CHLORMEPHOS Property

Melting point:

25°C

Boiling point:

bp1mm 93-95°; bp0.1 Torr 81-85°

Density 

d20 1.260

vapor pressure 

7.6 Pa (30 °C)

refractive index 

nD220 1.5244

Flash point:

100 °C

storage temp. 

0-6°C

Water Solubility 

60 mg l^-1(20 °C)

form 

liquid

EPA Substance Registry System

Chlormephos (24934-91-6)

Safety

Hazard Codes 

T+,N

Risk Statements 

27/28-50/53

Safety Statements 

28-36/37-45-60-61-27

RIDADR 

3018

RTECS 

TD5170000

HazardClass 

6.1(a)

PackingGroup 

II

Hazardous Substances Data

24934-91-6(Hazardous Substances Data)

Toxicity

LD50 in rats (mg/kg): 7 orally; 27 dermally; LC50 in fish: 1.5 mg/l (Lynch)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P391Collect spillage. Hazardous to the aquatic environment

P501Dispose of contents/container to..…

CHLORMEPHOS Chemical Properties,Usage,Production

Description

Chlormephos is an organophosphate, colorlessliquid. Molecular weight=234.70; Boiling point =81-85℃ at 0.1 mmHg. Hazard Identification (based onNFPA 704 M Rating System): Health 3, Flammability 2,Reactivity 0. Soluble in water; solubility=60 mg/L at20℃.

Uses

Insecticide primarily for soil applications.

Uses

Chlormephos is used to control soil insects such as wireworms in a number of crops.

Uses

Chlormefos has agricultural applications. Useful for preparing compositions for controlling plant diseases.

Definition

ChEBI: Chlormephos is an organic thiophosphate, an organothiophosphate insecticide and an organochlorine insecticide. It has a role as an agrochemical and an EC 3.1.1.7 (acetylcholinesterase) inhibitor.

General Description

Colorless liquid. Used as a soil insecticide. Not registered as a pesticide in the U.S.

Air & Water Reactions

Slightly soluble in water [Farm Chemicals Handbook].

Reactivity Profile

Organophosphates, such as CHLORMEPHOS, 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.

Health Hazard

(Non-Specific -- Organophosphorus Pesticide, Liquid, n.o.s.) CHLORMEPHOS is poisonous; it may be fatal if inhaled, swallowed, or absorbed through the skin.

Fire Hazard

(Non-Specific -- Organophosphorus Pesticide, Liquid, n.o.s.) Container may explode in heat of fire. Fire and runoff from control water may produce irritating or poisonous gases.

Potential Exposure

This material is a soil insecticide. Notregistered as a pesticide in the US.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Speed in removing material from skinis of extreme importance. Shampoo hair promptly if contaminated. Seek medical attention immediately. If this chemicalhas been inhaled, remove from exposure, begin rescuebreathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart actionhas stopped. Transfer promptly to a medical facility. Whenthis chemical has been swallowed, get medical attention.Give large quantities of water and induce vomiting. Do notmake an unconscious person vomit. Medical observation isrecommended for 24-48 h after breathing overexposure, aspulmonary edema may be delayed. As first aid for pulmonary edema, a doctor or authorized paramedic may consideradministering a corticosteroid spray.

Metabolic pathway

Chlormephos is a soil insecticide with considerable vapour phase activity. The main soil metabolite is ethion. The mechanism of hydrolysis of chlormephos is mainly by the nucleophilic attack of OH- on the Smethylene carbon to yield O,O-diethyl phosphorodithioate and in this respect it is similar to mecarbam. This mechanism may afford ethion when the nucleophile is O,O-diethyl phosphorodithioate. The other mechanism of hydrolysis is by attack on phosphorus to yield O,O-diethyl phosphorothioate and these two routes of hydrolytic degradation apparently dominate the metabolism of the insecticide.

Metabolism

In soils, chlormephos is converted to ethion by reaction with the hydrolytic product, O,O-diethyl hydrogen phosphorothioate.

storage

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working withChlormephos you should be trained on its proper handlingand storage. Should be protected from moisture and storedin glass-lined or polyethylene-lined containers. Keep awayfrom strong oxidizers. Sources of ignition, such as smokingand open flames, are prohibited where this chemical isused, handled, or stored in a manner that could create apotential fire or explosion hazard.

Shipping

This chemical requires a shipping label of“POISONOUS/TOXIC MATERIALS” for organophosphorus pesticides, liquid, toxic. It falls in Hazard Class6.1.

Toxicity evaluation

The acute oral LD₅₀ for rats is 7 mg/kg. NOEL (90 d) for rats is 0.39 mg/kg diet (0.002 mg/kg/d). In rats, orally administered chlormephos is almost completely eliminated within 24 h in the urine as diethyl hydrogen phosphate and O,O-diethyl hydrogen phosphorothioate.

Degradation

In strongly basic solution (0.5 M aqueous KOH), hydroxide ion attack on chlormephos may occur on the phosphorus atom with P-C bond cleavage to yield O,O-diethyl phosphorothioate (2) or on the S-methylene carbon atom to give O,O-diethyl phosphorodithioate (3), both of which may react with chlormephos to give further products. Hudson et al. (1991) showed that both hydrolysis products 2 and 3 could react with chlormephos via attact on the ethoxy group to yield the transethylation products O,O,Striethyl phophorothioate (4) and O,O,S-triethyl phophoroditluoate (5) respectively. Compound 3 could also attack the phosphorus atom of chlormephos to yield O,O,O’,O’-tetraethyl trithiopyrophosphate (6) and the S-methylene carbon to give ethion (7). Reaction products were identified by GC-MS after conversion of the acidic products into their methyl esters by reaction with diazomethane. Routes by which these products may be formed in strongly basic solution are shown in Scheme 1.

Incompatibilities

Contact with oxidizers may cause therelease of phosphorous oxides. Contact with strong reducingagents, such as hydrides, may cause the formation of flammable and toxic phosphine gas. Contact with alkaline materials causes rapid hydrolysis. May corrode metals.