50790-93-7

Basic information

• Product Name: 2-Butyl-1-H-imidazole
• Synonyms: 2-Butyl-1H-imidazole;1H-imidazole, 2-butyl-
• CAS NO: 50790-93-7
• Molecular Formula: C₇H₁₂N₂
• Molecular Weight: 124.18358
• Mol File: 50790-93-7.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 279.3 °C at 760 mmHg
• Flash Point: 132.7 °C
• Appearance: /
• Density: 0.979 g/cm³
• Vapor Pressure: 0.00686mmHg at 25°C
• Refractive Index: 1.504
• CAS DataBase Reference: 2-Butyl-1-H-imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butyl-1-H-imidazole(50790-93-7)
• EPA Substance Registry System: 2-Butyl-1-H-imidazole(50790-93-7)

Safety Data

• Hazardous Substances Data: 50790-93-7(Hazardous Substances Data)

Usage

Description

2-Butyl-1-H-imidazole is a chemical compound with the molecular formula C7H12N2, belonging to the imidazole derivative family. It features a butyl group attached to the nitrogen atom, which endows it with a variety of potential applications across different industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Applications:
2-Butyl-1-H-imidazole is used as a chemical intermediate in the synthesis of various drugs and pharmaceuticals. Its structural characteristics make it a valuable component in the development of new medications.
Used in Anti-Inflammatory Applications:
2-Butyl-1-H-imidazole is used as an anti-inflammatory agent for its potential to reduce inflammation. Its imidazole structure may contribute to modulating inflammatory responses in biological systems.
Used in Anti-Bacterial Applications:
In the field of microbiology, 2-Butyl-1-H-imidazole is used as an anti-bacterial agent, leveraging its chemical properties to combat bacterial infections.
Used in Anti-Fungal Applications:
2-Butyl-1-H-imidazole is also utilized as an anti-fungal agent, indicating its broad-spectrum activity against fungal pathogens.
Used in Corrosion Inhibition:
In industrial applications, 2-Butyl-1-H-imidazole is used as a corrosion inhibitor to protect materials from degradation, particularly in environments where corrosion is a significant concern.
Each of these applications highlights the versatility and potential of 2-Butyl-1-H-imidazole in addressing various challenges in medicine, biology, and industry.

InChI:InChI=1/C7H12N2/c1-2-3-4-7-8-5-6-9-7/h5-6H,2-4H2,1H3,(H,8,9)

Downstream Products

• 133485-54-8 2-n-butyl-1-(2-chlorophenyl)-methyl-1H-imidazole 
• 1431152-75-8 2-butyl-N,N'-bis{[2'-(tert-butoxycarbonyl)biphenyl-4-yl]methyl}imidazolium bromide 
• 1431152-74-7 2-butyl-N,N'-bis{[2'-[2-(trityl)tetrazol-5-yl]biphenyl-4-yl]methyl}imidazolium bromide 
• 1431152-77-0 2-butyl-N,N'-bis{[2'-carboxybiphenyl-4-yl]methyl}imidazolium bromide 
• 1431152-76-9 C₃₅H₃₃N₁₀⁽¹⁺⁾*Br^(1-) 
• 912962-79-9 3-(3-(2-butylimidazol-1-ylmethyl)phenyl)-5-isobutylthiophene-2-(N-tert-butyl)sulfonamide 
• 125665-49-8 N-[4-(2-Butyl-imidazol-1-ylmethyl)-phenyl]-phthalamic acid 
• 134405-94-0 ethyl (E)-3-<2-butyl-1-<<2-(trimethylsilyl)ethoxy>methyl>imidazol-5-yl>-2-benzyl-2-butenoate 
• 143564-86-7 ethyl (Z)-3-<2-butyl-1-<<2-(trimethylsilyl)ethoxy>methyl>imidazol-5-yl>-2-benzyl-2-butenoate 
• 134405-55-3 (E)-3-<2-butyl-1-<(2-chlorophenyl)methyl>imidazol-5-yl>-2-benzyl-2-butenoic acid 
• 142893-54-7 2-<2-butyl-1-<(2-chlorophenyl)methyl>imidazol-5-yl>benzoic acid 
• 142893-53-6 3-[2-n-butyl-1-{(2-chlorophenyl)-methyl }-1H-imidazol-5-yl]benzoic acid 
• 143110-76-3 4-<2-butyl-1-<(2-chlorophenyl)methyl>imidazol-5-yl>benzoic acid 

Relevant articles and documents

MANUFACTURING METHOD OF 2-SUBSTITUTED IMIDAZOLE COMPOUND

PROBLEM TO BE SOLVED: To provide a high-yield manufacturing method of a 2-substituted imidazole which is expected to be useful as a curing agent for epoxy resins, polyurethane resins or the like, as an intermediate of various agrochemicals, antibiotics or pharmaceuticals such as anti-AIDS agents or the like, or as dye intermediates. SOLUTION: An aldehyde compound is reacted with ammonia (I) to give an imine compound, and subsequently an α,β-dicarbonyl compound and ammonia (II) are added and allowed to react with the imine compound. Preferably, the α,β-dicarbonyl compound and ammonia (II) are simultaneously added.