(S)-2-((5-Methylisoxazol-3-yl)amino)propanoic acid CAS 100960-41-6

Purity 97%+In StockPharmaceutical Standards
CAS No.100960-41-6
Molecular FormulaC7H10N2O3
Molecular Weight170.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-((5-Methylisoxazol-3-yl)amino)propanoic acid CAS 100960-41-6 chemical structure

Description

Based on its molecular formula C7H10N2O3, (S)-2-((5-Methylisoxazol-3-yl)amino)propanoic acid contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 170.17 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

(S)-2-((5-Methylisoxazol-3-yl)amino)propanoic acid (CAS 100960-41-6) is a high-purity analytical reference standard with the molecular formula C7H10N2O3 and a molecular weight of 170.17 g/mol.

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-((5-Methylisoxazol-3-yl)amino)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 FormulaC7H10N2O3
Molecular Weight170.17 g/mol
AppearanceOff-white to pale yellow crystalline powder. (faint amine-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
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.)1985
Nitrogen Atoms2

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