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230669

Sigma-Aldrich

4-Phenoxyphenol

99%

Synonym(s):

Hydroquinone monophenyl ether

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About This Item

Linear Formula:
C6H5OC6H4OH
CAS Number:
831-82-3
Molecular Weight:
186.21
Beilstein/REAXYS Number:
2047182
EC Number:
212-611-1
MDL number:
MFCD00002331
UNSPSC Code:
12352100
PubChem Substance ID:
24853827
NACRES:
NA.22

assay

99%

form

solid

mp

80-84 °C (lit.)

SMILES string

Oc1ccc(Oc2ccccc2)cc1

InChI

1S/C12H10O2/c13-10-6-8-12(9-7-10)14-11-4-2-1-3-5-11/h1-9,13H

InChI key

ZSBDGXGICLIJGD-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

338.0 °F - closed cup

flash_point_c

170 °C - closed cup

ppe

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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Victoria B F Custodis et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(36), 8658-8668 (2017-04-08)
One of the key challenges in renewable chemical production is the conversion of lignin, especially by fast pyrolysis. The complexity of the lignin pyrolysis process has hindered the elucidation of the mechanism, inhibiting further industrial implementation. By combining pyrolysis of
Kyoungseon Min et al.
Biotechnology for biofuels, 10, 212-212 (2017-09-16)
In the biorefinery utilizing lignocellulosic biomasses, lignin decomposition to value-added phenolic derivatives is a key issue, and recently biocatalytic delignification is emerging owing to its superior selectivity, low energy consumption, and unparalleled sustainability. However, besides heme-containing peroxidases and laccases, information
Xiaolu Jiang et al.
Bioorganic & medicinal chemistry letters, 18(24), 6549-6552 (2008-10-28)
The synthesis and biological evaluation of a series of diphenyl ether derivatives were described. The compounds can either activate or inhibit the aminopeptidase activity of leukotriene A(4) hydrolase, while at the same time do not influence the hydrolase activity. Further
Cynthia D Selassie et al.
Journal of medicinal chemistry, 48(23), 7234-7242 (2005-11-11)
In this comprehensive study on the caspase-mediated apoptosis-inducing effect of 51 substituted phenols in a murine leukemia cell line (L1210), we determined the concentrations needed to induce caspase activity by 50% (I50) and utilized these data to develop the following

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