(R)-tert-Butyl 3-((S)-2-amino-N-cyclopropylpropanamido)pyrrolidine-1-carboxylate CAS 1401666-96-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1401666-96-3
Molecular FormulaC15H27N3O3
Molecular Weight297.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-tert-Butyl 3-((S)-2-amino-N-cyclopropylpropanamido)pyrrolidine-1-carboxylate CAS 1401666-96-3 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 (R)-tert-Butyl 3-((S)-2-amino-N-cyclopropylpropanamido)pyrrolidine-1-carboxylate (CAS 1401666-96-3), a certified reference material (molecular formula C15H27N3O3, MW 297.39 g/mol) for analytical method development and quality control.

The molecular framework of (R)-tert-Butyl 3-((S)-2-amino-N-cyclopropylpropanamido)pyrrolidine-1-carboxylate (C15H27N3O3) is characterized by a nitrogen-containing heterocyclic scaffold, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

As a certified reference material (CRM), (R)-tert-Butyl 3-((S)-2-amino-N-cyclopropylpropanamido)pyrrolidine-1-carboxylate 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 FormulaC15H27N3O3
Molecular Weight297.39 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms3

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