Skip to Content
Merck
All Photos(1)

Documents

134341

Sigma-Aldrich

4-Phenylphenol

97%

Synonym(s):

4-Hydroxybiphenyl

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

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

Assay

97%

bp

321 °C (lit.)

mp

164-166 °C (lit.)

solubility

methanol: soluble 50 mg/mL, clear, colorless

SMILES string

Oc1ccc(cc1)-c2ccccc2

InChI

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

InChI key

YXVFYQXJAXKLAK-UHFFFAOYSA-N

Gene Information

rat ... Ar(24208)

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

Signal Word

Warning

Hazard Statements

H315,H317,H411

Hazard Classifications

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

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 2

Flash Point(F)

320.0 °F - closed cup

Flash Point(C)

160 °C - closed cup

Personal Protective Equipment

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
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
T Yoshimura et al.
Journal of pharmacobio-dynamics, 15(8), 387-393 (1992-08-01)
The apparent in vitro kinetic constants of uridine diphosphate-glucuronyltransferase (UDP-GT) activities towards E6080, 1-naphthol (1-N) and 4-hydroxybiphenyl (4-HB) were determined using microsomes, to assess the effect of inducing agents and evaluate species and tissue differences. In rats, the 3-methylcholanthrene and
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service