INT (chemical)
{{chembox
| Name = INT
| Verifiedfields =
| Watchedfields =
| verifiedrevid =
| ImageFile = Iodonitrotetrazolium chloride.svg
| ImageSize =
| IUPACName = 3-(4-Iodophenyl)-2-(4-nitrophenyl)-5-phenyl-2H-tetrazol-3-ium chloride
| OtherNames = 2-(4-Iodophenyl)-3-(4-nitrophenyl)-5-phenyltetrazolium chloride
| Section1 = {{Chembox Identifiers
| ChemSpiderID_Ref =
| ChemSpiderID = 58482
| InChI =
| InChIKey =
| StdInChI_Ref =
| StdInChI = 1S/C19H13IN5O2.ClH/c20-15-6-8-16(9-7-15)23-21-19(14-4-2-1-3-5-14)22-24(23)17-10-12-18(13-11-17)25(26)27;/h1-13H;1H/q+1;/p-1
| StdInChIKey_Ref =
| StdInChIKey = JORABGDXCIBAFL-UHFFFAOYSA-M
| CASNo = 146-68-9
| CASNo_Ref = {{cascite|correct|CAS}}
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = XY3JA5594E
| PubChem = 629284
| SMILES = [Cl-].[O-][N+](=O)c1ccc(cc1)n3nc(n[n+]3c2ccc(I)cc2)c4ccccc4
}}
| Section2 = {{Chembox Properties
| C=19|H=13|Cl=1|I=1|N=5|O=2
| Appearance =
| Density =
| MeltingPtC = 240
| MeltingPt_notes = (decomposes)
| BoilingPt =
| SolubleOther = 50 mg/mL hot, very faintly turbid, very deep yellow
| Solvent = methanol: water (1:1)
| LogP = −2.4
}}
| Section3 = {{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt =
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INT (iodonitrotetrazolium or 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyl-2H-tetrazolium) is a commonly used tetrazolium salt (usually prepared with chloride ions), similar to tetrazolium chloride that on reduction produces a red formazan dye that can be used for quantitative redox assays. It is also toxic to prokaryotes.{{cite journal|title=INT (2-(4-Iodophenyl)-3-(4-Nitrophenyl)-5-(Phenyl) Tetrazolium Chloride) Is Toxic to Prokaryote Cells Precluding Its Use with Whole Cells as a Proxy for In Vivo Respiration|journal=Microbial Ecology|volume=70|issue=4|pages=1004–1011|doi=10.1007/s00248-015-0626-3|pmid=25991603|year=2015|last1=Villegas-Mendoza|first1=Josué|last2=Cajal-Medrano|first2=Ramón|last3=Maske|first3=Helmut|s2cid=15264318}}
INT is an artificial electron acceptor that can be utilized in a colorimetric assay to determine the concentration of protein in a solution. It can be reduced by succinate dehydrogenase to furazan, the formation of which can be measured by absorbance at 490 nm. The activity of succinate dehydrogenase is readily observed by the naked eye as the solution turns from colorless to rusty red.
See also
References
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Category:Biochemistry detection reactions
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