Skip to content
luminol

Structure via PubChem · Public domain (PubChem)

EntityQ408061· pop 39· linked from 79 articles

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.

OverviewAI-generated

Luminol is a chemical compound with the formula C₈H₇N₃O₂. Its IUPAC name is 5-amino-2,3-dihydrophthalazine-1,4-dione. The substance has a melting point of 328 and a mass of 177.054. It possesses a charge of 0, with three hydrogen bond donors and three hydrogen bond acceptors. The calculated xlogp value is 0.3, and the topological polar surface area is 84.2.

The compound has a PubChem weight of 177.16. A search for luminol in PubMed yields a count of 6451 entries. The subject is referenced by 79 other encyclopedia articles.

Synthesized by Vinony from 18 facts across 4 sources: Wikidata, PubMed, PubChem, Vinony graph. Generated from structured data (not the Wikipedia text) and checked against those facts — may still contain errors.

Chemical data

Formula
C8H7N3O2
Molecular weight
177.16 g/mol
IUPAC name
5-amino-2,3-dihydrophthalazine-1,4-dione
SMILES
C1=CC2=C(C(=C1)N)C(=O)NNC2=O
InChIKey
HWYHZTIRURJOHG-UHFFFAOYSA-N
XLogP
0.3
Polar surface area
84.2 Ų
H-bond donors
3
H-bond acceptors
3
Formal charge
0

via PubChem

Research

6,451 papers

via PubMed

~4 min read

Encyclopedic overview

10 sections
Contents
  • Synthesis
  • Chemiluminescence
  • Use in criminal investigation
  • History
  • Theory
  • Drawbacks
  • Related molecules
  • See also
  • References
  • External links

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. Biologists use it in cellular assays to detect copper, iron, and cyanides as well as specific proteins via western blotting.

Excerpted from Wikipedia’s “luminol” article, available under the CC BY-SA 4.0 licence.

Gallery (5)