1-[4-(6-Chloro-pyridazin-3-ylmethyl)-piperidin-1-yl]-ethanone CAS 1316222-53-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1316222-53-3
Molecular FormulaC12H16ClN3O
Molecular Weight253.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-[4-(6-Chloro-pyridazin-3-ylmethyl)-piperidin-1-yl]-ethanone CAS 1316222-53-3 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies 1-[4-(6-Chloro-pyridazin-3-ylmethyl)-piperidin-1-yl]-ethanone (CAS 1316222-53-3), a certified reference material (molecular formula C12H16ClN3O, MW 253.73 g/mol) for analytical method development and quality control.

Structurally, 1-[4-(6-Chloro-pyridazin-3-ylmethyl)-piperidin-1-yl]-ethanone (C12H16ClN3O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 253.73 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

As a certified reference material (CRM), 1-[4-(6-Chloro-pyridazin-3-ylmethyl)-piperidin-1-yl]-ethanone 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 FormulaC12H16ClN3O
Molecular Weight253.73 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl-containing
Nitrogen Atoms3

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