183725
4-(Imidazol-1-yl)phenol
97%
Sinónimos:
1-(4-Hydroxyphenyl)imidazole
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About This Item
Productos recomendados
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
Categorías relacionadas
Application
4-(Imidazol-1-yl)phenol was used in evaluation of estrogenicity of phenolic xenoestrogens by Saccharomyces cerevisiae-based Lac-Z reporter assay.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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
Effect of substituent size and dimensionality on potency of phenolic xenoestrogens evaluated with a recombinant yeast assay.
Environmental Toxicology and Chemistry / Setac, 19(11), 2637-2642 (2000)
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In this study, a molecularly imprinted polymer capable of recognizing 8 benzimidazoles was first synthesized. The computation simulation showed that the shape and size of used template were the main factors influencing its recognition ability. Then the polymer was used
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