| Weight | 268.099 g/mol |
|---|---|
| Formula | C12H7Cl2NO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2,6-DICHLOROINDOPHENOL (620-45-1, 956-48-9)
Dichlorophenolindophenol · Dichlorophenol Indophenol · 2,6 Dichlorophenolindophenol
Score:
#2259 in Biochemistry
,
#4539 in Biology
,
#5756 in Chemistry
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- Test reactions for a stopped-flow apparatus: Reduction of 2,6-dichlorophenolindophenol and potassium ferricyanide by l-ascorbic acid (Analytical Biochemistry, 1978)
- The molar extinction coefficient of 2,6-dichlorophenol indophenol (Biochimica et Biophysica Acta, 1964)
- Photoreduction of 2,6-Dichlorophenolindophenol by Diphenylcarbazide: A Photosystem 2 Reaction Catalyzed by Tris-Washed Chloroplasts and Subchloroplast Fragments (Plant Physiology, 1969)
- Photoreductions by fresh and aged chloropasts: requirement for ascorbate and 2, 6-dichlorophenolindophenol with aged chloroplasts. (Journal of Biological Chemistry, 1960)
- The reactivation of EPR signal II in chloroplasts treated with reduced dichlorophenol-indophenol: Evidence against a dark equilibrium between two oxidation states of the oxygen evolving system (FEBS Letters, 1975)
- Flow electrochemical determination of ascorbic acid in real samples using a glassy carbon electrode modified with a cellulose acetate film bearing 2,6-dichlorophenolindophenol (Analytica Chimica Acta, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Dichlorophenolindophenol
- Dichlorophenol Indophenol
- 2,6 Dichlorophenolindophenol
- 2,6 Dichloroindophenol
- Sodium 2,6-Dichloroindophenol
- Tillmans' Reagent
- Tillmans Reagent
- 2,6-Dichlorobenzenoneindophenol Dye
- 2,6-Dichlorophenolindophenol
- Tillman Reagent
- Tillman's Reagent
- Sodium 2,6 Dichloroindophenol
- 2,6 Dichlorobenzenoneindophenol Dye
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SMILESC1=CC(=O)C=CC1=NC2=CC(=C(C(=C2)Cl)O)Cl
-
InChIKeyFBWADIKARMIWNM-UHFFFAOYSA-N
- Pubchem - 2,6-DICHLOROINDOPHENOL
- Wikipedia - dichlorphenolindophenol
2,6-Dichlorophenolindophenol (DCPIP, DCIP or DPIP) is a chemical compound used as a redox dye. When oxidized, DCPIP is blue with a maximal absorption at 600nm; when reduced, DCPIP is colorless. DCPIP can be used to measure the rate of photosynthesis.
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