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Merck
CN

175161

6,6,7,7,8,8,8-Heptafluoro-2,2-dimethyl-3,5-octanedione

98%

Synonym(s):

2,2-Dimethyl-6,6,7,7,8,8,8-heptafluoro-3,5-octanedione

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About This Item

Linear Formula:
CF3CF2CF2COCH2COC(CH3)3
CAS Number:
Molecular Weight:
296.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-556-6
Beilstein/REAXYS Number:
2056991
MDL number:
Assay:
98%
Form:
liquid
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assay

98%

form

liquid

impurities

0.1% 4,4′-methylenebis(2,6-di-tert-butylphenol)

refractive index

n20/D 1.379 (lit.)

bp

46-47 °C/5 mmHg (lit.)

density

1.273 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)C(=O)CC(=O)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C10H11F7O2/c1-7(2,3)5(18)4-6(19)8(11,12)9(13,14)10(15,16)17/h4H2,1-3H3

InChI key

SQNZLBOJCWQLGQ-UHFFFAOYSA-N

Application

6,6,7,7,8,8,8-Heptafluoro-2,2-dimethyl-3,5-octanedione (2,2-Dimethyl-6,6,7,7,8,8,8-heptafluoro-3,5-octanedione) was used as a co-inducer in the production of human γ interferon (HuIFN-γ). It was also used as a beta-diketone chelating agent in the extraction of supercritical carbon dioxide.


pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

127.4 °F - closed cup

flash_point_c

53 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品

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M Deleers et al.
Chemistry and physics of lipids, 33(1), 11-20 (1983-07-01)
The beta-diketone 1,1,1,2,2,3,3-heptafluoro-7,7-dimethyloctane-4,6-dione (FOD) translocates calcium from an aqueous medium into an organic phase. FOD is less efficient than but acts synergistically with A23187 in causing calcium translocation. The FOD-mediated process of calcium translocation is inhibited by NaCl, although the
B D Gomperts et al.
European journal of biochemistry, 117(3), 559-562 (1981-07-01)
We show that the relatively simple beta-diketone, 1.1.1.2.2.3.3-heptafluoro-7,7-dimethyloctane-4,6-dione, known as "fod", will solvate Ca2+ ions in an organic phase. In consequence it will transport Ca2+ across phospholipid bilayers. It acts as predicted for a Ca2+-transporting ionophore in two biological systems:
A Kreutzberger et al.
Arzneimittel-Forschung, 31(2), 288-290 (1981-01-01)
Since in the compound class of 2-ureidopyrimidines accessible through condensation of guanidinecarboxamide (1) with beta-diketones, representatives occur possessing hypnotic activity, the range of applicability of this synthesis on the one hand and the properties of the end products as related



Global Trade Item Number

SKUGTIN
175161-5G04061836682804