2-Hydroxy-3-methylcholanthrene CAS 3308-64-3

Purity 97%+In StockPharmaceutical Standards
CAS No.3308-64-3
Molecular FormulaC21H16O
Molecular Weight284.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Hydroxy-3-methylcholanthrene CAS 3308-64-3 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2-Hydroxy-3-methylcholanthrene.

2-Hydroxy-3-methylcholanthrene (CAS 3308-64-3), molecular formula C21H16O and molecular weight 284.35 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a steroid core, a hydroxyl group, an ether linkage, 2-Hydroxy-3-methylcholanthrene is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 284.35 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

CATO manufactures 2-Hydroxy-3-methylcholanthrene 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 FormulaC21H16O
Molecular Weight284.35 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957

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Why CATO?