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Documentos

374776

Sigma-Aldrich

4-Methoxybiphenyl

97%

Sinónimos:

4-Phenylanisole

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About This Item

Fórmula lineal:
C6H5C6H4OCH3
Número de CAS:
613-37-6
Peso molecular:
184.23
EC Number:
210-339-8
MDL number:
MFCD00014897
UNSPSC Code:
12171500
PubChem Substance ID:
24863335
NACRES:
NA.47

assay

97%

form

powder, crystals or chunks

mp

86-90 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

COc1ccc(cc1)-c2ccccc2

InChI

1S/C13H12O/c1-14-13-9-7-12(8-10-13)11-5-3-2-4-6-11/h2-10H,1H3

InChI key

RHDYQUZYHZWTCI-UHFFFAOYSA-N

Application

4-Methoxybiphenyl has been used as a standard reagent whose fluorescence intensity is associated with the fluorescence characteristics of the products of derivatization reaction for aryl halides with phenylboronic acid (PBA).

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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J R Fry
Xenobiotica; the fate of foreign compounds in biological systems, 17(6), 751-758 (1987-06-01)
1. The metabolism of 4-methoxybiphenyl to 4-hydroxybiphenyl and its sulphate and glucuronic acid conjugates has been studied in rat isolated hepatocytes at various concentrations of 4-methoxybiphenyl. 2. The proportions of metabolites produced remained constant at concentrations of 4-methoxybiphenyl less than
A comparison of biphenyl 4-hydroxylation and 4-methoxybiphenyl O-demethylation in rat liver microsomes.
J R Fry
Biochemical pharmacology, 30(14), 1915-1919 (1981-07-15)
P Paterson et al.
Xenobiotica; the fate of foreign compounds in biological systems, 15(6), 493-502 (1985-06-01)
The rate of production of 4-hydroxybiphenyl from 4-methoxybiphenyl in hepatocytes isolated from untreated rats was essentially identical to that from biphenyl in hepatocytes isolated from rats pretreated with beta-naphthoflavone at 40 mg/kg. Similar results were obtained using liver microsomes isolated
Influence of the sulphation inhibitor, 2,6-dichloro-4-nitrophenol, on the production and conjugation, of 4-hydroxybiphenyl generated from 4-methoxybiphenyl by rat isolated hepatocytes.
J R Fry et al.
Biochemical pharmacology, 36(18), 3090-3092 (1987-09-15)

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