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Merck
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Documenti

175161

Sigma-Aldrich

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

98%

Sinonimo/i:

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

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About This Item

Formula condensata:
CF3CF2CF2COCH2COC(CH3)3
Numero CAS:
17587-22-3
Peso molecolare:
296.18
Beilstein:
2056991
Numero CE:
241-556-6
Numero MDL:
MFCD00000435
Codice UNSPSC:
12352100
ID PubChem:
24850490
NACRES:
NA.22

Saggio

98%

Forma fisica

liquid

Impurezze

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

Indice di rifrazione

n20/D 1.379 (lit.)

P. eboll.

46-47 °C/5 mmHg (lit.)

Densità

1.273 g/mL at 25 °C (lit.)

Stringa SMILE

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
SQNZLBOJCWQLGQ-UHFFFAOYSA-N

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Applicazioni

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.

Pittogrammi

Flame
GHS02

Avvertenze

Warning

Indicazioni di pericolo

H226

Classi di pericolo

Flam. Liq. 3

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

127.4 °F - closed cup

Punto d’infiammabilità (°C)

53 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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Chia-Chan Wu et al.
Journal of hazardous materials, 163(2-3), 1239-1245 (2008-09-06)
This study presents supercritical carbon dioxide (scCO(2)) extraction as an inherently safer and cleaner sample treatment method for identifying trace gallium in urine samples. Extraction is performed in the presence of a fluorinated beta-diketones chelating agent, 2,2-dimethyl-6,6,7,7,8,8,8-heptafluoro-3,5-octanedione (HFOD), by unmodified
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:
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
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
I A Braude
Journal of immunological methods, 63(2), 237-246 (1983-10-14)
A method for the production of human gamma interferon (HuIFN-gamma), which is both simple and efficient, has been developed. The 2 co-inducers, A-23187 and mezerein, stimulate human peripheral blood lymphocytes to produce high levels of HuIFN-gamma in both stationary cultures
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