvents may be flammable. Gives off irritating or toxic fumes (or gases) in a fire.

Fire PotentialNot combustible. Liquid formulations containing organic solvents may be flammable.
Health HazardsIt is very toxic. The probable oral lethal dose is 50 to 500 mg/kg, or 1 teaspoonful to 1 ounce for a 150 lb. person. (EPA, 1998)

Safety & protection

Fire Fighting · 2 items

Keep unnecessary people away; isolate hazard area and deny entry. Stay upwind; keep out of low areas. Ventilate closed spaces before entering them. Wear positive pressure breathing apparatus and special protective clothing. Remove and isolate contaminated clothing at the site.;Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) Use water in flooding quantities as fog. Use alcohol foam, carbon dioxide or dry chemical. (EPA, 1998)

In case of fire in the surroundings, use appropriate extinguishing media. In case of fire: keep drums, etc., cool by spraying with water.

First Aid Measures · 4 items

Fresh air, rest. Refer for medical attention.

Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .

First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.

Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Rest. Refer for medical attention .

First Aid · 2 items

Signs and Symptoms of Acute Endosulfan Exposure: Ingestion of endosulfan may result in nausea, vomiting, and diarrhea. Dizziness, agitation, nervousness, tremor, incoordination, and convulsions may also occur. Central nervous system depression may terminate in respiratory failure. Contact with endosulfan may irritate or burn the skin, eyes, and mucous membranes.;Emergency Life-Support Procedures: Acute exposure to endosulfan may require decontamination and life support for the victims. Emergency personnel should wear protective clothing appropriate to the type and degree of contamination. Air-purifying or supplied-air respiratory equipment should also be worn, as necessary. Rescue vehicles should carry supplies such as plastic sheeting and disposable plastic bags to assist in preventing spread of contamination.;Inhalation Exposure:;1. Move victims to fresh air. Emergency personnel should avoid self-exposure to endosulfan.;2. Evaluate vital signs including pulse and respiratory rate, and note any trauma. If no pulse is detected, provide CPR. If not breathing, provide artificial respiration. If breathing is labored, administer oxygen or other respiratory support.;3. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures.;4. Transport to a health care facility.;Dermal/Eye Exposure:;1. Remove victims from exposure. Emergency personnel should avoid self- exposure to endosulfan.;2. Evaluate vital signs including pulse and respiratory rate, and note any trauma. If no pulse is detected, provide CPR. If not breathing, provide artificial respiration. If breathing is labored, administer oxygen or other respiratory support.;3. Remove contaminated clothing as soon as possible.;4. If eye exposure has occurred, eyes must be flushed with lukewarm water for at least 15 minutes.;5. Wash exposed skin areas three times. An initial soap and water wash should be followed by an alcohol wash. The third wash should again be with soap and water.;6. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures.;7. Transport to a health care facility.;Ingestion Exposure:;1. Evaluate vital signs including pulse and respiratory rate, and note any trauma. If no pulse is detected, provide CPR. If not breathing, provide artificial respiration. If breathing is labored, administer oxygen or other respiratory support.;2. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures.;3. Vomiting may be induced with syrup of Ipecac. If elapsed time since ingestion of endosulfan is unknown or suspected to be greater than 30 minutes, do not induce vomiting and proceed to Step;4.Ipecac should not be administered to children under 6 months of age.Warning: Ingestion of endosulfan may result in sudden onset of seizures or loss of consciousness. Syrup of Ipecac should be administered only if victims are alert, have an active gag-reflex, and show no signs of impending seizure or coma. If ANY uncertainty exists, proceed to Step

(General first aid procedures);Eye: Irrigate immediately - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately.;Skin: Soap flush immediately - If this chemical contacts the skin, immediately flush the contaminated skin with soap and water. If this chemical penetrates the clothing, immediately remove the clothing and flush the skin with water. If irritation persists after washing, get medical attention.;Breathing: Respiratory support;Swallow: Medical attention immediately - If this chemical has been swallowed, get medical attention immediately.

