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177741

Sigma-Aldrich

Perfluorodecanoic acid

98%

Synonyme(s) :

Nonadecafluorodecanoic acid, Nonadecafluorocapric acid, Perfluorocapric acid, Perfluorodecanoic acid

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About This Item

Formule linéaire :
CF3(CF2)8CO2H
Numéro CAS:
Poids moléculaire :
514.08
Numéro Beilstein :
1810811
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Pression de vapeur

~10 mmHg ( 0 °C)

Pureté

98%

Point d'ébullition

218 °C/740 mmHg (lit.)

Pf

77-81 °C (lit.)

Solubilité

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

Chaîne SMILES 

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)

Clé InChI

PCIUEQPBYFRTEM-UHFFFAOYSA-N

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Description générale

The electrochemical mineralization of environmentally persistent perfluorodecanoic acid was studied.

Application

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).

Pictogrammes

Skull and crossbonesHealth hazard

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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


Certificats d'analyse (COA)

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Changhui Liu et al.
Environmental science & technology, 45(22), 9758-9764 (2011-10-13)
The effects of exposure concentration on the bioaccumulation of four perfluorinated chemicals (PFCs): perfluorooctanesulfonate (PFOS), perfluoroocanoic acid (PFOA), perfluorononanoic acid (PFNA), and perfluorodecanoic acid (PFDA), was investigated using green mussels, Perna viridis. Mussels were exposed to concentrations of 1 μgL(-1)
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
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
Hoon Yoo et al.
Environmental science & technology, 42(15), 5821-5827 (2008-08-30)
Concentrations of perfluoroalkyl acids (PFAs) were measured in egg yolks of three species of birds, the little egret (Egretta garzetta), little ringed plover (Charadrius dubius), and parrot bill (Paradoxornis webbiana), collected in and around Lake Shihwa, Korea, which receives wastewaters
Ingrid Nobels et al.
Toxicology in vitro : an international journal published in association with BIBRA, 24(6), 1768-1774 (2010-07-14)
Perfluorinated compounds are widely distributed in the environment; good knowledge about the toxic mode of action of these compounds can contribute to improved molecular design and risk assessment. The studied compounds were evaluated with a bacterial multiple endpoint reporter assay

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