N-(3-Methoxybenzyl)-1-butanamine hydrochloride CAS 935250-88-7

Purity 97%+In StockPharmaceutical Standards
CAS No.935250-88-7
Molecular FormulaC12H19NO
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-Methoxybenzyl)-1-butanamine hydrochloride CAS 935250-88-7 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including N-(3-Methoxybenzyl)-1-butanamine hydrochloride.

CATO supplies N-(3-Methoxybenzyl)-1-butanamine hydrochloride (CAS 935250-88-7), a certified reference material (molecular formula C12H19NOHCl, MW 229.75 g/mol) for analytical method development and quality control.

N-(3-Methoxybenzyl)-1-butanamine hydrochloride (C12H19NOHCl) contains an amide group, a hydroxyl group, an ether linkage, 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. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures N-(3-Methoxybenzyl)-1-butanamine 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 FormulaC12H19NO HCl
Molecular Weight229.75 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms1

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