产品名称
2,6-二氯-4-氨基苯酚, 98%
InChI
1S/C6H5Cl2NO/c7-4-1-3(9)2-5(8)6(4)10/h1-2,10H,9H2
InChI key
KGEXISHTCZHGFT-UHFFFAOYSA-N
SMILES string
Nc1cc(Cl)c(O)c(Cl)c1
assay
98%
form
powder
mp
167-170 °C (lit.)
Quality Level
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Benoît Limoges et al.
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
Daniel Aigner et al.
Journal of materials chemistry. C, 1(36), 5685-5693 (2013-10-01)
New optical pH-sensors relying on 1,4-diketopyrrolo-[3,4-
Gary O Rankin et al.
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
Benoît Limoges et al.
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
S K Hong et al.
Toxicology and applied pharmacology, 147(1), 115-125 (1997-11-14)
A halogenated derivative of 4-aminophenol, 4-amino-2, 6-dichlorophenol (ADCP), is a potent nephrotoxicant and a weak hepatotoxicant in Fischer 344 rats. Although the mechanism of ADCP nephrotoxicity is unknown, ADCP could undergo oxidation to a reactive intermediate, such as a 4-amino-2,6-dichlorophenoxy
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