Safe StorageProvision to contain effluent from fire extinguishing. Separated from acids, bases, iron and food and feedstuffs. Dry. Well closed.
Exposure Control and Personal Protection · 1 item

TIH (Toxic Inhalation Hazard) - Term used to describe gases and volatile liquids that are toxic when inhaled. Some are TIH materials themselves, e.g., chlorine, and some release TIH gases when spilled in water, e.g., chlorosilanes. [ERG 2016].

Fire Fighting Procedures · 1 item

If material involved in fire: Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) Use "alcohol" foam, dry chemical, or carbon dioxide. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Keep run-off watter out of sewers and water sources. /Endosulfan (organochlorine pesticides, liquid, toxic); Endosulfan (organochlorine pesticides, solid, toxic)/

Toxicology

Toxicological InformationCDC-ATSDR Toxicological Profile
Interactions · 5 items

Citrinin (CIT) (10 mg/kg feed) and endosulfan (1 mg/kg body weight) were administered orally alone and in combination to pregnant Wistar rats from gestational day 6 to 20 and their fetuses were collected to evaluate the histopathological alterations in hepatic and renal tissues. In CIT-fed group fetal liver, the changes were less marked, showing only sinusoidal dilation and mild vacuolar degeneration, whereas the consistent changes in the fetal kidney included tubular degeneration, medullary tubular necrosis, cystic dilatation of tubules, distortion of glomerulur capillary tuft and interstitial fibroblastic proliferation which separated clusters of tubules. In the endosulfan group, the liver was predominantly affected, showing vacuolar degeneration, karyomegaly and severe sinusoidal dilation, whereas the renal changes were mainly confined to tubular degeneration and varying degree of interstitial fibrosis. In the combination group, the hepatic and renal histopathological alterations in the fetus, though of similar nature to those of the individual groups, were more severe.

The protective effects of vitamin E was investigated on the cardiotoxicity induced by endosulfan administration. Male rats in different groups were given endosulfan (2 mg/kg bw/day in corn oil through gavage), vitamin E (200 mg/kg bw twice a week in corn oil through gavage) and endosulfan and vitamin E at the same dose and route, to the control group corn oil is given at the dose rate of 2 mL per rat per day through gavage, for a period of 28 days. The animals were sacrificed and heart tissues were collected and subjected to histopathology. The result indicated, severe congestion, hemorrhages with interstitial edema. In some places there was diapedesis of leukocytes. Myocardium showed different degrees of degeneration, some of the myofibrils were found to be granular with pyknotic nuclei. Thickening of wall of arteries were seen. In the Vitamin E and endosulfan treated group the above mentioned lesions were significantly decreased in their severity.

... Livers of /New Zealand white/ rabbits were examined grossly and histopathologically, and caspase-3 activity was detected by immunohistochemical methods. A total of twenty-four rabbits were divided into four groups (n=6). Rabbits in Group I (endosulfan (END)) were daily given a sublethal dose of endosulfan (1mg/kgbw) in corn oil by oral gavage for 6 weeks. Group II (END+C) received the same dose of endosulfan and additionally Vit C (20mg/kgbw) every other day during this period. Group III (OIL+C) received corn oil daily by oral gavage and vitamin C every other day for 6 weeks. Group IV (OIL), the control group, received only corn oil daily, by oral gavage throughout the experiment. The concentration of alpha-endosulfan in the END group was higher in livers (0.102+/-0.012 ppb) than the beta-endosulfan (0.072+/-0.001 ppb). Decreased accumulation of alpha and beta endosulfan was observed in the END+C group (0.025+/-0.003 and 0.016+/-0.002 ppb, respectively) (p<0.0001). The most prominent gross findings at the necropsy were seen in the END group, in which swollen and pale livers were commonly observed. Hemorrhages, degenerations, necrosis, and in some rabbits bile duct hyperplasia were the marked histopathological findings of the END group. Caspase-3 positive reaction was more severe in this group than in the others. An ameliorating effect of Vit C on gross, histopathological and immunohistochemical findings was observed in the END+C group. The results revealed that endosulfan is highly toxic for rabbit livers. However, toxicity was decreased by Vit C treatment, which reduced the accumulation of endosulfan in livers four-fold.

