Basic information Safety Supplier Related

4-(PHENYLAZO)DIPHENYLAMINE

Basic information Safety Supplier Related

4-(PHENYLAZO)DIPHENYLAMINE Basic information

Product Name:
4-(PHENYLAZO)DIPHENYLAMINE
Synonyms:
  • 4-(phenylamino)azobenzene
  • 4-(phenylazo)-diphenylamin
  • 4-anilino-azobenzen
  • Azobenzene, 4-anilino-
  • Diphenylamine, 4-(phenylazo)-
  • N-Phenyl-4-[(E)-phenyldiazenyl]aniline
  • N-Phenyl-4-aminoazobenzene
  • 4-Azobenzeneaniline
CAS:
101-75-7
MF:
C18H15N3
MW:
273.33
EINECS:
202-972-3
Product Categories:
  • Azo
  • Anilines, Aromatic Amines and Nitro Compounds
Mol File:
101-75-7.mol
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4-(PHENYLAZO)DIPHENYLAMINE Chemical Properties

Melting point:
87-91 °C
Boiling point:
406.35°C (rough estimate)
Density 
1.0332 (rough estimate)
refractive index 
1.5480 (estimate)
solubility 
Solubility Insoluble in water; soluble in ethanol, methanol
pka
0.42(at 25℃)
form 
Fine Crystalline Powder
color 
Orange
PH Range
Red (1.2) to yellow (2.5)
λmax
411nm, 272nm
BRN 
749359
Major Application
Display device, nonlinear optial (NLO) material, photoresists, printing plates, lithographic plates, photosensitive materials, photography, markers
InChI
InChI=1S/C18H15N3/c1-3-7-15(8-4-1)19-16-11-13-18(14-12-16)21-20-17-9-5-2-6-10-17/h1-14,19H
InChIKey
VXLFYNFOITWQPM-UHFFFAOYSA-N
SMILES
C1(NC2=CC=CC=C2)=CC=C(N=NC2=CC=CC=C2)C=C1
CAS DataBase Reference
101-75-7(CAS DataBase Reference)
EPA Substance Registry System
Benzenamine, N-phenyl-4-(phenylazo)- (101-75-7)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
3234
WGK Germany 
1
RTECS 
JK0185000
TSCA 
Yes
HS Code 
29270000
Toxicity
LD50 ivn-mus: 56 mg/kg CSLNX* NX#03760

MSDS

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4-(PHENYLAZO)DIPHENYLAMINE Usage And Synthesis

Chemical Properties

orange fine crystalline powder

Uses

4-(Phenylazo)diphenylamine is a soluble azo dye and stain. Dyes and metabolites.

Safety Profile

Poison by intravenous route. When heated to decomposition it emits toxic vapors of NOx.

Purification Methods

Purify the dye by chromatography on neutral alumina using dry *C6H6 with 1% of dry MeOH. The major component, which gave a stationary band, is cut out and eluted with EtOH or MeOH. [H.gfeldt & Bigeleisen J Am Chem Soc 82 15 1960.] It crystallises from pet ether, EtOH or aqueous EtOH, and has max at 420nm ( 28,000) (aqueous EtOH) and 540nm (aqueous EtOH/H2SO4) [Badger et al. J Chem Soc 1888 1954, Beilstein 16 H 314, 16 III 343, 16 IV 457.]

4-(PHENYLAZO)DIPHENYLAMINESupplier

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