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Documenti fondamentali

177741

Sigma-Aldrich

Perfluorodecanoic acid

97%

Sinonimo/i:

Nonadecafluorodecanoic acid, Nonadecafluorocapric acid, Perfluorocapric acid, Perfluorodecanoic acid

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About This Item

Formula condensata:
CF3(CF2)8CO2H
Numero CAS:
Peso molecolare:
514.08
Beilstein:
1810811
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Tensione di vapore

~10 mmHg ( 0 °C)

Saggio

97%

P. ebollizione

218 °C/740 mmHg (lit.)

Punto di fusione

77-81 °C (lit.)

Solubilità

methanol: soluble 10%, clear to very slightly hazy, colorless to faintly yellow

Gruppo funzionale

carboxylic acid
fluoro

Stringa SMILE

OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C10HF19O2/c11-2(12,1(30)31)3(13,14)4(15,16)5(17,18)6(19,20)7(21,22)8(23,24)9(25,26)10(27,28)29/h(H,30,31)
PCIUEQPBYFRTEM-UHFFFAOYSA-N

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Descrizione generale

The electrochemical mineralization of environmentally persistent perfluorodecanoic acid was studied.

Applicazioni

Perfluorodecanoic acid was used to evaluate the effect of nonadecafluorocapric acid on the levels of six thyroid function variables (thyroid stimulating hormone, free and total thyroxine, free and total triiodothyronine and thyroglobulin).

Pittogrammi

Skull and crossbonesHealth hazard

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Acute Tox. 3 Oral - Carc. 2 - Lact. - Repr. 1B

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Anna Kärrman et al.
Environmental science and pollution research international, 17(3), 750-758 (2009-05-22)
Perfluorinated compounds (PFCs) are global environmental pollutants that bioaccumulate in wildlife and humans. Laboratory experiments have revealed toxic effects such as delayed development, humoral suppression, and hepatotoxicity. Although numerous human blood levels have been reported, little is known about distribution
Koichi Inoue et al.
Environmental health perspectives, 112(11), 1204-1207 (2004-08-04)
Fluorinated organic compounds (FOCs), such as perfluorooctane sulfonate (PFOS), perfluoro-octanoate (PFOA), and perfluorooctane sulfonylamide (PFOSA), are widely used in the manufacture of plastic, electronics, textile, and construction material in the apparel, leather, and upholstery industries. FOCs have been detected in
Laura A MacManus-Spencer et al.
Analytical chemistry, 82(3), 974-981 (2009-12-31)
Perfluorochemicals are globally pervasive contaminants that are persistent, bioaccumulative, and toxic. Perfluorocarboxylic acids (PFCAs) with 8-13 carbons accumulate in the liver and blood of aquatic organisms; PFCA-protein interactions may explain this accumulation pattern. Here, the interactions between PFCAs with 8-11
Hui Lin et al.
Environmental science & technology, 47(22), 13039-13046 (2013-10-30)
The electrochemical mineralization of environmentally persistent long-chain perfluorinated carboxylic acids (PFCAs), i.e., perfluorononanoic acid (C8F17COOH, PFNA) and perfluorodecanoic acid (C9F19COOH, PFDA) was investigated in aqueous solutions (0.25 mmol L(-1)) over Ti/SnO2-Sb-Ce (SnO2), Ti/SnO2-Sb/Ce-PbO2 (PbO2), and Ti/BDD (BDD) anodes under galvanostatic
Emanuela Corsini et al.
Toxicology and applied pharmacology, 258(2), 248-255 (2011-11-29)
We have previously shown that PFOA and PFOS directly suppress cytokine secretion in immune cells, with different mechanisms of action. In particular, we have demonstrated a role for PPAR-α in PFOA-induced immunotoxicity, and that PFOS has an inhibitory effect on

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