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175161

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

Name: 6,6,7,7,8,8,8-Heptafluoro-2,2-dimethyl-3,5-octanedione
Brand: ALDRICH

98%

Sinónimos:

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

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Acerca de este artículo

Fórmula lineal:

CF₃CF₂CF₂COCH₂COC(CH₃)₃

Número CAS:

17587-22-3

Peso molecular:

296.18

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24850490

EC Number:

241-556-6

Beilstein/REAXYS Number:

2056991

MDL number:

MFCD00000435

Assay:

98%

Form:

liquid

Este producto está descatalogado. Póngase en contacto con el Servicio técnicopara asistencia

Propiedades

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

Descripción

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)[1]. It was also used as a beta-diketone chelating agent in the extraction of supercritical carbon dioxide[2].

pictograms

GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Clase de almacenamiento

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

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A synthetic ionophore for Ca2+: studies with model and biological systems.

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:

[Hypnotic drugs. 2. Reaction of guanidine carboxamide with fluorinated beta-diketones].

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

Calcium transport by a beta-diketone in model membranes.

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

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SKU	GTIN
175161-5G	04061836682804

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