(S)-2-Amino-N-((S)-1-phenylethyl)butanamide CAS 1993390-30-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1993390-30-9
Molecular FormulaC12H18N2O
Molecular Weight206.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-Amino-N-((S)-1-phenylethyl)butanamide CAS 1993390-30-9 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including (S)-2-Amino-N-((S)-1-phenylethyl)butanamide.

CATO supplies (S)-2-Amino-N-((S)-1-phenylethyl)butanamide (CAS 1993390-30-9), a certified reference material (molecular formula C12H18N2O, MW 206.28 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, (S)-2-Amino-N-((S)-1-phenylethyl)butanamide is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 206.28 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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-((S)-1-phenylethyl)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 FormulaC12H18N2O
Molecular Weight206.28 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Nitrogen Atoms2

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