Iodonitrotetrazolium chloride - CAS 146-68-9
Catalog: |
BB010116 |
Product Name: |
Iodonitrotetrazolium chloride |
CAS: |
146-68-9 |
Synonyms: |
2H-Tetrazolium, 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyl-, chloride (1:1); 2H-Tetrazolium, 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyl-, chloride; 2H-Tetrazolium, 2-(p-iodophenyl)-3-(p-nitrophenyl)-5-phenyl-, chloride; [2-(p-Iodophenyl)-3-(p-nitrophenyl)-5-phenyl-2H-tetrazolium chloride]; 2-(4-Iodophenyl)-3-(4-nitrophenyl)-5-phenyl-2H-tetrazolium chloride; 2-(4-Iodophenyl)-3-(4-nitrophenyl)-5-phenyltetrazolium chloride; 2-(p-Iodophenyl)-3-(p-nitrophenyl)-5-phenyltetrazolium chloride; 3-(p-Nitrophenyl)-2-(p-iodophenyl)-5-phenyltetrazolium chloride; INT; Iodonitro tetrazolium; Iodonitrotetrazolium purple; Iodonitrotetrazolium violet; NSC 27620; p-Iodonitrotetrazolium violet |
Related CAS: | 7685-16-7 (free base)
|
IUPAC Name: | 2-(4-iodophenyl)-3-(4-nitrophenyl)-5-phenyltetrazol-3-ium;chloride |
Description: | Iodonitrotetrazolium chloride (INT) is a redox dye used extensively in biochemical and microbiological assays. It is known for its ability to serve as an electron acceptor in various redox reactions, forming a formazan product upon reduction, which is often used as an indicator in cell viability and enzymatic activity assays. |
Molecular Weight: | 505.70 |
Molecular Formula: | C19H13ClIN5O2 |
Canonical SMILES: | C1=CC=C(C=C1)C2=NN([N+](=N2)C3=CC=C(C=C3)[N+](=O)[O-])C4=CC=C(C=C4)I.[Cl-] |
InChI: | InChI=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 |
InChI Key: | JORABGDXCIBAFL-UHFFFAOYSA-M |
Melting Point: | 229 °C |
Appearance: | Yellow powder |
MDL: | MFCD00011961 |
LogP: | 1.25100 |
Publication Number | Title | Priority Date |
CN-112890195-A | Traditional Chinese medicine health product with function of enhancing immunity | 20210225 |
CN-112939239-A | Compound microbial preparation and application thereof in sewage treatment | 20210219 |
CN-112022846-A | Application of indoline derivative in preparation of medicine for treating sepsis | 20200923 |
CN-112076189-A | Application of amide compound in preparation of medicine for treating sepsis | 20200923 |
CN-111991377-A | Application of indanone derivative in preparation of medicine for treating sepsis | 20200923 |
PMID | Publication Date | Title | Journal |
22595184 | 20120901 | A blue native polyacrylamide gel electrophoretic technology to probe the functional proteomics mediating nitrogen homeostasis in Pseudomonas fluorescens | Journal of microbiological methods |
22539312 | 20120401 | A facile electrophoretic technique to monitor phosphoenolpyruvate-dependent kinases | Electrophoresis |
22326263 | 20120316 | Recombinant Nox4 cytosolic domain produced by a cell or cell-free base systems exhibits constitutive diaphorase activity | Biochemical and biophysical research communications |
22347309 | 20111201 | Superoxide Dismutase (SOD) Enzyme Activity Assay in Fasciola spp. Parasites and Liver Tissue Extract | Iranian journal of parasitology |
21463121 | 20110601 | Associations between regulators of extracellular matrix and hemostatic factors in hematologic neoplasias | Leukemia & lymphoma |
Complexity: | 497 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 2 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 504.98025 |
Formal Charge: | 0 |
Heavy Atom Count: | 28 |
Hydrogen Bond Acceptor Count: | 5 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 504.98025 |
Rotatable Bond Count: | 3 |
Topological Polar Surface Area: | 80.4 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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