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Merck
CN

29226

Undecafluorohexanoic acid

≥97.0% (T)

Synonym(s):

Perfluorocaproic acid, Perfluorohexanoic acid

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About This Item

Linear Formula:
CF3(CF2)4COOH
CAS Number:
307-24-4
Molecular Weight:
314.05
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57648349
EC Number:
206-196-6
Beilstein/REAXYS Number:
1805852
MDL number:
MFCD00198040

Key Documents

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Product Name

Undecafluorohexanoic acid, ≥97.0% (T)

InChI key

PXUULQAPEKKVAH-UHFFFAOYSA-N

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)

SMILES string

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

assay

≥97.0% (T)

solubility

water: insoluble

density

1.759 g/mL at 20 °C (lit.)

functional group

carboxylic acid
fluoro

Quality Level

200

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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
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCM8535
BCCL3724
BCCL6932
BCCL2144
BCCK8850

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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
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
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
Abdullah Akhdhar et al.
Talanta, 209, 120466-120466 (2020-01-02)
The determination of total fluorine content using high-resolution graphite furnace continuum source molecular absorption spectrometry (HR- MAS) has been employed in a variety of samples for over 10 years. However, most of the samples analysed by HR- MAS are rich
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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