42383-61-9

Basic information

• Product Name: imidazol-2-ylamine sulphate
• Synonyms: imidazol-2-ylamine sulphate;1H-Imidazole-2-amine/sulfuric acid,(1:x);4H-1,2,4-triazol-3-aminesulfate;imidazol-2-ylamine sulphate(1:)(HEMISULFATE form)
• CAS NO: 42383-61-9
• Molecular Formula: C₃H₅N₃*H₂O₄S
• Molecular Weight: 181.17038
• EINECS: 255-791-7
• Mol File: 42383-61-9.mol

Chemical Properties

• Boiling Point: 313.1 °C at 760 mmHg
• Flash Point: 168.9 °C
• Appearance: /
• CAS DataBase Reference: imidazol-2-ylamine sulphate(CAS DataBase Reference)
• NIST Chemistry Reference: imidazol-2-ylamine sulphate(42383-61-9)
• EPA Substance Registry System: imidazol-2-ylamine sulphate(42383-61-9)

Safety Data

• Hazardous Substances Data: 42383-61-9(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
Imidazol-2-ylamine sulphate is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the creation of a wide range of organic compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, imidazol-2-ylamine sulphate serves as a valuable reagent, aiding in the development and understanding of new drug candidates and their mechanisms of action.
Used as a Catalyst in Chemical Reactions:
Imidazol-2-ylamine sulphate is utilized as a catalyst to accelerate chemical reactions, enhancing the efficiency and speed of processes in the chemical and pharmaceutical industries.
Used in the Production of Pharmaceutical Compounds:
As a building block, imidazol-2-ylamine sulphate is instrumental in the synthesis of various pharmaceutical compounds, playing a crucial role in the development of new medications.
Used in Antimicrobial Applications:
Leveraging its antimicrobial properties, imidazol-2-ylamine sulphate is a potential candidate for the development of new antimicrobial agents, useful in combating resistant strains of bacteria.
Used in Anti-inflammatory Treatments:
Due to its anti-inflammatory characteristics, imidazol-2-ylamine sulphate may be employed in the development of treatments for inflammatory conditions, offering a new avenue for therapeutic intervention.
Overall, imidazol-2-ylamine sulphate is a multifaceted chemical with broad applications across different industries, particularly in the realms of organic synthesis, pharmaceuticals, and medicine. Its unique properties position it as a promising substance for future scientific and industrial advancements.

InChI:InChI=1/C3H5N3.H2O4S/c4-3-5-1-2-6-3;1-5(2,3)4/h1-2H,(H3,4,5,6);(H2,1,2,3,4)

Upstream product

• 52328-05-9 O-methylisourea hemisulfate 
• 645-36-3 2,2-diethoxy-ethanamine 
• 22483-09-6 2,2-dimethoxyethylamine 

Downstream Products

• 169298-50-4 5-oxo-1H-imidazo<1,2-a>pyrimidine-6-carbonitrile 
• 112273-77-5 ethyl 5-oxo-1H-imidazo<1,2-a>pyrimidine-6-carboxylate 
• 1054644-10-8 3-[(4R,5S,6S,7R)-4,7-Dibenzyl-3-butyl-5,6-bis-(2-methoxy-ethoxymethoxy)-2-oxo-[1,3]diazepan-1-ylmethyl]-N-(1H-imidazol-2-yl)-benzamide 
• 1054620-91-5 3-[(4R,5S,6S,7R)-4,7-Dibenzyl-3-cyclopropylmethyl-5,6-bis-(2-methoxy-ethoxymethoxy)-2-oxo-[1,3]diazepan-1-ylmethyl]-N-(1H-imidazol-2-yl)-benzamide 
• 197089-38-6 4-nitro-3-(2'-amino-imidazol-1'-yl)-benzoic acid t-butyl ester 
• 218301-91-8 4-(2'-amino-imidazol-1'-yl)nitrobenzene 
• 7720-39-0 1H-imidazol-2-amine 
• 588942-81-8 3-Cyclopentyl-N-(1 H-imidazol-2-yl)-2-(4-methanesulfonyl-3-nitro-phenyl)-propionamide 
• 588941-68-8 2-(3-Bromo-4-methanesulfonyl-phenyl)-3-cyclopentyl-N-(1 H-imidazol-2-yl)-propionamide 
• 502506-57-2 6-phenylimidazo[1,2-a]pyrimidine-5,7-diol 

Relevant articles and documents

Efficient and environmentally friendly synthesis of 2-amino-imidazole

A new and efficient method for the preparation of 2-amino-imidazole 3 was developed. Starting from cheap commodities O-methyl-iso-urea sulphate and 2-aminoacetaldehyde-acetales the desired product is isolated through a very simple work-up in a good yield.

Method for inhibiting advanced glycosylation of proteins using aminosubstituted imidazoles

The present invention relates to compositions and methods for inhibiting nonenzymatic cross-linking (protein aging), Accordingly, a composition is disclosed which comprises 2-aminoimidazoles capable of inhibiting the formation of advanced glycosylation endproducts of target proteins by reacting with the carbonyl moiety of the early glycosylation product of such target proteins formed by their initial glycosylation, The method comprises contacting the target protein with the composition, Both industrial and therapeutic applications for the invention are envisioned, as food spoilage and animal protein aging can be treated.