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P5360

Sigma-Aldrich

2,3,4,5,6-Pentafluorobenzoic acid

99%

Synonym(s):

pentafluorobenzoic acid, perfluorobenzoic acid

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About This Item

Linear Formula:
C6F5CO2H
CAS Number:
602-94-8
Molecular Weight:
212.07
Beilstein:
2054395
EC Number:
210-026-6
MDL number:
MFCD00002406
UNSPSC Code:
12352100
PubChem Substance ID:
24898625
NACRES:
NA.22

Assay

99%

form

powder

bp

220 °C (lit.)

mp

100-102 °C (lit.)

SMILES string

OC(=O)c1c(F)c(F)c(F)c(F)c1F

InChI

1S/C7HF5O2/c8-2-1(7(13)14)3(9)5(11)6(12)4(2)10/h(H,13,14)

InChI key

YZERDTREOUSUHF-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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M Palit et al.
Journal of chromatography. A, 1043(2), 275-284 (2004-08-28)
A method based on gas chromatography-mass spectrometry (GC/MS) has been evaluated and standardized for the analysis of pentafluorobenzyl (PFB) derivatives of alkylphosphonic, O-alkyl alkylphosphonic and phosphonothioic acids. The pentafluorobenzyl (PFB) derivatives are much more stable as compared to the conventionally
Paolo Guidetti et al.
Brain research. Molecular brain research, 118(1-2), 132-139 (2003-10-16)
alpha-Aminoadipic acid (alphaAA) is a structural homolog of the excitatory amino acid glutamate and a natural product of lysine metabolism in mammalian cells. Under experimental conditions, alphaAA can influence various elements of glutamatergic neurotransmission. Moreover, as a selective inhibitor of
Tinne Geens et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 877(31), 4042-4046 (2009-11-04)
The development and validation of an analytical method is presented for the determination of bisphenol-A (BPA) and triclosan (TCS), two ubiquitous contaminants, in serum and urine. The glucuronidated metabolites were first turned into their free forms to determine total BPA
Paul W Reimus et al.
Journal of contaminant hydrology, 62-63, 613-636 (2003-04-26)
Two cross-hole tracer tests involving the simultaneous injection of two nonsorbing solute tracers with different diffusion coefficients (bromide and pentafluorobenzoate) and one weakly sorbing solute tracer (lithium ion) were conducted in two different intervals at the C-wells complex near the
Nathan W Haws et al.
Journal of contaminant hydrology, 75(3-4), 257-280 (2004-12-22)
Soil macropore networks establish a dual-domain transport scenario in which water and solutes are preferentially channeled through soil macropores while slowly diffusing into and out of the bulk soil matrix. The influence of macropore networks on intra-ped solute diffusion and
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