5-(piperidin-4-yl)-1,3,4-oxadiazol-2-amine dihydrochloride CAS 1909337-36-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1909337-36-5
Molecular FormulaC7H12N4O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(piperidin-4-yl)-1,3,4-oxadiazol-2-amine dihydrochloride CAS 1909337-36-5 chemical structure

Description

CATO supplies 5-(piperidin-4-yl)-1,3,4-oxadiazol-2-amine dihydrochloride (CAS 1909337-36-5), a certified reference material (molecular formula C7H12N4OHCl, MW 204.66 g/mol) for analytical method development and quality control.

The molecular framework of 5-(piperidin-4-yl)-1,3,4-oxadiazol-2-amine dihydrochloride (C7H12N4OHCl) is characterized by an amide group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

As a certified reference material (CRM), 5-(piperidin-4-yl)-1,3,4-oxadiazol-2-amine 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 FormulaC7H12N4O 2*HCl
Molecular Weight204.66 g/mol
AppearanceWhite to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor)
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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1995
Halogen ContentCl-containing
Nitrogen Atoms4

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