Chloropicrin
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| Names | |||
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| IUPAC name
Trichloro(nitro)methane
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Other names
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| Identifiers | |||
CAS Number
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3D model (JSmol)
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Beilstein Reference
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1756135 | ||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.000.847 | ||
| EC Number |
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Gmelin Reference
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240197 | ||
| KEGG | |||
PubChem CID
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| RTECS number |
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| UNII | |||
| UN number | 1580 | ||
CompTox Dashboard (EPA)
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InChI
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SMILES
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| Properties | |||
Chemical formula
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CCl3NO2 | ||
| Molar mass | 164.375 g/mol | ||
| Appearance | colorless liquid | ||
| Odor | irritating[1] | ||
| Density | 1.692 g/ml | ||
| Melting point | −69 °C (−92 °F; 204 K) | ||
| Boiling point | 112 °C (234 °F; 385 K) (decomposes) | ||
Solubility in water
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0.2%[1] | ||
| Vapor pressure | 18 mmHg (20°C)[1] | ||
Magnetic susceptibility (χ)
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−75.3·10−6 cm3/mol | ||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards
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Extremely toxic and irritating to skin, eyes, and lungs. | ||
| GHS labelling: | |||
Pictograms
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Signal word
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Danger | ||
Hazard statements
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H301, H314, H330, H370, H372, H410 | ||
Precautionary statements
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P260, P264, P270, P271, P273, P280, P284, P301+P310, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P307+P311, P310, P314, P320, P321, P330, P363, P391, P403+P233, P405, P501 | ||
| NFPA 704 (fire diamond) | |||
| Lethal dose or concentration (LD, LC): | |||
LC50 (median concentration)
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9.7 ppm (mouse, 4 hr) 117 ppm (rat, 20 min) 14.4 ppm (rat, 4 hr)[2] | ||
LCLo (lowest published)
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293 ppm (human, 10 min) 340 ppm (mouse, 1 min) 117 ppm (cat, 20 min)[2] | ||
| NIOSH (US health exposure limits): | |||
PEL (Permissible)
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TWA 0.1 ppm (0.7 mg/m3)[1] | ||
REL (Recommended)
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TWA 0.1 ppm (0.7 mg/m3)[1] | ||
IDLH (Immediate danger)
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2 ppm[1] | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Chloropicrin, also known as PS (from Port Sunlight[3]) and nitrochloroform, is a chemical compound currently used as a broad-spectrum antimicrobial, fungicide, herbicide, insecticide, and nematicide.[4] It was used as a poison gas in World War I and the Russian military has been accused of using it in the Russo-Ukrainian War.[5][6][7] Its chemical structural formula is Cl3C−NO2.
- ^ a b c d e f NIOSH Pocket Guide to Chemical Hazards. "#0132". National Institute for Occupational Safety and Health (NIOSH).
- ^ a b "Chloropicrin". Immediately Dangerous to Life or Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
- ^ Foulkes, C. H. (31 January 2012). "GAS!" – The Story of the Special Brigade. Andrews UK Limited. p. 193.
- ^ "RED Fact Sheet: Chloropicrin" (PDF). US Environmental Protection Agency. 10 July 2008. p. 2. Archived from the original (PDF) on October 31, 2008. Retrieved 20 September 2013.
- ^ Office of the Spokesperson (1 May 2024). "Imposing New Measures on Russia for its Full-Scale War and Use of Chemical Weapons Against Ukraine". U.S. Department of State. Archived from the original on 23 May 2024. Retrieved 23 May 2024.
- ^ "A top Russian general is killed in a Moscow bombing claimed by Ukraine". Associated Press News. 2024-12-17. Retrieved 2024-12-18.
- ^ Quell, Molly (2025-07-04). "Dutch intelligence services say Russia has stepped up use of banned chemical weapons in Ukraine". Reuters. Retrieved 2025-07-05.