(S)-2-Amino-N,3-dimethyl-N-(2-oxo-2-(1H-pyrrol-2-yl)ethyl)butanamide CAS 1353994-61-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1353994-61-2
Molecular FormulaC12H19N3O2
Molecular Weight237.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-Amino-N,3-dimethyl-N-(2-oxo-2-(1H-pyrrol-2-yl)ethyl)butanamide CAS 1353994-61-2 chemical structure

Description

CATO supplies (S)-2-Amino-N,3-dimethyl-N-(2-oxo-2-(1H-pyrrol-2-yl)ethyl)butanamide (CAS 1353994-61-2), a certified reference material (molecular formula C12H19N3O2, MW 237.30 g/mol) for analytical method development and quality control.

(S)-2-Amino-N,3-dimethyl-N-(2-oxo-2-(1H-pyrrol-2-yl)ethyl)butanamide (C12H19N3O2) contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

As a certified reference material (CRM), (S)-2-Amino-N,3-dimethyl-N-(2-oxo-2-(1H-pyrrol-2-yl)ethyl)butanamide 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 FormulaC12H19N3O2
Molecular Weight237.30 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms3

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