User:Ejhoekstra/List of natural halogenated substances
This list contains halogenated substances that are formed in natural processes or that are suspected to have a natural origin.
- aerothionin, produced by the Red Sea sponge Suberea mollis [1]
- barettin and 8,9-dihydrobarettin, produced by the cold water marine sponge Geodia barretti Bowerbank act in synergy to deter larvae of surface settlers and may also be involved in defense against grazers[2].
- bromodichloromethane
- bromomethane
- chlorodibromomethane
- chlorodifluoromethane
- chloromethane
- 4-chlorophenol
- chlorotrifluoroethene
- dichloroacetamide
- dichloroacetone isomers
- dichloroacetonitrile
- dichlorodifluoromethane
- dichlorofluoromethane
- dichloromethane
- dichloropyruvic acid
- 2,4-dichlorophenol and/or 2,5-dichlorophenol
- 2,6-dichlorophenol
- dichloroverongiaquinol, produced by the Red Sea sponge Suberea mollis [1]
- difluorodimethylsilane
- dioxine, produced by
- 1,2,3,7,8,9-hexachlorodibenzo-p-dioxin
- hexafluoropropene isomers
- iodomethane
- pentachloroacetone
- 1,2,3,7,8-pentachlorodibenzo-p-dioxin
- purealdin L, produced by the Red Sea sponge Suberea mollis [1]
- subereamine A and subereamine B, produced by the Red Sea sponge Suberea mollis [1].
- subereaphenol D, produced by the Red Sea sponge Suberea mollis [1]
- tetrachloroacetone isomers
- 2,3,7,8-tetrachlorodibenzo-p-dioxin
- tetrachloromethane
- tetrachloroethene
- tetrafluoroethene
- tribromomethane
- trichloroacetic acid
- trichloroacetone isomers
- trichloroacetonitrile
- 1,1,1-trichloroethane
- trichloroethene
- trichlorofluoromethane
- trichloromethane
- trichloropyruvic acid
- 2,4,5-trichlorophenol
- 1,1,2-trichloro-1,2,2-trifluoroethane
Chlorinated maleic acids (n(Cl)=1-2) and chlorinated fumaric acids (n(Cl)=1-2) have been identified.
groupparameters
References
[edit]- ^ a b c d e Shaala, Lamiaa A.; Bamane, Faida H.; Badr, Jihan M.; Youssef, Diaa T. A. (2011). "Brominated Arginine-Derived Alkaloids from the Red Sea Sponge Suberea mollis". J. Nat. Prod. 74 (6): 1517–1520. doi:10.1021/np200120d. PMID 21542602. Retrieved 24 June 2011.
{{cite journal}}: CS1 maint: date and year (link) - ^ Sjögren M. et al. (2011) Two Brominated Cyclic Dipeptides Released by the Coldwater Marine Sponge Geodia barretti Act in Synergy As Chemical Defense. J. Nat. Prod. 74(3), 449–454 [1]
- ^ Öberg, L.G. (1990). "Peroxisade-catalysed oxidation of chlorophenols to polychlorinated dibenzo-p-dioxins and dibenzofurans". Archives of Environmental Contamination and Toxicology. 19 (6): 930–938. doi:10.1007/BF01055064. PMID 2256708.
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