A study was conducted to determine the cumulative toxicity of manganese chloride (MnCl2), endosulfan, and a mixture of these compounds and also to suggest a cumulative toxicity rating. Male mice were fed mixtures of endosulfan powder suspended in peanut oil and manganese chloride dissolved in water for 6 day/wk until the cumulative LD50 remained constant for three consecutive weeks. The cumulative toxic factors were: 0-3.48 for manganese chloride, 1.30-2.46 for endosulfan, and 1.30-3.34 for a mixture of these compounds. Observed cumulative toxic factors for the mixture were higher than expected values, indicating a greatly reduced toxicity when these compounds are mixed.

For more Interactions (Complete) data for ENDOSULFAN (6 total), please visit the HSDB record page.

Target Organs · 3 items

Developmental (effects while organs are developing), Immunological (Immune System), Neurological (Nervous System)

Cardiovascular;Urinary

Skin, central nervous system, liver, kidneys, reproductive system

Ecotoxicity Values · 5 items

LC50; Species: Colinus virginianus (Bobwhite quail, age 9 days) oral (in food) 805 ppm for 5 days (95% confidence limit: 690-939 ppm)

LD50; Species: Colinus virginianus (Northern bobwhite) oral via capsule 42 mg/kg (95% confidence interval: 32-56 mg/kg)

LC50; Species: Coturnix japonica (Japanese quail, age 14 days) oral (in food) approx 1250 ppm for 5 days

LC50; Species: Coturnix japonica (Japanese quail, juvenile, age 14 days post hatch) oral in food 2160 ppm for 5 days (95% confidence interval: 1658-2815 ppm)

For more Ecotoxicity Values (Complete) data for ENDOSULFAN (82 total), please visit the HSDB record page.

Environmental Fate · 5 items

TERRESTRIAL FATE: Based on a classification scheme(1), Koc values of 350 to 19,953(2,3) indicate that endosulfan is expected to have moderate to no mobility in soil(SRC). Volatilization of endosulfan from moist soil surfaces may be an important fate process(SRC) given a Henry's Law constant of 6.5X10-5 atm-cu m/mole(4). Endosulfan is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure of 1.73X10-7 mm Hg at 25 °C(5). Endosulfan may undergo hydrolysis in moist soil surfaces based on half-lives of 9-533 hours in river water(3). The half-life of endosulfan in aerobic soil was reported as 32 days and in anaerobic soil was 150 days(6).

TERRESTRIAL FATE: Endosulfan was applied 3 times at a rate of 0.5 and 1.5 lb/acre to field tobacco, with max time to zero residue level estimated to be 10 days...

TERRESTRIAL FATE: Fifty percent of residues are lost in 3-7 days (depending on plant species).

TERRESTRIAL FATE: The persistence of greater than 0.05 ppm of total endosulfan residues under natural conditions of wet and dry cultivation was studied. When the initial dose of application was the same, the residues persisted for approx 120 days in wet soils and 100 days in dry soils. In 3 dry soils that received low, normal and high initial doses (41.88, 87.5, and 350 g AI/acre), residues persisted for 60, 100, and 160 days, respectively. Endosulfan sulfate was the principal metabolite except in dry soil receiving the high dose, where the endosulfan alc and endosulfan ether were principal metabolites for the first 50 days, after which endosulfan sulfate appeared.

For more Environmental Fate (Complete) data for ENDOSULFAN (8 total), please visit the HSDB record page.

