1-tert-Butyl 4-Methyl (S)-2-Aminosuccinate Hydrochloride CAS 34582-30-4

Purity 97%+In StockPharmaceutical Standards
CAS No.34582-30-4
Molecular FormulaC9H17NO4
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-tert-Butyl 4-Methyl (S)-2-Aminosuccinate Hydrochloride CAS 34582-30-4 chemical structure

Description

The molecular framework of 1-tert-Butyl 4-Methyl (S)-2-Aminosuccinate Hydrochloride (C9H17NO4HCl) is characterized by an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

1-tert-Butyl 4-Methyl (S)-2-Aminosuccinate Hydrochloride (CAS 34582-30-4) is a high-purity analytical reference standard with the molecular formula C9H17NO4HCl and a molecular weight of 239.70 g/mol.

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 1-tert-Butyl 4-Methyl (S)-2-Aminosuccinate 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 FormulaC9H17NO4 HCl
Molecular Weight239.70 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityLight-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)1.0
CAS Registry Year (est.)1966
Halogen ContentCl-containing
Nitrogen Atoms1

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