(S)-Fmoc-2-amino-6-tert-butoxy-hexanoic acid CAS 1354752-71-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1354752-71-8
Molecular FormulaC25H31NO5
Molecular Weight425.52 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-Fmoc-2-amino-6-tert-butoxy-hexanoic acid CAS 1354752-71-8 chemical structure

Description

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

(S)-Fmoc-2-amino-6-tert-butoxy-hexanoic acid (CAS 1354752-71-8) is a high-purity analytical reference standard with the molecular formula C25H31NO5 and a molecular weight of 425.52 g/mol.

The molecular framework of (S)-Fmoc-2-amino-6-tert-butoxy-hexanoic acid (C25H31NO5) is characterized by a flavonoid core, 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).

As a certified reference material (CRM), (S)-Fmoc-2-amino-6-tert-butoxy-hexanoic 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 FormulaC25H31NO5
Molecular Weight425.52 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms1

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