295388
Hexafluoropropene
≥99%
Synonym(s):
Hexafluoropropylene, Perfluoropropene
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About This Item
Linear Formula:
CF3CF=CF2
CAS Number:
Molecular Weight:
150.02
Beilstein:
1705671
EC Number:
MDL number:
UNSPSC Code:
12142100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥99%
bp
−28 °C (lit.)
mp
−153 °C (lit.)
functional group
fluoro
SMILES string
F\C(F)=C(/F)C(F)(F)F
InChI
1S/C3F6/c4-1(2(5)6)3(7,8)9
InChI key
HCDGVLDPFQMKDK-UHFFFAOYSA-N
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Packaging
Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve
Compatible with the following:
Compatible with the following:
Legal Information
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Inhalation - Press. Gas Liquefied gas - STOT RE 2 - STOT SE 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
2A - Gases
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Jenny W Reboredo et al.
Advanced healthcare materials, 5(17), 2191-2198 (2016-05-18)
Cartilage degeneration is the major cause of chronic pain, lost mobility, and reduced quality of life for over estimated 150 million osteoarthritis sufferers worldwide. Despite intensive research, none of the available therapies can restore the hyaline cartilage surface beyond just
Xiuzhi Tian et al.
Journal of hazardous materials, 153(1-2), 128-135 (2007-09-22)
In this study, poly(vinylidene fluoride-co-hexafluoropropene) (PVDF-HFP) with low crystallinity was applied as the membrane material for pervaporative separating ethyl acetate (EtAc) from its aqueous solutions. The drying conditions during membrane fabrication by means of casting the PVDF-HFP solution dominated the
Rafał Loska et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(8), 2577-2589 (2008-01-15)
Hexafluoropropene reacts with aromatic azine N-oxides under mild conditions to produce fluorides of 2-heteroarylperfluoropropionic acids. The reaction proceeds as 1,3-dipolar cycloaddition followed by spontaneous scission of the N--O bond in the isoxazolidine ring and elimination of HF. When the reaction
M Koob et al.
Drug metabolism and disposition: the biological fate of chemicals, 18(6), 911-916 (1990-11-01)
We investigated the metabolism of hexafluoropropene, a nephrotoxic fluoroalkene, in rat liver and kidney subcellular fractions and in rats in vivo. Incubation of hexafluoropropene (1 mM) with microsomes and cytosol in the presence of glutathione (GSH) yielded S-(1,2,3,3,3-pentafluoropropenyl)glutathione (PPFG) and
Effects of inhaled chlorotrifluoroethylene and hexafluoropropene on the rat kidney.
C L Potter et al.
Toxicology and applied pharmacology, 59(3), 431-440 (1981-07-01)
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