tert-Butyl (2-(2-aminoacetamido)cyclohexyl)carbamate CAS 1353947-44-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1353947-44-0
Molecular FormulaC13H25N3O3
Molecular Weight271.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl (2-(2-aminoacetamido)cyclohexyl)carbamate CAS 1353947-44-0 chemical structure

Description

Based on its molecular formula C13H25N3O3, tert-Butyl (2-(2-aminoacetamido)cyclohexyl)carbamate contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 271.36 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

tert-Butyl (2-(2-aminoacetamido)cyclohexyl)carbamate (CAS 1353947-44-0) is a high-purity analytical reference standard with the molecular formula C13H25N3O3 and a molecular weight of 271.36 g/mol.

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 (2-(2-aminoacetamido)cyclohexyl)carbamate 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 FormulaC13H25N3O3
Molecular Weight271.36 g/mol
AppearanceWhite 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)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1991
Nitrogen Atoms3

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