V900088
1-Methylimidazole
98%, Vetec™, reagent grade
Synonym(s):
N-Methylimidazole
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About This Item
Empirical Formula (Hill Notation):
C4H6N2
CAS Number:
Molecular Weight:
82.10
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
210-484-7
Beilstein/REAXYS Number:
105197
MDL number:
Assay:
98%
Product Name
1-Methylimidazole, Vetec™, reagent grade, 98%
grade
reagent grade
vapor pressure
0.4 mmHg ( 20 °C)
product line
Vetec™
assay
98%
autoignition temp.
977 °F
expl. lim.
15.7 %
greener alternative product characteristics
Catalysis
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Greener Alternative Product
refractive index
n20/D 1.495 (lit.)
bp
198 °C (lit.)
mp
−6 °C (lit.)
density
1.03 g/mL at 25 °C (lit.)
greener alternative category
SMILES string
Cn1ccnc1
InChI
1S/C4H6N2/c1-6-3-2-5-4-6/h2-4H,1H3
InChI key
MCTWTZJPVLRJOU-UHFFFAOYSA-N
General description
We are committed to bringing you Greener Alternative Products, which adhere to one or more of the 12 Principles of Green Chemistry. This product has been enhanced for catalysis. Find details here.
Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 2 - Skin Corr. 1B
Storage Class
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
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Pengfei Zhang et al.
Journal of chromatography. A, 1218(22), 3459-3465 (2011-04-19)
The development of mixed-mode stationary phase to achieve multiple separation capabilities in one column is very important for high performance liquid chromatography. In this paper, a new specific stationary phase based on grafting N-methylimidazolium to a monolithic silica column was
Sabesan Yoganathan et al.
Organic letters, 15(3), 602-605 (2013-01-19)
An efficient, one-pot, N-methylimidazole (NMI) accelerated synthesis of aromatic and aliphatic carbamates via the Lossen rearrangement is reported. NMI is a catalyst for the conversion of isocyanate intermediates to the carbamates. Moreover, the utility of arylsulfonyl chloride in combination with
Wen-Xin Chen et al.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| V900088-100ML | 04061838134585 |