tert-Butyl (4-benzylpiperidin-4-yl)methylcarbamate CAS 1707602-65-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1707602-65-0
Molecular FormulaC18H28N2O2
Molecular Weight304.43 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (4-benzylpiperidin-4-yl)methylcarbamate CAS 1707602-65-0 chemical structure

Description

The molecular framework of tert-Butyl (4-benzylpiperidin-4-yl)methylcarbamate (C18H28N2O2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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.

CATO supplies tert-Butyl (4-benzylpiperidin-4-yl)methylcarbamate (CAS 1707602-65-0), a certified reference material (molecular formula C18H28N2O2, MW 304.43 g/mol) for analytical method development and quality control.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC18H28N2O2
Molecular Weight304.43 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.)1994
Nitrogen Atoms2

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