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N-Methyldiphenylamine

Basic Information

  • CAS No.: 552-82-9

Physical properties

Product Description

Factory Sells Best Quality N-Methyldiphenylamine 552-82-9 with GMP standards

  • Molecular Formula: C13H13 N
  • Molecular Weight: 183.253
  • Appearance/Colour: yellow oil-like liquid 
  • Vapor Pressure: 0.00143mmHg at 25°C 
  • Melting Point: -7.6 ºC 
  • Refractive Index: n20/D 1.623(lit.) 
  • Boiling Point: 296-297 ºC 
  • PKA: 1.00±0.20(Predicted) 
  • Flash Point: 116.6 ºC 
  • PSA: 3.24000 
  • Density: 1.05 
  • LogP: 3.45450 

N-Methyldiphenylamine(Cas 552-82-9) Usage

Hazard

Toxic by ingestion.

General Description

N-Methyldiphenylamine is an aromatic tertiary amine. It undergoes transformation to N-methylcarbazole (C) via a photochemical reaction.

InChI:InChI=1/C13H13N/c1-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2-11H,1H3/p+1

552-82-9 Relevant articles

Three-Component Coupling Involving Arynes, Aromatic Tertiary Amines, and Aldehydes via Aryl-Aryl Amino Group Migration

Bhojgude, Sachin Suresh,Baviskar, Dnyaneshwar R.,Gonnade, Rajesh G.,Biju, Akkattu T.

, p. 6270 - 6273 (2015)

The transition-metal-free multicomponent...

Borane-Trimethylamine Complex as a Reducing Agent for Selective Methylation and Formylation of Amines with CO2

Zhang, Yanmeng,Zhang, He,Gao, Ke

supporting information, p. 8282 - 8286 (2021/10/25)

We report herein that a borane-trimethyl...

Effect of Precatalyst Oxidation State in C-N Cross-Couplings with 2-Phosphinoimidazole-Derived Bimetallic Pd(I) and Pd(II) Complexes

Martinez, Erin E.,Moreno, Mariur Rodriguez,Barksdale, Caleb A.,Michaelis, David J.

supporting information, p. 2763 - 2767 (2021/08/27)

We report the catalytic activity of two ...

Mesoionic N-heterocyclic olefin catalysed reductive functionalization of CO2for consecutiveN-methylation of amines

Das, Arpan,Maji, Subir,Mandal, Swadhin K.

, p. 12174 - 12180 (2021/09/28)

A mesoionic N-heterocyclic olefin (mNHO)...

Univariate classification of phosphine ligation state and reactivity in cross-coupling catalysis

Newman-Stonebraker, Samuel H.,Smith, Sleight R.,Borowski,Peters, Ellyn,Gensch, Tobias,Johnson, Heather C.,Sigman, Matthew S.,Doyle, Abigail G.

, p. 301 - 308 (2021/10/22)

Chemists often use statistical analysis ...

552-82-9 Process route

dichloromethane
75-09-2

dichloromethane

N-methylaniline
100-61-8

N-methylaniline

4,4'-methylenebis(N-methylaniline)
1807-55-2

4,4'-methylenebis(N-methylaniline)

benzhydrylidene(methyl)amine
552-82-9

benzhydrylidene(methyl)amine

N,N'-dimethyl-2,4'-diaminodiphenylmethane
4073-99-8

N,N'-dimethyl-2,4'-diaminodiphenylmethane

1,2,5,6-tetrahydro-1,5-dimethyl-3,4,7,8-dipheno-1,5-diazocine
7165-20-0

1,2,5,6-tetrahydro-1,5-dimethyl-3,4,7,8-dipheno-1,5-diazocine

Conditions
Conditions Yield
In benzene; at 15 ℃; for 48h; Further byproducts given; Irradiation;
12.7%
at 15 ℃; for 48h; Further byproducts given; Irradiation;
6.3%
4.1%
8.1%
N-methylaniline
100-61-8

N-methylaniline

4,4'-methylenebis(N-methylaniline)
1807-55-2

4,4'-methylenebis(N-methylaniline)

benzhydrylidene(methyl)amine
552-82-9

benzhydrylidene(methyl)amine

N,N'-dimethyl-2,4'-diaminodiphenylmethane
4073-99-8

N,N'-dimethyl-2,4'-diaminodiphenylmethane

1,2,5,6-tetrahydro-1,5-dimethyl-3,4,7,8-dipheno-1,5-diazocine
7165-20-0

1,2,5,6-tetrahydro-1,5-dimethyl-3,4,7,8-dipheno-1,5-diazocine

Conditions
Conditions Yield
With dichloromethane; at 15 ℃; for 48h; Further byproducts given; Irradiation;
6.3%
4.1%
8.1%

552-82-9 Upstream products

  • 67-56-1
    67-56-1

    methanol

  • 537-67-7
    537-67-7

    diphenylamine hydrochloride

  • 607-00-1
    607-00-1

    diphenylformamide

  • 603-52-1
    603-52-1

    ethyl diphenylcarbamate

552-82-9 Downstream products

  • 382165-80-2
    382165-80-2

    N-nitrosodiphenylamine

  • 68258-04-8
    68258-04-8

    N-methyl-N-phenylaniline N-oxide

  • 20349-66-0
    20349-66-0

    (4‐(methyl(phenyl)amino)phenyl)(phenyl)methanone

  • 73323-82-7
    73323-82-7

    2-(N-Methyl-N-phenylamino)-benzoic acid

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