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ChemicalBook >> CAS DataBase List >>Fenpropathrin

Fenpropathrin suppliers

Fenpropathrin

CAS:
39515-41-8
MF:
C22H23NO3
MW:
349.42

Company Type

Properties

Melting point:
47 °C
Boiling point:
483.6°C (rough estimate)
Density 
1.1700 (rough estimate)
refractive index 
nD26 1.5283
Flash point:
100 °C
storage temp. 
-20°C
solubility 
DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 15 mg/ml
form 
A solid
Water Solubility 
14.24ug/L(temperature not stated)

Safety Information

Symbol(GHS) 
GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS09
Signal word 
Danger
Hazard statements 
H301-H312-H330-H410
Precautionary statements 
P260-P264-P273-P280-P302+P352+P312-P304+P340+P310
Hazard Codes 
T+,N
Risk Statements 
21-25-26-50/53
Safety Statements 
28-36/37-38-45-60-61
RIDADR 
UN 2811 6.1/PG 2
RTECS 
GZ2090000
HS Code 
29269090
Toxicity
LC50 (24 hr) in rainbow trout: 76.7 ppb (Coats); LD50 in rats (mg/kg): 2.5 i.v. (Verschoyle); in male, female rats (mg/kg): 24-36, 18-24 orally (Crawford)

Use

A pyrethroid. Fenpropathrin is an ester and nitrile. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Nitriles may polymerize in the presence of metals and some metal compounds. They are incompatible with acids; mixing nitriles with strong oxidizing acids can lead to extremely violent reactions. Nitriles are generally incompatible with other oxidizing agents such as peroxides and epoxides. The combination of bases and nitriles can produce hydrogen cyanide. Nitriles are hydrolyzed in both aqueous acid and base to give carboxylic acids (or salts of carboxylic acids). These reactions generate heat. Peroxides convert nitriles to amides. Nitriles can react vigorously with reducing agents. Acetonitrile and propionitrile are soluble in water, but nitriles higher than propionitrile have low aqueous solubility. They are also insoluble in aqueous acids.

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