Benzyl 4-(3-aminoazetidin-1-yl)piperidine-1-carboxylate dihydrochloride CAS 1179362-99-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1179362-99-2
Molecular FormulaC16H23N3O2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Benzyl 4-(3-aminoazetidin-1-yl)piperidine-1-carboxylate dihydrochloride CAS 1179362-99-2 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 Benzyl 4-(3-aminoazetidin-1-yl)piperidine-1-carboxylate dihydrochloride (CAS 1179362-99-2), a certified reference material (molecular formula C16H23N3O2HCl, MW 325.84 g/mol) for analytical method development and quality control.

The molecular framework of Benzyl 4-(3-aminoazetidin-1-yl)piperidine-1-carboxylate dihydrochloride (C16H23N3O2HCl) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures Benzyl 4-(3-aminoazetidin-1-yl)piperidine-1-carboxylate dihydrochloride 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 FormulaC16H23N3O2 2*HCl
Molecular Weight325.84 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms3

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