3-(Trifluoromethyl)pyridine-4-thiol CAS 1806316-97-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1806316-97-1
Molecular FormulaC6H4F3NS
Molecular Weight179.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(Trifluoromethyl)pyridine-4-thiol CAS 1806316-97-1 chemical structure

Description

The occurrence of 3-(Trifluoromethyl)pyridine-4-thiol is closely related to a nitrile group, sulfur-containing functionality, fluorine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 3-(Trifluoromethyl)pyridine-4-thiol (CAS 1806316-97-1), a certified reference material (molecular formula C6H4F3NS, MW 179.16 g/mol) for analytical method development and quality control.

3-(Trifluoromethyl)pyridine-4-thiol (C6H4F3NS) contains a nitrile group, sulfur-containing functionality, fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

CATO manufactures 3-(Trifluoromethyl)pyridine-4-thiol 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 FormulaC6H4F3NS
Molecular Weight179.16 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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-containing
Nitrogen Atoms1
Sulfur Atoms1

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