(E)-1-methyl-3-(4-methyl-5-(3-(phenylamino)acryloyl)thiazol-2-yl)pyridin-1-ium iodide CAS 477713-54-5

Purity 97%+In StockPharmaceutical Standards
CAS No.477713-54-5
Molecular FormulaC19H18N3OS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-1-methyl-3-(4-methyl-5-(3-(phenylamino)acryloyl)thiazol-2-yl)pyridin-1-ium iodide CAS 477713-54-5 chemical structure

Description

The molecular framework of (E)-1-methyl-3-(4-methyl-5-(3-(phenylamino)acryloyl)thiazol-2-yl)pyridin-1-ium iodide (C19H18N3OSI) is characterized by a steroid core, an amide group, sulfur-containing functionality, 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).

CATO supplies (E)-1-methyl-3-(4-methyl-5-(3-(phenylamino)acryloyl)thiazol-2-yl)pyridin-1-ium iodide (CAS 477713-54-5), a certified reference material (molecular formula C19H18N3OSI, MW 463.33 g/mol) for analytical method development and quality control.

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 (E)-1-methyl-3-(4-methyl-5-(3-(phenylamino)acryloyl)thiazol-2-yl)pyridin-1-ium iodide 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 FormulaC19H18N3OS I
Molecular Weight463.33 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentI-containing
Nitrogen Atoms3
Sulfur Atoms1

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