Food Survey Values · 3 items

Endosulfan was detected in 95 of 3,281 large domestic fruits (avg 0.005 ppm), 20 of 1,048 imported large fruits (avg 0.0008 ppm), 89 of 1,445 small domestic fruits (avg 0.007 ppm), 720 of 2,119 imported small fruits (avg 0.122 ppm), 718 of 5,319 domestic leaf and stem vegetables (avg 0.031 ppm), 41 of 312 imported leaf and stem vegetables (avg 0.444 ppm), 100 of 2,954 domestic vine and ear vegetables (avg 0.004 ppm), 342 of 4,117 imported vine and ear vegetables (avg 0.004 ppm), 5 of 499 domestic beans (avg 0.001 ppm), 41 of 365 imported beans (avg 0.005 ppm), 62 of 3,248 domestic root vegetables (avg 0.0005 ppm), 18 of 609 imported root vegetables (avg 0.004 ppm), 27 of 631 domestic processed vegetable products (avg 0.002 ppm), 22 of 929 imported vegetable products (avg 0.003 ppm), 8 of 210 domestic processed fruit products (avg 0.002 ppm), and 36 of 634 imported processed fruit products (avg 0.004 ppm)(1). Endosulfan was infrequently detected in eggs and egg products, fish, shellfish and hay(1). Seventeen of 240 food composites contained beta- endosulfan at concns ranging from 0.001-0.006 ppm and 13 of 240 food composites contained alpha-endosulfan at 0.001-0.006 ppm(2). Two of 110 toddler food composites contained from 0.001-0.004 ppm beta-endosulfan(3).

Endosulfan was identified, not quantified, in 7% of adult foods during an FDA survey from 1978-1982(1) and in 5% of adult foods from 1982-1986(2). During an FDA survey of domestic foods from 1985-1991 endosulfan was detected in an apple juice sample at 0.01 ppm, 222 of 2,464 apples at a max concn of 0.33 ppm, 1 of 2,739 milk samples at trace concns, and 59 of 571 pears at a max concn of 1.1 ppm(3). In an FDA survey of imported foods from 1985-1991, endosulfan was detected in 7 of 735 apples at a max concn of 0.15 ppm, 1 of 474 oranges at trace levels and 4 of 816 pears at a max concn of 0.29 ppm(3). In an FDA survey of children foods, endosulfan was detected in cereals (max concn 0.007 ppm), deserts (max concn 0.001 ppm), fruits and juices (max concn 0.053 ppm) and vegetables (max concn 0.004 ppm)(3). Endosulfan was detected in 144 of 710 domestic pears at a max concn of 1.1 ppm and in 4 of 949 imported pears at a max concn of 0.13 ppm during a 1992-1993 FDA survey(4). Endosulfan was detected in 471 of 1,219 domestic tomatoes at a max concn of 0.2 ppm and in 80 of 144 imported tomatoes at a max concn of 0.55 ppm during a 1992-1993 FDA survey(4). In an FDA survey of foods in 1993-1994, endosulfan was detected in 76 of 769 domestic apples at a max concn of 0.20 ppm and in 45 of 1,062 imported apples at a max concn of 0.10 ppm(5).

Endosulfan was detected in 111 out of 2,223 total samples of the following fruits and vegetables from Sao Paulo, Brazil from 1994-2001, at a mean residue concentration (range) of 0.11 (0.01-1.56) mg/kg: apple, carrot, cucumber, grape, green bean, guava, melon, onion, papaya, peach, summer squash, strawberry, sweet pepper, tomato(1). Out of 270 apple and citrus fruit samples collected from Karachi, Pakistan from 1999 to 2001, 11 apples, and 16 citrus fruits were contaminated with endosulfan at 0.05-13.07 ppm(2). Out of 206 samples of 27 different vegetables collected from Karachi, Pakistan from 2001 to 2003, endosulfan was detected one time each in sugarbeet, mint, bitterguord, french bean, Indian squash, cucumber, lady's finger, lufa, tomato and cabbage, and twice each in turnip and pumpkin; the MRL was exceeded in 7 of these samples(3). From April 1995 to March 2000, in a study of 765 total samples of agricultural products in Japan, endosulfan was detected in 6 out of 237 cucumbers, with one detection each at residue levels <0.01, <0.05 and <0.5 ug/g, and 3 detections at concentrations <0.1 ug/g(4). Out of 235 fish samples from Calcutta, analyzed between 1993-95 to 1997-98, 131 were contaminated with endosulfan residues from 0.01 to 1.41 ug/g, with about 16% above the maximum residue limit of 0.2 ug/g prescribed for meat on fat basis(5).

