ChemicalBook--->CAS DataBase List--->35454-39-8

35454-39-8

35454-39-8 Structure

35454-39-8 Structure
IdentificationBack Directory
[Name]

1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE
[CAS]

35454-39-8
[Synonyms]

1-METHYL-4-IMIDAZOLE ACETIC ACID HCL
1-Methyl-15N2-imidazol-4-yl acetic acid HCl
2-(1-METHYL-1H-IMIDAZOL-4-YL)ACETIC ACID HCL
1-MethyliMidazole-4-acetic acid hydrochloride
1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE
MECHAN. MEASURING STATION, AMELUNG*NO. D10013
1-METHYL-4-IMIDAZOLEACETIC ACID HYDROGEN CHLORIDE
1-methyl-1H-imidazol-4-acetic acid monohydrochloride
(1-Methyl-1H-imidazol-4-yl)-acetic acid hydrochloride
2-(1-Methyl-1H-imidazol-4-yl)acetic acid hydrochloride
2-(1-Methyl-1H-imidazol-4-yl)ethanoic acid hydrochloride
1H-Imidazole-4-aceticacid, 1-methyl-, hydrochloride (1:1)
[EINECS(EC#)]

252-577-5
[Molecular Formula]

C6H9ClN2O2
[MDL Number]

MFCD00036998
[MOL File]

35454-39-8.mol
[Molecular Weight]

176.6
Chemical PropertiesBack Directory
[Melting point ]

204-206℃
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

DMSO (Slightly), Methanol (Slightly), Water (Slightly)
[form ]

Solid
[color ]

Light Beige to Beige
[Stability:]

Hygroscopic
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P305+P351+P338
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

1-Methyl-4-imidazoleacetic acid (MIMA) is a stable metabolite of histamine that is produced by the oxidation of the primary metabolite, N-methylhistamine. Urinary levels of MIMA are commonly measured to evaluate histamine secretion, particularly in the context of systemic mastocytosis.
[Uses]

1-Methyl-4-imidazoleacetic Acid Hydrochloride is a metabolite of histamine (H436500), which is produced by mast cells and involved with the inflammatory response. 1-Methyl-4-imidazoleacetic Acid Hydrochloride can also be used to synthesize N-[1-(9,10-methano-9-anthracenylmethyl)-4-piperidinyl]alkanamides and analogs as dopamine D2 receptor antagonists.
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