tert-Butyl N-(4-hydroxyphenyl)-N-propylcarbamate CAS 1881292-47-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1881292-47-2
Molecular FormulaC14H21NO3
Molecular Weight251.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl N-(4-hydroxyphenyl)-N-propylcarbamate CAS 1881292-47-2 chemical structure

Description

CATO manufactures tert-Butyl N-(4-hydroxyphenyl)-N-propylcarbamate 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.

CATO supplies tert-Butyl N-(4-hydroxyphenyl)-N-propylcarbamate (CAS 1881292-47-2), a certified reference material (molecular formula C14H21NO3, MW 251.32 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, tert-Butyl N-(4-hydroxyphenyl)-N-propylcarbamate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 251.32 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

Physical & Chemical Properties

Molecular FormulaC14H21NO3
Molecular Weight251.32 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Nitrogen Atoms1

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