(4-Benzyl-3,5-bis(benzyloxy)phenyl)methanol CAS 1199274-62-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1199274-62-8
Molecular FormulaC28H26O3
Molecular Weight410.50 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4-Benzyl-3,5-bis(benzyloxy)phenyl)methanol CAS 1199274-62-8 chemical structure

Description

The occurrence of (4-Benzyl-3,5-bis(benzyloxy)phenyl)methanol is closely related to a steroid core, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies (4-Benzyl-3,5-bis(benzyloxy)phenyl)methanol (CAS 1199274-62-8), a certified reference material (molecular formula C28H26O3, MW 410.50 g/mol) for analytical method development and quality control.

Based on its molecular formula C28H26O3, (4-Benzyl-3,5-bis(benzyloxy)phenyl)methanol contains a steroid core, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 410.50 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

CATO manufactures (4-Benzyl-3,5-bis(benzyloxy)phenyl)methanol 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 FormulaC28H26O3
Molecular Weight410.50 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, 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
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989

Recommended Standards

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