benzyl N-[cis-4-hydroxycyclopent-2-en-1-yl]carbamate CAS 205675-68-9

Purity 97%+In StockPharmaceutical Standards
CAS No.205675-68-9
Molecular FormulaC13H21NO3
Molecular Weight239.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

benzyl N-[cis-4-hydroxycyclopent-2-en-1-yl]carbamate CAS 205675-68-9 chemical structure

Description

benzyl N-[cis-4-hydroxycyclopent-2-en-1-yl]carbamate (C13H21NO3) contains a nitrogen-containing heterocyclic scaffold, an amide 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

benzyl N-[cis-4-hydroxycyclopent-2-en-1-yl]carbamate (CAS 205675-68-9), molecular formula C13H21NO3 and molecular weight 239.31 g/mol, is a CATO reference standard with documented purity and traceability.

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.

As a certified reference material (CRM), benzyl N-[cis-4-hydroxycyclopent-2-en-1-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.

Physical & Chemical Properties

Molecular FormulaC13H21NO3
Molecular Weight239.31 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; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2015
Nitrogen Atoms1

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