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336092

Sigma-Aldrich

1-Methylimidazole

≥99%, purified by redistillation

Synonym(s):

N-Methylimidazole

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About This Item

Empirical Formula (Hill Notation):
C4H6N2
CAS Number:
Molecular Weight:
82.10
Beilstein:
105197
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

vapor pressure

0.4 mmHg ( 20 °C)

Quality Level

Assay

≥99%

form

liquid

autoignition temp.

977 °F

purified by

redistillation

expl. lim.

15.7 %

impurities

≤19 ppm Triazine
<0.005% water

refractive index

n20/D 1.495 (lit.)

bp

198 °C (lit.)

mp

−6 °C (lit.)

density

1.03 g/mL at 25 °C (lit.)
1.034-1.036 g/mL

SMILES string

Cn1ccnc1

InChI

1S/C4H6N2/c1-6-3-2-5-4-6/h2-4H,1H3

InChI key

MCTWTZJPVLRJOU-UHFFFAOYSA-N

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General description

1-Methylimidazole is an N-donor ligand generally used in the preparation of coordinate complexes.

Application

1-Methylimidazole may be used as a starting material to synthesize:
  • 1-(2-hydroxypropyl)-3-methylimidazolium salts used as ionic liquids
  • 1,3-dimethylimidazoyl-2-ylidene borane, a stable and easy to handle N-heterocyclic carbene borane
  • It can act both as a catalyst and a solvent in the synthesis of aldononitrile acetates from aldoses.

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Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flash Point(F)

197.6 °F - closed cup

Flash Point(C)

92 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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The use of 1-methylimidazole as a solvent and catalyst for the preparation of aldononitrile acetates of aldoses.
Chen CC & McGinnis GD
Carbohydrate Research, 90(1), 127-130 (1981)
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Green Chemistry, 5(6), 731-736 (2003)
1,3-Dimethylimidazoyl-2-ylidene borane
Gardner S, et al.
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The Journal of organic chemistry, 77(20), 9236-9239 (2012-10-02)
We report herein that amides are excellent N-sources in the NHC-Pd(II)-Im complex 1 catalyzed amination of aryl chlorides. In the presence of KO(t)Bu, various aryl chlorides and amides can react smoothly to give the corresponding aminated products in moderate to

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