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Ethoprophos

Ethoprophos Structure
CAS No.
13194-48-4
Chemical Name:
Ethoprophos
Synonyms
PROPHOS;ETHOPROP;MOCAP;Profos;Ethoprofos;Jolt;Rovokil;vc9-104;v-c9-104;MOCAP(R)
CBNumber:
CB0155120
Molecular Formula:
C8H19O2PS2
Molecular Weight:
242.34
MOL File:
13194-48-4.mol
MSDS File:
SDS
Modify Date:
2024/3/14 15:18:25

Ethoprophos Properties

Melting point -13 °C
Boiling point 86-91°C
Density d420 1.094
vapor pressure 4.65 x 10-2 Pa (26 °C)
Flash point 100 °C
storage temp. APPROX 4°C
solubility DMF: 5mg/mL; DMSO: 5mg/mL; Ethanol: 1.6mg/mL
Water Solubility 700 mg l-1 (20 °C)
Merck 13,3782
BRN 8139788
Stability Hygroscopic
CAS DataBase Reference 13194-48-4(CAS DataBase Reference)
NIST Chemistry Reference Ethoprophos(13194-48-4)
EPA Substance Registry System Ethoprop (13194-48-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS09
Signal word  Danger
Hazard statements  H300+H310+H330-H317-H410
Precautionary statements  P262-P264-P273-P280-P302+P352+P310-P304+P340+P310
Hazard Codes  T+;N,N,T+
Risk Statements  25-26/27-43-50/53
Safety Statements  27-28-36/37/39-45-60-61-27/28
RIDADR  UN 2810
WGK Germany  3
RTECS  TE4025000
HazardClass  6.1(a)
PackingGroup  II
HS Code  29309090
Toxicity LC50 (96-hour) for rainbow trout 13.8 mg/L, bluegill sunfish 2.1 mg/L and goldfish 13.6 mg/L (Hartley and Kidd, 1987); acute oral LD50 for rats 262 mg/kg (Hartley and Kidd, 1987), 34 mg/kg (RTECS, 1985).
NFPA 704
0
4 0

Ethoprophos price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 45306 Ethoprophos PESTANAL?, analytical standard 13194-48-4 100MG ₹9655.9 2022-06-14 Buy
Product number Packaging Price Buy
45306 100MG ₹9655.9 Buy

Ethoprophos Chemical Properties,Uses,Production

Description

Introduced in the 1960s, ethoprop is a nonsystemic insecticide/nematicide. The mobility of ethoprop in soil and its half-life are strongly dependent on soil organic matter (21). It is not known to be carcinogenic and is available as granules or emulsifiable concentrates.

Chemical Properties

Ethoprophos is a pale yellow liquid.

Uses

Ethoprophos is an organophosphate non-systemic nematicide and soil insecticide. Ethoprophos is an acetylcholinesterase (AChE) inhibitor.

General Description

Ethorop is one of a family of organophosphorus pesticides. Mocap is combustible though Mocap may require some effort to ignite. Mocap is very toxic by skin absorption and inhalation. Mocap may or may not be water soluble.

Air & Water Reactions

Hydrolyzed in alkali.

Reactivity Profile

Organothiophosphates, such as Mocap, 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

Mocap is extremely toxic; the probable oral lethal dose for humans is 5-50 mg/kg, or between 7 drops and 1 teaspoonful for a 150 lb. person. It is a cholinesterase inhibitor which affects the nervous system.

Fire Hazard

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

Agricultural Uses

Nematicide, Insecticide: Ethoprop is used as a pre-plant soil application to control wireworms and nematodes in potatoes, sugar cane, sweet potatoes, and tobacco, with lesser usage on corn (field and sweet), beans (lima and snap), cucumbers, and cabbage. In addition, it is used to treat pineapples, bananas, and plantains, as well as fieldgrown ornamentals and non-bearing citrus trees, and commercial turf. Roughly 60% of ethoprop is applied to potatoes.

Trade name

AI3-27318®; CASWELL No. 434C®; JOLT®[C]; MENAP®; MOBIL V-C 9-104®; MOCAP®[C]; MOCAP 10G®[C]; PHOSETHOPROP®; ROVOKIL®; V-C 9-104®[C]; V-C CHEMICAL V-C 9-104®[C]; VIRGINIA-CAROLINA VC 9-104®

Safety Profile

Poison by ingestion and skin contact. A cholinesterase inhibitor type of insecticide. When heated to decomposition it emits very toxic fumes of POx and SOx. See also PARATHION.

Potential Exposure

A potential danger to those involved in the manufacture, formulation and application of this nematocide and soil insecticide

Carcinogenicity

In a combined chronic feeding/ carcinogenicity study, when rats were fed diets with 0, 1, 10, or 100 ppm ethoprop in the diet for 24 months (equivalent to 0, 0.041, 0.40, or 4.19 mg/kg/day (males); 0, 0.052, 0.51, or 5.12 mg/kg/day (females)), adrenal gland malignant pheochromocytomas were increased in males and thyroid C-cell carcinomas were increased slightly in males . When ethoprop was administered in the diet to mice for 104 weeks at 0, 0.2, 2.0, or 30 ppm (males: 0, 0.026, 0.254, or 3.96 mg/ kg/day; females: 0, 0.032, 0.318, or 4.9 mg/kg/day), survival was unaffected at any dose level and no statistically significant dose-related incidence of tumors were seen in males or females.

Environmental Fate

Soil. The reported half-life in humus-containing soil (pH 4.5) and a sandy loam (pH 7.2–7.3) are 87 and 14–28 days, respectively (Hartley and Kidd, 1987). The rate of degradation increased in soils that had been treated annually four times (Smelt et al., 1987).
Chemical/Physical. Emits toxic fumes of phosphorus and sulfur oxides when heated to decomposition (Sax and Lewis, 1987).

Metabolic pathway

Ethoprophos is a soil-acting insecticide and nematicide which is generally incorporated into the soil in the form of a granular formulation. Volatilisation is a factor involved in the loss and movement of the compound in the environment. The major route of degradation of ethoprophos in both plants and mammals is via hydrolysis to give O-ethyl S-propyl phosphorothioate through loss of propanethiol. Propanethiol has been shown to react as a nucleophile to yield ethyl propyl sulfide through attack on the phosphorus atom and dipropyl disulfide through attack on the sulfur atom of ethoprophos. The sulfide metabolites are further metabolised via oxidation to sulfoxides and sulfones. In mammals, an additional important route of detoxification is through de-ethylation via glutathione- S-alkyl transferase, a route common to many organophosphorus insecticides.

Shipping

UN3018 Organophosphorus pesticides, liquid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, and epoxides. Strong oxidizers may cause release of toxic phosphorus oxides. Organophosphates, in the presence of strong reducing agents such as hydrides, may form highly toxic and flammable phosphine gas. Keep away from alkaline materials

Waste Disposal

In accordance with 40CFR 165 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

Global( 127)Suppliers
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Appolo Biotech 08046051566 Gujarat, India 2 58 Inquiry
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Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
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