ChemicalBook--->CAS DataBase List--->13194-48-4

13194-48-4

13194-48-4 Structure

13194-48-4 Structure
IdentificationMore
[Name]

Mocap
[CAS]

13194-48-4
[Synonyms]

EPHOPROPHOS(R)
ETHOPROP
Ethoprop(content>3%)
ETHOPROPHOS
Ethoprophos(content>3%)
Ethoprophos powder(content3%-10%)
ETHOPROPHOS(R)
Ethoprop powder
ETHOPROP(R)
MOCAP
MOCAP(R)
O-ETHYL-S,S-DIPROPYLPHOSPHORODITHIOATE
PHOPHOS(R)
PHOSETHOPROP
PROPHOS
ENT 27,318
ent27,318
Ethopropho
Jolt
MOBIL V-C 9-104
[EINECS(EC#)]

236-152-1
[Molecular Formula]

C8H19O2PS2
[MDL Number]

MFCD00055333
[Molecular Weight]

242.34
[MOL File]

13194-48-4.mol
Chemical PropertiesBack Directory
[Appearance]

Ethoprophos is a pale yellow liquid.
[Melting point ]

-13 °C
[Boiling point ]

86-91°C
[density ]

d420 1.094
[vapor pressure ]

4.65 x 10-2 Pa (26 °C)
[Fp ]

100 °C
[storage temp. ]

APPROX 4°C
[solubility ]

DMF: 5mg/mL; DMSO: 5mg/mL; Ethanol: 1.6mg/mL
[form ]

neat
[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]

13194-48-4(EPA Substance)
Safety DataBack Directory
[Hazard Codes ]

T+;N,N,T+
[Risk Statements ]

R25:Toxic if swallowed.
R26/27:Very Toxic by inhalation and in contact with skin .
R43:May cause sensitization by skin contact.
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
[Safety Statements ]

S27:Take off immediately all contaminated clothing .
S28:After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S60:This material and/or its container must be disposed of as hazardous waste .
S61:Avoid release to the environment. Refer to special instructions safety data sheet .
S27/28:After contact with skin, take off immediately all contaminated clothing and wash imediately with plenty of.... (to be specified by the manufacturer) .
[RIDADR ]

UN 2810
[WGK Germany ]

3
[RTECS ]

TE4025000
[HazardClass ]

6.1(a)
[PackingGroup ]

II
[HS Code ]

29309090
[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.
[Hazardous Substances Data]

13194-48-4(Hazardous Substances Data)
[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).
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethanol-->Phosphorus oxychloride-->Phosphorus pentasulfide-->SULPHOSUCCINIC ACID ESTER-->1-Bromopropane-->1-Propanethiol-->Ethyl dichlorophosphate-->Diethylphosphorodithioate-->Phosphorodithioic acid, mixed O,O-bis(1,3-dimethylbutyl and iso-Pr) esters, zinc salts-->potassium O-ethyl-S-propyldithiophosphate-->POTASSIUM HYDROGENSULFIDE,
[Preparation Products]

potassium O-ethyl-S-propyldithiophosphate
Hazard InformationBack Directory
[General Description]

Ethorop is one of a family of organophosphorus pesticides. ETHOPROPHOS(13194-48-4) is combustible though ETHOPROPHOS(13194-48-4) may require some effort to ignite. ETHOPROPHOS(13194-48-4) is very toxic by skin absorption and inhalation. ETHOPROPHOS(13194-48-4) may or may not be water soluble.
[Reactivity Profile]

Organothiophosphates, such as ETHOPROPHOS, 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.
[Air & Water Reactions]

Hydrolyzed in alkali.
[Health Hazard]

This material 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.
[Potential Exposure]

A potential danger to those involved in the manufacture, formulation and application of this nematocide and soil insecticide
[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.
[First aid]

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Speed in removing material from skin is of extreme importance. Shampoo hair promptly if contaminated. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit. Remove and isolate contaminated clothing and shoes at the site. Keep victim quiet and maintain normal body temperature. Effects may be delayed; keep victim under observation
[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
[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]

Clear Colorless Oil
[Chemical Properties]

Ethoprophos is a pale yellow liquid.
[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
[Uses]

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

Ethoprophos is used to control plant parasitic nematodes and soil insects.
[Uses]

Insecticide; nematocide.
[Uses]

Nonsystemic, nonfumigant nematocide and soil insecticide for control of insects in ornamentals, potatoes, sweet potatoes, tomatoes, strawberries, bananas, pineapples, sugar cane, turf and many other crops.
[Definition]

ChEBI:Ethoprophos is an organic thiophosphate and an organothiophosphate insecticide. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an agrochemical and an antinematodal drug.
[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®
[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.
[storage]

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling andstorage. Store in tightly closed containers in a cool, well-ventilated area. Where possible, automatically pump liquidfrom drums or other storage containers to processcontainers.
[Degradation]

Ethoprophos is very stable in neutral and weakly acidic media but it is hydrolysed rapidly in alkaline solutions (PM). The DT50 of ethoprophos in 0.05M NaOH solution at 25 °C was 35 min and the hydrolysis product was identified as O-ethyl S-propyl phosphorothioate (2), indicating the greater susceptibility of the P-S bond to hydrolysis over the P-O bond. There was no measurable hydrolysis in 0.1M HCl after 1 hour (Menzer et al., 1971). The route of the base-catalysed hydrolysis of ethoprophos is shown in Scheme 1.
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

13194-48-4(sigmaaldrich)
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