Tert-butyl (6-(piperidin-1-yl)pyridin-3-yl)carbamate CAS 849353-29-3

Purity 97%+In StockPharmaceutical Standards
CAS No.849353-29-3
Molecular FormulaC15H23N3O2
Molecular Weight277.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Tert-butyl (6-(piperidin-1-yl)pyridin-3-yl)carbamate CAS 849353-29-3 chemical structure

Description

CATO supplies Tert-butyl (6-(piperidin-1-yl)pyridin-3-yl)carbamate (CAS 849353-29-3), a certified reference material (molecular formula C15H23N3O2, MW 277.36 g/mol) for analytical method development and quality control.

Structurally, Tert-butyl (6-(piperidin-1-yl)pyridin-3-yl)carbamate (C15H23N3O2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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 277.36 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.

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

CATO manufactures Tert-butyl (6-(piperidin-1-yl)pyridin-3-yl)carbamate 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 FormulaC15H23N3O2
Molecular Weight277.36 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 Atoms3

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