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134341

Sigma-Aldrich

4-Phenylphenol

97%

Sinônimo(s):

4-Hydroxybiphenyl

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About This Item

Fórmula linear:
C6H5C6H4OH
Número CAS:
92-69-3
Peso molecular:
170.21
Beilstein:
1907452
Número CE:
202-179-2
Número MDL:
MFCD00002347
Código UNSPSC:
12352100
eCl@ss:
39023323
ID de substância PubChem:
24848146
NACRES:
NA.22

Ensaio

97%

pb

321 °C (lit.)

pf

164-166 °C (lit.)

solubilidade

methanol: soluble 50 mg/mL, clear, colorless

cadeia de caracteres SMILES

Oc1ccc(cc1)-c2ccccc2

InChI

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

chave InChI

YXVFYQXJAXKLAK-UHFFFAOYSA-N

Informações sobre genes

rat ... Ar(24208)

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Categorias relacionadas

Descrição geral

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.

Aplicação

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

Pictogramas

Exclamation markEnvironment
GHS07,GHS09

Palavra indicadora

Warning

Frases de perigo

H315,H317,H411

Classificações de perigo

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

Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

320.0 °F - closed cup

Ponto de fulgor (°C)

160 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análise (COA)

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Sigma-Aldrich

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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)
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
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
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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