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1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE

1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE Structure
CAS No.
35454-39-8
Chemical Name:
1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE
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-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE;MECHAN. MEASURING STATION, AMELUNG*NO. D10013;1-MethyliMidazole-4-acetic acid hydrochloride;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
CBNumber:
CB7759318
Molecular Formula:
C6H9ClN2O2
Molecular Weight:
176.6
MOL File:
35454-39-8.mol
MSDS File:
SDS
Modify Date:
2023/5/18 11:31:05
Request For Quotation

1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE Properties

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

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P280-P305+P351+P338
WGK Germany  3

1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE Chemical Properties,Uses,Production

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.

1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE Preparation Products And Raw materials

Raw materials

Preparation Products

1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE Suppliers

Global( 42)Suppliers
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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
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Aladdin Scientific +1-+1(833)-552-7181 United States 52927 58 Inquiry
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Shanghai Sunway Pharmaceutical Technology Co.,Ltd. 021-51816796-820 13611835272 China 44462 58 Inquiry
Nanjing Norris-Pharm Technology Co., Ltd 13901585132 China 8888 55 Inquiry
Supplier Advantage
CLEARSYNTH LABS LTD. 58
Career Henan Chemica Co 58
Aladdin Scientific 58
Suzhou ARTK Medchem Co., Ltd. 58
Amadis Chemical Company Limited 58
Shanghai Hao Zhun Biological Technology Co., Ltd. 58
PharmaBlock Sciences (Nanjing), Inc. 58
TargetMol Chemicals Inc. 58
Shanghai Sunway Pharmaceutical Technology Co.,Ltd. 58
Nanjing Norris-Pharm Technology Co., Ltd 55

35454-39-8(1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE)Related Search:

METHYL 2-(6-CHLOROIMIDAZO[1,2-A]PYRIDIN-2-YL)ACETATE (1H-IMIDAZOL-4-YL)-ACETALDEHYDE Imidazole-4-acetic acid (1-METHYL-1H-IMIDAZOL-4-YL)-ACETIC ACID 2-(3H-imidazol-4-yl)acetic acid
4-IMIDAZOLEACETIC ACID HYDROCHLORIDE (1-METHYL-1H-IMIDAZOL-4-YL)-ACETALDEHYDE 1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE Imidazolyl-4-ethanol 2-(1,7-diazabicyclo[4.3.0]nona-2,4,6,8-tetraen-8-yl)acetic acid
BASIONIC(TM) AC 75 (6-CHLORO-IMIDAZO[1,2-A]PYRIDIN-2-YL)-ACETIC ACID
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1-METHYL-4-IMIDAZOLE ACETIC ACID HCL 1-METHYL-4-IMIDAZOLEACETIC ACID HYDROCHLORIDE 1-methyl-1H-imidazol-4-acetic acid monohydrochloride MECHAN. MEASURING STATION, AMELUNG*NO. D10013 1-METHYL-4-IMIDAZOLEACETIC ACID HYDROGEN CHLORIDE 1-MethyliMidazole-4-acetic acid hydrochloride 2-(1-Methyl-1H-imidazol-4-yl)ethanoic acid hydrochloride 2-(1-Methyl-1H-imidazol-4-yl)acetic acid hydrochloride (1-Methyl-1H-imidazol-4-yl)-acetic acid hydrochloride 2-(1-METHYL-1H-IMIDAZOL-4-YL)ACETIC ACID HCL 1H-Imidazole-4-aceticacid, 1-methyl-, hydrochloride (1:1) 1-Methyl-15N2-imidazol-4-yl acetic acid HCl 35454-39-8 Heterocyclic Building Blocks Imidazoles Building Blocks Heterocyclic Compounds