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Key Documents

190276

Sigma-Aldrich

3-Phenoxybenzoic acid

98%

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About This Item

Linear Formula:
C6H5OC6H4CO2H
CAS Number:
Molecular Weight:
214.22
Beilstein/REAXYS Number:
2105574
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

mp

147-149 °C (lit.)

SMILES string

OC(=O)c1cccc(Oc2ccccc2)c1

InChI

1S/C13H10O3/c14-13(15)10-5-4-8-12(9-10)16-11-6-2-1-3-7-11/h1-9H,(H,14,15)

InChI key

NXTDJHZGHOFSQG-UHFFFAOYSA-N

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Application

3-Phenoxybenzoic acid was used as standard in the determination of urinary residues of 3-phenoxybenzoic acid by GLC with electron-capture detection method. It was also used in the synthesis of poly(ether-ketones).

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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Grafting of vapor-grown carbon nanofibers via in-situ polycondensation of 3-phenoxybenzoic acid in poly (phosphoric acid).
Baek J-B, et al.
Macromolecules, 37(22), 8278-8285 (2004)
C Aprea et al.
Journal of chromatography. B, Biomedical sciences and applications, 695(2), 227-236 (1997-08-01)
The determination of urinary 3-phenoxybenzoic acid enables exposure to pyrethroid insecticides to be evaluated. A method for the quantitative determination of this metabolite in urine is described. The compound and the internal standard (2-phenoxybenzoic acid) are derivatized with pentafluorobenzylbromide and
Idalina Bragança et al.
Environmental science and pollution research international, 26(3), 2987-2997 (2018-12-07)
3-Phenoxybenzoic acid (3-PBA) is a shared metabolite of several synthetic pyrethroid pesticides (SPs) resulting from environmental degradation of parent compounds and thus occurs frequently as a residue in samples. Hence, the importance of 3-PBA evaluation after pyrethroid application. There is
Improved syntheses of poly (oxy-1, 3-phenylenecarbonyl-1, 4-phenylene) and related poly (ether-ketones) using polyphosphoric acid/P 2 O 5 as polymerization medium.
Baek J-B and Tan L-S.
Polymer, 44(15), 4135-4147 (2003)
Guixiang Ji et al.
Reproductive toxicology (Elmsford, N.Y.), 31(2), 171-176 (2010-10-20)
Observations in several western and Asiatic countries point toward a decline in semen quality which may be associated with environmental exposures. To investigate the effect of environmental exposure to pyrethroids on sperm DNA integrity and semen quality, 240 men were

Articles

Friedel-Crafts acylation with Lewis acid catalysts forms monoacylated products via electrophilic aromatic substitution of arenes.

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