52516
六氟丙烯
purum, ≥99.0%
别名:
Hexafluoropropylene, 全氟丙烯
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关于此项目
线性分子式:
CF3CF=CF2
化学文摘社编号:
分子量:
150.02
EC Number:
204-127-4
UNSPSC Code:
12142100
PubChem Substance ID:
Beilstein/REAXYS Number:
1705671
MDL number:
grade
purum
assay
≥99.0%
bp
−28 °C (lit.)
mp
−153 °C (lit.)
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
Packaging
罐装，净重 50g
法规信息
新产品
此项目有
Meng Cheng et al.
Nanotechnology, 31(42), 425401-425401 (2020-06-27)
A ceramic in polymer hybrid solid electrolyte (HSE) based on a poly vinylidene fluoride-hexafluoropropylene (PVDF-HFP) polymer comprising Na3Zr2Si2PO12 (NASICON) ceramic particles was prepared by a simple solution casting method followed by activation in a liquid electrolyte. The prepared HSE exhibits
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
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)
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
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