2-(1h-1,3-Benzodiazol-1-yl)pyridine-4-carboximidamide hydrochloride CAS 1221725-54-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1221725-54-7
Molecular FormulaC13H11N5
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(1h-1,3-Benzodiazol-1-yl)pyridine-4-carboximidamide hydrochloride CAS 1221725-54-7 chemical structure

Description

CATO supplies 2-(1h-1,3-Benzodiazol-1-yl)pyridine-4-carboximidamide hydrochloride (CAS 1221725-54-7), a certified reference material (molecular formula C13H11N5HCl, MW 273.72 g/mol) for analytical method development and quality control.

Based on its molecular formula C13H11N5HCl, 2-(1h-1,3-Benzodiazol-1-yl)pyridine-4-carboximidamide hydrochloride contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 273.72 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 2-(1h-1,3-Benzodiazol-1-yl)pyridine-4-carboximidamide hydrochloride 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 FormulaC13H11N5 HCl
Molecular Weight273.72 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms5

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