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ChemicalBook--->CAS DataBase List--->41198-08-7

41198-08-7

41198-08-7 Structure

41198-08-7 Structure
IdentificationMore
[Name]

Profenofos
[CAS]

41198-08-7
[Synonyms]

CURACRON
CURACRON(R)
FERTIFENOPHOS
FORNOFOS
O-(4-BROMO-2-CHLOROPHENYL)-O-ETHYL-S-PROPYL PHOSPHOROTHIOATE
POLYCRON
POLYCRON(R)
PRAHAR
PROFENOFOS
PROFENOPHOS
PROFENPHOS
ROMIFOS
SANOFOS
Selecron
SELECRON(R)
cga15324
phosphorothioicacid,o-(4-bromo-2-chlorophenyl)-o-ethyl-s-propylester
S-n-Propyl-O-ethyl-O-2-chloro-4-bromo phenyl thiophosphate
Curacron(Ciba-Geigy) Polycron
Nonacron
[EINECS(EC#)]

255-255-2
[Molecular Formula]

C11H15BrClO3PS
[MDL Number]

MFCD00078736
[Molecular Weight]

373.63
[MOL File]

41198-08-7.mol
Chemical PropertiesBack Directory
[Melting point ]

<25 °C
[Boiling point ]

110°C (0.001 torr)
[density ]

d20 1.455
[vapor pressure ]

1.24×10-4 Pa (25 °C)
[refractive index ]

n20D 1.5466
[Fp ]

124℃
[storage temp. ]

APPROX 4°C
[solubility ]

DMSO: 50 mg/mL (133.82 mM)
[form ]

Oily Liquid
[Water Solubility ]

28 mg l-1 (25 °C)
[color ]

Colorless to light yellow
[Specific Gravity]

1.455 (20℃)
[Merck ]

13,7860
[BRN ]

2150258
[LogP]

4.2 at 25℃
[CAS DataBase Reference]

41198-08-7(CAS DataBase Reference)
[NIST Chemistry Reference]

Phosphorothioic acid, o-(4-bromo-2-chlorophenyl) o-ethyl s-propyl ester(41198-08-7)
[EPA Substance Registry System]

Profenofos (41198-08-7)
Safety DataBack Directory
[Hazard Codes ]

Xn,N,T
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R50/53:Very Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
R24:Toxic in contact with skin.
R20/22:Harmful by inhalation and if swallowed .
[Safety Statements ]

S36/37:Wear suitable protective clothing and gloves .
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 .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S9:Keep container in a well-ventilated place .
S7:Keep container tightly closed .
[RIDADR ]

3018
[WGK Germany ]

3
[RTECS ]

TE6975000
[HazardClass ]

6.1(b)
[PackingGroup ]

III
[HS Code ]

29309090
[Hazardous Substances Data]

41198-08-7(Hazardous Substances Data)
[Toxicity]

LD50 in rat (mg/kg): 358-400 orally; ~3300 dermally; LC50 (4 hr) in rat (mg/m3): ~3000 by inhalation (Buholzer); LC50 (96 hr) in rainbow fish: 0.91 mg/l (Kumar, Chapman).
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Government regulation-->Chlorobenzene-->EMULSIFIER-->THIOPHOSPHORYL CHLORIDE-->Solvent-->1-Bromopropane-->SULPHOSUCCINIC ACID ESTER-->Diethyl chlorothiophosphate-->2-Chlorophenol-->4-Bromo-2-chlorophenol-->POTASSIUM HYDROGENSULFIDE,-->Phenylphosphonic acid
[Preparation Products]

Prothiofos-->1-Propanesulfonic acid
Hazard InformationBack Directory
[General Description]

Pale yellow liquid with garlic-like odor. Corrosive. Used as an insecticide.
[Reactivity Profile]

Organophosphates 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 under alkaline conditions.
[Description]

Profenofos is a pale yellow liquid, bp 100 ?C/1.80 Pa, vp 0.124 mPa (25 ?C). Solubility in water is 28 mg/L (25 ?C). It is miscible with most organic solvents. Log Kow = 4.44. It is relatively stable in neutral and mild acid media but hydrolyzed in alkaline media; DT50 values (20 ?C) at pH 5, 7, and 9 are 93 d, 14.6 d, and 5.7 h, respectively.
[Chemical Properties]

