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m-Tolidine

m-Tolidine Structure
CAS No.
84-67-3
Chemical Name:
m-Tolidine
Synonyms
NZ066;APB-144;M-TOLIDINE;2,2'-Tolidine;m-Tolidine;2,2’-dimethylbenzidine;2,2'-dimethyl benzidine;2,2'-DIMETHYL-4,4'-DIAMINOBIPHENYL;4,4'-Diamino-2,2'-dimethylbiphenyl;2,2'-Dimethyl-4,4'-biphenyldiamine
CBNumber:
CB0320487
Molecular Formula:
C14H16N2
Molecular Weight:
212.29
MOL File:
84-67-3.mol
Modify Date:
2024/5/29 17:03:55

m-Tolidine Properties

Melting point 105-106℃
Boiling point 344.4±37.0 °C(Predicted)
Density 1.106
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka 4.89±0.10(Predicted)
color White to Off-White
Stability Incompatible with oxidising agents
InChI InChI=1S/C14H16N2/c1-9-7-11(15)3-5-13(9)14-6-4-12(16)8-10(14)2/h3-8H,15-16H2,1-2H3
InChIKey QYIMZXITLDTULQ-UHFFFAOYSA-N
SMILES C1(C2=CC=C(N)C=C2C)=CC=C(N)C=C1C
CAS DataBase Reference 84-67-3

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319
Precautionary statements  P305+P351+P338
Safety Statements  24/25
HS Code  29215900
NFPA 704
0
1 0

m-Tolidine price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemicals (India) T3098 m-Tolidine min. 98.0 % 84-67-3 25G ₹6200 2022-05-26 Buy
Product number Packaging Price Buy
T3098 25G ₹6200 Buy

m-Tolidine Chemical Properties,Uses,Production

Chemical Properties

m-Tolidine is pink particles and can form prisms when exposed to water. It is soluble in cold water, alcohol, and ether. In the presence of iron(III) chloride, m-Tolidine does not produce any color. It is tetrazotized with nitrite and acid and couples to form dyes.

Uses

M-TOLIDINE is used for preparation polyimide and epoxy resin material.

Definition

M-Tolidine gives no color in the presence of iron(III) chloride. It is tetrazotized with nitrite and acid and couples to form dyes. M-Tolidine was used in the past for the production of azo dyes.

Preparation

M-Tolidine is made by the reduction of m-nitrotoluene with zinc dust and sodium hydroxide solution. The subsequent rearrangement is carried out with hydrochloric acid or sulfuric acid and gives rise to m-tolidine dihydrochloride or m-tolidine sulfate, which are isolated as salts. The free base is diffificult to isolate and is therefore not a commercial product.

Chemical Reactivity

M-Tolidine gives no color in the presence of iron(III) chloride. It is tetrazotized with nitrite and acid and couples to form dyes.

Global( 202)Suppliers
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KPCL Industries (part of Benzo Products (I) Pvt Ltd) +91-7948989351 +91-9924992995 Gujarat, India 51 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
CHINATECH(TIANJIN) CHEMICAL CO.,LTD. +86-18222270857 +86-18222265956 China 64 58 Inquiry
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Shanghai Daken Advanced Materials Co.,Ltd +86-371-66670886 China 16220 58 Inquiry
2,2'-dimethyl[1,1'-biphenyl]-4,4'-diamine 4-(4-amino-2-methylphenyl)-3-methylbenzenamine 4,4'-Diamino-2,2'-dimethylbiphenyl 2,2'-DIMETHYL-4,4'-DIAMINOBIPHENYL APB-144 M-TOLIDINE 1’-Biphenyl]-4,4’-diamine,2,2’-dimethyl-[1 2,2’-dimethylbenzidine 2,2'-diMethyl-4,4'-diaMinobiphenyl(M-TB) 2,2'-diMethyl-4,4'-diaMinobiphenyl (M-tolidine m-Tolidine 2,2'-Dimethyl-[1,1'-biphenyl]-4,4'-Diamine(M-Tolidine) [1,1'-Biphenyl]-4,4'-diamine,2,2'-dimethyl- 2,2'-dimethyl-[1,1'-Biphenyl]-4,4'-diamine 2,2'-dimethyl benzidine 2,2'-Dimethyl-4,4'-biphenyldiamine 2,2'-Dimethyl-4,4'-diamino-1,1'-biphenyl 2,2'-Tolidine [4-(4-amino-2-methyl-phenyl)-3-methyl-phenyl]amine 4-(4-amino-2-methylphenyl)-3-methylaniline 4-(4-azanyl-2-methyl-phenyl)-3-methyl-aniline NZ066 2,2'-DIMETHYL-4,4'-DIAMINOBIPHENYL(M-TOLIDINE/M-TB) 2,2'-Dimethyl-[1,1'-biphenyl] -4,4'-Diamine (M-Tolidine) CAS 2,2'-Dimethyl-[1,1'-biphenyl] -4,4'-Diamine (M-Tolidine) 2,2'-Dimethyl-[1,1'-biphenyl]-4,4'-diamine 2,2'-dimethyl benzidine 4,4'-Diamino-2,2'-dimethylbiphenyl 2,2'-diMethyl-4,4'-diaMinobiphenyl 84-67-3 C6H3NH2CH32 Intermediates of Dyes and Pigments fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis, functional materials 84-67-3