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56-72-4

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56-72-4 Usage

Description

Technical coumaphos is a tan crystalline solid with a slight sulphur odour. It is insoluble in water; slightly soluble in acetone, chloroform, and ethanol; and soluble in organic solvents. Coumaphos when heated undergoes decomposition and releases very toxic fumes of sulphur oxides, phosphorous oxides, and chlorides. It is used for the control of a wide variety of livestock insects, including cattle grubs, screwworms, lice, scabies, flies, and ticks. It is used against ectoparasites, which are insects that live on the outside of host animals such as sheep, goats, horses, pigs, and poultry. Coumaphos is incompatible with alkalis, strong oxidising agents, pyrethroids, and piperonyl butoxide. The U.S. EPA has grouped coumaphos as RUP.

Chemical Properties

Different sources of media describe the Chemical Properties of 56-72-4 differently. You can refer to the following data:
1. coumaphos is a tan crystalline solid with a slight sulfur odor. It is insoluble in water, slightly soluble in acetone, chloroform, and ethanol, and soluble in organic solvents. It is used for the control of a wide variety of livestock insects, including cattle grubs, screwworms, lice, scabies, fl ies, and ticks. It is used against ectoparasites, which are insects that live outside the host animals, such as sheep, goats, horses, pigs, and poultry. Coumaphos is incompatible with pyrethroids and piperonyl butoxide. The US EPA has grouped coumaphos as an RUP. Acute dermal exposures to occupational workers occur during mixing, loading, and application of coumaphos, especially in the livestock dip-vat and hand-held sprayer uses
2. Coumaphos is a white to brownish crystalline solid with a slight sulfurous odor
3. tan or beige solid

Uses

Coumaphos is used to control larvae of Diptera and ticks on cattle. It has also recently been used to control Varroa mite in honeybees.

Brand name

Baymix (Bayer AnimalHealth); Meldane (Bayer Animal Health).

General Description

Slightly brownish crystals with a slight sulfurous odor. Used for the control of a wide variety of livestock insects including cattle grubs, lice, scabies, flies, and ticks; the common ectoparasites of sheep, goats, horse, swine, and poultry as well as for screwworms in all these animals.

Air & Water Reactions

Insoluble in water. Coumaphos hydrolyzes slowly under alkaline conditions.

Reactivity Profile

Organothiophosphates, such as Coumaphos, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides. Coumaphos reacts with strong oxidizing agents and alkaline materials.

Hazard

Use may be restricted; cholinesterase inhibitor. Questionable carcinogen.

Health Hazard

Different sources of media describe the Health Hazard of 56-72-4 differently. You can refer to the following data:
1. Highly toxic compound; choline stearaseinhibitor; toxic symptoms include headache,dizziness, blurred vision, muscle spasm,vomiting, abdominal pain, diarrhea, chestpain, and shortness of breath; high dose maycause seizure, respiratory paralysis, comaand death; ingestion of 15–20 g can be fatalto adult humans.LD50 oral (rat): 13 mg/kgLD50 skin (rat): 860 mg/kgLC50 inhalation (rat): ~300 mg/m3.
2. Very toxic, probable oral lethal dose is 50-500 mg/kg, or between 1 teaspoonful and 1 oz. for a 70 kg (150 lb.) person. May be fatal if inhaled, swallowed, or absorbed through skin. Contact may cause burns to skin and eyes.
3. Exposures to coumaphos cause signs of poisoning such as diarrhea, drooling, diffi culty in breathing, leg and neck stiffness among occupational workers. Acute inhalation of coumaphos causes headaches, dizziness, and incoordination. Moderate poisoning causes muscle twitching and vomiting while severe poisoning leads to fever, toxic psychosis, lung edema, and high blood pressure. Repeated exposures cause irritability, confusion, headache, speech diffi culties, effects on memory concentration, disorientation, severe depressions, sleepwalking, and drowsiness or insomnia among occupational workers. Coumaphos has been classifi ed as non-carcinogenic to humans

Fire Hazard

When heated to decomposition, Coumaphos emits very toxic fumes of sulfur oxides, phosphorus oxides, and chlorides. Incompatible with piperonyl butoxide. Stable in water.

