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form
liquid
availability
available only in Japan
pH
4.2-6.2
SMILES string
CN(C)c1ccc(cc1)\N=N\c2ccccc2C(O)=O
InChI
1S/C15H15N3O2/c1-18(2)12-9-7-11(8-10-12)16-17-14-6-4-3-5-13(14)15(19)20/h3-10H,1-2H3,(H,19,20)/b17-16+
InChI key
CEQFOVLGLXCDCX-WUKNDPDISA-N
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Suitability
for titration
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
55.4 °F
Flash Point(C)
13 °C
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Journal of neuro-oncology, 102(1), 9-18 (2010-07-17)
A major focus of brain cancer research today is to translate understanding of glioma biology into advances in treatment, by exploring the potential of target therapy. Here we investigated the ability of three compounds belonging to the chemical class of
Bioresource technology, 130, 517-521 (2013-01-17)
Azo dyes are toxic and carcinogenic and are often present in industrial effluents. In this research, azoreductase and glucose 1-dehydrogenase were coupled for both continuous generation of the cofactor NADH and azo dye removal. The results show that 85% maximum
Nanoscale, 3(8), 3269-3276 (2011-07-01)
Nanoporous and nonporous three-dimensional silicon nanowire arrays (SiNWAs) prepared with metal-assisted chemical etching method were investigated as photocatalysts in dye photodegradation systematically. In comparison with nonporous SiNWAs, nanoporous SiNWAs have higher surface area, larger pore volume, stronger light absorption and
Proceedings of the National Academy of Sciences of the United States of America, 108(52), 20891-20896 (2011-12-14)
Noncontact optical trapping and manipulation of micrometer- and nanometer-sized particles are typically achieved by use of forces and torques exerted by tightly focused high-intensity laser beams. Although they were instrumental for many scientific breakthroughs, these approaches find few technological applications
Chemistry (Weinheim an der Bergstrasse, Germany), 18(35), 10865-10872 (2012-07-26)
Asymmetric dye clusters with a single fluorophore (Cy3) and multiple quenchers (4'-methylthioazobenzene-4-carboxylate, methyl red, and 4'-dimethylamino-2-nitroazobenzene-4-carboxylate) were prepared. The dye and one-to-five quenchers were tethered through D-threoninol to opposite strands of a DNA duplex. NMR analysis revealed that the clusters
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