(S)-2-amino-2-(5-chlorothiophen-2-yl)propanoic acid CAS 68056-35-9

Purity 97%+In StockPharmaceutical Standards
CAS No.68056-35-9
Molecular FormulaC7H8ClNO2S
Molecular Weight205.66 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-amino-2-(5-chlorothiophen-2-yl)propanoic acid CAS 68056-35-9 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.

(S)-2-amino-2-(5-chlorothiophen-2-yl)propanoic acid (CAS 68056-35-9), molecular formula C7H8ClNO2S and molecular weight 205.66 g/mol, is a CATO reference standard with documented purity and traceability.

(S)-2-amino-2-(5-chlorothiophen-2-yl)propanoic acid (C7H8ClNO2S) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, 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.

As a certified reference material (CRM), (S)-2-amino-2-(5-chlorothiophen-2-yl)propanoic acid 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 FormulaC7H8ClNO2S
Molecular Weight205.66 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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