Copper(I) iodide

99.999% trace metals basis

Reagent Code: #162493
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Alias Copper iodide (I)
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CAS Number 7681-65-4

science Other reagents with same CAS 7681-65-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.45 g/mol
Formula CuI
badge Registry Numbers
EC Number 231-674-6
MDL Number MFCD00010978
thermostat Physical Properties
Melting Point 605 °C(lit.)
Boiling Point 1290 °C
inventory_2 Storage & Handling
Density 5.62 g/mL at 25 °C(lit.)
Storage Room temperature, light-proof, inert gas storage

description Product Description

Used as a catalyst in coupling reactions such as Ullmann (for aryl halides) and Glaser (for terminal alkynes), enabling carbon-carbon bond formation in organic synthesis, commonly in laboratory and pharmaceutical industries. Employed in photovoltaic cells, thin-film solar cells, and semiconductor devices due to its favorable electronic properties, including good electrical conductivity and light absorption. Acts as a source of iodide ions in the preparation of radiopharmaceuticals. Utilized in luminescent materials and sensors because of its light-emitting characteristics under certain conditions. Also applied in wood preservatives and antifouling coatings for marine paints to prevent microbial and algal growth. In animal nutrition, serves as a supplement providing both copper and iodine to prevent deficiencies in livestock feed.

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Test Parameter Specification
Appearance Off-white to grey-brown powder
Purity 99.999-100%
XRD Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,790.00
inventory 5g
10-20 days ฿3,740.00
inventory 25g
10-20 days ฿14,960.00
inventory 100g
10-20 days ฿38,480.00

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Copper(I) iodide
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Used as a catalyst in coupling reactions such as Ullmann (for aryl halides) and Glaser (for terminal alkynes), enabling carbon-carbon bond formation in organic synthesis, commonly in laboratory and pharmaceutical industries. Employed in photovoltaic cells, thin-film solar cells, and semiconductor devices due to its favorable electronic properties, including good electrical conductivity and light absorption. Acts as a source of iodide ions in the preparation of radiopharmaceuticals. Utilized in luminescen

Used as a catalyst in coupling reactions such as Ullmann (for aryl halides) and Glaser (for terminal alkynes), enabling carbon-carbon bond formation in organic synthesis, commonly in laboratory and pharmaceutical industries. Employed in photovoltaic cells, thin-film solar cells, and semiconductor devices due to its favorable electronic properties, including good electrical conductivity and light absorption. Acts as a source of iodide ions in the preparation of radiopharmaceuticals. Utilized in luminescent materials and sensors because of its light-emitting characteristics under certain conditions. Also applied in wood preservatives and antifouling coatings for marine paints to prevent microbial and algal growth. In animal nutrition, serves as a supplement providing both copper and iodine to prevent deficiencies in livestock feed.

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