(E)-3,5-di-tert-butyl-4-hydroxybenzaldehyde O-methyl oxime CAS 14446-64-1

Purity 97%+In StockPharmaceutical Standards
CAS No.14446-64-1
Molecular FormulaC16H25NO2
Molecular Weight263.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-3,5-di-tert-butyl-4-hydroxybenzaldehyde O-methyl oxime CAS 14446-64-1 chemical structure

Description

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.

(E)-3,5-di-tert-butyl-4-hydroxybenzaldehyde O-methyl oxime (CAS 14446-64-1) is a high-purity analytical reference standard with the molecular formula C16H25NO2 and a molecular weight of 263.38 g/mol.

The molecular framework of (E)-3,5-di-tert-butyl-4-hydroxybenzaldehyde O-methyl oxime (C16H25NO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures (E)-3,5-di-tert-butyl-4-hydroxybenzaldehyde O-methyl oxime 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 FormulaC16H25NO2
Molecular Weight263.38 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.)1961
Nitrogen Atoms1

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