1-Methyl-2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole hydrochloride CAS 1185293-95-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1185293-95-1
Molecular FormulaC12H15N3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Methyl-2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole hydrochloride CAS 1185293-95-1 chemical structure

Description

1-Methyl-2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole hydrochloride (C12H15N3HCl) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies 1-Methyl-2-(pyrrolidin-2-yl)-1H-benzo[d]imidazole hydrochloride (CAS 1185293-95-1), a certified reference material (molecular formula C12H15N3HCl, MW 237.73 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 1-Methyl-2-(pyrrolidin-2-yl)-1H-benzo[d]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 FormulaC12H15N3 HCl
Molecular Weight237.73 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 Atoms3

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