79917-90-1

  • Product Name:1-Butyl-3-methylimidazolium chloride
  • Molecular Formula:C8H15ClN2
  • Purity:99%
  • Molecular Weight:174.673
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Product Details;

CasNo: 79917-90-1

Molecular Formula: C8H15ClN2

Appearance: colorless to straw yellow liquid

factory and manufacture 79917-90-1 1-Butyl-3-methylimidazolium chloride lonic liquid

  • Molecular Formula:C8H15ClN2
  • Molecular Weight:174.673
  • Appearance/Colour:colorless to straw yellow liquid 
  • Melting Point:~70 °C 
  • Flash Point:192 °C 
  • PSA:8.81000 
  • Density:d25 1.08 (dried) 
  • LogP:-1.88330 

1-Butyl-3-methylimidazolium chloride(Cas 79917-90-1) Usage

General Description

1-Butyl-3-methylimidazolium chloride ([BMIM]Cl) is an organic chloride salt used as a precursor in synthesizing chloroindate(III) ionic liquids, which serve as recyclable and efficient media for Friedel-Crafts acylation reactions. These ionic liquids overcome limitations of traditional Lewis acid catalysts by providing a stable, reusable system for producing aromatic ketones.

InChI:InChI=1/C8H15N2/c1-3-4-5-10-7-6-9(2)8-10/h6-8H,3-5H2,1-2H3/q+1

79917-90-1 Relevant articles

Experimental measurement and modeling of vapor-liquid equilibrium for the ternary system water + ethanol + 1-Butyl-3-methylimidazolium chloride

Geng, Wei,Zhang, Lianzhong,Deng, Dongshun,Ge, Yun,Ji, Jianbing

, p. 1679 - 1683 (2010)

Vapor-liquid equilibrium (VLE) data were...

Various metal organic frameworks combined with imidazolium, quinolinum and benzothiazolium ionic liquids for removal of three antibiotics from water

Yohannes, Alula,Li, Jing,Yao, Shun

, (2020/10/02)

In this research, imidazolium, quinolinu...

Method for synthesizing antioxygen 1076

-

Paragraph 0020; 0021, (2017/07/21)

The invention belongs to the technical f...

Recyclable zinc (II) ionic liquid catalyzed synthesis of azides by direct azidation of alcohols using trimethylsilylazide at room temperature

Singh, Ashima,Singh, Harjinder,Khurana

, p. 2498 - 2502 (2017/05/31)

A new efficient method has been reported...

A New Mode of Operation of Pd-NHC Systems Studied in a Catalytic Mizoroki-Heck Reaction

Astakhov, Alexander V.,Khazipov, Oleg V.,Chernenko, Andrey Yu.,Pasyukov, Dmitry V.,Kashin, Alexey S.,Gordeev, Evgeniy G.,Khrustalev, Victor N.,Chernyshev, Victor M.,Ananikov, Valentine P.

, p. 1981 - 1992 (2017/06/14)

Metal complexes bearing N-heterocyclic c...

79917-90-1 Process route

1-n-butyl-3-methylimidazolim bromide
85100-77-2

1-n-butyl-3-methylimidazolim bromide

1-butyl-3-methylimidazolium chloride
79917-90-1

1-butyl-3-methylimidazolium chloride

Conditions
Conditions Yield
With hydrogenchloride; In acetone; at 40 ℃; for 10h;
n-Butyl chloride
109-69-3

n-Butyl chloride

1-butyl-3-methylimidazolium chloride
79917-90-1

1-butyl-3-methylimidazolium chloride

Conditions
Conditions Yield
With 1-methyl-1H-imidazole;
98%

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