Methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate CAS 92136-56-6

Purity 97%+In StockPharmaceutical Standards
CAS No.92136-56-6
Molecular FormulaC16H23NO4
Molecular Weight293.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate CAS 92136-56-6 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.

Methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate (CAS 92136-56-6), molecular formula C16H23NO4 and molecular weight 293.36 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of Methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate (C16H23NO4) is characterized by a nitrogen-containing heterocyclic scaffold, 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).

CATO manufactures Methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-4-phenylbutanoate 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 FormulaC16H23NO4
Molecular Weight293.36 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1983
Nitrogen Atoms1

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