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134341

Sigma-Aldrich

4-Phenylphenol

97%

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Synonym(s):
4-Hydroxybiphenyl
Linear Formula:
C6H5C6H4OH
CAS Number:
Molecular Weight:
170.21
Beilstein:
1907452
EC Number:
MDL number:
eCl@ss:
39023323
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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)

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1 of 4

This Item
CRM69184424625P28263
4-Phenylphenol 97%

Sigma-Aldrich

134341

4-Phenylphenol

4-Phenylphenol certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

CRM69184

4-Phenylphenol

4-Phenylphenol purified by sublimation, 99%

Sigma-Aldrich

424625

4-Phenylphenol

2-Phenylphenol 99%

Sigma-Aldrich

P28263

2-Phenylphenol

bp

321 °C (lit.)

bp

321 °C (lit.)

bp

321 °C (lit.)

bp

282 °C (lit.)

mp

164-166 °C (lit.)

mp

164-166 °C (lit.)

mp

164-166 °C (lit.)

mp

57-59 °C (lit.)

solubility

methanol: soluble 50 mg/mL, clear, colorless

solubility

-

solubility

water: soluble 0.7 g/L at 20 °C

solubility

-

Gene Information

rat ... Ar(24208)

Gene Information

-

Gene Information

rat ... Ar(24208)

Gene Information

-

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

Signal Word

Warning

Hazard Statements

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

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Customers Also Viewed

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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)
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

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