(6-Iodo-5-methylpyridin-3-yl)(phenyl)methanone CAS 1355182-85-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1355182-85-2
Molecular FormulaC13H10INO
Molecular Weight323.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(6-Iodo-5-methylpyridin-3-yl)(phenyl)methanone CAS 1355182-85-2 chemical structure

Description

Structurally, (6-Iodo-5-methylpyridin-3-yl)(phenyl)methanone (C13H10INO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. 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 323.13 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies (6-Iodo-5-methylpyridin-3-yl)(phenyl)methanone (CAS 1355182-85-2), a certified reference material (molecular formula C13H10INO, MW 323.13 g/mol) for analytical method development and quality control.

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 (6-Iodo-5-methylpyridin-3-yl)(phenyl)methanone 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 FormulaC13H10INO
Molecular Weight323.13 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
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentI-containing
Nitrogen Atoms1

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