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Merck
CN

134341

4-Phenylphenol

97%

Synonym(s):

4-Hydroxybiphenyl

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About This Item

Linear Formula:
C6H5C6H4OH
CAS Number:
92-69-3
Molecular Weight:
170.21
NACRES:
NA.22
PubChem Substance ID:
24848146
eCl@ss:
39023323
UNSPSC Code:
12352100
EC Number:
202-179-2
MDL number:
MFCD00002347
Beilstein/REAXYS Number:
1907452
Assay:
97%

Key Documents

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InChI key

YXVFYQXJAXKLAK-UHFFFAOYSA-N

InChI

1S/C12H10O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9,13H

SMILES string

Oc1ccc(cc1)-c2ccccc2

assay

97%

bp

321 °C (lit.)

Quality Level

100

Gene Information

rat ... Ar(24208)

solubility

methanol: soluble 50 mg/mL, clear, colorless

functional group

phenyl

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General description

4-Phenylphenol undergoes enzymatic polymerization and polymer developed is characterized by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. It is the intermediate in manufacture of 4-alkyl substituted phenol-formaldehyde resins.

Application

4-Phenylphenol was used in the synthesis of a novel polyphosphazene polyelectrolyte as a dispersing agent of single-walled carbon nanotubes in water.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Aquatic Chronic 2 - Skin Irrit. 2 - Skin Sens. 1B

Storage Class

13 - Non Combustible Solids

wgk

WGK 2

flash_point_f

320.0 °F - closed cup

flash_point_c

160 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB7231
SDBB6357
STBK7705
STBK5298
STBK2154

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MALDI-TOF mass spectrometry characterization of 4-alkyl substituted phenol-formaldehyde novalac type resins.
Mandal H and Hay AS.
Polymer, 38(26), 6267-6271 (1997)
Dispersion of single-walled carbon nanotubes in water with polyphosphazene polyelectrolyte.
Park HJ, et al.
Journal of Inorganic and Organometallic Polymers and Materials, 16(4), 359-364 (2006)
Enzymatic polymerization of p-phenylphenol in aqueous micelles.
W H Liu et al.
Annals of the New York Academy of Sciences, 750, 138-145 (1995-03-31)
C K Kuo et al.
Journal of pharmacobio-dynamics, 14(4), 187-193 (1991-04-01)
Species difference in glucuronidation of morphine was studied using mice, rats, guinea pigs and rabbits in vivo and in vitro. Morphine-3-glucuronide (M-3-G) and morphine-6-glucuronide (M-6-G) were determined by high-performance liquid chromatography. M-3-G was the major urinary metabolite of morphine in
R H Tukey et al.
The Journal of biological chemistry, 268(20), 15260-15266 (1993-07-15)
A polyclonal antibody generated against rabbit liver p-nitrophenol UDP-glucuronosyltransferase (UGT) was used to screen a rabbit liver cDNA expression library constructed in lambda gt11. A 500-base pair cDNA clone, termed pPNP, generated a fusion protein that was antigenic with the
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