Weight | 200.028 g/mol |
---|---|
Formula | C4F8 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Perfluoroisobutylene (382-21-8)
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- Short-Term Inhalation Toxicity of Perfluoroisobutylene (Drug and Chemical Toxicology, 1982)
- High-performance capillary electrophoresis of proteins from the fluid lining of the lungs of rats exposed to perfluoroisobutylene (Journal of Chromatography A, 1991)
- Electron microscopy of rat lung following a single acute exposure to perfluoroisobutylene (PFIB). A sequential study of the first 24 hours following exposure. (International Journal of Experimental Pathology, 1991)
- Lung Injury After Acute Inhalation Of Perfluoroisobutylene: Exposure Concentration-Response Relationships (Inhalation Toxicology, 1993)
- The synthesis of perfluoroisobutylene from perfluoropropylene (Journal of Organic Chemistry, 1967)
- Analysis of chemical warfare agents III. Use of bis-nucleophiles in the trace level determination of phosgene and perfluoroisobutylene (Journal of Chromatography A, 2005)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H330: Fatal if inhaled
Danger Acute toxicity, inhalation - Category 1, 2 - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 -
SMILESC(=C(F)F)(C(F)(F)F)C(F)(F)F
-
InChIKeyDAFIBNSJXIGBQB-UHFFFAOYSA-N
- Pubchem - Perfluoroisobutylene
- Wikipedia - perfluoroisobutylene
Perfluoroisobutene (PFIB), also known as 1,1,3,3,3-pentafluoro-2-(trifluoromethyl)prop-1-ene, is a fluorocarbon alkene. It is a hydrophobic reactive gas with boiling point at 7 C. It is a strong electrophile.
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3 suppliers
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hexafluoroisopropyl methyl ether
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2252-84-8
(2252-84-8, 33660-75-2)
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1H,1H,2H-Heptafluoropent-1-ene
(355-08-8, 71164-40-4)
1 alternate name
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1 alternate name
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1 alternate name
3 suppliers
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(64712-27-2)
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1 alternate name
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1 alternate name
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(819-46-5)
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382-26-3
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382-31-0
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1,1,1-Trichlorotrifluoroacetone
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