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2,2-Dimethyl-3-methylen-norbornan,chloriertes
CAMPHECHLOR · Motox · TOXAPHEN · TOXAPHANE · CHLORINATED CAMPHENE · Toxaphene camphechlor · 3956 · PChK

Identifikatoren & physikalische Daten
| CAS No. | 1852481-29-8 |
|---|---|
| Summenformel | C10H8Cl8 |
| Durchschnittliche Molmasse | 411,8 g/mol |
| Monoisotopische Masse | 407,813422 g/mol |
| SMILES | C=C1C(CCl)(CCl)C2(Cl)C(Cl)C(Cl)C1(Cl)C2(Cl)Cl |
| InChIKey | OEJNXTAZZBRGDN-UHFFFAOYSA-N |
| PubChem CID | 5284469 |
| ChEMBL | CHEMBL1339089 |
| EC No. | 232-283-3 |
| DTXSID | DTXSID90858936 |
| Lokaler Name | 2,2-Dimethyl-3-methylen-norbornan,chloriertes |
Chemische & physikalische Eigenschaften
| XLogP | 4,7 |
|---|---|
| Polarare Oberfläche (TPSA) | 0 |
| H-Brücken-Donoren | 0 |
| H-Brücken-Akzeptoren | 0 |
| Frei drehbare Bindungen | 2 |
| Schwere Atome | 18 |
| Formalladung | 0 |
| Komplexität | 403 |
| Stoffklassen | Hazardous Air Pollutants (HAPs)Carcinogens |
| Kosmetika | Cosmetics ingredient -> Fragrance |
| Pestizide | Pesticide -> EPA IRISAgrochemicals -> Pesticide active substancesActive substance -> EU Pesticides database: Not approvedPesticides -> Organochlorine PesticidesPesticide (Toxaphene) -> USDA PDB |
| LogP (Verteilungskoeffizient) | The median log Kow for toxaphene is 5.90.3.35.5 |
| Geruch | Pleasant piney odorMild odor of chlorine and camphorMild, turpentine-like odorMild, piney, chlorine- and camphor-like odor. |
| Dichte | 1.65 (EPA, 1998) - Denser than waterwill sink1.65 @ 25 °CRelative density (water = 1): 1.651.65 @25 °C |
| Color/Form | Yellow waxy solid.Amber, waxy solid. |
| Löslichkeit | less than 1 mg/mL at 66 °F (NTP, 1992)Clear, amber-colored, and viscous liquid, mild terpene odor, specific gravity: 1.519-1.567 at 25 °C/25 °Creadily sol in most commercial organic solvents and is more sol in aromatic than in aliphatic hydrocarbons /Strobane T-90/Freely sol in aromatic hydrocarbonsREADILY SOL IN ORG SOLVENTS INCL PETROLEUM OILS3 mg/l water @ room temp> 450 g/100 ml benzene120 g/L in alcohol at 25–30 °C (quoted, Meites, 1963)0.4mg/L(25 ºC) |
| Corrosivity | Noncorrosive in the absence of moistureCorrosive to ironSolution in xylene may produce corrosive products when heated. |
| Flammpunkt | 84 °F (EPA, 1998)135 °C, 275 °F (closed cup) /Chlorinated camphene 60%/115 °C (tag closed cup) /Toxaphene 90% soln/34-46 °C (tag closed cup) /Strobane T-90/4 °C |
| Siedepunkt | Decomposes (NTP, 1992)Decomposes near boiling point |
| Schmelzpunkt | 149 to 194 °F (EPA, 1998)65-90 °C149-194 °F65-90℃ |
| Dampfdruck | 15.8 at 25 °C (2,2,5-endo-6-exo-8,9,10-heptachlorobornane, toxaphene component, Hinckley etal., 1990) |
| Lagerbedingungen | 2-8°C |
| Aggregatzustand | Yellow waxy solid |
| Merck | 13,9633 |
| Henry-Konstante | 0.99 at 10 °C, 3.56 at 20 °C, 6.81 at 30 °C, 8.49 at 35 °C, 14.8 at 40 °C (gas stripping, Jantunen and Bidleman, 2000) |
| Stabilität | Stable. Incompatible with alkali, strong oxidizers. Heat and light sensitive. |
| EPA chemische Informationen | Toxaphene (8001-35-2) |
Sicherheit & Vorschriften
| GHS-Einstufung | DangerH301: Toxic if swallowed [Danger Acute toxicity, oral]P203, P261, P264, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P317, P318, P319, P321, P330, P332+P317, P362+P364, P391, P403+P233, P405, and P501 (click each P-code to see the statement)H301 (97.6%): Toxic if swallowed [Danger Acute toxicity, oral] |
|---|---|
| Regulatorische Informationen | Hazard Traits - BioaccumulationCarcinogenicityEnvironmental PersistenceNeurotoxicityRespiratory ToxicityRegulation (EC) No 178/2002 (amended)Substance: ToxapheneThe New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.) |
| Weitere Sicherheitsinformationen | IMAP assessments - Toxaphene: Human health tier I assessment |
| DOT-Kennzeichnung | Poison |
| Brandgefahren | Container may explode in heat of fire. Toxic vapors are generated when heated. Releases hydrochloric acid in the presence of alkali, on prolonged exposure to sunlight, and at temperatures above 311F. Avoid strong oxidizers, corrosive to iron. (EPA, 1998)Liquid formulations containing organic solvents may be flammable. Gives off irritating or toxic fumes (or gases) in a fire. |
| Brandpotenzial | Solid /is/ not flammable, but /it is/ usually dissolved in combustible liquid. |
| Gesundheitsgefahren | Camphechlor is extremely toxic: the probable oral lethal dose (human) is 5-50 mg/kg or between 7 drops and 1 teaspoonful for 70 kg (150 lb.) person. (EPA, 1998) |
| Gefahrenübersicht | Toxaphene was one of the most heavily used pesticides in the United States in the 1970s and early 1980s. It was used primarily to control insect pests on cotton and other crops in the southern United States. Other uses included controlling insect pests on livestock and killing unwanted fish in lakes. Toxaphene was banned for all registered uses by 1990. Toxaphene is made by reacting chlorine gas with a substance called camphene. The resulting product (toxaphene) is a mixture of hundreds of different chlorinated camphenes and related chemicals. |
Anwendungen & Verwendung
Verwenden
Toxaphene is an insecticide that contains over 200–700 chemicals and can exist as an yellow to amber solid or gas. Heavily used in the United States until 1982, its use was completely banned in 1990. Toxaphene was used primarily to control insects on cotton crops in the southern United States; it has also been used to control pests on livestock and to control unwanted fish in aquatic environments. Reports have indicated that fish are low metabolizers of toxaphene, whereas other aquatic life such as snails can be extensive metabolizers, thus reducing the toxicity of toxaphene to aquatic life other than fish (Isensee et al., 1979).