Regulatory information

Regulatory Information · 6 items

Hazard Traits - Bioaccumulation; Environmental Persistence; Environmental tox; Neurotoxicity;Authoritative List - ATSDR Neurotoxicants; CWA 303(d); EC PBTs; OSPAR Priority Action Part A;Report - if used as a fragrance or flavor ingredient

Regulation (EC) No 1107/2009 (amended)

Endosulfan is listed in the dataset of EPA Human Health Benchmarks for Pesticides under the Safe Drinking Water Act (40 eCFR 141)

05/864/EC

Substance: Endosulfan;EC: 204-079-4;Date of inclusion in the POPs Regulation: 19-Jun-2012;POPs Regulation Annex: Annex I, part A; Annex IV

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

RCRA Requirements · 1 item

P050; As stipulated in 40 CFR 261.33, when endosulfan, as a commercial chemical product or manufacturing chemical intermediate or an off-specification commercial chemical product or a manufacturing chemical intermediate, becomes a waste, it must be managed according to federal and/or state hazardous waste regulations. Also defined as a hazardous waste is any container or inner liner used to hold this waste or any residue, contaminated soil, water, or other debris resulting from the cleanup of a spill, into water or on dry land, of this waste. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (40 CFR 261.5(e)).

FIFRA Requirements · 4 items

Tolerances are established for the combined residues of the insecticide endosulfan, 6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide (alpha and beta isomers), and its metabolite endosulfan sulfate, 6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3,3-dioxide, in or on the following food commodities: [Table#1172]

A tolerances of 24 parts per million (ppm) is established for the combined residues of the insecticide endosulfan, 6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3-oxide (alpha and beta isomers), and its metabolite endosulfan sulfate, 6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin-3,3-dioxide, in or on dried tea (reflecting less than 0.1 ppm residues in beverage tea) resulting from application of the insecticide to growing tea.

The Agency has previously identified and required the submission of the generic (i.e., an active ingredient specific) data required to support reregistration of products containing endosulfan active ingredients. The Agency has completed its assessment of the dietary (food and drinking water), ecological and occupational risks associated with the use of currently registered pesticides containing the active ingredient endosulfan. Based on a review of these data and public comments on the Agency's assessments for the active ingredient endosulfan, EPA has sufficient information on the human health and ecological effects of endosulfan to make decisions as part of the tolerance reassessment process under FFDCA and reregistration under FIFRA, as amended by FQPA. The Agency has reassessed all 80 tolerances for endosulfan and can make a FQPA safety determination ... The Agency has determined that agricultural use of endosulfan, based on the currently approved labeling, pose occupational and ecological risks that constitute unreasonable adverse effects on the environment. However, the Agency believes that these risks can likely be acceptably mitigated through routine changes to pesticide labeling and formulations. Accordingly, the Agency has determined that endosulfan is eligible for reregistration provided that: (i) additional data that the Agency intends to require confirm this decision for occupational exposures associated with the application of dip treatment to roots or whole plants and ecological risks; and (ii) the risk mitigation measures outlined in this document are adopted, and label amendments are made to reflect these measures. ... Further mitigation measures and additional data requirements, however, may be warranted following the completion of the stakeholder process outlined in this document. Based on its evaluation of endosulfan, the Agency has determined that endosulfan products, unless labeled and used as specified in this document, would present risks inco

