Chemical Properties of 1,4-Benzenediamine, N-phenyl- (CAS 101-54-2)

1,4-Benzenediamine, N-phenyl-

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InChI
InChI=1S/C12H12N2/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9,14H,13H2
InChI Key
ATGUVEKSASEFFO-UHFFFAOYSA-N
Formula
C12H12N2
SMILES
Nc1ccc(Nc2ccccc2)cc1
Molecular Weight1
184.24
CAS
101-54-2
Other Names
  • 1,4-Benzenediamine, N1-phenyl-
  • 4-(Phenylamino)aniline
  • 4-Aminodiphenylamine
  • Acna Black DF Base
  • Azosalt R
  • C.I. 37240
  • C.I. 76085
  • C.I. Azoic Diazo Component 22
  • C.I. Developer 15
  • C.I. Oxidation Base 2
  • Diphenyl Black
  • Diphenylamine, 4-amino-
  • Diphenylamine, p-amino-
  • Fast Blue R Salt
  • Luxan Black R
  • N-(4-Aminophenyl)aniline
  • N-4'-Bianiline
  • N-Fenyl-p-fenylendiamin
  • N-Phenyl-1,4-benzenediamine
  • N-Phenyl-1,4-phenylenediamine
  • N-Phenyl-p-aminoaniline
  • N-Phenyl-p-phenylenediamine
  • NCI-C02233
  • NSC 3401
  • Naphthoelan Navy Blue
  • Oxy Acid Black Base
  • Peltol BR
  • Peltol BR II
  • Semidin
  • Semidine
  • UBOB
  • Variamine Blue RT
  • Variamine Blue Salt RT
  • p-(Phenylamino)aniline
  • p-Aminodifenylamin
  • p-Aminodiphenylamine
  • p-Anilinoaniline
  • p-Phenylenediamine, N-phenyl-
  • p-Semidine
Sources

Physical Properties

Property Value Unit Source
Δf 421.19 kJ/mol Joback Calculated Property
Δfgas 257.84 kJ/mol Joback Calculated Property
Δfus 24.83 kJ/mol Joback Calculated Property
Δvap 64.60 kJ/mol Joback Calculated Property
logPoct/wat 3.01 Crippen Calculated Property
Pc 3659.77 kPa Joback Calculated Property
Tboil 627.00 K NIST
Tboil 428.00 K NIST
Tc 910.40 K Joback Calculated Property
Tfus 339.00 K NIST
Vc 0.56 m3/kg-mol Joback Calculated Property

Temperature Dependent Properties

Property Value Unit Temperature (K) Source
Cp,gas 384.08 J/mol×K 655.0 Joback Calculated Property

Molecular Descriptors

Joback and Reid Groups
=C< (ring) 3
=CH- (ring) 9
-NH2 1
>NH 1

Similar Compounds

Diphenylamine, 4-amino-, mono-hydrochloride. 1,4-Benzenediamine, N,N'-diphenyl-. Benzenamine, n-phenyl-, hydrochloride. Diphenylamine. Benzenamine, 4-nitroso-N-phenyl-. Benzenamine, N,N-diphenyl-. 1,3-Benzenediamine, n,n'-diphenyl-, monohydrochloride. Benzenamine, n-phenyl-4-(phenylazo)-. N,N'-di-2-Naphthyl-p-phenylenediamine. p,p'-Ditolylamine. Benzenamine, 4-methyl-N-phenyl-. P-phenylenediamine, n-isopropyl-n'-phenyl-. Phenol, 4-(phenylamino)-. P-phenylenediamine, n,n'-dimethyl-n,n'-diphenyl-. 1,2-Benzenediamine, N-phenyl-.

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