3,5-Dimethoxy-2-iodobenzophenone CAS 951892-13-0

Purity 97%+In StockPharmaceutical Standards
CAS No.951892-13-0
Molecular FormulaC15H13IO3
Molecular Weight368.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,5-Dimethoxy-2-iodobenzophenone CAS 951892-13-0 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 3,5-Dimethoxy-2-iodobenzophenone.

3,5-Dimethoxy-2-iodobenzophenone (CAS 951892-13-0) is a high-purity analytical reference standard with the molecular formula C15H13IO3 and a molecular weight of 368.17 g/mol.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, a polycyclic aromatic system, 3,5-Dimethoxy-2-iodobenzophenone is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 368.17 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures 3,5-Dimethoxy-2-iodobenzophenone 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 FormulaC15H13IO3
Molecular Weight368.17 g/mol
AppearancePale yellow to 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentI-containing

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