As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their continued use. Under this pesticide reregistration program, EPA examines newer health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether the use of the pesticide does not pose unreasonable risk in accordance to newer saftey standards, such as those described in the Food Quality Protection Act of 1996. Endosulfan is found on List A, which contains most pesticides that are used on foods and, hence, have a high potential for human exposure. List A consists of the 194 chemical cases (or 350 individual active ingredients) for which EPA issued registration standards prior to FIFRA '88. Case No: 0014; Pesticide type: Insecticide (Acaricide); Registration Standard Date: 04/01/82; Case Status: OPP is reviewing data from the pesticide's producers regarding its human health and/or environmental effects, or OPP is determining the pesticide's eligibility for reregistration and developing the Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): Endosulfan; Data Call-in (DCI) Date(s): 05/10/94, 10/13/95; AI Status: The producers of the pesticide has made commitments to conduct the studies and pay the fees required for reregistration, and are meeting those commitments in a timely manner.

CERCLA Reportable Quantities · 2 items

Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 1 lb or 0.454 kg. The toll free number of the NRC is (800) 424-8802. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).

[40 CFR 355 (7/1/2000)] Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Endosulfan is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 10 or 10,000 lbs. Extremely hazardous substances that are solids are subject to either of two threshold planning quantities ... The lower quantity applies only if the solid exists in powdered form and has a particle size less than 100 microns; or is handled in solution or in molten form; or meets the criteria for a National Fire Protection Association (NFPA) rating of 2, 3 or 4 for reactivity. If the solid does not meet any of these criteria, it is subject to the upper ... threshold planning quantity ... .

Clean Water Act Requirements · 2 items

Endosulfan is designated as a hazardous substance under section 311(b)(2)(A) of the Federal Water Pollution Control Act and further regulated by the Clean Water Act Amendments of 1977 and 1978. These regulations apply to discharges of this substance. This designation includes any isomers and hydrates, as well as any solutions and mixtures containing this substance.

Toxic pollutant designated pursuant to section 307(a)(1) of the Federal Water Pollution Control Act and is subject to effluent limitations. /Endosulfan and metabolites/

State Drinking Water Guidelines · 3 items

(AZ) ARIZONA 74 ug/L

(FL) FLORIDA 42 ug/L

(ME) MAINE 42 ug/L

Safety data

OEB
D
OEL
TWA: 0.1 mg/m3 [skin]
wgk
3
rtecs
RB9275000
ridadr
UN 2761
hs_code
29209090

Chemistry & industry

Pharmacology

Mechanism of Action · 2 items

Endosulfan interferes with energy metabolism in vivo of the fresh water teleost fish, Chana gachua, following chronic exposure to various sublethal concentrations. The marked sensitivity of mitochondrial magnesium2+ atpase to endosulfan is suggestive of the potential for endosulfan to interfere markedly with various energy requiring processes in the fish body.

Endosulfan is a chlorinated cyclodiene pesticide, and like other members of this chemical group, the predominant toxicological effect is over stimulation of the CNS [by inhibiting Ca2+, Mg2+ - ATPase and antagonizing chloride ion transport in gamma-aminobutyric acid (GABA) receptors] with little or no peripheral component.

Biological Half-Life · 4 items

No reports found; [TDR, p. 607]

Total endosulfan residue levels in postmortem samples from carcass of poisoned dairy cows were 1270 ppm in rumen content & 4.2, 1.1, & 0.6 ppm in liver, kidney, & muscle tissue, respectively. Analysis of milk from cows which survived the poisoning revealed level of greater than 1 ppm endosulfan immediately following the intoxication. This level decreased to 1 ppb at the end of 35 days & half-life of approx 3.9 days was calculated for endosulfan in milk.

