2-[(4-Iodophenyl)amino]-4-methoxypyridine-3-carbonitrile CAS 341966-85-6

Purity 97%+In StockPharmaceutical Standards
CAS No.341966-85-6
Molecular FormulaC13H10IN3O
Molecular Weight351.14 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[(4-Iodophenyl)amino]-4-methoxypyridine-3-carbonitrile CAS 341966-85-6 chemical structure

Description

CATO manufactures 2-[(4-Iodophenyl)amino]-4-methoxypyridine-3-carbonitrile 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.

2-[(4-Iodophenyl)amino]-4-methoxypyridine-3-carbonitrile (CAS 341966-85-6), molecular formula C13H10IN3O and molecular weight 351.14 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution, 2-[(4-Iodophenyl)amino]-4-methoxypyridine-3-carbonitrile is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 351.14 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.

Physical & Chemical Properties

Molecular FormulaC13H10IN3O
Molecular Weight351.14 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 DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentI-containing
Nitrogen Atoms3

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