Chloropicrin
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| Names | |||
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IUPAC name
trichloro(nitro)methane
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| Other names
PS, Nitrochloroform, Trichloronitromethane, Nitrotrichloromethane
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| Identifiers | |||
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3D model (Jmol)
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| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.000.847 | ||
| KEGG | |||
| UNII | |||
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| Properties | |||
| CCl3NO2 | |||
| Molar mass | 164.375 g/mol | ||
| Appearance | colorless liquid | ||
| Odor | irritating | ||
| Density | 1.692 g/ml | ||
| Melting point | −69 °C (−92 °F; 204 K) | ||
| Boiling point | 112 °C (234 °F; 385 K) (decomposes) | ||
| 0.2% | |||
| Vapor pressure | 18 mmHg (20°C) | ||
| -75.3·10−6 cm3/mol | |||
| Hazards | |||
| Main hazards | Extremely toxic and irritating to skin, eyes, and lungs. | ||
| GHS pictograms |  |
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| GHS signal word | Danger | ||
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EU classification (DSD)
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 T+ |
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| R-phrases | R22, R26, R36/37/38, R43, R50/53 | ||
| S-phrases | S36/37, S38, S45 | ||
| NFPA 704 | |||
| Lethal dose or concentration (LD, LC): | |||
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LC50 (median concentration)
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9.7 ppm (mouse, 4 hr) 117 ppm (rat, 20 min) 14.4 ppm (rat, 4 hr) |
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LCLo (lowest published)
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293 ppm (human, 10 min) 340 ppm (mouse, 1 min) 117 ppm (cat, 20 min) |
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| US health exposure limits (NIOSH): | |||
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PEL (Permissible)
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TWA 0.1 ppm (0.7 mg/m3) | ||
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REL (Recommended)
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TWA 0.1 ppm (0.7 mg/m3) | ||
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IDLH (Immediate danger)
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2 ppm | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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 (what is   ?) |
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| Infobox references | |||
Chloropicrin, also known as PS and nitrochloroform, is a chemical compound currently used as a broad-spectrum antimicrobial, fungicide, herbicide, insecticide, and nematicide. Its chemical structural formula is Cl3CNO2.
Chloropicrin was discovered in 1848 by Scottish chemist John Stenhouse. He prepared it by the reaction of a chlorinating agent with picric acid:
Because of the precursor used, Stenhouse named the compound chloropicrin, although the two compounds are structurally dissimilar.
Chloropicrin’s chemical formula is CCl3NO2 and its molecular weight is 164.38 grams/mole. Pure chloropicrin is a colorless liquid, with a boiling point of 112 °C. Chloropicrin is sparingly soluble in water with solubility of 2000 mg/L at 25 °C. It is volatile, with a vapor pressure of 23.2 millimeters of mercury (mmHg) at 25 °C; the corresponding Henry’s Law Constant is 0.00251 atmosphere-cubic meter per mole. The octanol-water partition coefficient (Kow) of chloropicrin is estimated to be 269. Its soil adsorption coefficient (Koc; normalized to soil organic matter content) is 25 cm3/g.
Chloropicrin was manufactured for use as poison gas in World War I. In agriculture, chloropicrin is injected into soil prior to planting a crop in order to fumigate soil. Chloropicrin affects a broad spectrum of fungi, microbes, insects. It is commonly used as a stand alone treatment or in combination / co-formulation with methyl bromide and 1,3-Dichloropropene. Chloropicrin is used as an indicator and repellent while fumigating residences for insects with sulfuryl fluoride which is an odorless gas.
At the national level, chloropicrin is regulated by the United States Environmental Protection Agency as a restricted use pesticide. Because of its toxicity and carcinogenicity, distribution and use of chloropicrin is available only to licensed professionals and specially certified growers who are trained in its proper and safe use. In the US, occupational exposure limits have been set at 0.1 ppm over an eight-hour time-weighted average.
In 2008 the US EPA re-approved chloropicrin as safe for use in agricultural settings, stating that treatments "can provide benefits to both food consumers and growers. For consumers, it means more fresh fruits and vegetables can be cheaply produced domestically year-round because several severe pest problems can be efficiently controlled." To ensure chloropicrin is used safely, the EPA requires a strict set of protections for handlers, workers, and persons living and working in and around farmland during treatments. EPA protections were increased in both 2011 and 2012, reducing fumigant exposures and significantly improving safety. Protections include the training of certified applicators supervising pesticide application, the use of buffer zones, posting before and during pesticide application, fumigant management plans, and compliance assistance and assurance measures.
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