Urea,N-(aminoiminomethyl)-N'-(4-nitrophenyl)-, hydrochloride (1:1)

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Names

[ CAS No. ]:
51-58-1

[ Name ]:
Urea,N-(aminoiminomethyl)-N'-(4-nitrophenyl)-, hydrochloride (1:1)

[Synonym ]:
N-carbamimidoyl-N'-(4-nitro-phenyl)-urea,hydrochloride
Nitroguanil
N-Carbamimidoyl-N'-(4-nitro-phenyl)-harnstoff,Hydrochlorid

Chemical & Physical Properties

[ Boiling Point ]:
421.2ºC at 760mmHg

[ Molecular Formula ]:
C8H9ClN5O3-

[ Molecular Weight ]:
258.64200

[ Flash Point ]:
208.5ºC

[ Exact Mass ]:
258.03900

[ PSA ]:
136.82000

[ Index of Refraction ]:
1.695

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
YR8166000
CHEMICAL NAME :
Urea, 1-amidino-3-(p-nitrophenyl)-, monohydrochloride
CAS REGISTRY NUMBER :
51-58-1
LAST UPDATED :
199709
DATA ITEMS CITED :
3
MOLECULAR FORMULA :
C8-H9-N5-O3.Cl-H
MOLECULAR WEIGHT :
259.68
WISWESSER LINE NOTATION :
WNR DMVMYZUM &GH

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
240 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
PJPPAA Polish Journal of Pharmacology and Pharmacy. (ARS Polona, POB 1001, 00-068 Warsaw 1, Poland) V.25- 1973- Volume(issue)/page/year: 38,425,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
225 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JMCMAR Journal of Medicinal Chemistry. (American Chemical Soc., Distribution Office Dept. 223, POB POB 57136, West End Stn., Washington, DC 20037) V.6- 1963- Volume(issue)/page/year: 10,521,1967 ** REPRODUCTIVE DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
35 mg/kg
SEX/DURATION :
female 7 day(s) pre-mating
TOXIC EFFECTS :
Reproductive - Fertility - female fertility index (e.g. # females pregnant per # sperm positive females; # females pregnant per # females mated)
REFERENCE :
TXAPA9 Toxicology and Applied Pharmacology. (Academic Press, Inc., 1 E. First St., Duluth, MN 55802) V.1- 1959- Volume(issue)/page/year: 13,228,1968

Precursor & DownStream

Precursor

DownStream

  • 1-ethyl-3-(4-nitrophenyl)-1-phenylurea
  • Urea,N-(4-nitrophenyl)-N'-phenyl-
  • Urea,N-methyl-N'-(4-nitrophenyl)-N-phenyl-

Related Compounds

  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 2-Amino-4-(2-nitrophenyl)butyric acid
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • 4-Methyl-2-[(4-methylpyrimidin-2-yl)disulfanyl]pyrimidine
  • tert-Butyl-DL-alanine