CHLUMOFIUOR® CH-8 Perfluorooctyl iodide CAS 507-63-1

CH-8
Perfluorooctyl iodide
CAS No.: 507-63-1
Molecular Formula: C8F17I
Molecular weight: 545.96
EINECS No.: 208-079-5

Application Fields
Key intermediate in the production of fluorinated surfactants and low surface energy coatings.
Packing and Storage
This product is packed in 25L, 50L and 200L steel-plastic composite drums. The product is stored in a ventilated and cool place under airtight condition, see MSDS for details, shelf life is one year.

Description

Performance index
Appearance: colorless to light pink liquid
Boiling point (°C): 160-161@760mm Hg
Melting point (°C): 25
Density (g/mL): 2.067 @20°C
Refractive index: 1.329 @20°C
Flash Point (°C): None
Purity (GC): >99%
Other Name:

1-Iodoperfluorooctane”“Heptadecafluoro-1-iodooctane

Heptadecafluoro-n-octyl iodide

Perfluoro-n-octyl iodide

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Application scenarios

1. Fluoropolymer Modification:

As a fluoropolymer modifier, it enhances the weather resistance, hydrophobicity, and chemical stability of materials, suitable for high-end plastics, rubber, and other products.

2. Organic Synthesis Intermediate:

Used in the synthesis of fluorinated surfactants, low surface energy coatings, fluorinated pharmaceutical intermediates, and contrast agent intermediates, it is a key raw material for constructing fluorinated functional molecules.

3. Special Surface Treatment:

Used in the production of fluorinated surfactants, applied in textiles, leather, and paper industries, imparting waterproof, oil-repellent, and stain-resistant properties to substrates; also used in the preparation of low surface energy coatings, suitable for anti-fouling coating systems in construction, automotive, and other industries.

4. Electronic Chemicals:

Used as a photoresist sensitizer, optimizing the photosensitive performance of photoresists, facilitating the precision processing of semiconductors and microelectronic devices; also used as a special cleaning agent for high-precision cleaning of electronic components.

5. Catalysis and Fire Extinguishing Materials:

In organic catalysis, it achieves substrate activation through halogen bonding, improving reaction efficiency and selectivity; it is a potential alternative to Halon fire extinguishers, suitable for fire protection needs in special scenarios.

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