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      2,6-Dichloroindophenol sodium salt hydrate

      SKU
      D1204

      Category: Non Fluorescent Detection & Chromogene Detection

      Synonyms
      2,6-Dichloro-N-(4-hydroxyphenyl)-1,4-benzoquinoneimine sodium salt, 2,6-Dichlorobenzenone-indophenol sodium salt, 2,6-Dichlorophenolindophenol sodium salt hydrate, DCIP, DPIP, Tillmans' reagent
      1266615-56-8
      CAS-Number
      C12H6Cl2NNaO2 · xH2O
      Molecular Formula
      290.08 (anhydrous basis)
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥95 (NMR)
      Appearance
      Blue to dark-blue powder
      Identity
      1H-NMR

      Properties

      Solvents
      water (10mg/ml)
      Shipping
      AMBIENT
      Short Term Storage
      RT
      Long Term Storage
      RT
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at RT.
      Transportation
      Not dangerous goods
      Description
      2,6-Dichloroindophenol sodium salt hydrate (DCIP) is a blue redox dye. It is an oxidizing agent and can be used as a redox indicator. The color change occurs through a redox reaction. In the oxidized quinone imine form, dichlorophenol-indophenol is blue or red, in the reduced aminodiphenol form it is colorless. DCIP is suitable for the quantitative determination of ascorbic acid (vitamin C). The ascorbic acid is oxidized and in return the colored dichlorophenol-indophenol solution is reduced and thus decolorized. The consumption of the reagent in redox reactions can be determined photometrically. It has been used as a redox dye to investigate the efficiency of gold nanoparticles (Au-NP) for the enzymatic activity of glucose oxidase and to compose UVB specific dosimeter and to measure the rate of photosynthesis. DCIP has been used as substrate in NQO1 assays to investigate the liver cytosolic NQO1 activity spectrophotometrically and in mitochondrial succinate CoQ oxidoreductase (complex II) activity assay. In thin layer chromatography the compound serves as a reagent for organic acids and reducing compounds.
      Smiles
      [O-]C1=CC=C(/N=C2C=C(C(C(Cl)=C\2)=O)Cl)C=C1.O.[Na+]
      InChi Key
      XHSOLXWCGCVQHE-UHFFFAOYSA-M
      References
      (1) H. Yao, et al.; Clin. Chem. 41, 591 (1995) , (2) A. Ramanaviciene, et al.; Sens. Actuat. B Chem. 137, 483 (2009) , (3) A. Mills & P. Grosshans; Analyst. 134, 845 (2009) , (4) J. Qiu, et al.; Chemosphere 77, 129 (2009) , (5) G.P. Rizzi, et al.; J. Agric. Food Chem. 58, 9739 (2010) , (6) C.A. Vieira CA, et al.; Biosci. 26, 296 (2010) , (7) S. Han, et al.; J. Microbiol. Methods 90, 206 (2012) , (8) M. Pohanka & L. Drtinova; Talanta 106, 281 (2013) , (9) S.H. Chiu & P.L. Urban; Analyst 140, 5145 (2015) , (10) P. Bollella, et al.; Anal. Bioanal. Chem. 410, 3253 (2018)
      InChi
      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

      2,6-Dichloroindophenol sodium salt hydrate (DCIP) is a blue redox dye. It is an oxidizing agent and can be used as a redox indicator. The color change occurs through a redox reaction. In the oxidized quinone imine form, dichlorophenol-indophenol is blue or red, in the reduced aminodiphenol form it is colorless. DCIP is suitable for the quantitative determination of ascorbic acid (vitamin C). The ascorbic acid is oxidized and in return the colored dichlorophenol-indophenol solution is reduced and thus decolorized. The consumption of the reagent in redox reactions can be determined photometrically. It has been used as a redox dye to investigate the efficiency of gold nanoparticles (Au-NP) for the enzymatic activity of glucose oxidase and to compose UVB specific dosimeter and to measure the rate of photosynthesis. DCIP has been used as substrate in NQO1 assays to investigate the liver cytosolic NQO1 activity spectrophotometrically and in mitochondrial succinate CoQ oxidoreductase (complex II) activity assay. In thin layer chromatography the compound serves as a reagent for organic acids and reducing compounds.

      SKU: D1204 Category: Non Fluorescent Detection & Chromogene Detection
      • Additional information

      Additional information

      Synonyms

      2,6-Dichloro-N-(4-hydroxyphenyl)-1,4-benzoquinoneimine sodium salt, 2,6-Dichlorobenzenone-indophenol sodium salt, 2,6-Dichlorophenolindophenol sodium salt hydrate, DCIP, DPIP, Tillmans' reagent

      Purity

      ≥95 (NMR)

      Appearance

      Blue to dark-blue powder

      CAS-Number

      1266615-56-8

      Molecular Formula

      C12H6Cl2NNaO2 · xH2O

      Molecular Weight

      290.08 (anhydrous basis)

      Identity

      1H-NMR

      Solvents

      water (10mg/ml)

      Smiles

      [O-]C1=CC=C(/N=C2C=C(C(C(Cl)=C\2)=O)Cl)C=C1.O.[Na+]

      InChi Key

      XHSOLXWCGCVQHE-UHFFFAOYSA-M

      Shipping

      AMBIENT

      Short Term Storage

      RT

      Long Term Storage

      RT

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at RT.

      Transportation

      Not dangerous goods

      References

      (1) H. Yao, et al.; Clin. Chem. 41, 591 (1995), (2) A. Ramanaviciene, et al.; Sens. Actuat. B Chem. 137, 483 (2009), (3) A. Mills & P. Grosshans; Analyst. 134, 845 (2009), (4) J. Qiu, et al.; Chemosphere 77, 129 (2009), (5) G.P. Rizzi, et al.; J. Agric. Food Chem. 58, 9739 (2010), (6) C.A. Vieira CA, et al.; Biosci. 26, 296 (2010), (7) S. Han, et al.; J. Microbiol. Methods 90, 206 (2012), (8) M. Pohanka & L. Drtinova; Talanta 106, 281 (2013), (9) S.H. Chiu & P.L. Urban; Analyst 140, 5145 (2015), (10) P. Bollella, et al.; Anal. Bioanal. Chem. 410, 3253 (2018)

      InChi

      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

      Quantity

      5 g, 25 g, Bulk

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