5-Chloro-2-iodo-3-(trifluoromethyl)pyridine CAS 1807208-32-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1807208-32-7
Molecular FormulaC6H2ClF3IN
Molecular Weight307.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Chloro-2-iodo-3-(trifluoromethyl)pyridine CAS 1807208-32-7 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies 5-Chloro-2-iodo-3-(trifluoromethyl)pyridine (CAS 1807208-32-7), a certified reference material (molecular formula C6H2ClF3IN, MW 307.44 g/mol) for analytical method development and quality control.

Based on its molecular formula C6H2ClF3IN, 5-Chloro-2-iodo-3-(trifluoromethyl)pyridine contains a nitrile group, fluorine/chlorine/iodine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 307.44 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO manufactures 5-Chloro-2-iodo-3-(trifluoromethyl)pyridine 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 FormulaC6H2ClF3IN
Molecular Weight307.44 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 methanol, acetonitrile, DMSO
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.)1995
Halogen ContentF/Cl/I-containing
Nitrogen Atoms1

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