Phenyl (4-hydroxyphenyl)carbamate CAS 14235-95-1

Purity 97%+In StockPharmaceutical Standards
CAS No.14235-95-1
Molecular FormulaC13H11NO3
Molecular Weight229.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenyl (4-hydroxyphenyl)carbamate CAS 14235-95-1 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 229.23 g/mol gives Phenyl (4-hydroxyphenyl)carbamate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Phenyl (4-hydroxyphenyl)carbamate (CAS 14235-95-1), a certified reference material (molecular formula C13H11NO3, MW 229.23 g/mol) for analytical method development and quality control.

Phenyl (4-hydroxyphenyl)carbamate (C13H11NO3) 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).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC13H11NO3
Molecular Weight229.23 g/mol
AppearancePale yellow to 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Nitrogen Atoms1

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