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Merck
CN

690147

1-乙基咪唑

produced by BASF, ≥95.0% (HPLC)

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经验公式(希尔记法):
C5H8N2
化学文摘社编号:
分子量:
96.13
UNSPSC Code:
12352005
PubChem Substance ID:
EC Number:
230-403-9
MDL number:
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assay

≥95.0% (HPLC)

impurities

≤0.5% water

color

APHA: ≤100

SMILES string

CCn1ccnc1

InChI

1S/C5H8N2/c1-2-7-4-3-6-5-7/h3-5H,2H2,1H3

InChI key

IWDFHWZHHOSSGR-UHFFFAOYSA-N

Disclaimer

产品储存中可能变色

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 2

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

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Romain Lambert et al.
Macromolecular rapid communications, 37(14), 1143-1149 (2016-03-19)
Statistical copoly(ionic liquid)s (coPILs), namely, poly(styrene)-co-poly(4-vinylbenzylethylimidazolium acetate) are synthesized by free-radical copolymerization in methanolic solution. These coPILs serve to in situ generate polymer-supported N-heterocyclic carbenes (NHCs), referred to as polyNHCs, due to the noninnocent role of the weakly basic acetate
Srikanta Pal et al.
Ecotoxicology and environmental safety, 184, 109634-109634 (2019-09-15)
Imidazolium-based ionic liquids (IL) with short-alkyl side chain such as 1-ethyl-3-methyl-imidazolium chloride ([Emim]Cl) and 1-butyl-3-methyl-imidazolium chloride ([Bmim]Cl) has immense application potential including in lignocellulosic bioenergy production. But they are toxic to most microorganisms, and those isolated from different environments as
Niwanthi Dissanayake et al.
Carbohydrate polymers, 221, 63-72 (2019-06-23)
During the past decade, ionic liquids (ILs) have attracted increasing attention as efficient, novel solvents for dissolving cellulose. In this study, 1-butyl-3-methylimdazolium methylphosphonate ([C4C1im][(OMe)(H)PO2]) was used in the dissolution of cotton cellulose and the role of 1-methylimidazole, 1-ethylimidazole, 1-propylimidazole, and
Yuliang Yang et al.
Chemistry, an Asian journal, 13(19), 2923-2933 (2018-08-14)
A family of novel imine-N-heterocyclic carbene ruthenium(II) complexes of the general formula [(η6 -p-cymene)Ru(C^N)Cl]PF6- (where C^N is an imine-N-heterocyclic carbene chelating ligand with varying substituents) have been prepared and characterized. In this imine-N-heterocyclic carbene chelating ligand framework, there are three
Marilyne Sosson et al.
Nucleic acids research, 47(8), 3836-3845 (2019-03-15)
The template-directed formation of phosphodiester bonds between two nucleic acid components is a pivotal process in biology. To induce such a reaction in the absence of enzymes is a challenge. This challenge has been met for the extension of a

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