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FAMPHUR

Basic information Safety Supplier Related

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
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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)
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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)
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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

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