n-(Piperidin-4-yl)pyridine-3-carboxamide dihydrochloride CAS 1211811-66-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1211811-66-3
Molecular FormulaC11H15N3O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(Piperidin-4-yl)pyridine-3-carboxamide dihydrochloride CAS 1211811-66-3 chemical structure

Description

n-(Piperidin-4-yl)pyridine-3-carboxamide dihydrochloride (C11H15N3OHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

n-(Piperidin-4-yl)pyridine-3-carboxamide dihydrochloride (CAS 1211811-66-3), molecular formula C11H15N3OHCl and molecular weight 241.72 g/mol, is a CATO reference standard with documented purity and traceability.

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.

As a certified reference material (CRM), n-(Piperidin-4-yl)pyridine-3-carboxamide dihydrochloride meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H15N3O 2*HCl
Molecular Weight241.72 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms3

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