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Merck
CN

190276

3-Phenoxybenzoic acid

98%

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About This Item

Linear Formula:
C6H5OC6H4CO2H
CAS Number:
3739-38-6
Molecular Weight:
214.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24851425
EC Number:
223-121-2
Beilstein/REAXYS Number:
2105574
MDL number:
MFCD00002498

Key Documents

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Product Name

3-Phenoxybenzoic acid, 98%

InChI key

NXTDJHZGHOFSQG-UHFFFAOYSA-N

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)

SMILES string

OC(=O)c1cccc(Oc2ccccc2)c1

assay

98%

mp

147-149 °C (lit.)

functional group

carboxylic acid
phenoxy

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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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000255954
0000244702
0000244702
0000255954
0000193177

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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
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)
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
C Fortes et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 52, 91-96 (2012-11-14)
Concerns about pesticide exposure through food consumption have increased during the past several years. Pyrethroids are applied as insecticides throughout the world. Human metabolism of pyrethroids results in urinary metabolites that are suitable for biological monitoring. The objective of our
View All Related Papers

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傅-克酰基化反应

傅-克酰基化反应是一种芳烃与酰氯或酸酐使用强路易斯酸催化剂的反应。该反应通过亲电芳族取代进行，形成单酰化产物。

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