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246182

Sigma-Aldrich

4-Phenoxybenzoic acid

97%

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About This Item

Linear Formula:
C6H5OC6H4CO2H
CAS Number:
2215-77-2
Molecular Weight:
214.22
EC Number:
218-682-5
MDL number:
MFCD00002539
UNSPSC Code:
12352100
PubChem Substance ID:
24854791
NACRES:
NA.22

Assay

97%

mp

163-165 °C (lit.)

functional group

carboxylic acid

SMILES string

OC(=O)c1ccc(Oc2ccccc2)cc1

InChI

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

InChI key

RYAQFHLUEMJOMF-UHFFFAOYSA-N

General description

4-Phenoxybenzoic acid was converted to its corresponding amide by the soil bacterium Bacillus cereus Tim-r01.

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

246182-BULK:
246182-5G:
246182-25G:
246182-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBV1344
BCBJ4840V
BCBQ5420V
BCBC6763
BCBC6763V

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R Maruyama et al.
Bioscience, biotechnology, and biochemistry, 65(8), 1761-1765 (2001-10-02)
The soil bacterium Bacillus cereus Tim-r01 efficiently transformed polyaromatic carboxylic acids (PACA) such as 4-biphenylcarboxylic acid (4-BPCA), 4-biphenylacetic acid, and 4-phenoxybenzoic acid into their corresponding amides. The amidation activity was expressed at 37 degrees C (pH 7-8) in the presence
K H Engesser et al.
FEMS microbiology letters, 57(3), 317-321 (1990-06-01)
A bacterial strain, Pseudomonas sp. POB 310, was enriched with 4-carboxy biphenyl ether as sole source of carbon and energy. Resting cells of POB 310 co-oxidize a substrate analogue, 4-carboxybenzophenone, yielding 1,2-dihydro-1,2-dihydroxy-4-carboxy-benzophenone. The ether bond of 3- and 4-carboxy biphenyl
Hideki Moriyama et al.
Bioorganic & medicinal chemistry letters, 13(16), 2737-2740 (2003-07-23)
In order to investigate structure-activity relationships of azasugar series toward metalloproteinases, we synthesized and evaluated several azasugar-based compounds. As a result, it was found that 4-phenoxybenzene derivative 3 having 2R,3R,4R,5S-configurations exhibited most potent inhibitory activities against matrix metalloproteinase-1, -3 and
U Dehmel et al.
Archives of microbiology, 163(1), 35-41 (1995-01-01)
Pseudomonas pseudoalcaligenes strain POB310 degrades 3- and 4-carboxydiphenyl ether. The initial reaction involves an angular dioxygenation yielding an unstable hemiacetal that spontaneously decays to phenol and protocatechuate. We cloned a DNA fragment containing the gene encoding the initial dioxygenase from
Mikaela Nichkova et al.
Analytical chemistry, 77(21), 6864-6873 (2005-11-01)
Currently, detection in microarray bioanalysis is based mainly on the use of organic dyes. To overcome photobleaching and spectral overlaps we applied a new type of fluorophore, crystalline europium-doped gadolinium oxide (Eu:Gd2O3) nanoparticles, as labels in immunoassay microarrays. The Eu:Gd2O3
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