Fenuron
Title: Fenuron
CAS Registry Number: 101-42-8
CAS Name: N,N-Dimethyl-N-phenylurea
Additional Names: N-phenyl-N¢,N¢-dimethylurea
Trademarks: Dybar (DuPont)
Molecular Formula: C9H12N2O
Molecular Weight: 164.20
Percent Composition: C 65.83%, H 7.37%, N 17.06%, O 9.74%
Line Formula: C6H5NHCON(CH3)2
Literature References: Prepn: Crosby, Niemann, J. Am. Chem. Soc. 76, 4458 (1954); Gilbert, Sorma, US 2729677 (1956 to Allied Chem.); Jones, US 2768971 (1956 to ICI); Applegath et al., US 2857430 (1958 to Monsanto). Prepn of trichloroacetate: Gilbert et al., US 2782112 (1957 to Allied Chem.). Toxicity data: G. W. Bailey, J. L. White, Residue Rev. 10, 97 (1965).
Properties: Crystals, mp 131-133°. Sparingly sol in water (0.29% at 24°); in hydrocarbons. LD50 orally in rats: 7500 mg/kg (Bailey, White).
Melting point: mp 131-133°
Toxicity data: LD50 orally in rats: 7500 mg/kg (Bailey, White)
 
Derivative Type: Trichloroacetate
Additional Names: Fenuron TCA
Trademarks: Urab (Hopkins)
Molecular Formula: C10H14Cl3N2O3
Molecular Weight: 316.59
Percent Composition: C 37.94%, H 4.46%, Cl 33.60%, N 8.85%, O 15.16%
Properties: mp 65-68°. Esp effective in woody plant control.
Melting point: mp 65-68°
 
CAUTION: If hydrolyzed to aniline can cause methemoglobinemia: Clinical Toxicology of Commercial Products, R. E. Gosselin et al., Eds. (Williams & Wilkins, Baltimore, 5th ed., 1984) Section II, p 331.
Use: Herbicide.

Others monographs:
tert-Butyl HypochloriteNicofuranoseResibufogeninVinylidene Chloride
Methysergiden-HexaneGold TrichlorideDiponium Bromide
MonensinCinerinsAmmonium Ferric ChromateFormamide
Oil of Cherry LaurelLanthanum CarbonateChlorophyllThimerfonate Sodium
©2016 DrugLead US FDA&EMEA