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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

Quality Level

100

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

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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Certificates of Analysis (COA)

Lot/Batch Number
MKCW3054
MKCW8836
MKCV5334
MKCT7988
MKCM3935

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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
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
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
R Schwarz et al.
Magnetic resonance in medicine, 41(1), 80-86 (1999-02-20)
19F-Magnetic resonance imaging in conjunction with perfluorononane provides a new modality for gastrointestinal (GI) imaging as is demonstrated here with an animal model. Perfluorononane was found to be an ideal oral contrast agent since it is biologically inert, immiscible with
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