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394459

Sigma-Aldrich

Perfluorononanoic acid

97%

Sinónimos:

Heptadecafluorononanoic acid, Perfluorononanoic acid

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About This Item

Fórmula lineal:
CF3(CF2)7COOH
Número de CAS:
375-95-1
Peso molecular:
464.08
Beilstein/REAXYS Number:
1897287
EC Number:
206-801-3
MDL number:
MFCD00039605
UNSPSC Code:
12352106
PubChem Substance ID:
24864596
NACRES:
NA.22

assay

97%

form

solid

mp

59-62 °C (lit.)

SMILES string

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)F

InChI

1S/C9HF17O2/c10-2(11,1(27)28)3(12,13)4(14,15)5(16,17)6(18,19)7(20,21)8(22,23)9(24,25)26/h(H,27,28)

InChI key

UZUFPBIDKMEQEQ-UHFFFAOYSA-N

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pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Lact. - Repr. 1B - STOT RE 1

target_organs

Liver

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Lin Tao et al.
Environmental science & technology, 42(9), 3472-3478 (2008-06-05)
The collapse of the World Trade Center (WTC) on September 11, 2001 resulted in the release of several airborne pollutants in and around the site. Perfluorochemicals including perfluorooctanesulfonate (PFOS) and perfluorooctanoic acid (PFOA), which are used in soil- and stain-resistant
Katoria Tatum-Gibbs et al.
Toxicology, 281(1-3), 48-55 (2011-01-18)
Perfluorononanoic acid (PFNA) is a fluorinated organic chemical found at low levels in the environment, but is detectable in humans and wildlife. The present study compared the pharmacokinetic properties of PFNA in two laboratory rodent species. Male and female Sprague-Dawley
Xuemei Fang et al.
Toxicology, 294(2-3), 109-115 (2012-03-06)
Exposure to perfluorononanoic acid (PFNA), an increasingly persistent organic pollutant that has been detected in abiotic and biotic matrices, has been demonstrated to cause hepatotoxicity in animals. However, the effects of PFNA on hepatic glucose metabolism have not been fully
Marleen Maras et al.
Environmental health perspectives, 114(1), 100-105 (2006-01-06)
We investigated estrogen-like properties of five perfluorinated compounds using a combination of three in vitro assays. By means of an E-screen assay, we detected the proliferation-promoting capacity of the fluorotelomer alcohols 1H,1H,2H,2H-perfluorooctan-1-ol (6:2 FTOH) and 1H,1H,2H,2H-perfluoro-decan-1-ol (8:2 FTOH). The more
Xuemei Fang et al.
Toxicological sciences : an official journal of the Society of Toxicology, 108(2), 367-376 (2009-02-07)
Perfluorononanoate (PFNA), a perfluorinated alkyl acid containing nine carbon chains, has been detected in abiotic and biotic matrices worldwide. Although a few studies have reported toxic effects of PFNA, little information of the mechanism has been offered. In this study
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