• Product Name2-Methylimidazole
  • CasNo. 693-98-1
  • MFC4H6N2
  • MW82.105
  • Purity
  • Appearancewhite to light yellow crystalline powder
  • Packing
  • Contact usInquiry

Product Details

CasNo: 693-98-1

MF: C4H6N2

Appearance: white to light yellow crystalline powder

Factory Supply High Purity 99% 693-98-1 with Efficient Shipping

  • Molecular Formula:C4H6N2
  • Molecular Weight:82.105
  • Appearance/Colour:white to light yellow crystalline powder 
  • Vapor Pressure:<1 mm Hg ( 0 °C) 
  • Melting Point:142-143 °C(lit.) 
  • Refractive Index:1.523 
  • Boiling Point:267 °C at 760 mmHg 
  • PKA:14.44±0.10(Predicted) 
  • Flash Point:144.9 °C 
  • PSA:28.68000 
  • Density:1.062 g/cm3 
  • LogP:0.71810 

2-Methylimidazole(Cas 693-98-1) Usage

Preparation

2-Methylimidazole is prepared by condensation of glyoxal, ammonia and acetaldehyde, a Radziszewski reaction. It is widely used as a polymeriza tion cross-linking accelerator and a hardener for epoxy resin systems for semiconductor potting compounds and soldering masks. It is obtained by eliminating dehydrogenation of 2-methylimidazoline. 2-methylimidazoline heated to melt (melting point 107 ℃), carefully add active nickel, raise the temperature to 200-210 ℃ reaction 2h. cool down to below 150 ℃, add water to dissolve, while hot pressure filtration, separation of active nickel, the filter lookchem liquid concentrated to a temperature of 140 ℃ or more, put the material cooling that 2-methylimidazole. Use the method to produce purity of ≥ 98% of the product, 1t product consumption of ethylenediamine (95%) 1095kg, acetonitrile 975kg. better method is to use glyoxal and aldehyde as raw materials.

Hazard

Possible carcinogen.

Flammability and Explosibility

Notclassified

Purification Methods

Recrystallise 2-methylimidazole from *benzene or pet ether. The picrate has m 215o (from H2O). [Beilstein 23 III/IV 594, 23/5 V 35.]

General Description

It is a white or colorless solid that is highly soluble in polar organic solvents and water. It is a precursor to a range of drugs and is a ligand in coordination chemistry.

InChI:InChI=1/C4H6N2/c1-4-5-2-3-6-4/h2-3H,1H3,(H,5,6)

693-98-1 Relevant articles

Identification of Intermediates and Products of 2,4,6-Trimethyl-1,3,5-Hexahydrotriazine Trihydrate and Glyoxal Reaction in an Aqueous Solution by NMR Spectroscopy

Bakibaev, A. A.,Cheltygmasheva, R. S.,Fateev, A. V.,Kotelnikov, O. A.,Kotov, A. V.,Tuguldurova, V. P.,Vodyankina, O. V.

, p. 225 - 231 (2020)

In situ formation of 2-methylimidazole a...

Continuous synthesis method for 2-methyl-5-nitroimidazole

-

Paragraph 0016; 0042-0046; 0050-0054; 0058-0061; 0066-0070, (2020/07/15)

The invention provides a continuous synt...

Imprinted Apportionment of Functional Groups in Multivariate Metal-Organic Frameworks

Feng, Liang,Wang, Kun-Yu,Lv, Xiu-Liang,Powell, Joshua A.,Yan, Tian-Hao,Willman, Jeremy,Zhou, Hong-Cai

supporting information, p. 14524 - 14529 (2019/10/02)

Sophisticated chemical processes widely ...

Novel nitroimidazole drug as well as preparation method and application of novel nitroimidazole drug

-

Paragraph 0020, (2018/04/01)

The invention relates to a novel nitroim...

693-98-1 Process route

2,4-dimethyl-2-imidazoline
930-61-0

2,4-dimethyl-2-imidazoline

chloroform
67-66-3,8013-54-5

chloroform

2,4-dimethylpyrimidine
14331-54-5

2,4-dimethylpyrimidine

4-chloro-2-methylpyrimidine
4994-86-9

4-chloro-2-methylpyrimidine

2-methylimidazole
693-98-1

2-methylimidazole

5-Chloro-2,4-dimethylpyrimidine
75712-73-1

5-Chloro-2,4-dimethylpyrimidine

Conditions
Conditions Yield
at 550 ℃; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
 
2,4-dimethyl-2-imidazoline
930-61-0

2,4-dimethyl-2-imidazoline

chloroform
67-66-3,8013-54-5

chloroform

2,5-dimethyl-pyrazine
123-32-0

2,5-dimethyl-pyrazine

4-chloro-2-methylpyrimidine
4994-86-9

4-chloro-2-methylpyrimidine

2-methylimidazole
693-98-1

2-methylimidazole

5-Chloro-2,4-dimethylpyrimidine
75712-73-1

5-Chloro-2,4-dimethylpyrimidine

Conditions
Conditions Yield
at 550 ℃; Yield given. Further byproducts given. Yields of byproduct given. Title compound not separated from byproducts;
 

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693-98-1 Downstream products

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