3,5-Dimethyl-3-iodo-4-methoxybenzophenone CAS 951884-47-2

Purity 97%+In StockPharmaceutical Standards
CAS No.951884-47-2
Molecular FormulaC16H15IO2
Molecular Weight366.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,5-Dimethyl-3-iodo-4-methoxybenzophenone CAS 951884-47-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 366.19 g/mol gives 3,5-Dimethyl-3-iodo-4-methoxybenzophenone distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 3,5-Dimethyl-3-iodo-4-methoxybenzophenone (CAS 951884-47-2), a certified reference material (molecular formula C16H15IO2, MW 366.19 g/mol) for analytical method development and quality control.

Structurally, 3,5-Dimethyl-3-iodo-4-methoxybenzophenone (C16H15IO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, a polycyclic aromatic system. The molecule exhibits a degree of unsaturation (DBE) of 9.0, corresponding to approximately 9 ring(s) or double-bond equivalent(s). With a molecular weight of 366.19 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC16H15IO2
Molecular Weight366.19 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; 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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