Pentanoic acid, 5-[(3-iodobenzoyl)amino]- CAS 1458544-53-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1458544-53-0
Molecular FormulaC12H14INO3
Molecular Weight347.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Pentanoic acid, 5-[(3-iodobenzoyl)amino]- CAS 1458544-53-0 chemical structure

Description

CATO supplies Pentanoic acid, 5-[(3-iodobenzoyl)amino]- (CAS 1458544-53-0), a certified reference material (molecular formula C12H14INO3, MW 347.15 g/mol) for analytical method development and quality control.

The molecular framework of Pentanoic acid, 5-[(3-iodobenzoyl)amino]- (C12H14INO3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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).

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 Pentanoic acid, 5-[(3-iodobenzoyl)amino]- 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 FormulaC12H14INO3
Molecular Weight347.15 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentI-containing
Nitrogen Atoms1

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