(S)-2-((tert-butoxycarbonyl)amino)-3-(quinoxalin-2-yl)propanoic acid CAS 161453-38-9

Purity 97%+In StockPharmaceutical Standards
CAS No.161453-38-9
Molecular FormulaC16H19N3O4
Molecular Weight317.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-((tert-butoxycarbonyl)amino)-3-(quinoxalin-2-yl)propanoic acid CAS 161453-38-9 chemical structure

Description

CATO manufactures (S)-2-((tert-butoxycarbonyl)amino)-3-(quinoxalin-2-yl)propanoic acid 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.

(S)-2-((tert-butoxycarbonyl)amino)-3-(quinoxalin-2-yl)propanoic acid (CAS 161453-38-9) is a high-purity analytical reference standard with the molecular formula C16H19N3O4 and a molecular weight of 317.34 g/mol.

The molecular framework of (S)-2-((tert-butoxycarbonyl)amino)-3-(quinoxalin-2-yl)propanoic acid (C16H19N3O4) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage. 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. 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.

Physical & Chemical Properties

Molecular FormulaC16H19N3O4
Molecular Weight317.34 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2003
Nitrogen Atoms3

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