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Safety Information

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:
2047182
EC Number:
212-611-1
MDL number:
MFCD00002331
UNSPSC Code:
12352100
PubChem Substance ID:
24853827
NACRES:
NA.22

Quality Level

100

Assay

99%

form

solid

mp

80-84 °C (lit.)

functional group

phenoxy

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

338.0 °F - closed cup

Flash Point(C)

170 °C - closed cup

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

230669-5G:
230669-25G:
230669-100G:
230669-VAR:
230669-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
09616TF
11425LX
00523MR
06703HC
03005HX

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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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