2-[4-(chloromethyl)phenoxymethyl]-1-methyl-1H-imidazole hydrochloride CAS 1170478-93-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1170478-93-9
Molecular FormulaC12H13ClN2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[4-(chloromethyl)phenoxymethyl]-1-methyl-1H-imidazole hydrochloride CAS 1170478-93-9 chemical structure

Description

The molecular framework of 2-[4-(chloromethyl)phenoxymethyl]-1-methyl-1H-imidazole hydrochloride (C12H13ClN2OHCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 2-[4-(chloromethyl)phenoxymethyl]-1-methyl-1H-imidazole hydrochloride (CAS 1170478-93-9), a certified reference material (molecular formula C12H13ClN2OHCl, MW 273.16 g/mol) for analytical method development and quality control.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 2-[4-(chloromethyl)phenoxymethyl]-1-methyl-1H-imidazole hydrochloride under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC12H13ClN2O HCl
Molecular Weight273.16 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms2

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