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dithizone
Sign in to saveDithizone is a sulfur-containing organic compound. It is a good ligand, and forms complexes with many toxic metals such as lead, thallium and mercury.
In the Vinony graph
Within Vinony's link graph, dithizone is referenced by 5 other articles, and connects out to lead, mercury and thallium.
Vinony files it under Chembox image size set, ECHA InfoCard ID from Wikidata and Thiocarbonyl compounds.
Its subject is documented across 15 Wikipedia language editions.
Chemical data
- Formula
- C13H12N4S
- Molecular weight
- 256.33 g/mol
- IUPAC name
- 1-anilino-3-phenyliminothiourea
- SMILES
- C1=CC=C(C=C1)NNC(=S)N=NC2=CC=CC=C2
- InChIKey
- UOFGSWVZMUXXIY-UHFFFAOYSA-N
- XLogP
- 4.2
- Polar surface area
- 80.9 Ų
- H-bond donors
- 2
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Research
940 papers- Dithizone-functionalized C(18) online solid-phase extraction-HPLC-ICP-MS for speciation of ultra-trace organic and inorganic mercury in cereals and environmental samples.Journal of environmental sciences (China) · 2022
- Alleviation of Hepatic Steatosis: Dithizone-Related Gut Microbiome Restoration During Paneth Cell Dysfunction.Frontiers in microbiology · 2022
- [Dithizone diabetes].Naunyn-Schmiedebergs Archiv fur experimentelle Pathologie und Pharmakologie · 1952
- Dithizone-induced Paneth cell disruption significantly decreases intestinal perfusion in the murine small intestine.Journal of pediatric surgery · 2019
- Durable Nanocellulose-Stabilized Emulsions of Dithizone/Chloroform in Water for Hg(2+) Detection: A Novel Approach for a Classical Problem.ACS applied materials & interfaces · 2023
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 256.078267384
Show 5 more facts
- chemical formula
- C₁₃H₁₂N₄S
- canonical SMILES
- S=C(/N=N/c1ccccc1)NNc2ccccc2
- melting point
- 168
- Commons category
- Dithizon
- isomeric SMILES
- S=C(/N=N/c1ccccc1)NNc2ccccc2
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Dithizone is a sulfur-containing organic compound. It is a good ligand, and forms complexes with many toxic metals such as lead, thallium and mercury.
Dithizone may be prepared by reacting phenylhydrazine with carbon disulfide, followed by reaction with potassium hydroxide.
Excerpted from Wikipedia’s “dithizone” article, available under the CC BY-SA 4.0 licence.