Merck

374776

Sigma-Aldrich

4-甲氧基联苯

97%

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别名:
4-苄基苯基醚
线性分子式:
C6H5C6H4OCH3
CAS号:
分子量:
184.23
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.47

检测方案

97%

形式

powder, crystals or chunks

mp

86-90 °C (lit.)

application(s)

diagnostic assay manufacturing
hematology
histology

储存温度

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

相关类别

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1 of 4

此商品
411930262013371335
vibrant-m

374776

4-甲氧基联苯

vibrant-m

411930

4-Phenoxyphthalonitrile

vibrant-m

262013

-4-芪甲醇

vibrant-m

371335

4′-Hydroxy-4-biphenylcarboxylic acid

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

storage temp.

room temp

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

application(s)

diagnostic assay manufacturing
hematology
histology

form

powder, crystals or chunks

form

powder, crystals or chunks

form

powder or crystals

form

powder, crystals or chunks

mp

86-90 °C (lit.)

mp

98-100 °C (lit.)

mp

155-160 °C (lit.)

mp

295 °C (dec.) (lit.)

应用

4-甲氧基联苯已被用作标准试剂,其荧光强度与芳基卤化物和苯基硼酸(PBA)的衍生化反应产物的荧光特性有关。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Sigma-Aldrich

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Sigma-Aldrich

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联苯 ≥99%

Sigma-Aldrich

W312908

联苯

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
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)
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)

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