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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:
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 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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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)
Xiaojuan Qi et al.
International journal of hygiene and environmental health, 215(5), 487-495 (2012-01-06)
Pyrethroid pesticides are widely used throughout the world in agriculture to protect crops and in public health to control diseases. Of particular concern is exposure of pregnant women and their fetuses because little is known about the potential developmental hazards

Articles

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

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