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About This Item
Empirical Formula (Hill Notation):
C12H6Cl2NNaO2 · xH2O
CAS Number:
Molecular Weight:
290.08 (anhydrous basis)
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
210-640-4
MDL number:
Beilstein/REAXYS Number:
3641229
Product Name
2,6-Dichloroindophenol sodium salt hydrate, suitable for vitamin C determination, BioReagent
product line
BioReagent
Quality Level
form
powder
solubility
H2O: soluble 10 mg/mL, clear, blue to very deep blue
suitability
suitable for vitamin C determination
application(s)
diagnostic assay manufacturing
food and beverages
hematology
histology
storage temp.
room temp
SMILES string
O.[Na+].[O-]c1ccc(cc1)\N=C2/C=C(Cl)C(=O)C(Cl)=C2
InChI
1S/C12H7Cl2NO2.Na.H2O/c13-10-5-8(6-11(14)12(10)17)15-7-1-3-9(16)4-2-7;;/h1-6,16H;;1H2/q;+1;/p-1
InChI key
XHSOLXWCGCVQHE-UHFFFAOYSA-M
General description
2,6-Dichloroindophenol sodium salt hydrate is a blue redox dye.
Application
2,6-Dichloroindophenol sodium salt hydrate is suitable for vitamin C determination. 2,6-Dichloroindophenol (DCIP) may be used in the following studies:
- As redox dye to investigate the efficiency of gold nanoparticles (Au-NP) for enzymatic activity of glucose oxidase (GOx).
- To compose UVB specific dosimeter.
- Quantification of vitamin C (L-ascorbic acid) in fruit juices.
- As substrate in NQO1 assay to investigate the liver cytosolic NQO1 activity spectrophotometrically.
- Mitochondrial succinate CoQ oxidoreductase (complex II) activity assay.
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Spectrophotometric evaluation of gold nanoparticles as red-ox mediator for glucose oxidase.
Ramanaviciene A, et al.
Sensors and Actuators B, Chemical, 137(2), 483-489 (2009)
Hanit Brenner-Lavie et al.
Biochimica et biophysica acta, 1777(2), 173-185 (2007-11-13)
Deleterious effects of dopamine (DA) involving mitochondrial dysfunction have an important role in DA-associated neuronal disorders, including schizophrenia and Parkinson's disease. DA detrimental effects have been attributed to its ability to be auto-oxidized to toxic reactive oxygen species. Since, unlike
Misty Prince et al.
Toxicology letters, 185(3), 180-186 (2009-01-20)
Naturally occurring coumarins possess anti-carcinogenic activities in part by inducing carcinogen-detoxifying enzymes glutathione S-transferase (GST) and/or NAD(P)H quinone oxidoreductase (NQO1). Our goal was to determine whether citrus coumarins induce hepatic GST and/or NQO1 via activation of Nrf2 and the antioxidant