4-(3-Bromothiophene-2-carboxamido)pentanoic acid CAS 1340033-22-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1340033-22-8
Molecular FormulaC10H12BrNO3S
Molecular Weight306.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-Bromothiophene-2-carboxamido)pentanoic acid CAS 1340033-22-8 chemical structure

Description

CATO manufactures 4-(3-Bromothiophene-2-carboxamido)pentanoic 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.

4-(3-Bromothiophene-2-carboxamido)pentanoic acid (CAS 1340033-22-8) is a high-purity analytical reference standard with the molecular formula C10H12BrNO3S and a molecular weight of 306.18 g/mol.

The molecular framework of 4-(3-Bromothiophene-2-carboxamido)pentanoic acid (C10H12BrNO3S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine 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 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).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC10H12BrNO3S
Molecular Weight306.18 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentBr-containing
Nitrogen Atoms1
Sulfur Atoms1

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