Profenofos is a pale yellow liquid. Profenofos is relatively stable under neutral and slightly acidic conditions and unstable under alkaline conditions.Profenofos has a garlic-like odor.
Profenofos has limited solubility in water (28 mg/L at 25°C) but is completely soluble in organic solvents (ethanol, acetone, toluene, n-octanol and n-hexane) at 25°C.
[Uses]

A broad-spectrum organophosphorous pesticide that is used widely in cotton fields for insect control.
[Uses]

Insecticide; acaricide.
[Uses]

Profenofos is used to control insects (particularly caterpillars and Lepidoptera eggs) and mites on cotton, maize, sugar beet, soyabean, potatoes, vegetables, tobacco and a number of other crops
[Definition]

ChEBI: Profenofos is an organic thiophosphate, an organophosphate insecticide, an organochlorine insecticide and a member of monochlorobenzenes. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an acaricide and an agrochemical. It is functionally related to a 4-bromo-2-chlorophenol.
[Agricultural Uses]

Profenofos: Profenofos is A U.S. EPA restricted Use Pesticide (RUP) used solely on cotton to control a number of pests including tobacco budworm, cotton aphid and bollworm, armyworm, fleahopper and whiteflies. It is not registered for residential use. Not approved for use in EU countries. Registered for use in the U.S.
[Trade name]

CGA-15324®; CURACRON®; POLYCRON®; SELECRON®
[Carcinogenicity]

In a 2 year carcinogenicity study mice were given diets containing 0, 1, 30, or 100 ppm profenofos (equivalent to 0, 0.15, 4.5, or 15 mg/kg/day) for 85 weeks (males) or 97 weeks (females) . No treatment related clinical signs were observed. No treatment-related gross or microscopic lesions, tumors, or biologically significant differences in body weight or food consumption were observed between controls and profenofos-treated animals. Plasma and erythrocyte cholinesterase inhibition occurred at dose levels of 4.5 and 15 mg/kg/day. In another carcinogenicity study, rats were fed diets containing 0, 0.3, 10, or 100 ppm profenofos (equivalent to 0, 0.015, 0.5, or 5 mg/kg/day) for 2 years, and there was no increase in tumor incidence in any treated group compared to the control group .
[Environmental Fate]

Plant. Dislodgable residues of profenofos on cotton leaf 0, 24, 48, 72 and 96 hours after application (1.1 kg/ha) were 3.5, 1.1, 0.74, 0.51 and 0.35 μg/m2, respectively (Buck et al., 1980)
Photolytic. When profenofos in an aqueous buffer solution (pH 7.0) was exposed to filtered UV light (λ >290 nm) for 24 hours at 25 and 50°C, 29 and 61% respectively decomposed to 4-bromo-2-chlorophenol and 4-bromo-2-chlorophenyl ethyl hydrogen ph
Chemical/Physical. Emits toxic fumes of bromine, chlorine phosphorus and sulfur oxides when heated to decomposition (Sax and Lewis, 1987).
[Metabolic pathway]

The metabolic transformations of profenofos in plants and animals are similar and occur via hydrolysis to 4-bromo-2-chlorophenol which is then conjugated.
[Metabolism]

Profenofos orally administered to rats is rapidly excreted, mainly in the urine. The principal degradation route is hydrolysis to 4-bromo-2-chlorophenol followed by conjugation. DT50 in soil is about 1 week.
[Degradation]

Profenofos is stable under neutral and slightly acid conditions but it is hydrolysed in alkaline solution. The DT50 values at pH 5, 7 and 9 (20°C) were 93 days, 14.6 days and 5.7 hours, respectively (PM).
[Toxicity evaluation]

The acute oral LD50 for rats is 358 mg/kg. Inhalation LC50 (4 h) for rats is about 3 mg/L air. NOEL (2 yr) for rats is 0.3 mg/kg diet (0.015 mg/kg/d). ADI is 0.01 mg/kg b.w.
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

O-(4-Bromo-2-chlorophenyl)-O-ethyl-S-propyl phosphorothioate(41198-08-7).msds
Spectrum DetailBack Directory
[Spectrum Detail]

Profenofos(41198-08-7)MS
Profenofos(41198-08-7)IR1
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

41198-08-7(sigmaaldrich)
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