Weight | 177.163 g/mol |
---|---|
Formula | C8H7N3O2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 3 |
Aromatic Rings | 2 |
Rotatable Bonds | 0 |
LUMINOL (521-31-3)
5-amino-2,3-dihydrophthalazine-1,4-dione · 521-31-3
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- Phagocytic activation of a luminol-dependent chemiluminescence in rabbit alveolar and peritoneal macrophages (Biochemical and Biophysical Research Communications, 1976)
- Evaluation of the probes 2,7-dichlorofluorescin diacetate, luminol, and lucigenin as indicators of reactive species formation (Biochemical Pharmacology, 2003)
- Mechanism of the luminol-dependent chemiluminescence of human neutrophils. (Journal of Immunology, 1982)
- Gold nanoparticle-catalyzed luminol chemiluminescence and its analytical applications (Analytical Chemistry, 2005)
- Evaluation of total antioxidant potential (TRAP) and total antioxidant reactivity from luminol-enhanced chemiluminescence measurements (Free Radical Biology and Medicine, 1995)
- Peroxynitrite-induced luminol chemiluminescence. (Biochemical Journal, 1993)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 5-amino-2,3-dihydrophthalazine-1,4-dione
- 521-31-3
-
SMILESC1=CC2=C(C(=C1)N)C(=O)NNC2=O
-
InChIKeyHWYHZTIRURJOHG-UHFFFAOYSA-N
- Pubchem - LUMINOL
- Wikipedia - luminol
Luminol (C8H7N3O2) is a chemical that exhibits chemiluminescence, with a blue glow, when mixed with an appropriate oxidizing agent. Luminol is a white-to-pale-yellow crystalline solid that is soluble in most polar organic solvents, but insoluble in water. Forensic investigators use luminol to detect trace amounts of blood at crime scenes, as it reacts with the iron in hemoglobin.
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Estimated Properties
Boiling Point | 363.35 C | EPA T.E.S.T. |
---|---|---|
Boiling Point | 467.05 C | EPI Suite |
Density | 1.42 g/cm3 | EPA T.E.S.T. |
Flash Point | 230.16 C | EPA T.E.S.T. |
Melting Point | 197.21 C | EPI Suite |
Water Solubility | 2278.29 mg/L | EPA T.E.S.T. |
Water Solubility | 1e+06 mg/L | EPI Suite |
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