1,6,7,12-tetrabromoperylene-3,4,9,10-tetracarboxylic acid bisanhydride

95%

Reagent Code: #128190
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CAS Number 321945-85-1

science Other reagents with same CAS 321945-85-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 707.9 g/mol
Formula C₂₄H₄Br₄O₆
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an electron-accepting material in organic photovoltaics (OPVs), enabling efficient charge separation in solar cells. Acts as a precursor for perylene diimide derivatives, which are key in organic field-effect transistors (OFETs) due to their high electron mobility and stability. Employed in dye-sensitized solar cells and as a building block for functional dyes with strong absorption in the visible and near-infrared regions. Also utilized in research for developing n-type semiconducting materials in flexible electronics and optoelectronic devices. Its rigid, planar structure supports strong π-π stacking, enhancing charge transport in thin-film devices.

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Test Parameter Specification
Appearance Red Powder
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿32,000.00
inventory 5g
10-20 days ฿94,000.00

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1,6,7,12-tetrabromoperylene-3,4,9,10-tetracarboxylic acid bisanhydride
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Used as an electron-accepting material in organic photovoltaics (OPVs), enabling efficient charge separation in solar cells. Acts as a precursor for perylene diimide derivatives, which are key in organic field-effect transistors (OFETs) due to their high electron mobility and stability. Employed in dye-sensitized solar cells and as a building block for functional dyes with strong absorption in the visible and near-infrared regions. Also utilized in research for developing n-type semiconducting materials

Used as an electron-accepting material in organic photovoltaics (OPVs), enabling efficient charge separation in solar cells. Acts as a precursor for perylene diimide derivatives, which are key in organic field-effect transistors (OFETs) due to their high electron mobility and stability. Employed in dye-sensitized solar cells and as a building block for functional dyes with strong absorption in the visible and near-infrared regions. Also utilized in research for developing n-type semiconducting materials in flexible electronics and optoelectronic devices. Its rigid, planar structure supports strong π-π stacking, enhancing charge transport in thin-film devices.

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