2-METHYLIMIDAZOLE

PRODUCT IDENTIFICATION

CAS NO

693-98-1

2-METHYLIMIDAZOLE

EINECS NO. 211-765-7
FORMULA C4H6N2
MOL WT. 82.11
H.S. CODE 2933.29

TOXICITY

 
SYNONYMS 2-methyl-1H-imidazole;

SMILES

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES

PHYSICAL STATE

colorless to slightly yellow crystalline solod

MELTING POINT 142 - 143 C
BOILING POINT 267 - 268 C
SPECIFIC GRAVITY  
SOLUBILITY IN WATER

soluble

pH

 

VAPOR DENSITY  
AUTOIGNITION

 

NFPA RATINGS  

REFRACTIVE INDEX

 
FLASH POINT

155 C

STABILITY Stable under ordinary conditions

APPLICATIONS

2-Methylimidazole is used as an intermediate for pharmaceuticals, agrochemicals, dyes, textile auxiliaries, pigments and other organic chemicals. It is also used in polyurethane manufacturings and epoxy resins as a curing agent.
SALES SPECIFICATION

APPEARANCE

Clear to yellow solid

ASSAY

98.5% min

WATER

0.5% max

TRANSPORTATION
PACKING 25kgs in bag
HAZARD CLASS 8 (Packing group:III)
UN NO. 3263
DESCRIPTION OF IMIDAZOLE
Imidazole is a heterocyclic compound of five-membered diunsaturated ring structure composed of three carbon atoms and two nitrogen atoms at nonadjacent positions. The simplest member of the imidazole family is imidazole itself, colorless to pale yellow crystalline solid with a weak aminelike odor; soluble in water and alcohol, melts at 89 C, boils at 256 C. Imidazoles are poorly soluble in water generally, but are dissolved in organic solvents, such as chloroform, propylene glycol, and polyethoxylated castor oil. Imidazole ring is found in histidine (an essential amino acid) and histamine, the decarboxylated compound from histamine. Some imidazole compounds inhibit the biosynthesis of ergosterol, required in cell membrane in fungal. They have antibacterial, antifungal, antiprotozoal, and anthelmintic activity. Several distinct phenylimidazoles are therapeutically useful antifungal agents against either superficial or systemic infections. Thiabendazoles which have anthelmintic and antifungal properties are imidazole class compounds. Benzimidazole is a dicyclic compound having midazole ring fused to benzene. Benzimidazole structure is a part of the nucleotide portion of vitamin B12 and the nucleus in some drugs such as proton pump inhibitors and anthelmintic agents. Imidazole has two nitrogen atoms. The one is slightly acidic, while the other is basic. Imidazole and its derivatives are widely used as intermediates in synthesis of organic target compounds including pharmaceuticals, agrochemicals, dyes, photographic chemicals, corrosion inhibitors, epoxy curing agents, adhesives and plastic modifiers. Some imidazole analogues which contain nitrogen in five-membered ring structure are:
  • Triazole: An analog of imidazole.It has three nitrogen atoms and two carbon atoms at nonadjacent positions in the ring system.
  • Pyrrole: An analog of imidazole. It has only one nitrogen atom in the ring system. Pyrrole ring system is involved in coloured products (green pigment, chlorophyll; red, hemoglobin; , blue, indigo) in nature.
  • Pyrroline: A pyrrole in which one of the two solid bonds are hydrogenated.
  • Pyrrolidine: The saturated tetrahydropyrrole, a part of the structures of amino acids (proline, hydroxyproline and hygrine).
  • Pyrazole: 1,2-Diazole (Imidazole isomer). The nitrogen positions are 1 and 2. It is not found in nature
  • Pyrazolone: Pyrazole analog with ketone group at 5 positon
  • Oxazole: an analog of imidazole. The nitrogen atom in position 1 is replaced by oxygen.
  • Isoxazole: an analog of pyrazole. The nitrogen atom at position 1 is replaced by oxygen.
  • Isothiazole:an analog of pyrazole. The nitrogen atom at position 1 is replaced by sulfur.

Triazole

Pyrrole

1-Pyrroline

3-Pyrroline

1,2,4-Triazole

Pyrrole

1-Pyrroline

3-Pyrroline

Pyrrolidine

Pyrazole

Pyrazolone

Oxazole

Pyrrolidine

Pyrazole

Pyrazolone

Oxazole

Isoxazole

Isothiazole

BENZIMIDAZOLE

Thiabendazole

Isoxazole

Isothiazole

Benzimidazole

Thiabendazole