Methyl 3-amino-2,2-bis(4-methylbenzyl)propanoate hydrochloride CAS 1255099-51-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1255099-51-4
Molecular FormulaC20H25NO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-amino-2,2-bis(4-methylbenzyl)propanoate hydrochloride CAS 1255099-51-4 chemical structure

Description

Methyl 3-amino-2,2-bis(4-methylbenzyl)propanoate hydrochloride (CAS 1255099-51-4) is a high-purity analytical reference standard with the molecular formula C20H25NO2HCl and a molecular weight of 347.88 g/mol.

Based on its molecular formula C20H25NO2HCl, Methyl 3-amino-2,2-bis(4-methylbenzyl)propanoate hydrochloride contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 347.88 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 Methyl 3-amino-2,2-bis(4-methylbenzyl)propanoate 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 FormulaC20H25NO2 HCl
Molecular Weight347.88 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms1

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