CAS 1184-43-6: Tetranitro Blue Tetrazolium
Formula:C40H28N12O10·2Cl
InChI:InChI=1S/C40H28N12O10.2ClH/c1-61-37-23-27(7-21-35(37)47-43-39(25-3-9-31(10-4-25)49(53)54)41-45(47)29-13-17-33(18-14-29)51(57)58)28-8-22-36(38(24-28)62-2)48-44-40(26-5-11-32(12-6-26)50(55)56)42-46(48)30-15-19-34(20-16-30)52(59)60;;/h3-24H,1-2H3;2*1H/q+2;;/p-2
InChI key:InChIKey=VCESGVLABVSDRO-UHFFFAOYSA-L
SMILES:O(C)C1=C(N2[N+](=NC(=N2)C3=CC=C(N(=O)=O)C=C3)C4=CC=C(N(=O)=O)C=C4)C=CC(=C1)C5=CC(OC)=C(C=C5)N6[N+](=NC(=N6)C7=CC=C(N(=O)=O)C=C7)C8=CC=C(N(=O)=O)C=C8.[Cl-]
Synonyms:- 2,2′,5,5′-Tetra-p-nitrophenyl-3,3′-(3,3′-dimethoxy-4,4′-biphenylene)ditetrazolium chloride
- 2,2′,5,5′-Tetrakis(p-nitrophenyl)-3,3′-(3,3′-dimethoxy-4,4′-diphenylene)ditetrazolium chloride
- 2,2′,5,5′-Tetrakis-p-(nitrophenyl)-3,3′-bis(3,3′-dimethoxy-4,4′-diphenylene)ditetrazolium chloride
- 2H-Tetrazolium, 2,2'-(3,3'-dimethoxy(1,1'-biphenyl)-4,4'-diyl)bis(3,5-bis(4-nitrophenyl)-, chloride (1:2)
- 2H-Tetrazolium, 2,2'-(3,3'-dimethoxy(1,1'-biphenyl)-4,4'-diyl)bis(3,5-bis(4-nitrophenyl)-, dichloride
- 2H-Tetrazolium, 3,3′-(3,3′-dimethoxy-4,4′-biphenylylene)bis[2,5-bis(p-nitrophenyl)-, dichloride
- 3,3'-(3,3'-Dimethoxy(1,1'-biphenyl)-4,4'-diyl)bis(2,5-bis(p-nitrophenyl)-2H-tetrazolium) dichloride
- 3,3'-(3,3'-dimethoxybiphenyl-4,4'-diyl)bis[2,5-bis(4-nitrophenyl)-2H-tetrazol-3-ium]
- 3,3'-(3,3'-dimethoxybiphenyl-4,4'-diyl)bis[2,5-bis(4-nitrophenyl)-2H-tetrazol-3-ium] dichloride
- Blue p-nitrotetrazolium chloride
- Nitroblue monotetrazolium chloride
- See more synonyms
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Found 4 products.
Tetranitroblue tetrazolium chloride
CAS:Formula:C40H28Cl2N12O10·2C2H6OPurity:(HPLC) ≥ 96.0%Color and Shape:Yellow crystalline powderMolecular weight:999.78Tetranitroblue tetrazolium chloride
CAS:Tetranitroblue tetrazolium chloride (TNBT) is a reagent that is used to measure the activity of enzymes in biological samples. TNBT can be used as a histological stain for myocardial infarcts and other areas of necrosis. It has been shown to be reactive with toll-like receptors, which are proteins that play a role in the immune response. The reaction mechanism of TNBT starts with its conversion to blue formazan crystals by peroxidase or other oxidizing enzymes. These crystals are reduced back to their original colorless form by reducing agents such as NADH or glutathione, which are present in most cells. This reduction process generates an electron that is then transferred to NAD+, forming NADH and releasing H2O2 as a byproduct.Formula:C40H28Cl2N12O10Purity:Min. 95%Color and Shape:PowderMolecular weight:907.63 g/molTetranitro blue tetrazolium chloride, 97%
CAS:Redox indicator for enzymes This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C40H28Cl2N12O10Purity:97%Color and Shape:Yellow, Powder or crystals or crystalline powderMolecular weight:907.64Tetranitroblue tetrazolium chloride
CAS:Formula:C40H28Cl2N12O10Purity:96%Color and Shape:SolidMolecular weight:907.6307200000005
