benzyl N-[cis-3-(hydroxymethyl)cyclopentyl]carbamate CAS 1380486-16-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1380486-16-7
Molecular FormulaC14H25NO3
Molecular Weight255.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

benzyl N-[cis-3-(hydroxymethyl)cyclopentyl]carbamate CAS 1380486-16-7 chemical structure

Description

benzyl N-[cis-3-(hydroxymethyl)cyclopentyl]carbamate (CAS 1380486-16-7), molecular formula C14H25NO3 and molecular weight 255.35 g/mol, is a CATO reference standard with documented purity and traceability.

benzyl N-[cis-3-(hydroxymethyl)cyclopentyl]carbamate (C14H25NO3) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, 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).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), benzyl N-[cis-3-(hydroxymethyl)cyclopentyl]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.

Physical & Chemical Properties

Molecular FormulaC14H25NO3
Molecular Weight255.35 g/mol
AppearanceWhite 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; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1991
Nitrogen Atoms1

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