(S)-2-(Benzylamino)-3-methylbutanoic acid CAS 15363-84-5

Purity 97%+In StockPharmaceutical Standards
CAS No.15363-84-5
Molecular FormulaC7H6F3NO3S
Molecular Weight241.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-(Benzylamino)-3-methylbutanoic acid CAS 15363-84-5 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 241.19 g/mol gives (S)-2-(Benzylamino)-3-methylbutanoic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

(S)-2-(Benzylamino)-3-methylbutanoic acid (CAS 15363-84-5), molecular formula C7H6F3NO3S and molecular weight 241.19 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, (S)-2-(Benzylamino)-3-methylbutanoic acid (C7H6F3NO3S) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 241.19 g/mol, it falls into the medium-molecular-weight range. 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-(Benzylamino)-3-methylbutanoic 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 FormulaC7H6F3NO3S
Molecular Weight241.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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; 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.)1961
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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