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374776

4-甲氧基联苯

Name: 4-甲氧基联苯
Brand: ALDRICH

97%

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所有图片(3)

别名:

4-苄基苯基醚

线性分子式:

C₆H₅C₆H₄OCH₃

CAS号:

613-37-6

分子量:

184.23

EC 号:

210-339-8

MDL编号:

MFCD00014897

PubChem化学物质编号:

24863335

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

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)

分析证书(COA)

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示例

T1503

货号

25G

包装规格/数量

其它示例：

705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

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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)

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)

Influence of substrate concentration on the phase I and phase II metabolism of 4-methoxybiphenyl by rat isolated hepatocytes.

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

Influence of cytochrome P-450 type on the pattern of conjugation of 4-hydroxybiphenyl generated from biphenyl or 4-methoxybiphenyl.

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

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