Tert-butyl (4-(tert-butyl)phenyl)carbamate CAS 110969-43-2

Purity 97%+In StockPharmaceutical Standards
CAS No.110969-43-2
Molecular FormulaC15H23NO2
Molecular Weight249.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl (4-(tert-butyl)phenyl)carbamate CAS 110969-43-2 chemical structure

Description

The occurrence of Tert-butyl (4-(tert-butyl)phenyl)carbamate is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

Tert-butyl (4-(tert-butyl)phenyl)carbamate (CAS 110969-43-2) is a high-purity analytical reference standard with the molecular formula C15H23NO2 and a molecular weight of 249.35 g/mol.

Tert-butyl (4-(tert-butyl)phenyl)carbamate (C15H23NO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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.

CATO manufactures Tert-butyl (4-(tert-butyl)phenyl)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 FormulaC15H23NO2
Molecular Weight249.35 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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