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29226

Sigma-Aldrich

Undecafluorohexanoic acid

≥97.0% (T)

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Synonym(s):
Perfluorocaproic acid, Perfluorohexanoic acid
Linear Formula:
CF3(CF2)4COOH
CAS Number:
Molecular Weight:
314.05
Beilstein/REAXYS Number:
1805852
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥97.0% (T)

solubility

water: insoluble

density

1.759 g/mL at 20 °C (lit.)

SMILES string

OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C6HF11O2/c7-2(8,1(18)19)3(9,10)4(11,12)5(13,14)6(15,16)17/h(H,18,19)

InChI key

PXUULQAPEKKVAH-UHFFFAOYSA-N

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This Item
34204178610171468
Undecafluorohexanoic acid ≥97.0% (T)

29226

Undecafluorohexanoic acid

Perfluoroheptanoic acid ≥97.0%

342041

Perfluoroheptanoic acid

Phenylglyoxylic acid purum, ≥98.0% (T)

78610

Phenylglyoxylic acid

Perfluorooctanoic acid 95%

171468

Perfluorooctanoic acid

solubility

water: insoluble

solubility

-

solubility

methanol: 0.1 g/mL, clear

solubility

-

density

1.759 g/mL at 20 °C (lit.)

density

1.792 g/mL at 25 °C (lit.)

density

-

density

-

Application

Undecafluorohexanoic acid, a volatile ion-pair reagent, has been used as mobile phase for LC-MS analysis of highly polar sulfonium pseudo-sugar constituents neosalacinol and neokotalanol, potential α-glucosidase inhibitors isolated from ayurvedic traditional medicine Salacia species.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible, corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Customers Also Viewed

Osamu Muraoka et al.
Journal of natural medicines, 65(1), 142-148 (2010-10-29)
A quantitative analytical method for the highly polar sulfonium pseudo-sugar constituents neosalacinol (3) and neokotalanol (4), another two potent α-glucosidase inhibitors isolated from Ayurvedic traditional medicine Salacia species, was developed by employing an ion pair reagent upon chromatographic separation. The
Álvaro Soriano et al.
Water research, 112, 147-156 (2017-02-06)
The present study was aimed at the development of a strategy for removing and degrading perfluorohexanoic acid (PFHxA) from industrial process waters at concentrations in the range 60-200 mg L
Yanping Cai et al.
International journal of environmental research and public health, 16(1) (2019-01-10)
Perfluorocarboxylic acid compounds (PFCAs) and copper have been regarded as ubiquitous environmental contaminants in aquatic ecosystems worldwide. However, data on their possible joint toxic effects on microorganisms are still lacking. To study the combined effects of four PFCAs with different
Qian S Liu et al.
Environmental science & technology, 51(17), 10173-10183 (2017-07-27)
Per- and polyfluoroalkyl substances (PFASs) are a global concern because of their ubiquitous occurrence and high persistence in human blood, and increasing amounts of unidentified fluorinated compounds are now becoming new exposure issues. This study aims to investigate the structure-related
Lei Wang et al.
Journal of chromatography. A, 1515, 45-53 (2017-08-15)
Ionic liquids have been used to efficiently extract a wide range of polar and nonpolar organic contaminants from water. In this study, imidazole ionic liquids immobilized on silica gel were synthesized through a chemical bonding method, and the immobilized dodecylimidazolium

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