Alpha and beta-isomers of endosulfan, following iv administration in rabbits, showed marked differences in their pharmacokinetic profile. Beta-endosulfan was cleared from the plasma much more rapidly than alpha-endosulfan, the terminal slope half-life being 5.97 and 235 hr, respectively. These dissimilarities may partly explain reported differences in their toxicity.

The half lives for urinary and fecal elimination for males and female rats were biphasic, with an earlier half-life of 6 to 14 hour and a later half life of 33 to 67.5 hour

Metabolism/Metabolites · 5 items

In temp stressed rats orally dosed with endosulfan I or II, endosulfan sulfate was the metabolite most commonly recovered from tissues, organs and feces regardless of temp stress. The diol, alpha-hydroxy ether and lactone ... were found in most urine and feces samples.

... White mice (balb/c strain) were fed (14)C-labeled endosulfan. The two isomers were not completely absorbed from GI tract but, along with endosulfan sulfate and diol, were excreted in feces. Only a trace of oxidized endosulfan was found in kidney & muscle extracts but neither of the two known metabolites nor endosulfan was found in blood or brain extracts. ... Large amounts of endosulfan sulfate were detected in the liver & traces in the kidney 24 hr after /mice/ ... received a single doses of endosulfan.

(14)C-Endosulfan was fed to milk sheep. Analysis of milk samples showed that up to 88% of radioactive materials remained in cream. Gas liquid chromatograhpy and thin layer chromatograhy showed that the radioactive material was almost entirely endosulfan sulfate. Analyses of urine samples showed the presence of endosulfan alcohol & alpha-hydroxyendosulfan ether. Other metabolites present were not identified.

After peroral, cutaneous, & subcutaneous application of endosulfan to male imagos of the locust (pachytilus migratorius migratorioides), four metabolites were ... Identified as: endosulfan sulfate; endosulfan ether; endosulfan hydroxyether; & endosulfan lactone.

For more Metabolism/Metabolites (Complete) data for ENDOSULFAN (13 total), please visit the HSDB record page.

MeSH Pharmacological ClassificationPesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics.
Absorption, Distribution and Excretion · 5 items

Endosulfan was differentially distributed in CNS of the cat brain with concentration pattern changing with time. White matter had slower uptake & release with lower max concentration of endosulfan than did gray matter.

The A and B-isomers of (14)C-endosulfan were administered to rats separately as single 2 mg/kg oral doses in corn oil. No appreciable differences were observed in the fecal (or urine) elimination of radioactivity of the two isomers. Approximately 11 and 13%, 55 and 62%, and 68 and 75% of the administered radioactivity was eliminated in the feces at 24, 48, and 120 hours after treatment with the alpha and beta-isomers, respectively. Analyses of bile collected for 48 hours showed that 47% of the alpha-endosulfan dose and 29% of the beta-endosulfan dose was eliminated by this route.

In studies with sheep receiving a single oral dose of radiolabeled endosulfan, 92 percent of the dose was eliminated in 22 days. The organ with the highest concentration of radiolabeled endosulfan after 40 days was the liver. Major metabolites did not persist in the fat or in the organs.

The principal route of excretion for endosulfan and endosulfan sulfate is in the feces.

For more Absorption, Distribution and Excretion (Complete) data for ENDOSULFAN (12 total), please visit the HSDB record page.

Uses & manufacturing

Uses · 6 items

Used as an insecticide on various crops including tea, coffee, fruits, vegetables, rice, corn, and sorghum; [EXTOXNET]

Farming (Pesticides) [Category: Industry]

For endosulfan (USEPA/OPP PC Code: 079401) Active products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

Non-systemic insecticide and acaricide

Insecticide used to control the Colorado potato beetle, flea beetle, cabbageworm, peach tree borer, and the tarnished plant bug.

Endosulfan is a broad spectrum contact insecticide and acaricide registered for use on a wide variety of vegetables, fruits, cereal grains, and cotton, as well as ornamental shrubs, trees, vines, and ornamentals for use in commercial agricultural settings.

