Fmoc-2-amino-5-phenyl(4-I)-L-pentanoic acid CAS 2055144-89-1

Purity 97%+In StockPharmaceutical Standards
CAS No.2055144-89-1
Molecular FormulaC26H24INO4
Molecular Weight541.38 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Fmoc-2-amino-5-phenyl(4-I)-L-pentanoic acid CAS 2055144-89-1 chemical structure

Description

The molecular framework of Fmoc-2-amino-5-phenyl(4-I)-L-pentanoic acid (C26H24INO4) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

Fmoc-2-amino-5-phenyl(4-I)-L-pentanoic acid (CAS 2055144-89-1), molecular formula C26H24INO4 and molecular weight 541.38 g/mol, is a CATO reference standard with documented purity and traceability.

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.

As a certified reference material (CRM), Fmoc-2-amino-5-phenyl(4-I)-L-pentanoic 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 FormulaC26H24INO4
Molecular Weight541.38 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997
Halogen ContentI-containing
Nitrogen Atoms1

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