Tert-butyl (S)-(3-oxo-1-phenylbutan-2-yl)carbamate CAS 85613-64-5

Purity 97%+In StockPharmaceutical Standards
CAS No.85613-64-5
Molecular FormulaC15H21NO3
Molecular Weight263.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl (S)-(3-oxo-1-phenylbutan-2-yl)carbamate CAS 85613-64-5 chemical structure

Description

As a certified reference material (CRM), Tert-butyl (S)-(3-oxo-1-phenylbutan-2-yl)carbamate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Tert-butyl (S)-(3-oxo-1-phenylbutan-2-yl)carbamate (CAS 85613-64-5), molecular formula C15H21NO3 and molecular weight 263.33 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, Tert-butyl (S)-(3-oxo-1-phenylbutan-2-yl)carbamate (C15H21NO3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 263.33 g/mol, it falls into the medium-molecular-weight range. 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 FormulaC15H21NO3
Molecular Weight263.33 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 chloroform, dichloromethane, ethyl acetate, DMSO
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.)1981
Nitrogen Atoms1

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