3-Fluoroisonicotinic acid CAS 393-53-3

Purity 97%+In StockPharmaceutical Standards
CAS No.393-53-3
Molecular FormulaC6H4FNO2
Molecular Weight141.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Fluoroisonicotinic acid CAS 393-53-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 141.10 g/mol gives 3-Fluoroisonicotinic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 3-Fluoroisonicotinic acid (CAS 393-53-3), a certified reference material (molecular formula C6H4FNO2, MW 141.10 g/mol) for analytical method development and quality control.

Structurally, 3-Fluoroisonicotinic acid (C6H4FNO2) contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 141.10 g/mol, it falls into the low-molecular-weight range. 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).

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-Fluoroisonicotinic acid 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 FormulaC6H4FNO2
Molecular Weight141.10 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Halogen ContentF-containing
Nitrogen Atoms1

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