1,10-Diiododecane

98%

Reagent Code: #174722
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CAS Number 16355-92-3

science Other reagents with same CAS 16355-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 394.08 g/mol
Formula C₁₀H₂₀I₂
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MDL Number MFCD00001086
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a crosslinking agent in perovskite solar cells to improve device stability and efficiency by passivating defects at grain boundaries and interfaces. It helps enhance charge transport and reduces non-radiative recombination, leading to better photovoltaic performance. Also employed in surface modification of nanomaterials due to its bifunctional iodine termini, enabling controlled assembly and electronic coupling in molecular junctions. Additionally, serves as a bifunctional alkylating agent in organic synthesis for preparing polymers and cyclic compounds via nucleophilic substitution reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿162.00
25g
10-20 days ฿3,800.00
5g
10-20 days ฿860.00
1,10-Diiododecane
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Used as a crosslinking agent in perovskite solar cells to improve device stability and efficiency by passivating defects at grain boundaries and interfaces. It helps enhance charge transport and reduces non-radiative recombination, leading to better photovoltaic performance. Also employed in surface modification of nanomaterials due to its bifunctional iodine termini, enabling controlled assembly and electronic coupling in molecular junctions. Additionally, serves as a bifunctional alkylating agent in or

Used as a crosslinking agent in perovskite solar cells to improve device stability and efficiency by passivating defects at grain boundaries and interfaces. It helps enhance charge transport and reduces non-radiative recombination, leading to better photovoltaic performance. Also employed in surface modification of nanomaterials due to its bifunctional iodine termini, enabling controlled assembly and electronic coupling in molecular junctions. Additionally, serves as a bifunctional alkylating agent in organic synthesis for preparing polymers and cyclic compounds via nucleophilic substitution reactions.

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