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Merck
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文件

374776

Sigma-Aldrich

4-甲氧基联苯

97%

别名:

4-苄基苯基醚

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About This Item

线性分子式:
C6H5C6H4OCH3
CAS号:
613-37-6
分子量:
184.23
EC號碼:
210-339-8
MDL號碼:
MFCD00014897
分類程式碼代碼:
12171500
PubChem物質ID:
24863335
NACRES:
NA.47

化驗

97%

形狀

powder, crystals or chunks

mp

86-90 °C (lit.)

應用

diagnostic assay manufacturing
hematology
histology

儲存溫度

room temp

SMILES 字串

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 密鑰

RHDYQUZYHZWTCI-UHFFFAOYSA-N

相关类别

應用

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。

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)

分析证书(COA)

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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)
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)

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