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Home > Encyclopedia > 2,4-Diaminotoluene

2,4-Diaminotoluene

2,4-Diaminotoluene structure

2,4-Diaminotoluene 

structure
  • CAS No:

    95-80-7

  • Formula:

    C7H10N2

  • Chemical Name:

    2,4-Diaminotoluene

  • Synonyms:

    1,3-Benzenediamine,4-methyl-;Toluene-2,4-diamine;4-Methyl-1,3-benzenediamine;2,4-Diaminotoluene;Fouramine J;Fourrine M;Fourrine 94;4-Methyl-m-phenylenediamine;Nako TMT;Pelagol J;Pelagol Grey J;Pontamine Developer TN;Renal MD;m-Toluenediamine;m-Tolylenediamine;2,4-Tolylenediamine;Zoba GKE;2,4-Diamino-1-methylbenzene;C.I. Oxidation Base 35;Eucanine GB;1,3-Diamino-4-methylbenzene;TDA;4-Methyl-1,3-phenylenediamine;Brown for Fur T;TDA (diamine);3-Amino-4-methylaniline;4-Methyl-1,3-diaminobenzene;2-Methyl-1,5-benzenediamine;12236-56-5;85898-88-0

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

brown crystalline powder, crystals or flakes Toluene-2,4-diamine takes the form of colorless needles.

2,4-Diaminotoluene Basic Attributes

122.17

122.17

2205839

202-453-1

29331990

Characteristics

52

0.35

Brown to dark gray Powder, Crystals and/or Chunks

1.05 (Liquid at 212°F)

99 °C

292 °C

149 °C

1.636

H2O: 50 g/l (25 ºC)

room temp

Vapour pressure, kPa at 106.5°C: 0.13

Relative vapour density (air = 1): 4.2

Abdominal snatch-rat LD50: 325 mg/kg; abdominal cavity-mouse LD50: 480 mg/kg

Open flame is flammable; high heat decomposes toxic nitrogen oxide fumes

Safety Information

III

6.1(b)

UN 1709 6.1/PG 3

3

45-21-25-36-43-51/53-68-62-48/22

53-45-61

XS9625000

T,N

The warehouse is ventilated, low temperature and dry; stored separately from oxidants, food additives and acids

Readily becomes oxidized in neutral or alkaline soln to form dark products

P201-P273-P280-P301 + P310-P308 + P313

H301-H312-H317-H341-H350-H361f-H373-H411

Toxicity

highly toxic

2,4-Diaminotoluene Use and Manufacturing

Methods of Manufacturing

Nitrification of p-nitrotoluene with mixed acid yields 2, 4-dinitrotoluene, which is then reduced with iron powder to obtain crude product, which is then concentrated and distilled to obtain finished product. Raw material consumption quota: p-nitrotoluene 1600kg/t, sulfuric acid (98%) 1616kg/t, nitric acid (98%) 760kg/t, iron powder (90%) 2700kg/t.

Uses

Aromatic amines likely to have high carcinogenic potency. QSARs of aromatic amines.

Computed Properties

Molecular Weight:122.17
XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Exact Mass:122.084398327
Monoisotopic Mass:122.084398327
Topological Polar Surface Area:52
Heavy Atom Count:9
Complexity:92.9
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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