5-(3-Fluorophenyl)pyridine-3,4-diamine dihydrochloride CAS 1956307-53-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1956307-53-1
Molecular FormulaC11H10FN3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(3-Fluorophenyl)pyridine-3,4-diamine dihydrochloride CAS 1956307-53-1 chemical structure

Description

Based on its molecular formula C11H10FN3HCl, 5-(3-Fluorophenyl)pyridine-3,4-diamine dihydrochloride contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 239.68 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).

5-(3-Fluorophenyl)pyridine-3,4-diamine dihydrochloride (CAS 1956307-53-1) is a high-purity analytical reference standard with the molecular formula C11H10FN3HCl and a molecular weight of 239.68 g/mol.

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.

CATO manufactures 5-(3-Fluorophenyl)pyridine-3,4-diamine dihydrochloride 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 FormulaC11H10FN3 2*HCl
Molecular Weight239.68 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentF/Cl-containing
Nitrogen Atoms3

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