(S)-2-((tert-Butoxycarbonyl)amino)hex-4-ynoic acid CAS 98254-05-8

Purity 97%+In StockPharmaceutical Standards
CAS No.98254-05-8
Molecular FormulaC11H17NO4
Molecular Weight227.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-((tert-Butoxycarbonyl)amino)hex-4-ynoic acid CAS 98254-05-8 chemical structure

Description

CATO supplies (S)-2-((tert-Butoxycarbonyl)amino)hex-4-ynoic acid (CAS 98254-05-8), a certified reference material (molecular formula C11H17NO4, MW 227.26 g/mol) for analytical method development and quality control.

The molecular framework of (S)-2-((tert-Butoxycarbonyl)amino)hex-4-ynoic acid (C11H17NO4) is characterized by an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures (S)-2-((tert-Butoxycarbonyl)amino)hex-4-ynoic acid under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC11H17NO4
Molecular Weight227.26 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 methanol, ethanol, DMSO
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 Atoms1

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