Tert-butyl 4-(hydroxymethyl)-4-(pyridin-2-yl)piperidine-1-carboxylate CAS 853576-51-9

Purity 97%+In StockPharmaceutical Standards
CAS No.853576-51-9
Molecular FormulaC16H24N2O3
Molecular Weight292.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl 4-(hydroxymethyl)-4-(pyridin-2-yl)piperidine-1-carboxylate CAS 853576-51-9 chemical structure

Description

Tert-butyl 4-(hydroxymethyl)-4-(pyridin-2-yl)piperidine-1-carboxylate (CAS 853576-51-9), molecular formula C16H24N2O3 and molecular weight 292.37 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of Tert-butyl 4-(hydroxymethyl)-4-(pyridin-2-yl)piperidine-1-carboxylate (C16H24N2O3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), Tert-butyl 4-(hydroxymethyl)-4-(pyridin-2-yl)piperidine-1-carboxylate 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 FormulaC16H24N2O3
Molecular Weight292.37 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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