tert-Butyl (5-bromo-2-hydroxybenzyl)carbamate CAS 1392846-44-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1392846-44-4
Molecular FormulaC12H16BrNO3
Molecular Weight302.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (5-bromo-2-hydroxybenzyl)carbamate CAS 1392846-44-4 chemical structure

Description

As a certified reference material (CRM), tert-Butyl (5-bromo-2-hydroxybenzyl)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.

CATO supplies tert-Butyl (5-bromo-2-hydroxybenzyl)carbamate (CAS 1392846-44-4), a certified reference material (molecular formula C12H16BrNO3, MW 302.16 g/mol) for analytical method development and quality control.

tert-Butyl (5-bromo-2-hydroxybenzyl)carbamate (C12H16BrNO3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, 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).

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.

Physical & Chemical Properties

Molecular FormulaC12H16BrNO3
Molecular Weight302.16 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentBr-containing
Nitrogen Atoms1

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