4-(2-Ethoxy-5-(tert-pentyl)phenyl)thiazol-2-amine hydrobromide CAS 1049749-13-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1049749-13-4
Molecular FormulaC16H22N2OS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(2-Ethoxy-5-(tert-pentyl)phenyl)thiazol-2-amine hydrobromide CAS 1049749-13-4 chemical structure

Description

4-(2-Ethoxy-5-(tert-pentyl)phenyl)thiazol-2-amine hydrobromide (C16H22N2OSHBr) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, bromine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

4-(2-Ethoxy-5-(tert-pentyl)phenyl)thiazol-2-amine hydrobromide (CAS 1049749-13-4), molecular formula C16H22N2OSHBr and molecular weight 371.34 g/mol, is a CATO reference standard with documented purity and traceability.

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 4-(2-Ethoxy-5-(tert-pentyl)phenyl)thiazol-2-amine hydrobromide 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 FormulaC16H22N2OS HBr
Molecular Weight371.34 g/mol
Purity97%+
StorageStore at 2-8°C, 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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