40-1012
Methyl Red solution
pH 4.2-6.2
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About This Item
Empirical Formula (Hill Notation):
C15H15N3O2
CAS Number:
Molecular Weight:
269.30
PubChem Substance ID:
UNSPSC Code:
12352107
Beilstein/REAXYS Number:
1843037
MDL number:
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
form
liquid
availability
available only in Japan
pH
4.2-6.2
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Application
for titration
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
55.4 °F
flash_point_c
13 °C
Regulatory Information
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Chan-Ju Wang et al.
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Yuyi Yang et al.
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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
X D Zhang et al.
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Taiga Fujii et al.
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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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