4-Chloro-3-iodo-6-methyl-5-(trifluoromethyl)pyridin-2-amine CAS 2852767-62-3

Purity 97%+In StockPharmaceutical Standards
CAS No.2852767-62-3
Molecular FormulaC7H5ClF3IN2
Molecular Weight336.48 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-3-iodo-6-methyl-5-(trifluoromethyl)pyridin-2-amine CAS 2852767-62-3 chemical structure

Description

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.

4-Chloro-3-iodo-6-methyl-5-(trifluoromethyl)pyridin-2-amine (CAS 2852767-62-3) is a high-purity analytical reference standard with the molecular formula C7H5ClF3IN2 and a molecular weight of 336.48 g/mol.

Owing to a nitrile group, fluorine/chlorine/iodine substitution, an aromatic ring system, 4-Chloro-3-iodo-6-methyl-5-(trifluoromethyl)pyridin-2-amine is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 336.48 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.

CATO manufactures 4-Chloro-3-iodo-6-methyl-5-(trifluoromethyl)pyridin-2-amine 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 FormulaC7H5ClF3IN2
Molecular Weight336.48 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2003
Halogen ContentF/Cl/I-containing
Nitrogen Atoms2

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