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295388

Sigma-Aldrich

Hexafluoropropene

≥99%

Sinónimos:

Hexafluoropropylene, Perfluoropropene

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About This Item

Fórmula lineal:
CF3CF=CF2
Número de CAS:
116-15-4
Peso molecular:
150.02
Beilstein/REAXYS Number:
1705671
EC Number:
204-127-4
MDL number:
MFCD00000447
UNSPSC Code:
12142100
PubChem Substance ID:
24857779
NACRES:
NA.22

Quality Level

100

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:

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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signalword

Warning

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

2A - Gases

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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Elija entre una de las versiones más recientes:

Certificados de análisis (COA)

Lot/Batch Number
SHBR7794
SHBQ2215
STBJ2481
SHBL6348
STBH1448

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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)
Jenny W Reboredo et al.
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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
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