Phenylmethanamine (2S,4S)-1-(tert-butoxycarbonyl)-4-hydroxypiperidine-2-carboxylate CAS 441044-14-0

Purity 97%+In StockPharmaceutical Standards
CAS No.441044-14-0
Molecular FormulaC11H19NO5
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Phenylmethanamine (2S,4S)-1-(tert-butoxycarbonyl)-4-hydroxypiperidine-2-carboxylate CAS 441044-14-0 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.

Phenylmethanamine (2S,4S)-1-(tert-butoxycarbonyl)-4-hydroxypiperidine-2-carboxylate (CAS 441044-14-0) is a high-purity analytical reference standard with the molecular formula C11H19NO5C7H9N and a molecular weight of 352.43 g/mol.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, Phenylmethanamine (2S,4S)-1-(tert-butoxycarbonyl)-4-hydroxypiperidine-2-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 352.43 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC11H19NO5 C7H9N
Molecular Weight352.43 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.)2025
Nitrogen Atoms2

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