(3-Hydroxypiperidin-1-yl)(5-iodothiophen-3-yl)methanone CAS 1355935-33-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1355935-33-9
Molecular FormulaC10H12INO2S
Molecular Weight337.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-Hydroxypiperidin-1-yl)(5-iodothiophen-3-yl)methanone CAS 1355935-33-9 chemical structure

Description

As a certified reference material (CRM), (3-Hydroxypiperidin-1-yl)(5-iodothiophen-3-yl)methanone 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.

(3-Hydroxypiperidin-1-yl)(5-iodothiophen-3-yl)methanone (CAS 1355935-33-9) is a high-purity analytical reference standard with the molecular formula C10H12INO2S and a molecular weight of 337.18 g/mol.

The molecular framework of (3-Hydroxypiperidin-1-yl)(5-iodothiophen-3-yl)methanone (C10H12INO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC10H12INO2S
Molecular Weight337.18 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentI-containing
Nitrogen Atoms1
Sulfur Atoms1

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