FAMPHUR
FAMPHUR Basic information
- Product Name:
- FAMPHUR
- Synonyms:
-
- BO-ANA
- FAMOPHOS
- FAMOPHOS(R)
- FAMPHUR
- O,O-DIMETHYL-O-P-(DIMETHYLSULFAMOYL)PHENYL PHOSPHOROTHIOATE
- WARBEXOL
- WARBEX(R)
- AC 38023
- CAS:
- 52-85-7
- MF:
- C10H16NO5PS2
- MW:
- 325.34
- EINECS:
- 200-154-0
- Mol File:
- 52-85-7.mol
FAMPHUR Chemical Properties
- Melting point:
- 53℃
- Boiling point:
- 394.2±52.0 °C(Predicted)
- Density
- 1.354±0.06 g/cm3(Predicted)
- vapor pressure
- 3 x 10-5 Pa (est. 20 °C)
- Flash point:
- >100 °C
- storage temp.
- APPROX 4°C
- Water Solubility
- 5000 (est. 20 °C)
- form
- Liquid
- pka
- -5.18±0.70(Predicted)
- Merck
- 13,3963
- BRN
- 2224254
- EPA Substance Registry System
- Famphur (52-85-7)
Safety Information
- Hazard Codes
- T,Xn,F
- Risk Statements
- 24/25-36/38-63-43-36/37/38-23/24/25-45-67-40-39/23/24/25-11
- Safety Statements
- 22-24/25-45-36/37-23-53-16-7
- RIDADR
- 2783
- WGK Germany
- 3
- RTECS
- TF7650000
- HazardClass
- 6.1(a)
- PackingGroup
- II
- HS Code
- 29350090
- Hazardous Substances Data
- 52-85-7(Hazardous Substances Data)
- Toxicity
- LD50 orally in rats: 35 mg/kg (Schafer)
FAMPHUR Usage And Synthesis
Chemical Properties
Crystalline powder. Very soluble in chloroform and carbon tetrachloride; slightly soluble in water.
Uses
Insecticide.
Definition
ChEBI: Famphur 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 anthelminthic drug. It is functionally related to a 4-hydroxy-N,N-dimethylbenzenesulfonamide.
General Description
Crystalline powder. Very toxic. Cholinesterase inhibitor. Restricted use as insecticide.
Air & Water Reactions
Slightly soluble in water.
Reactivity Profile
Organothiophosphates, such as FAMPHUR, 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.
Hazard
Cholinesterase inhibitor, use may be restricted.
Metabolism
The principal degradation routes in mammals are P?Ophenyl bond cleavage and O-demethylation. Oxidative desulfuration and N-demethylation also take place to form toxic metabolites.
Toxicity evaluation
The acute oral LD50 for rats is 35–62 mg/kg.
FAMPHURSupplier
- Tel
- info@syntechem.com
- Tel
- 400-1166-196 18981987031
- cdhxsj@163.com
- Tel
- 021-021-021-67601398-809-809-809 15221380277
- marketing_china@spectrumchemical.com
- Tel
- 025-57798810
- sales@sunlidabio.com
- Tel
- 022-65378550-8551
- contact@altascientific.com
FAMPHUR(52-85-7)Related Product Information
- ATRAZINE-DESETHYL
- Trichlorfon
- ATRAZINE SOLUTION 100UG/ML IN T-BUTYLMETHYL ETHER 1ML
- Prometryn
- ETOXAZOLE
- CYFLUFENAMID
- FAMPHUR
- 4-Hydroxybenzenesulfonamide
- Cythioate
- TRIMETHYL THIOPHOSPHATE
- FAMPHUR-O-ANALOG,FAMPHUR-O-ANALOGUE,FAMPHUR-OXON
- P-HYDROXY-N,N-DIMETHYLBENZENE SULFONAMIDE
- N,N-Dipentyl-p-hydroxybenzenesulfonamide O,O-dimethyl phosphorothioate
- FAMPHUR SOLUTION 5X1ML
- FAMPHUR SOLUTION 100UG/ML IN ISOOCTANE 5X1ML
- FAMPHUR MIX 5X1ML MEOH 100UG/ML
- FAMPHUR SOLUTION 100UG/ML IN ISOOCTANE 5ML
- FAMPHUR SOLUTION 100UG/ML IN ISOOCTANE 1ML