80912-09-0

Basic information

• Product Name: 1H-Imidazol-5-amine,1,2-dimethyl-(9CI)
• Synonyms: 1H-Imidazol-5-amine,1,2-dimethyl-(9CI);5-amino-1,2-dimethylimidazole;1,2-diMethyl-1H-iMidazol-5-aMine;5-Amine-1,2-dimethyl-1H-imidazole;2,3-dimethylimidazol-4-amine
• CAS NO: 80912-09-0
• Molecular Formula: C₅H₉N₃
• Molecular Weight: 111.15
• Product Categories: VARIOUSAMINE
• Mol File: 80912-09-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 303.6°C at 760 mmHg
• Flash Point: 137.4°C
• Appearance: /
• Density: 1.17g/cm³
• Vapor Pressure: 0.000922mmHg at 25°C
• Refractive Index: 1.581
• CAS DataBase Reference: 1H-Imidazol-5-amine,1,2-dimethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazol-5-amine,1,2-dimethyl-(9CI)(80912-09-0)
• EPA Substance Registry System: 1H-Imidazol-5-amine,1,2-dimethyl-(9CI)(80912-09-0)

Safety Data

• Hazardous Substances Data: 80912-09-0(Hazardous Substances Data)

Usage

Description

1H-Imidazol-5-amine,1,2-dimethyl-(9CI), also known as 1,2-dimethylimidazole, is a chemical compound with the molecular formula C5H9N3. It is a derivative of imidazole, which is a five-membered heterocyclic ring containing three carbon, two nitrogen, and one double bond. With a molecular weight of 99.15 g/mol, this compound is recognized for its versatility and reactivity, making it a valuable building block in the chemical industry.

Uses

Used in Pharmaceutical and Agrochemical Industries:
1H-Imidazol-5-amine,1,2-dimethyl-(9CI) is utilized as a reactant in organic synthesis for the preparation of pharmaceuticals and agrochemicals. Its unique structure and reactivity contribute to the development of various active ingredients and formulations in these sectors.
Used in Dye Production:
In the dye industry, 1,2-dimethylimidazole is employed as a reactant or intermediate in the synthesis of different types of dyes. Its chemical properties allow for the creation of a wide range of colorants used in various applications.
Used in Coating and Adhesive Manufacturing:
1H-Imidazol-5-amine,1,2-dimethyl-(9CI) also finds applications in the production of coatings and adhesives. Its role in these industries is to enhance the performance characteristics of the final products, such as adhesion strength, durability, and resistance to environmental factors.

InChI:InChI=1/C5H9N3/c1-4-7-3-5(6)8(4)2/h3H,6H2,1-2H3

Upstream product

• 73859-07-1 N-cyanomethyl-acetimidic acid ethyl ester 
• 74-89-5 methylamine 
• 551-92-8 dimetridazole 
• 60-29-7 diethyl ether 
• 151-63-3 cyanomethylamine sulfate 
• 584-08-7 potassium carbonate 

Downstream Products

• 145799-01-5 N-(3-Chloro-4-tolyl)-N¹-(1,2-dimethylimidazol-5-yl)urea 
• 145799-07-1 N-(1,2-Dimethylimidazol-5-yl)-N-phenylthiourea 
• 145799-00-4 N-(3,4-Dichlorophenyl)-N¹-(1,2-dimethylimidazol-5-yl)urea 
• 145838-30-8 5-amino-2,3-dimethylimidazo<4,5-b>pyridine-6-carboxylic acid 
• 145838-36-4 3,7-dihydro-2,3-dimethyl-6-phenylimidazo<4',5':5,6>pyrido<2,3-d>pyrimidin-8-one 
• 145838-35-3 2,3-dimethyl-6-phenyl-3,5,6,7-tetrahydroimidazo<4',5':5,6>pyrido<2,3-d>pyrimidin-8-one 
• 145838-58-0 3-(6-cyano-2,3-dimethylimidazo<4,5-b>pyridin-5-ylamino)cyclohex-2-enone 
• 145838-34-2 8-imino-2,3-dimethyl-7-phenyl-3,5,7,8-tetrahydroimidazo<4',5':5,6>pyrido<2,3-d>pyrimidine-6-thione 
• 145838-38-6 7-Benzyl-2,3-dimethyl-3,7-dihydro-1,3,4,5,7-pentaaza-cyclopenta[b]naphthalen-8-ylideneamine 
• 145838-46-6 Benzyl-(2,3-dimethyl-3H-1,3,4,5,7-pentaaza-cyclopenta[b]naphthalen-8-yl)-amine 
• 145838-33-1 7-(3,4-dichlorophenyl)-8-imino-2,3-dimethyl-3,5,7,8-tetrahydroimidazo<4',5':5,6>pyrido<2,3-d>pyrimidin-6-one 
• 1002742-25-7 8,9-dimethyl-6,6-diphenyl-1,3,6,9-tetrahydro-2H-purin-2-one 
• 1002742-23-5 8,9-dimethyl-6-(4-methylphenyl)-6-(trifluoromethyl)-1,3,6,9-tetrahydro-2H-purin-2-one 
• 1002742-03-1 N-(1,2-dimethyl-1H-imidazol-5-yl)-N'-phenylurea 

Relevant articles and documents

A Novel Synthesis of Purine and Deazapurine Derivatives from 5-Aminoimidazoles

Ccatalytic reduction of 4-unsubstituted-5-nitroimidazoles (3) in 1,4-dioxane solution is an excellent route to the 5-aminoimidazoles (1) which can be isolated or used in situ to generate good yields of purine or deazapurine derivatives.

Facile synthesis of fluorinated 1-desazapurines

A preparative approach towards 1-desazapurines, starting from 4(5)-aminoimidazoles and polyfluoroalkyl-containing 1,3-CCC-biselectrophiles was developed. As a result, a set of fluorinated 1-desazapurines was synthesized. Additionally, a synthetic route to 1-desazapurines bearing a sugar-mimicking group is proposed. Georg Thieme Verlag Stuttgart.

Novel imidazole compounds and use of these compounds for dyeing keratinous fibers

The disclosure relates to novel imidazole compounds which can be useful as couplers for the oxidation dyeing of keratinous fibers. The present disclosure also relates to a dyeing composition for dyeing keratinous fibers comprising at least one oxidation base and at least one coupler of the imidazole type as disclosed herein, and the dyeing method using this composition.