Oxalic acid tert-Butyl N-[(2S)-morpholin-2-ylmethyl]carbamate CAS 1820575-28-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1820575-28-7
Molecular FormulaC10H20N2O3
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Oxalic acid tert-Butyl N-[(2S)-morpholin-2-ylmethyl]carbamate CAS 1820575-28-7 chemical structure

Description

As a certified reference material (CRM), Oxalic acid tert-Butyl N-[(2S)-morpholin-2-ylmethyl]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.

CATO supplies Oxalic acid tert-Butyl N-[(2S)-morpholin-2-ylmethyl]carbamate (CAS 1820575-28-7), a certified reference material (molecular formula C10H20N2O3C2H2O4, MW 306.31 g/mol) for analytical method development and quality control.

The molecular framework of Oxalic acid tert-Butyl N-[(2S)-morpholin-2-ylmethyl]carbamate (C10H20N2O3C2H2O4) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. 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. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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

Physical & Chemical Properties

Molecular FormulaC10H20N2O3 C2H2O4
Molecular Weight306.31 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.)1995
Nitrogen Atoms2

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