N-phenyl-p-phenylenediamine

p-phenylenediamine, N-phenyl-

CAS: 101-54-2 C12 H12 N2 MW: 184.24164000

Identification

Name	N-phenyl-p-phenylenediamine
CAS Number	101-54-2
EINECS	202-951-9
FDA UNII	007X4XXS71
Molecular Formula	C12 H12 N2
Molecular Weight	184.24164000
MDL Number	MFCD00007850
Nikkaji Number	J4.017G
Beilstein	908935
XlogP3	2.50 (est)

Regulatory

Physical Properties

Appearance	purple-black solid or flake (est)
Assay	95.00 to 100.00
Food Chemicals Codex Listed	No
Melting Point	66.00 °C. @ 760.00 mm Hg
Boiling Point	354.00 °C. @ 760.00 mm Hg
Flash Point	388.00 °F. TCC ( 197.80 °C. ) (est)
logP (o/w)	1.290 (est)
Soluble in	water, 1453 mg/L @ 25 °C (est)

Cosmetic Information

CosIng	cosmetic data
Cosmetic Uses	hair dyeing agents

No sensory data available

Safety Information

Preferred SDS	View
Oral/Parenteral Toxicity	oral-cat LDLo 100 mg/kg
Dermal Toxicity	skin-rabbit LD50 > 5000 mg/kg
Inhalation Toxicity	Not determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Category	hair dyeing agents
Recommendation for N-phenyl-p-phenylenediamine usage levels up to	not for fragrance use.
Recommendation for N-phenyl-p-phenylenediamine flavor usage levels up to	not for flavor use.

TCI AMERICA

Moving Your Chemistry Forward

We continuously strive to advance our technology.

P0203 Azoic Diazo Component 22 >98.0%(HPLC)(T)

View All Website 1-800-423-8616 Sales-US@TCIchemicals.com;

Potential Uses

hair dyeing agents

Natural Occurrence

not found in nature

Synonyms

acna black DF base p- aminodifenylamin p- aminodiphenylamine N-(4- aminophenyl) aniline (c.i. 76085) N-(4- aminophenyl)aniline (4- aminophenyl)phenylamine azoic diazo component 22 azoic diazo no. 22 azosalt R 1,4- benzenediamine, N-phenyl- 1,4- benzenediamine, N1-phenyl- black base P c.i. 76085 C.I. azoic diazo component 22 C.I. developer 15 C.I. oxidation base 2 ci 76085 CI azoic diazo component 22 CI developer 15 CI oxidation base 2 developer 15 diphenyl black base P diphenylamine, 4-amino- diphenylamine, p-amino- fast blue R salt N- fenyl-p-fenylendiamin luxan black R naphthoelan navy blue oxidation base 2 oxy acid black base peltol BR N- phenyl-1,4-benzenediamine N- phenyl-1,4-phenylene diamine N- phenyl-1,4-phenylenediamine N- phenyl-1,4-phenylenediamine sulfate N- phenyl-p-aminoaniline 4-( phenylamino)aniline p-( phenylamino)aniline 1-N- phenylbenzene-1,4-diamine N- phenylbenzene-1,4-diamine p- phenylenediamine, N-phenyl- rodol gray B base p- semidine variamine blue RT variamine blue RT salt variamine blue salt RT Try the PubMed Search.