Fmoc-3-iodo-Tyr-OH CAS 134486-00-3

Purity >95%In StockPharmaceutical Standards
CAS No.134486-00-3
Molecular FormulaC24H20INO5
Molecular Weight529.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Fmoc-3-iodo-Tyr-OH CAS 134486-00-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 529.32 g/mol gives Fmoc-3-iodo-Tyr-OH distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Fmoc-3-iodo-Tyr-OH (CAS 134486-00-3) is a high-purity analytical reference standard with the molecular formula C24H20INO5 and a molecular weight of 529.32 g/mol.

The molecular framework of Fmoc-3-iodo-Tyr-OH (C24H20INO5) is characterized by a flavonoid 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

CATO manufactures Fmoc-3-iodo-Tyr-OH 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 FormulaC24H20INO5
Molecular Weight529.32 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity>95%
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.)1995
Halogen ContentI-containing
Nitrogen Atoms1

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