4-(Aminomethyl)-2-methoxyphenol hydrochloride CAS 7149-10-2

Purity >95%In StockPharmaceutical Standards
CAS No.7149-10-2
Molecular FormulaC8H11NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Aminomethyl)-2-methoxyphenol hydrochloride CAS 7149-10-2 chemical structure

Description

CATO supplies 4-(Aminomethyl)-2-methoxyphenol hydrochloride (CAS 7149-10-2), a certified reference material (molecular formula C8H11NO2HCl, MW 189.64 g/mol) for analytical method development and quality control.

4-(Aminomethyl)-2-methoxyphenol hydrochloride (C8H11NO2HCl) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; 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.

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 4-(Aminomethyl)-2-methoxyphenol 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 FormulaC8H11NO2 HCl
Molecular Weight189.64 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
Purity>95%
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1959
Halogen ContentCl-containing
Nitrogen Atoms1

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