- Product Name:
- Polycron E.C.
- Profenofos E.C.
- O-(4-bromo-2-chlorophenyl) O-ethyl S-propyl phosphorothioate profenofos (ISO)
- CGA 15324S
- O-Ethyl S-propyl O-(2-chloro-4-bromophenyl)thiophosphate
- Product Categories:
- Intermediates & Fine Chemicals
- Phosphorylating and Phosphitylating Agents
- Sulfur & Selenium Compounds
- Oeko-Tex Standard 100
- OrganophorousMethod Specific
- Alpha sort
- PON - PT
- Mol File:
Profenofos Chemical Properties
- Melting point:
- <25 °C
- Boiling point:
- 110°C (0.001 torr)
- d20 1.455
- vapor pressure
- 1.24×10-4 Pa (25 °C)
- refractive index
- n20D 1.5466
- Flash point:
- storage temp.
- APPROX 4°C
- Oily Liquid
- Water Solubility
- 28 mg l-1 (25 °C)
- Specific Gravity
- 1.455 (20℃)
- 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)
- Hazard Codes
- Risk Statements
- Safety Statements
- WGK Germany
- HS Code
- Hazardous Substances Data
- 41198-08-7(Hazardous Substances Data)
- 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).
- Language:English Provider:O-(4-Bromo-2-chlorophenyl)-O-ethyl-S-propyl phosphorothioate
Profenofos Usage And Synthesis
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.
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.
A broad-spectrum organophosphorous pesticide that is used widely in cotton fields for insect control.
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
Pale yellow liquid with garlic-like odor. Corrosive. Used as an insecticide.
Air & Water Reactions
Hydrolyzed under alkaline conditions.
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.
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.
CGA-15324®; CURACRON®; POLYCRON®; SELECRON®
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 .
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).
The metabolic transformations of profenofos in plants and animals are similar and occur via hydrolysis to 4-bromo-2-chlorophenol which is then conjugated.
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.
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.
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).
Profenofos Preparation Products And Raw materials
- 0513-85056018 13328062001
- 010-82848833 400-666-7788
- 400-1166196 18981987031
- 4008-755-333 18080918076
- 40%PROFENOFOS+BETA-CYPERMETHRIN EC
- PROFENOFOS SOLUTION 100UG/ML IN ACETONITRILE 1ML
- Ethyl acrylate
- O,O,S-trimethyl phosphorothioate
- O,O-dimethyl S-ethyl phosphorothioate
- Ethyl acetate
- Propyl butyrate
- Propyl gallate