Structure via PubChem · Public domain (PubChem)
crimidine
Sign in to saveCrimidine is a convulsant poison used as a rodenticide. Crimidine was originally known by its product name, Castrix. It was originally produced in the 1940s by the conglomerate, IG Farben. It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities. It is also no longer used in the United States as a rodenticide, but is still used to this day in other coun
Chemical data
- Formula
- C7H10ClN3
- Molecular weight
- 171.63 g/mol
- IUPAC name
- 2-chloro-N,N,6-trimethylpyrimidin-4-amine
- SMILES
- CC1=CC(=NC(=N1)Cl)N(C)C
- InChIKey
- HJIUPFPIEBPYIE-UHFFFAOYSA-N
- XLogP
- 2
- Polar surface area
- 29 Ų
- H-bond donors
- 0
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 171.056
Show 3 more facts
- canonical SMILES
- CC1=CC(=NC(=N1)Cl)N(C)C
- chemical formula
- C₇H₁₀ClN₃
- Commons category
- Crimidine
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
4 sectionsContents
- Mechanism of action
- Toxicity
- References
- External links
Crimidine is a convulsant poison used as a rodenticide. Crimidine was originally known by its product name, Castrix. It was originally produced in the 1940s by the conglomerate, IG Farben. It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities. It is also no longer used in the United States as a rodenticide, but is still used to this day in other countries.
==Mechanism of action== Crimidine is a highly reactive compound. The main mechanism of toxicity with crimidine is that it inhibits vitamin B6, which is used in the metabolism of carbohydrates and amino acids. This is due to the pyrimidine ring that both compounds contain. Although, the exact mechanism of how crimidine antagonizes vitamin B6 is unknown. Another mechanism of toxicity with crimidine is due to its deactivating effect on acetylcholinesterase
Excerpted from Wikipedia’s “crimidine” article, available under the CC BY-SA 4.0 licence.
Gallery (2)
Available in 11 languages
via Wikidata sitelinks · CC0