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134341

Sigma-Aldrich

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
Beilstein:
1907452
EC Number:
202-179-2
MDL number:
MFCD00002347
UNSPSC Code:
12352100
eCl@ss:
39023323
PubChem Substance ID:
24848146
NACRES:
NA.22

Quality Level

100

Assay

97%

bp

321 °C (lit.)

mp

164-166 °C (lit.)

solubility

methanol: soluble 50 mg/mL, clear, colorless

functional group

phenyl

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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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

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

134341-500G:
134341-3KG:
134341-VAR:
134341-BULK:
134341-100G:
134341-1KG:
134341-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
STBK7705
STBK5298
STBK2154
STBJ8945
STBJ8059

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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)
Peng Xu et al.
Biomacromolecules, 3(5), 889-893 (2002-09-10)
Matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF) mass spectrometry is a powerful tool for polymer characterization. It has been used to understand the enzymatic polymerization of 4-phenylphenol and to monitor number average molecular weight and weight average molecular weight of the
Minoru Yamaji
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 7(6), 711-717 (2008-06-06)
The photochemical properties of alpha-cleavage of C-O bond in highly excited triplet states (T(n) with n>2) of p-biphenyl acetate and p-biphenyl benzoate (Me-OBP and Ph-OBP) in solution were investigated in comparison with those in the lowest excited singlet and triplet
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
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