Agricultural Uses

Insecticide, Nematocide; Veterinary medication: The U.S. EPA classifies the formulations 11.6% EC and 42% flowable concentrate end-use products as Restricted Use Pesticides (RUPs) because they pose a hazard of acute poisoning from ingestion. Coumaphos is an insecticide/acaricide used to control a wide variety of liver stock insects including cattle grubs, fleeceworms, lice scabies, flies, and ticks; the common ectoparasites of beef cattle, dairy cows, sheep, goats, horse, swine, and poultry as well as for screw worms in all these animals. The USDA uses coumaphos in dip vats along the U.S.-Texas border to control ticks that carry Texas Cattle Fever. It is added to cattle and poultry feed to control the development of fly larvae that breed in manure. It has applications in beekeeping.

Trade name

AGRIDIP?; ASUNTOL?; AZUNTHOL?; BAY? 21/199; BAYER? 21/199; BAYMIX?; BAYMIX? 50; CHECKMITE?; CO-RAL?[C]; DELICE?; MELDANE?; MELDONE?; MUSCATOX?; NEGASHUNT?; DIOLICE?; RESITOX?; SUNTOL?; UMBETHION?

Safety Profile

Poison by ingestion, sktn contact, inhalation, and intraperitoneal routes. Mutation data reported. When heated to decomposition, it emits very toxic fumes of SOx, PO,, and Cl-. See also COUMARIN.

Potential Exposure

A potential danger to those involved in the manufacture, formulation, and application of this material which is used for control of a wide variety of livestock insects including cattle grubs, lice scabies, flies, and ticks; the common ectoparasites of sheep, goats, horse, swine, and poultry; as well as for screw worms in all these animals.

Carcinogenicity

There was no evidence of carcinogenicity at any dose in rats fed diets that contained 1, 5, or 25 ppm coumaphos (0.05, 0.25, or 1.22 mg/kg/day (males); 0.07, 0.36, or 1.70 mg/kg/day (females)) for 2 years . There was no evidence of carcinogenicity in another study when rats were given diets that contained 10 or 20 ppm coumaphos for 103 weeks .

Metabolic pathway

By UV irradiation of coumaphos in solutions, three dimeric products are isolated and identified as the head-to-tail anti-dimer, its oxidation product, and the head-to-tail syn-dimer.

Metabolism

Degradation occurs rapidly in the liver of the cow and rat. The principal metabolite excreted in urine is diethyl hydrogen phosphorothioate. Deethylation products are also found in lesser amounts. Photolytic DT50 on soil surface is 23.8 d.

Shipping

UN2783 Organo phosphorus pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous material. UN3018 Organophosphorus pesticides, liquid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Toxicity evaluation

The acute oral LD50 values for male and female rats are 41 and 16 mg/kg, respectively. Inhalation LC50 values (1 h) for male and female rats are >1081 and 341 mg/m3 air. In 2-yr trials, rats tolerated 100 mg/kg diet.

Degradation

Note that technical coumaphos may contain the dechlorinated analogue 'Potasan' (O-4-methyl-2-oxo-2H-chromen-7-yl O,O-diethyl phosphorothioate) (2) as an impurity (Waleski, 1966; Volpk and Mallet, 1976). Coumaphos is stable to hydrolysis in aqueous media although the pyrone ring opens in dilute alkali and re-closes on acidification (PM). In water at pH 4.0, 5.5, 6.3, 7.0 and 8.5, the DT50 values were 33, 67, 124, 347 and 29 days, respectively. Coumaphos degraded first to coroxon (coumaphos oxon) (3), presumably by an oxidative mechanism and this was hydrolysed to chlorferon (3-chloro-4-methyl-7-hydroxycoumarin)(4). The analysis was by TLC (Mallet and Volpe,1978).

