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Merck
CN

89483

Sigma-Aldrich

1-乙基-3-甲基溴化咪唑

≥97.0% (T)

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别名:
1-Ethyl-3-methyl-1H-imidazolium bromide, 1-Methyl-3-ethylimidazolium bromide
经验公式(希尔记法):
C6H11BrN2
CAS号:
分子量:
191.07
Beilstein:
5162084
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

≥97.0% (T)

形式

crystals

SMILES字符串

[Br-].CCn1cc[n+](C)c1

InChI

1S/C6H11N2.BrH/c1-3-8-5-4-7(2)6-8;/h4-6H,3H2,1-2H3;1H/q+1;/p-1

InChI key

GWQYPLXGJIXMMV-UHFFFAOYSA-M

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应用

1-乙基-3-甲基咪唑溴化物可用于制备:
  • 1-乙基-3-甲基咪唑鎓双((三氟甲基)磺酰基)酰亚胺
  • 1-乙基-3-甲基咪唑四氟硼酸盐
  • (EMI)[Cd(BTC)](EMI = 1-乙基-3-甲基咪唑鎓,BTC = 1,3,5-苯三甲酸酯),配位聚合物

其他说明

在室温下熔化的疏水性、高导电性咪唑熔盐

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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Voltammetry of oxygen in the room-temperature ionic liquids 1-ethyl-3-methylimidazolium bis ((trifluoromethyl) sulfonyl) imide and hexyltriethylammonium bis ((trifluoromethyl) sulfonyl) imide: one-electron reduction to form superoxide. Steady-state and transient behavior......
Buzzeo MC, et al.
The Journal of Physical Chemistry A, 107(42), 8872-8878 (2003)
Ionic liquid as solvent for the synthesis and crystallization of a coordination polymer:(EMI)[Cd(BTC)](EMI=1-ethyl-3-methylimidazolium,BTC=1,3,5 benzenetricarboxylate).
Liao JH, et al.
Crystal Growth & Design, 6(5), 1062-1063 (2006)
The phase behaviour of 1-alkyl-3-methylimidazolium tetrafluoroborates; ionic liquids and ionic liquid crystals.
J. Chem. Soc., Dalton Trans., 13, 2133-2140 (1999)
Pierre Bonhôte et al.
Inorganic chemistry, 35(5), 1168-1178 (1996-02-28)
New, hydrophobic ionic liquids with low melting points (<-30 degrees C to ambient temperature) have been synthesized and investigated, based on 1,3-dialkyl imidazolium cations and hydrophobic anions. Other imidazolium molten salts with hydrophilic anions and thus water-soluble are also described.
Seungmin Oh et al.
The journal of physical chemistry. B, 123(39), 8274-8284 (2019-09-11)
Ionic liquids with aprotic heterocyclic anions (AHAs) have been developed for CO2 capture but have been considered for other applications as well. Previously, we have shown that AHA ILs, where the only site for reaction with CO2 is the anion

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