478935-29-4

Basic information

• Product Name: 1-Hexyl-3-MethyliMidazoliuM hydrosulfate
• Synonyms: 1-Hexyl-3-MethyliMidazoliuM hydrosulfate
• CAS NO: 478935-29-4
• Molecular Formula: C₁₀H₁₉N₂*HO₄S
• Molecular Weight: 264.3418
• Mol File: 478935-29-4.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Hexyl-3-MethyliMidazoliuM hydrosulfate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Hexyl-3-MethyliMidazoliuM hydrosulfate(478935-29-4)
• EPA Substance Registry System: 1-Hexyl-3-MethyliMidazoliuM hydrosulfate(478935-29-4)

Safety Data

• Hazardous Substances Data: 478935-29-4(Hazardous Substances Data)

Usage

General Description

1-Hexyl-3-MethyliMidazoliuM hydrosulfate is a chemical compound that belongs to the class of imidazole derivatives. It is a hydrosulfate salt of midazolam, which is a short-acting benzodiazepine central nervous system depressant. This chemical is used as a sedative and anesthetic agent in medical settings. It acts on the GABA receptors in the brain to produce its calming and relaxing effects. It is commonly used in medical procedures such as surgery, dental work, and diagnostic procedures to reduce anxiety and induce sedation. However, it is important to use this chemical under the supervision of a medical professional, as it can have potential side effects and interactions with other medications.

Upstream product

• 171058-17-6 1-hexyl-3-methylimidazol-1-ium chloride 
• 616-47-7 1-methyl-1H-imidazole 
• 85100-78-3 1-hexyl-3-methyl-1-imidazolium bromide 
• 111-25-1 1-bromo-hexane 

Downstream Products

• 1361123-97-8 3-((2E,4Z)-5-chloro-2-(ethoxycarbonyl)-5-(4-fluorophenyl)penta-2,4-dienyl)-1-methyl-1H-imidazol-3-iumhydrogensulfate 
• 1361123-93-4 3-((2E,4Z)-5-chloro-2-(ethoxycarbonyl)-5-(4-nitrophenyl)penta-2,4-dienyl)-1-methyl-1H-imidazol-3-iumhydrogensulfate 
• 1361123-87-6 3-((2E,4Z)-5-chloro-2-(methoxycarbonyl)-5-(4-nitrophenyl)penta-2,4-dienyl)-1-methyl-1H-imidazol-3-iumhydrogensulfate 
• 1361123-91-2 3-((2E,4Z)-5-chloro-5-(3-chlorophenyl)-2-(methoxycarbonyl)penta-2,4-dienyl)-1-methyl-1H-imidazol-3-iumhydrogensulfate 
• 1361123-95-6 3-((2E,4Z)-5-chloro-5-(4-fluorophenyl)-2-(methoxycarbonyl)penta-2,4-dienyl)-1-methyl-1H-imidazol-3-iumhydrogensulfate 
• 1361123-85-4 methyl 6-phenyl-2H-pyran-3-carboxylate 
• 1361123-89-8 3-((2E,4Z)-5-chloro-2-(methoxycarbonyl)-5-phenylpenta-2,4-dienyl)-1-methyl-1H-imidazol-3-iumhydrogensulfate 

Relevant articles and documents

Acid-induced chemoselective arylthiolations of electron-rich arenes in ionic liquids from sodium arylsulfinates: The reducibility of halide anions in [Hmim]Br

An acid-induced protocol for the chemoselective arylthiolations of electron-rich arenes in ionic liquids from sodium arylsulfinates is introduced. The chemistry, in which [Hmim]Br (heaxylmethylimidazolium bromide) is used as both a solvent and a reducer, provides several advantages including odorless and simple operation, inexpensive reagents, recyclable solvents and gram-scale synthesis.

Dual functionality of amphiphilic 1-alkyl-3-methylimidazolium hydrogen sulfate ionic liquids: Surfactants with catalytic function

A series of amphiphilic 1-alkyl-3-methylimidazolium hydrogen sulfate ionic liquids were synthesized. Acidic hydrogen sulfate ionic liquids with the alkyl chains C6-C14 are characterized by good surface properties. Their surface properties (adsorption and micellization parameters, degree of ionization of micelles, Krafft temperatures and thermodynamic parameters) were determined. Synthesized ionic liquids were applied as a co-catalyst in an oxirane ring opening reaction in epoxidized fatty acid methyl esters (FAME). Their co-catalytic activities were determined and discussed as a function of their structure and surface properties. It was found that the co-catalytic properties, both conversion and selectivity, of alkylimidazolium hydrogen sulfate ionic liquids noticeably depended on the alkyl chain lengths, and in consequence their properties.

Acidic-functionalized ionic liquid as an efficient, green, and metal-free catalyst for benzylation of sulfur, nitrogen, and carbon nucleophiles to benzylic alcohols

A series of HSO4- functionalized ILs was synthesized and used as efficient, green, and metal-free catalysts for benzylation. Notably, the catalytic system has wide substrate scopes and the ionic liquid catalysts were applied to investigate three different types of nucleophiles to give the desired benzylation products with moderate to excellent yields.