3,5-Bis(tert-butyl)-4-hydroxybenzene-propanoyl chloride CAS 3062-64-4

Purity 97%+In StockPharmaceutical Standards
CAS No.3062-64-4
Molecular FormulaC17H25ClO2
Molecular Weight296.83 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,5-Bis(tert-butyl)-4-hydroxybenzene-propanoyl chloride CAS 3062-64-4 chemical structure

Description

As a certified reference material (CRM), 3,5-Bis(tert-butyl)-4-hydroxybenzene-propanoyl chloride 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.

3,5-Bis(tert-butyl)-4-hydroxybenzene-propanoyl chloride (CAS 3062-64-4) is a high-purity analytical reference standard with the molecular formula C17H25ClO2 and a molecular weight of 296.83 g/mol.

The molecular framework of 3,5-Bis(tert-butyl)-4-hydroxybenzene-propanoyl chloride (C17H25ClO2) is characterized by a steroid core, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC17H25ClO2
Molecular Weight296.83 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; 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.)1957
Halogen ContentCl-containing

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