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Merck
CN

183725

4-(咪唑-1-基)苯酚

97%

别名:

1-(4-羟基苯基)咪唑

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关于此项目

经验公式(希尔记法):
C9H8N2O
化学文摘社编号:
分子量:
160.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
EC Number:
233-121-4
MDL number:
Assay:
97%
Form:
powder
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assay

97%

form

powder

mp

204-206 °C (lit.)

SMILES string

Oc1ccc(cc1)-n2ccnc2

InChI

1S/C9H8N2O/c12-9-3-1-8(2-4-9)11-6-5-10-7-11/h1-7,12H

InChI key

CYKCUAPYWQDIKR-UHFFFAOYSA-N

Application

4-(咪唑-1-基)苯酚通过基于 酿酒酵母 - Lac - Z 报告基因分析 用于评价酚类外源性雌激素的雌激素活性。


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Effect of substituent size and dimensionality on potency of phenolic xenoestrogens evaluated with a recombinant yeast assay.
Schultz TW, et al.
Environmental Toxicology and Chemistry / Setac, 19(11), 2637-2642 (2000)
Wan Qiu Xia et al.
Analytical biochemistry, 554, 9-15 (2018-05-29)
In this study, a molecularly imprinted polymer based chemiluminescence array capable of simultaneous determining phenothiazines and benzodiazepines was first reported. Two polymers were coated in different wells of the conventional 96-well microtiter plate as the recognition reagents, and the added
Marimuthu Senthilkumaran et al.
Journal of fluorescence, 27(6), 2159-2168 (2017-09-10)
The interaction of n-(4-hydroxyphenyl)-imidazole with p-sulfonatocalix[4]arene is studied using fluorescence technique. The quenching of fluorescence intensity explains the efficiency of binding via binding constant and quenching constant. The excited state lifetime of n-(4-hydroxyphenyl)-imidazole is decreased upon interaction with p-sulfonatocalix[4]arene. The



全球贸易项目编号

货号GTIN
183725-1G04061826652428