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Source: The Open Library
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1Hexachlorocyclopentadiene
By World Health Organization (WHO)
“Hexachlorocyclopentadiene” Metadata:
- Title: Hexachlorocyclopentadiene
- Author: ➤ World Health Organization (WHO)
- Language: English
- Number of Pages: Median: 126
- Publisher: World Health Organization
- Publish Date: 1991
“Hexachlorocyclopentadiene” Subjects and Themes:
- Subjects: ➤ Chlorinated Hydrocarbons - Umweltbelastung - Farmacologia - Bewertung - Gesundheitsgefährdung - Hidrocarbonetos - Pollutants - Hexachlorocyclopentadien - Hydrocarbons - Hexachlorocyclopentadiène - Hexachlorcyclopentadien - Gezondheidseffecten - Toxicologie - Hexachloorcyclopentadieen - Saude Ambiental - Toxiciteit - Blootstelling - Aspect de l'environnement - Adverse effects - Environmental Exposure - Arbeidshygiëne - Environmental Health - Toxicity - Environmental Pollutants
Edition Identifiers:
- The Open Library ID: OL12898421M
- Online Computer Library Center (OCLC) ID: 24223003 - 27978317
- All ISBNs: 9241571209 - 9789241571203
Author's Alternative Names:
"W.H.O.", "W. H. O.", "World Health Organization WHO", "WORLD HEALTH ORGANISATION.", "World Health Organisation.", "World Health Oganisation.", "World Health World Health Organization", "WORLD HEALTH ORGANIZATION.", "World health organisation.", "World Health Organisation", "WORLD Health Organization.", "World Health Organisation Staff", "Who", "Health Organization World", "World Health Organization Staff", "WHO", "World Health Organization. Executive Board.", "World Health Organization (Who)", "World Health Organization.",Access and General Info:
- First Year Published: 1991
- Is Full Text Available: Yes
- Is The Book Public: No
- Access Status: Printdisabled
Online Access
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Wiki
Source: Wikipedia
Wikipedia Results
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Hexachlorocyclopentadiene
Hexachlorocyclopentadiene (HCCPD), also known as C-56, Graphlox, and HRS 1655, is an organochlorine compound with the formula C5Cl6. It is a precursor
Cis-Butene-1,4-diol
compound used in the production of endosulfan. It reacts with hexachlorocyclopentadiene to form endosulfan diol. Endosulfan diol then reacts with thionyl
Dieldrin
which is used to form aldrin from a mixture of norbornadiene and hexachlorocyclopentadiene. Originally developed in the 1940s as an alternative to DDT, dieldrin
Aldrin
related "cyclodiene" pesticides (a term for pesticides derived from Hexachlorocyclopentadiene) became notorious as persistent organic pollutants. Pure aldrin
Dechlorane plus
is produced by the Diels-Alder reaction of two equivalents of hexachlorocyclopentadiene with one equivalent of cyclooctadiene. The syn and anti isomer
Chlordecone
Organic Pollutants in 2009. Chlordecone is made by dimerizing hexachlorocyclopentadiene and hydrolyzing to a ketone. It is also the main degradation product
Chlordane
Cyclodiene derives its name from hexachlorocyclopentadiene, a precursor in its production. Hexachlorocyclopentadiene forms a Diels-Alder adduct with cyclopentadiene
National Emissions Standards for Hazardous Air Pollutants
118-74-1 Hexachlorobenzene 87-68-3 Hexachlorobutadiene 77-47-4 Hexachlorocyclopentadiene 67-72-1 Hexachloroethane 822-06-0 Hexamethylene-1,6-diisocyanate
EPA list of extremely hazardous substances
Formparanate Fosthietan Fuberidazole Furan Gallium trichloride Hexachlorocyclopentadiene Hexamethylenediamine, N,N'-dibutyl- Hydrazine Hydrocyanic acid
Endosulfan
tonnes per year.[citation needed] Endosulfan is a derivative of hexachlorocyclopentadiene, and is chemically similar to aldrin, chlordane, and heptachlor