tert-Butyl 2-(4-bromobenzyl)-3-(methylamino)propanoatehydrochloride CAS 1159822-24-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1159822-24-8
Molecular FormulaC15H22BrNO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 2-(4-bromobenzyl)-3-(methylamino)propanoatehydrochloride CAS 1159822-24-8 chemical structure

Description

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

CATO supplies tert-Butyl 2-(4-bromobenzyl)-3-(methylamino)propanoatehydrochloride (CAS 1159822-24-8), a certified reference material (molecular formula C15H22BrNO2HCl, MW 364.71 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/bromine substitution, tert-Butyl 2-(4-bromobenzyl)-3-(methylamino)propanoatehydrochloride is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 364.71 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures tert-Butyl 2-(4-bromobenzyl)-3-(methylamino)propanoatehydrochloride 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 FormulaC15H22BrNO2 HCl
Molecular Weight364.71 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl/Br-containing
Nitrogen Atoms1

Recommended Standards

Why CATO?