Incompatibilities

Organophosphates are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrideds and active metals. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides. Keep away from piperonyl butoxide, oxidizers, strong bases, water, and heat

Waste Disposal

Coumaphos can be decomposed by heating with concentrated alkali. Large amounts should be incinerated in a unit equipped with effluent gas scrubbing. Do not discharge into drains or sewers. Dispose of waste material as hazardous waste using a licensed disposal contractor to an approved landfill. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (>=100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal. Incineration with effluent gas scrubbing is recommended. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office

Check Digit Verification of cas no

The CAS Registry Mumber 56-72-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 6 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56-72:
(4*5)+(3*6)+(2*7)+(1*2)=54
54 % 10 = 4
So 56-72-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H16ClO5PS/c1-4-17-21(22,18-5-2)20-10-6-7-11-9(3)13(15)14(16)19-12(11)8-10/h6-8H,4-5H2,1-3H3

56-72-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name coumaphos

1.2 Other means of identification

Product number -
Other names Agridip

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Insecticide
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:56-72-4 SDS

56-72-4Synthetic route

diethyl phosphorochloridothioate
2524-04-1

diethyl phosphorochloridothioate

Sodium; 3-chloro-4-methyl-2-oxo-2H-chromen-7-olate

Sodium; 3-chloro-4-methyl-2-oxo-2H-chromen-7-olate

coumaphos
56-72-4

coumaphos

Conditions
ConditionsYield
In N,N-dimethyl-formamide64%
3-chloro-4-methylumbelliferone
6174-86-3

3-chloro-4-methylumbelliferone

diethyl phosphorochloridothioate
2524-04-1

diethyl phosphorochloridothioate

coumaphos
56-72-4

coumaphos

Conditions
ConditionsYield
Stage #1: 3-chloro-4-methylumbelliferone With n-butyllithium In tetrahydrofuran; hexane for 1h;
Stage #2: diethyl phosphorochloridothioate In tetrahydrofuran; hexane at 20℃; for 12h;
58%
With copper; potassium carbonate; butanone
coumaphos
56-72-4

coumaphos

o,o-diethyl 6a,12a-dichloro-6a,6b,12a,12b-tetrahydro-6b,12b-dimethyl-6,12(6H,12H)-dioxocyclobuta<1,2-c:3,4-c'>bis<1>benzopyran-3,9-di-o-thiophosphate

o,o-diethyl 6a,12a-dichloro-6a,6b,12a,12b-tetrahydro-6b,12b-dimethyl-6,12(6H,12H)-dioxocyclobuta<1,2-c:3,4-c'>bis<1>benzopyran-3,9-di-o-thiophosphate

Conditions
ConditionsYield
In chloroform for 250h; Irradiation;20%
coumaphos
56-72-4

coumaphos

O,O,O,O-tetraethyl-O,O-4,4'-dimethyl-2,2'-dioxo-(3,3'-bi-2H-1-benzopyran-7,7'-diyl)-diphosphorothioate

O,O,O,O-tetraethyl-O,O-4,4'-dimethyl-2,2'-dioxo-(3,3'-bi-2H-1-benzopyran-7,7'-diyl)-diphosphorothioate

Conditions
ConditionsYield
With oxygen In chloroform Irradiation;
coumaphos
56-72-4

coumaphos

A

O-(4-Acetyl-3-hydroxyphenyl) O,O-diethyl thiophosphate

O-(4-Acetyl-3-hydroxyphenyl) O,O-diethyl thiophosphate

B

thiophosphoric acid O-[6a,12a-dichloro-9-(diethoxy-thiophosphoryloxy)-6b,12b-dimethyl-6,12-dioxo-6a,12,12a,12b-tetrahydro-6H,6bH-5,11-dioxa-dibenzo[a,b]biphenylen-3-yl] ester O',O''-diethyl ester

thiophosphoric acid O-[6a,12a-dichloro-9-(diethoxy-thiophosphoryloxy)-6b,12b-dimethyl-6,12-dioxo-6a,12,12a,12b-tetrahydro-6H,6bH-5,11-dioxa-dibenzo[a,b]biphenylen-3-yl] ester O',O''-diethyl ester

C

thiophosphoric acid O-[6a,12a-dichloro-9-(diethoxy-thiophosphoryloxy)-6b,12b-dimethyl-6,12-dioxo-6a,12,12a,12b-tetrahydro-6H,6bH-5,11-dioxa-dibenzo[a,b]biphenylen-3-yl] ester O',O''-diethyl ester

thiophosphoric acid O-[6a,12a-dichloro-9-(diethoxy-thiophosphoryloxy)-6b,12b-dimethyl-6,12-dioxo-6a,12,12a,12b-tetrahydro-6H,6bH-5,11-dioxa-dibenzo[a,b]biphenylen-3-yl] ester O',O''-diethyl ester

