Phenylmethyl N-[(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutyl]carbamate CAS 197892-14-1

Purity 97%+In StockPharmaceutical Standards
CAS No.197892-14-1
Molecular FormulaC17H26N2O5
Molecular Weight338.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenylmethyl N-[(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutyl]carbamate CAS 197892-14-1 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.

CATO supplies Phenylmethyl N-[(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutyl]carbamate (CAS 197892-14-1), a certified reference material (molecular formula C17H26N2O5, MW 338.40 g/mol) for analytical method development and quality control.

Phenylmethyl N-[(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutyl]carbamate (C17H26N2O5) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 Phenylmethyl N-[(3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutyl]carbamate 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 FormulaC17H26N2O5
Molecular Weight338.40 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 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2013
Nitrogen Atoms2

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