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394459

Sigma-Aldrich

Perfluorononanoic acid

97%

Synonym(s):

Heptadecafluorononanoic acid, Perfluorononanoic acid

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About This Item

Linear Formula:
CF3(CF2)7COOH
CAS Number:
375-95-1
Molecular Weight:
464.08
Beilstein:
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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Related Categories

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Danger

Hazard Classifications

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

Target Organs

Liver

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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
Xuemei Fang et al.
Toxicology, 267(1-3), 54-59 (2009-11-03)
Perfluoroalkyl acid (PFAA)-induced apoptosis has been reported in many cell types. However, minimal information on its mode of action is available. This study explored the possible involvement of apoptotic signaling pathways in a nine-carbon-chain length PFAA-perfluorononanoic acid (PFNA)-induced splenocyte apoptosis.
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
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.
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
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