2,7-Dibromo-4,4,9,9-tetrakis(4-hexylphenyl)-4,9-s-benzoindeno[1,2-b:5,6-b']di Thiophene CAS 1049034-71-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1049034-71-0
Molecular FormulaC64H72Br2S2
Molecular Weight1065.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,7-Dibromo-4,4,9,9-tetrakis(4-hexylphenyl)-4,9-s-benzoindeno[1,2-b:5,6-b']di Thiophene CAS 1049034-71-0 chemical structure

Description

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 supplies 2,7-Dibromo-4,4,9,9-tetrakis(4-hexylphenyl)-4,9-s-benzoindeno[1,2-b:5,6-b']di Thiophene (CAS 1049034-71-0), a certified reference material (molecular formula C64H72Br2S2, MW 1065.19 g/mol) for analytical method development and quality control.

2,7-Dibromo-4,4,9,9-tetrakis(4-hexylphenyl)-4,9-s-benzoindeno[1,2-b:5,6-b']di Thiophene (C64H72Br2S2) contains sulfur-containing functionality, bromine substitution, a polycyclic aromatic system. 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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 2,7-Dibromo-4,4,9,9-tetrakis(4-hexylphenyl)-4,9-s-benzoindeno[1,2-b:5,6-b']di Thiophene 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 FormulaC64H72Br2S2
Molecular Weight1065.19 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)28.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing
Sulfur Atoms2

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