Conditions
ConditionsYield
With sodium dodecyl-sulfate In phosphate buffer at 30℃; pH=7.4; Dimerization; UV-irradiation;
coumaphos
56-72-4

coumaphos

A

3-chloro-4-methylumbelliferone
6174-86-3

3-chloro-4-methylumbelliferone

B

O,O'-diethyl thiophosphoric acid
2465-65-8

O,O'-diethyl thiophosphoric acid

Conditions
ConditionsYield
With sodium perchlorate; cycloplatinated aryl ketoxime In acetonitrile at 25℃; pH=8.5; Kinetics;
methanol
67-56-1

methanol

coumaphos
56-72-4

coumaphos

Thiophosphorsaeure-O,O-diethyl-O-methylester
15959-01-0

Thiophosphorsaeure-O,O-diethyl-O-methylester

Conditions
ConditionsYield
With triethylamine; Pd(dmba)(py)(OTf) at 25℃; pH=10.80; Kinetics;
coumaphos
56-72-4

coumaphos

A

Coralox
321-54-0

Coralox

B

3-chloro-4-methylumbelliferone
6174-86-3

3-chloro-4-methylumbelliferone

C

phosphonic acid diethyl ester
762-04-9

phosphonic acid diethyl ester

Conditions
ConditionsYield
With water; dihydrogen peroxide In ethanol at 40℃; Kinetics; Temperature; Reagent/catalyst;

56-72-4Relevant articles and documents

Analogues with fluorescent leaving groups for screening and selection of enzymes that efficiently hydrolyze organophosphorus nerve agents

Brise?o-Roa, Luis,Hill, Jim,Notman, Stuart,Sellers, David,Smith, Andy P.,Timperley, Christopher M.,Wetherell, Janet,Williams, Nichola H.,Williams, Gareth R.,Fersht, Alan R.,Griffiths, Andrew D.

, p. 246 - 255 (2007/10/03)

Enzymes that efficiently hydrolyze highly toxic organophosphorus nerve agents could potentially be used as medical countermeasures. As sufficiently active enzymes are currently unknown, we synthesized twelve fluorogenic analogues of organophosphorus nerve agents with the 3-chloro-7-oxy-4- methylcoumarin leaving group as probes for high-throughput enzyme screening. This set included analogues of the pesticides paraoxon, parathion, and dimefox, and the nerve agents DFP, tabun, sarin, cyclosarin, soman, VX, and Russian-VX. Data from inhibition of acetylcholinesterase, in vivo toxicity tests of a representative analogue (cyclosarin), and kinetic studies with phosphotriesterase (PTE) from Pseudomonas diminuta, and a mammalian serum paraoxonase (PON1), confirmed that the analogues mimic the parent nerve agents effectively. They are suitable tools for high-throughput screens for the directed evolution of efficient nerve agent organophosphatases.

Compositions against wood-destroying insects

-

, (2008/06/13)

The present invention relates to long-acting compositions against wood-destroying insects, characterized in that they contain a) insecticidally active compounds, b) organic natural compounds or organic synthetic compounds or mixtures thereof as carrier material, c) optionally microbicidally active compounds, d) optionally attractants or development-inhibitory compounds for insects, e) and optionally formulation auxiliaries.

Biocidal macroemulsions containing polyvinyl alcohol

-

, (2008/06/13)

The present invention relates to new macroemulsions which contain 0.001 to 60 percent by weight of at least one active compound from the class comprising the phosphates and/or carbamates, 0 to 50 percent by weight of aromatic diluents, 0.001 to 20 percent by weight of polyvinyl alcohol having a mean molecular weight of between 5,000 and 150,000 and a content of acetate groups of between 2 and 30 mol %, and/or 0.001 to 20 percent by weight of a nonlphenol/propylene oxide/ethylene oxide adduct of the formula STR1 in which X represents integers from 10 to 50 and Y represents integers from 15 to 65, and/or 0.001 to 20 percent by weight of ethylene oxide/propylene oxide/ethylene oxide block copolymers having a mean molecular weight of between 2,000 and 8,000 and HLB values of between 8 and 30, and water and, if appropriate, additives, and in which the oil phase is dispersed in the aqueous phase in the form of droplets having a mean particle diameter of 0.1 to 3.0 μm.

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