Structure via PubChem · Public domain (PubChem)
aldrina
Sign in to saveAlso known as HHDN, 1,2,3,4,10,10-hexachloro-1,4,4a,5,8,8a-hexahydro-endo-1,4-exo-5,8-dimethanonaphthalene, hexachlorohexahydro-endo-exo-dimethanonaphthalene
composto chimico
Chemical data
- Formula
- C12H8Cl6
- Molecular weight
- 364.9 g/mol
- IUPAC name
- (1S,2S,3S,6R,7R,8R)-1,8,9,10,11,11-hexachlorotetracyclo[6.2.1.13,6.02,7]dodeca-4,9-diene
- SMILES
- C1[C@@H]2C=C[C@H]1[C@H]3[C@@H]2[C@]4(C(=C([C@@]3(C4(Cl)Cl)Cl)Cl)Cl)Cl
- InChIKey
- QBYJBZPUGVGKQQ-SJJAEHHWSA-N
- XLogP
- 4.5
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Formal charge
- 0
via PubChem
Research
1,767 papers- Aldrin and dieldrin: a review of research on their production, environmental deposition and fate, bioaccumulation, toxicology, and epidemiology in the United States.Environmental health perspectives · 2001
- Monograph: reassessment of human cancer risk of aldrin/dieldrin.Toxicology letters · 1999
- Human aldrin poisoning.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 1991
- Toxicological profile of organochlorines aldrin and dieldrin: an Indian perspective.Reviews on environmental health · 2017
- The genetic toxicology of aldrin and dieldrin.Mutation research · 1981
via PubMed
Wikidata facts
- Has part
- chlorine
- Named after
- Kurt Alder
- Mass
- 361.875716336
- Has use
- insecticide
Show 14 more facts
- chemical formula
- C₁₂H₈Cl₆
- NIOSH Pocket Guide ID
- 0016
- density
- 1.60
- immediately dangerous to life or health
- 25
- melting point
- 219
- vapor pressure
- 0.00008
- solubility
- 0.003
- time-weighted average exposure limit
- 0.01
- median lethal dose (LD50)
- 44
- minimal lethal dose
- 5.8
- short-term exposure limit
- 0.03
- Commons category
- Aldrin
- isomeric SMILES
- C1[C@@H]2C=C[C@H]1[C@H]3[C@@H]2[C@]4(C(=C([C@@]3(C4(Cl)Cl)Cl)Cl)Cl)Cl
- canonical SMILES
- ClC1=C(Cl)C2(Cl)C3C4C=CC(C4)C3C1(Cl)C2(Cl)Cl
Sources (7)
via Wikidata · CC0
Article · Italiano
L'aldrina o aldrin è un insetticida organoclorurato che è stato ampiamente usato negli anni settanta e il cui uso è ora proibito in molti paesi, negli Stati Uniti dal 1974. L'aldrina è uno degli inquinanti organici persistenti. L'aldrina viene ossidata a dieldrina dal metabolismo degli insetti, è quest'ultimo composto ad essere tossico per gli insetti. L'aldrina è prodotta da e norbornadiene per reazione di Diels-Alder. La DL50 di questa sostanza è di 39–60 mg/kg (nei ratti per via orale).
Abstract from DBpedia / Wikipedia · CC BY-SA