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Sigma-Aldrich

Pentadecafluorooctanoic acid ammonium salt

≥98.0% (NT)

Synonym(s):

Ammonium pentadecafluorooctanoate, Perfluorocaprylic acid ammonium salt, Perfluorooctanoic acid ammonium salt

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About This Item

Linear Formula:
CF3(CF2)6COONH4
CAS Number:
3825-26-1
Molecular Weight:
431.10
Beilstein:
4286466
EC Number:
223-320-4
MDL number:
MFCD00042599
UNSPSC Code:
12352100
PubChem Substance ID:
57652683
NACRES:
NA.22

Assay

≥98.0% (NT)

form

powder

functional group

carboxylic acid
fluoro

SMILES string

N.OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C8HF15O2.H3N/c9-2(10,1(24)25)3(11,12)4(13,14)5(15,16)6(17,18)7(19,20)8(21,22)23;/h(H,24,25);1H3

InChI key

YOALFLHFSFEMLP-UHFFFAOYSA-N

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General description

Pentadecafluorooctanoicacid ammonium salt (Ammonium pentadecafluorooctanoate) is commonly used in the polymerization of fluorinated monomers. It is also used as a surfactant during chemical synthesis.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - 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
BCCM3051
BCCG1071
BCCG1628
BCCF9958
BCCF6623

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Synthesis, interfacial property, and application of new hybrid anion surfactant containing fluorocarbon and hydrocarbon chains
Kang EK, et al.
Journal of Industrial and Engineering Chemistry, 67, 72-79 (2018)
Hydrocarboxylation of terminal alkenes in supercritical carbon dioxide using perfluorinated surfactants
Tortosa-Estorach C, et al.
Chemical Communications (Cambridge, England), 26, 2789-2791 (2006)
Anne Vested et al.
Environmental health perspectives, 121(4), 453-458 (2013-01-31)
Perfluorinated alkyl acids (PFAAs), persistent chemicals with unique water-, dirt-, and oil-repellent properties, are suspected of having endocrine-disrupting activity. The PFAA compounds perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) are found globally in humans; because they readily cross the
Mei-Huei Chen et al.
Epidemiology (Cambridge, Mass.), 24(6), 800-808 (2013-09-17)
Epidemiologic data regarding the potential neurotoxicity of perfluorinated compounds (PFCs) are inconclusive. We investigated the associations between in utero exposure to perfluorooctanoic acid (PFOA) and perfluorooctyl sulfonate (PFOS) and early childhood neurodevelopment. We recruited 239 mother-infant pairs in northern Taiwan
A K Rosenmai et al.
Toxicology and applied pharmacology, 266(1), 132-142 (2012-11-13)
Polyfluoroalkyl phosphate surfactants (PAPS) are widely used in food contact materials (FCMs) of paper and board and have recently been detected in 57% of investigated materials. Human exposure occurs as PAPS have been measured in blood; however knowledge is lacking
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