Structure via PubChem · Public domain (PubChem)
Diazinon
Sign in to saveAlso known as Basudin, Diazide, O,O-Diethyl-O-2-isopropyl-4-methyl-6-pyrimidinyl-phosphorothioate, Spectracide, O,O-diethyl O-[6-methyl-2-(1-methylethyl)pyrimidin-4-yl] thiophosphate, Dimpylate, O,O-Diethyl 2-isopropyl-4-methylpyrimidyl-6-thiophosphate, O,O-Diethyl O-(2-isopropyl-4-methyl-6-pyrimidyl) thionophosphate
chemische Verbindung
Chemical data
- Formula
- C12H21N2O3PS
- Molecular weight
- 304.35 g/mol
- IUPAC name
- diethoxy-(6-methyl-2-propan-2-ylpyrimidin-4-yl)oxy-sulfanylidene-lambda5-phosphane
- SMILES
- CCOP(=S)(OCC)OC1=NC(=NC(=C1)C)C(C)C
- InChIKey
- FHIVAFMUCKRCQO-UHFFFAOYSA-N
- XLogP
- 3.8
- Polar surface area
- 85.6 Ų
- H-bond donors
- 0
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
2,575 papers- In Vitro Activity of Beauvericin against All Developmental Stages of Sarcoptes scabiei.Antimicrobial agents and chemotherapy · 2020
- Atypical ocular bobbing in acute organophosphate poisoning.Archives of neurology · 1986
- Diazinon poisoning.Quarterly medical review · 1978
- Percutaneous organophosphate poisoning.Southern medical journal · 1987
- Severe post-dipping dermatitis.The Veterinary record · 1995
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 304.101
- Has use
- insecticide
Show 11 more facts
- MCN code
- 2933.59.32
- canonical SMILES
- CCOP(=S)(OCC)OC1=NC(=NC(=C1)C)C(C)C
- chemical formula
- C₁₂H₂₁N₂O₃PS
- Commons category
- Diazinon
- NIOSH Pocket Guide ID
- 0181
- density
- 1.12
- flash point
- 180
- solubility
- 0.004
- vapor pressure
- 0.0001
- time-weighted average exposure limit
- 0.1
- subject has role
- acetylcholinesterase inhibitor
via Wikidata · CC0
Article · Deutsch
Diazinon ist ein Thiophosphorsäureester, der als nicht-systemisches Insektizid und Akarizid eingesetzt wird. Entwickelt wurde Diazinon 1952 von H. Gysin beim Schweizer Unternehmen Geigy, das später in Novartis und danach in Syngenta überging.
Abstract from DBpedia / Wikipedia · CC BY-SA