1,7-Dibromo-3,4,9,10-perylenetetracarboxylic Dianhydride

95%

Reagent Code: #173928
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CAS Number 118129-60-5

science Other reagents with same CAS 118129-60-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 550.11 g/mol
Formula C₂₄H₆Br₂O₆
badge Registry Numbers
MDL Number MFCD11870875
thermostat Physical Properties
Boiling Point 840.2°C
inventory_2 Storage & Handling
Density 2.159g/mL
Storage Room temperature, dry

description Product Description

Used as an electron-accepting material in organic photovoltaics due to its strong electron-deficient character and extended π-conjugation, enabling efficient charge separation in solar cells. Also employed in organic field-effect transistors (OFETs) as a n-type semiconductor, offering good electron mobility and ambient stability. Its deep LUMO energy level makes it suitable for use in near-infrared (NIR) dyes and photodetectors. Additionally, it serves as a precursor for synthesizing perylene diimide derivatives used in fluorescent sensors and bioimaging, leveraging its high thermal and chemical stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,130.00
inventory 5g
10-20 days ฿5,500.00
inventory 25g
10-20 days ฿21,260.00

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1,7-Dibromo-3,4,9,10-perylenetetracarboxylic Dianhydride
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Used as an electron-accepting material in organic photovoltaics due to its strong electron-deficient character and extended π-conjugation, enabling efficient charge separation in solar cells. Also employed in organic field-effect transistors (OFETs) as a n-type semiconductor, offering good electron mobility and ambient stability. Its deep LUMO energy level makes it suitable for use in near-infrared (NIR) dyes and photodetectors. Additionally, it serves as a precursor for synthesizing perylene diimide der

Used as an electron-accepting material in organic photovoltaics due to its strong electron-deficient character and extended π-conjugation, enabling efficient charge separation in solar cells. Also employed in organic field-effect transistors (OFETs) as a n-type semiconductor, offering good electron mobility and ambient stability. Its deep LUMO energy level makes it suitable for use in near-infrared (NIR) dyes and photodetectors. Additionally, it serves as a precursor for synthesizing perylene diimide derivatives used in fluorescent sensors and bioimaging, leveraging its high thermal and chemical stability.

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