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537-67-7

537-67-7 Structure

537-67-7 Structure
IdentificationMore
[Name]

DIPHENYLAMINE HYDROCHLORIDE
[CAS]

537-67-7
[Synonyms]

DIPHENYLAMINE HYDROCHLORIDE
n-phenyl-benzenaminhydrochloride
diphenylammonium chloride
DiphenylamineHCl
N-PHENYLANILINE HYDROCHLORIDE
[EINECS(EC#)]

208-675-5
[Molecular Formula]

C12H12ClN
[MDL Number]

MFCD00042007
[Molecular Weight]

205.68
[MOL File]

537-67-7.mol
Chemical PropertiesBack Directory
[Appearance]

white crystalline powder
[Melting point ]

180 °C
[storage temp. ]

<0°C
[form ]

powder to crystal
[color ]

White to Almost white
[InChIKey]

JEFJSEIUEJBMSR-UHFFFAOYSA-N
[CAS DataBase Reference]

537-67-7(CAS DataBase Reference)
[EPA Substance Registry System]

Benzenamine, N-phenyl-, hydrochloride (537-67-7)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
[HS Code ]

2921.44.7000
Hazard InformationBack Directory
[Chemical Properties]

white crystalline powder
[Uses]

Diphenylamine hydrochloride (N-Phenylaniline hydrochloride) is an antihyperglycemic agent with oral activity and a common structure in non-steroidal anti-inflammatory drugs (NSAIDs) that uncouples oxidative phosphorylation in mitochondria, leading to a decrease in hepatic cell ATP levels and causing liver cell damage. Diphenylamine hydrochloride is also an industrial antioxidant, a dyeing mordant, and is used in agriculture as an antifungal and antibacterial agent[1][2][3][4].
[in vivo]

Diphenylamine hydrochloride is excreted in rats through urine and bile[1].
Diphenylamine (10 mg/kg, orally, single dose) hydrochloride lowers blood sugar in hyperglycemic rabbits[2].

Animal Model:Hyperglycemic rabbit[2]
Dosage:10 mg/kg; single dose
Administration:Oral
Result:Reduced blood sugar by 61.4% two hours after administration.
[References]

[1] W E Alexander, et al. Metabolism of diphenylamine in the rat, rabbit and man. Food Cosmet Toxicol. 1965 Oct;3(4):571-9. DOI:10.1016/s0015-6264(65)80203-6
[2] M S Karawya, wt al. Diphenylamine, an antihyperglycemic agent from onion and tea. J Nat Prod. 1984 Sep-Oct;47(5):775-80. DOI:10.1021/np50035a003
[3] Safe S, et al. Identification of toxic impurities in commercial diphenylamine. Bull Environ Contam Toxicol. 1977 Feb;17(2):204-7. DOI:10.1007/BF01685551
[4] Masubuchi Y, et al. Possible mechanism of hepatocyte injury induced by diphenylamine and its structurally related nonsteroidal anti-inflammatory drugs. J Pharmacol Exp Ther. 2000 Mar;292(3):982-7. PMID:10688613
Spectrum DetailBack Directory
[Spectrum Detail]

DIPHENYLAMINE HYDROCHLORIDE(537-67-7)1HNMR
DIPHENYLAMINE HYDROCHLORIDE(537-67-7)IR1
DIPHENYLAMINE HYDROCHLORIDE(537-67-7)IR2
Well-known Reagent Company Product InformationBack Directory
[TCI AMERICA]

Diphenylamine Hydrochloride,>99.0%(LC)(N)(537-67-7)
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