(S)-2-(Fmoc-amino)-4-iodobutanoic acid CAS 1932598-55-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1932598-55-4
Molecular FormulaC19H18INO4
Molecular Weight451.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(S)-2-(Fmoc-amino)-4-iodobutanoic acid CAS 1932598-55-4 chemical structure

Description

CATO manufactures (S)-2-(Fmoc-amino)-4-iodobutanoic 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.

CATO supplies (S)-2-(Fmoc-amino)-4-iodobutanoic acid (CAS 1932598-55-4), a certified reference material (molecular formula C19H18INO4, MW 451.25 g/mol) for analytical method development and quality control.

Structurally, (S)-2-(Fmoc-amino)-4-iodobutanoic acid (C19H18INO4) contains a flavonoid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 451.25 g/mol, it falls into the moderately-high-molecular-weight range. 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).

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.

Physical & Chemical Properties

Molecular FormulaC19H18INO4
Molecular Weight451.25 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1996
Halogen ContentI-containing
Nitrogen Atoms1

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