| Weight | 727.656 g/mol |
|---|---|
| Formula | C40H32Cl2N8O2 |
| Hydrogen Acceptors | 8 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 8 |
| Rotatable Bonds | 9 |
1871-22-3 (1871-22-3)
Tetrazolium blue · 4-anisyltetrazolium blue · p-anisyltetrazolium blue
Score:
#2892 in Biochemistry
,
#5350 in Biology
,
#7067 in Chemistry
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- Reduction of nitro blue tetrazolium by CO/sub 2//sup -/ and O/sub 2//sup -/ radicals (The Journal of Physical Chemistry, 1980)
- Failure of Nitro Blue Tetrazolium reduction in the phagocytic vacuoles of leukocytes in chronic granulomatous disease (Journal of Clinical Investigation, 1969)
- Determination of reducing sugars in the nanomole range with tetrazolium blue (Journal of Biochemical and Biophysical Methods, 1985)
- THE CYTOCHEMICAL REDUCTION OF NITRO BLUE TETRAZOLIUM AS AN INDEX OF POLLEN VIABILITY1 2 (American Journal of Botany, 1964)
- Triazolyl blue tetrazolium bromide as a novel corrosion inhibitor for steel in HCl and H2SO4 solutions (Corrosion Science, 2011)
- Preparation of a New Tetrazolium Salt Which Yields a Blue Pigment on Reduction and Its Use in the Demonstration of Enzymes in Normal and Neoplastic Tissues (Cancer Research, 1950)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Tetrazolium blue
- 4-anisyltetrazolium blue
- p-anisyltetrazolium blue
-
SMILESCOC1=C(C=CC(=C1)C2=CC(=C(C=C2)[N+]3=NC(=NN3C4=CC=CC=C4)C5=CC=CC=C5)OC)[N+]6=NC(=NN6C7=CC=CC=C7)C8=CC=CC=C8.[Cl-].[Cl-]
-
InChIKeyMUUHXGOJWVMBDY-UHFFFAOYSA-L
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