36443-80-8

Basic information

• Product Name: 1-BENZYL-3-METHYLIMIDAZOLIUM CHLORIDE
• Synonyms: 1-benzyl-3-Methyl-1H-iMidazol-3-iuM chloride;BzMIMCl;1-Benzyl-3-methylimidazolium chloride >=97.0%;1-Benzyl-3-methylimidazolium chloride: 1-Methyl-3-benzylimidazolium chloride;1H-Imidazolium,1-methyl-3-(phenylmethyl)-, chloride (1:1);1-Benzyl-3-methylimidazolium chloride, 97% solid
• CAS NO: 36443-80-8
• Molecular Formula: C₁₁H₁₃N₂*Cl
• Molecular Weight: 208.691
• EINECS: 200-144-5
• Mol File: 36443-80-8.mol
• Article Data: 28

Chemical Properties

• Melting Point: 70 °C
• Appearance: /
• Storage Temp.: Inert atmosphere,Room Temperature
• Sensitive: Moisture Sensitive
• CAS DataBase Reference: 1-BENZYL-3-METHYLIMIDAZOLIUM CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BENZYL-3-METHYLIMIDAZOLIUM CHLORIDE(36443-80-8)
• EPA Substance Registry System: 1-BENZYL-3-METHYLIMIDAZOLIUM CHLORIDE(36443-80-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26
• WGK Germany: 3
• F: 3-10
• Hazardous Substances Data: 36443-80-8(Hazardous Substances Data)

Usage

General Description

1-Benzyl-3-methylimidazolium chloride is a chemical compound that belongs to the class of imidazolium salts. It is a white crystalline solid with the molecular formula C11H14ClN2. 1-BENZYL-3-METHYLIMIDAZOLIUM CHLORIDE is widely used as a precursor for the synthesis of various organic and inorganic compounds. It is also used as an ionic liquid in various chemical processes, such as catalysis and electrochemistry. Additionally, 1-Benzyl-3-methylimidazolium chloride has been studied for its potential antimicrobial and antifungal properties, making it a versatile and important chemical in various industries and scientific research.

InChI:InChI=1/C11H13N2.ClH/c1-12-7-8-13(10-12)9-11-5-3-2-4-6-11;/h2-8,10H,9H2,1H3;1H/q+1;/p-1

Upstream product

• 3459-92-5 DBC 
• 35487-17-3 1-methylimidazolium chloride 
• 616-47-7 1-methyl-1H-imidazole 
• 100-44-7 benzyl chloride 

Downstream Products

• 1331734-75-8 1-benzyl-3-methylimidazolium O,Se-dimethylphosphoroselenoate 
• 1331734-64-5 1-benzyl-3-methylimidazolium O,S-dimethylphosphorothioate 
• 1379371-68-2 [Benz-SO₃Hmim][Cl] 
• 500996-04-3 1-methyl-3-(phenylmethyl)-1H-imidazolium tetrafluoroborate 

Relevant articles and documents

Imidazolium salt-modified porous hypercrosslinked polymers for synergistic CO2 capture and conversion

A new type of imidazolium salt-modified porous hypercrosslinked polymer (BET surface area up to 926 m2 g-1) was reported. These porous materials exhibited good CO2 capture capacities (14.5 wt%) and catalytic activities for the conversion of CO2 into various cyclic carbonates under metal-free conditions. The synergistic effect of CO2 capture and conversion was observed.

Electronic excitations in homopolyatomic bismuth cations: Spectroscopic measurements in molten salts and an ab initio CI-Singles study

The electronic excitations of the low-valence bismuth cluster cations Bi53+, Bi82+, and Bi95+ have been studied with experimental and theoretical techniques. The UV-visible spectra of the b

Characterizing Cation Chemistry for Anion Exchange Membranes - A Product Study of Benzylimidazolium Salt Decompositions in the Base

Imidazolium functionality has played a prominent role in research on anion exchange membranes for use in alkaline electrochemical devices. Base stability and degradation of these materials has been much studied, but in many instances, product pathways have not been thoroughly delineated. We report an NMR study of base-induced decomposition products from three benzylimidazolium salts bearing varying extents of methyl substitution on the imidazolium ring. The major products are consistent with a hydrolytic ring fragmentation pathway as the principal mode of decomposition. We observe several new products not previously reported in the literature on imidazolium salt degradation, including benzilic acid rearrangement products formally derived from intermediate 1,2-dicarbonyl compounds or their equivalents. However, the overall reactions are complex, the yields of observed products do not account for all consumed starting materials, and mechanistic ambiguities remain.

PHOTOBASE GENERATOR

There is provided a photobase generator and a photosensitive resin composition containing the photobase generator. The photobase generator includes an ammonium salt represented by general formula (1). In formula (1), R1 to R4 independently represent an alkyl group having 1 to 18 carbon atoms or Ar, wherein at least one of R1 to R4 represents Ar; Ar represents an aryl group having 6 to 14 carbon atoms (excluding carbon atoms contained in a substituent as mentioned below), wherein some of hydrogen atoms in the aryl group may be independently substituted by an alkyl group having 1 to 18 carbon atoms or the like; Y+ represents an ammonio group represented by general formula (2) or (3); and E represents a hydrogen atom or a group represented by general formula (5).