ImpuritiesTechnical endosulfan according to The Food and Agricultural Organization specifications must contain 94% endosulfan as the active ingredient and impurities may not exceed 2% endosulfan alcohol and 1% endosulfan ether.
U.S. Imports · 2 items

(1978) 4.41X10+8 g (princpl custms dists)

(1982) 1.82X10+8 g (princpl custms dists)

U.S. Production · 2 items

(1977) Probably greater than 2.27x10+6 g

(1982) Not produced commercially in US

Consumption Patterns · 3 items

Insecticide used on deciduous fruits/nuts, 50%; insecticide used on vegetables, 50% (1982)

Endosulfan use in US agriculture was 1.1X10+6 kg (1989); 9.77X10+5 kg (1982); 1.653X10+6 kg (1976) 8.82X10+5 kg (1971); 7.91X10+5 kg (1966)

Total average annual use of endosulfan is estimated at approximately 1.38 million pounds of active ingredient (lbs. ai).

Methods of Manufacturing · 2 items

Endosulfan is produced by reaction of 1,2,3,4,7,7-hexachloro-5,6-dihydroxymethylbicylo[2,2,1]-hept-5-ene, obtained by condensation of cis-1,4-dihydroxybut-2-ene with hexachlorocyclopentadiene, with thionyl chloride.

Prepared by reaction of hexachlorocyclopentadiene with cis-butene-1,4-diol to form bicyclic dialcohol followed by esterification and cyclization with SOCl2.

Applications · 4 items

DescriptionEndosulfan (70) [115-29-7], 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3,- benzo-dioxathiepine 3-oxide (IUPAC) [The technical product is a mixture of two isomers: α-endosulfan: 3α,5αβ,6α, 9α,9αβ (64–67%) (70a) and β-endosulfan 3α,5aα,6β,9β, 9aα, (29–32%) (70b)]; [959-98-8] (formerly [33213-66- 0]) (β-endosulfan);[33213-65-9] (formerly [891-86-1] and [19670-15-6]) (β-endosulfan) is the adduct of hexachlorocyclopentadiene and 1,4-dihydroxy-2-butene reacted further with SOCl2 to produce 6,7,8,9,10,10-hexachloro- 1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxa thiepin-3-oxide. The technical product is a brownish solid, mp 70–100 C, vapor pressure 1.3 mPa at 25 C, soluble in petroleum solvents but having low solubility in water. It consists of about four parts of α-isomer (mp 108 C, cis with regard to the sulfite group) and one part of the β-isomer (mp 206 C, trans with regard to the sulfite group). The α-isomer, which is somewhat more insecticidal, is slowly converted to the more stable β-isomer at high temperature, and both isomers are oxidized slowly to endosulfan sulfate [1031-07-8] (mp 181 C). In acid media, both isomers form endosulfan diol [2157-19-9] (mp 203 C).

UsesEndosulfan is used for the control of sucking, chewing, boring insects and mites on a wide variety of crops. It also controls tsetse flies.

UsesInsecticide.

General DescriptionEndosulfan is a pesticide. It is a cream- to brown-coloured solid that may appear in the form of crystals or flakes. It has a smell like turpentine, but does not burn. It does not occur naturally in the environment. It is a restricted use pesticide, meaning that it can only be used by professional applicators.

Suppliers37 total

阿诺西(上海)生物技术有限公司400-1107768 15058188853 · [email protected]
广州佳途科技股份有限公司81960175 18933936954 · [email protected]
杭州品高化工有限公司0571-87658025 · [email protected]
常州市华阳科技有限公司+8615250961469 · [email protected]
四川库利南科技有限公司400-1166-196 18981987031 · [email protected]

Additional notes

DefinitionChEBI: A cyclic sulfite ester that is 1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepine 3-oxide substituted by chloro groups at positions 6, 7, 8, 9, 10 and 10.

Related reactions

1 records

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