A48407
4-Amino-2,6-dichlorophenol
98%
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About This Item
Productos recomendados
assay
98%
form
powder
mp
167-170 °C (lit.)
SMILES string
Nc1cc(Cl)c(O)c(Cl)c1
InChI
1S/C6H5Cl2NO/c7-4-1-3(9)2-5(8)6(4)10/h1-2,10H,9H2
InChI key
KGEXISHTCZHGFT-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Journal of the American Chemical Society, 130(23), 7259-7275 (2008-05-21)
The use of enzyme labeling techniques to convert biorecognition events into high sensitivity electrochemical signals may follow two different strategies. One, in which the current is the electrocatalytic response of a redox couple serving as cosubstrate to a redox enzyme
Journal of materials chemistry. C, 1(36), 5685-5693 (2013-10-01)
New optical pH-sensors relying on 1,4-diketopyrrolo-[3,4-
Toxicology, 245(1-2), 123-129 (2008-02-05)
4-Amino-2,6-dichlorophenol (ADCP) is a potent acute nephrotoxicant in vivo inducing prominent renal corticomedullary necrosis. In vitro, ADCP exposure increases lactate dehydrogenase (LDH) release from rat renal cortical slices at 0.05 mM or greater. The purpose of this study was to
Journal of the American Chemical Society, 130(23), 7276-7285 (2008-05-22)
The two articles in this series are dedicated to bioaffinity electrodes with in situ detection of the product of the enzyme label after recognition by its conjugate immobilized on the electrode. Part 1 was devoted to direct electrochemical detection, whereas
Toxicology, 90(1-2), 115-128 (1994-05-31)
Halogenated anilines and aminophenols are nephrotoxicants and hepatotoxicants in mammals. The purpose of this study was to determine the in vivo and in vitro nephrotoxic and hepatotoxic potential of 4-amino-2,6-dichlorophenol, a putative metabolite of 3,5-dichloroaniline. In the in vivo experiments
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