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Dimethyl(trifluoromethylthio)arsine
Dimethyl(trifluoromethylthio)arsine is an arsenical compound developed by the United States military chemical weapon research program, which is described as "one of the most potent lung irritants known." See also * Cacodyl * Cacodyl cyanide * Diphenylchlorarsine * Lewisite * Methyldichloroarsine * Tetrachlorodinitroethane * Bis(trifluoromethyl) disulfide Bis(trifluoromethyl) disulfide (TFD) is a fluorinated organosulfur compound that was used as a fumigant. It is also an intermediate in the synthesis of triflic acid. It is a volatile liquid that is extremely toxic by inhalation. Synthesis TFD can ... References Arsenical vesicants Arsenic(III) compounds Vomiting agents Trifluoromethylthio compounds Cacodyl compounds {{Organic-compound-stub ...
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Cacodyl
Cacodyl, also known as dicacodyl or tetramethyldiarsine, (CH3)2As–As(CH3)2, is an organoarsenic compound that constitutes a major part of "Cadet's fuming liquid" (named after the French chemist Louis Claude Cadet de Gassicourt). It is a poisonous oily liquid with an extremely unpleasant garlicky odor. Cacodyl undergoes spontaneous combustion in dry air. Cacodyl is also the name of the functional group or radical (CH3)2As. Preparation A mixture of dicacodyl and cacodyl oxide ((CH3)2As–O–As(CH3)2) was first prepared by Cadet by the reaction of potassium acetate with arsenic trioxide. A subsequent reduction yields a mixture of several methylated arsenic compounds including dicacodyl. The global reaction (mass balance) corresponding to the oxide formation is the following: : A more efficient synthesis was later developed which started from the dimethyl arsine chloride and dimethyl arsine: : History Robert Wilhelm Bunsen coined the name kakodyl (later modified to cacodyl ...
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Cacodyl Cyanide
Cacodyl cyanide is a highly poisonous organoarsenic compound discovered by Robert Bunsen in the 1840s. It is very volatile and flammable, as it shares the chemical properties of both arsenic and cyanide. Synthesis Cacodyl cyanide can be prepared by reaction of cacodyl oxide with hydrogen cyanide or mercuric cyanide. Properties Cacodyl cyanide is a white solid that is only slightly soluble in water, but very soluble in alcohol and ether. Cacodyl cyanide is highly toxic, producing symptoms of both cyanide and arsenic poisoning. Bunsen described it in the following terms; It is also explosive, and Bunsen himself was severely injured in the course of his experiments with cacodyl cyanide. The Russian military tested cacodyl cyanide on cats as a potential chemical weapon for filling shells in late 1850s, but while it was found to be a potent lachrymatory agent, all cats survived and it was ultimately considered unsuitable for military use.https://www.supotnitskiy.ru/stat/stat72.htm ...
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Bis(trifluoromethyl) Disulfide
Bis(trifluoromethyl) disulfide (TFD) is a fluorinated organosulfur compound that was used as a fumigant. It is also an intermediate in the synthesis of triflic acid. It is a volatile liquid that is extremely toxic by inhalation. Synthesis TFD can be produced by reaction of perchloromethyl mercaptan or thiophosgene with sodium fluoride. Toxicity TFD is extremely toxic by inhalation. TFD is a powerful pulmonary agent that can cause severe pulmonary edema. TFD is about half as toxic as perfluoroisobutene. See also *Dimethyl(trifluoromethylthio)arsine * Perchloromethyl mercaptan *Thiophosgene *Perfluoroisobutene *Phosgene Phosgene is the organic chemical compound with the formula COCl2. It is a toxic, colorless gas; in low concentrations, its musty odor resembles that of freshly cut hay or grass. Phosgene is a valued and important industrial building block, espe ... Reference Organic disulfides Trifluoromethylthio compounds Pulmonary agents Fumigants {{Organohalid ...
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Arsenical
Arsenicals are chemical compounds that contain arsenic. In a military context, the term arsenical refer to toxic arsenic compounds that are used as chemical warfare agents. This include blister agents, blood agents and vomiting agents. Examples Blister agents * Ethyldichloroarsine * Lewisite *Methyldichloroarsine *Phenyldichloroarsine Blood agents *Arsine Vomiting agents *Adamsite *Diphenylchlorarsine *Diphenylcyanoarsine *Phenyldichloroarsine Phenyldichloroarsine, also known by its wartime name phenyl Dick and its NATO abbreviation PD, is an organic arsenical vesicant and vomiting agent developed by Germany and France for use as a chemical warfare agent during World War I. The agent is ... References Arsenic compounds Chemical weapons Poisons {{Chem-stub ...
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Chemical Weapon
A chemical weapon (CW) is a specialized munition that uses chemicals formulated to inflict death or harm on humans. According to the Organisation for the Prohibition of Chemical Weapons (OPCW), this can be any chemical compound intended as a weapon "or its precursor that can cause death, injury, temporary incapacitation or sensory irritation through its chemical action. Munitions or other delivery devices designed to deliver chemical weapons, whether filled or unfilled, are also considered weapons themselves." Chemical weapons are classified as weapons of mass destruction (WMD), though they are distinct from nuclear weapons, biological weapons, and radiological weapons. All may be used in warfare and are known by the military acronym NBC (for nuclear, biological, and chemical warfare). Weapons of mass destruction are distinct from conventional weapons, which are primarily effective due to their explosive, kinetic, or incendiary potential. Chemical weapons can be widely dispe ...
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Diphenylchlorarsine
Diphenylchloroarsine (DA) is the organoarsenic compound with the formula (C6H5)2AsCl. It is highly toxic and was once used in chemical warfare. It is also an intermediate in the preparation of other organoarsenic compounds. The molecule consists of a pyramidal As(III) center attached to two phenyl rings and one chloride. It was also known as sneezing oil during World War I by the Allies. Preparation and structure It was first produced in 1878 by the German chemists August Michaelis (1847–1916) and Wilhelm La Coste (1854–1885). It is prepared by the reduction of diphenylarsinic acid with sulfur dioxide. An idealized equation is shown: :Ph2AsO2H + SO2 + HCl → Ph2AsCl + H2SO4 The process adopted by Edgewood Arsenal for the production of DA for chemical warfare purposes employed a reaction between chlorobenzene and arsenic trichloride in the presence of sodium. The structure consists of pyramidal As centre. The As-Cl distance is 2.26 A and the Cl-As-C and C-As-C angles are 96 ...
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Lewisite
Lewisite (L) (A-243) is an organoarsenic compound. It was once manufactured in the U.S., Japan, Germany and the Soviet Union for use as a Chemical warfare, chemical weapon, acting as a vesicant (blister agent) and lung irritant. Although the substance is colorless and odorless in its pure form, impure samples of lewisite are a yellow, brown, violet-black, green, or amber oily liquid with a distinctive odor that has been described as similar to Pelargonium, geraniums. Chemical reactions The compound is prepared by the addition of arsenic trichloride to acetylene in the presence of a suitable catalyst: :AsCl3 + C2H2 → ClCHCHAsCl2 (Lewisite) Lewisite, like other arsenous chlorides, hydrolysis, hydrolyses in water to form hydrochloric acid and chlorovinylarsenous oxide (a less-powerful blister agent): :ClCHCHAsCl2 + 2 H2O → ClCHCHAs(OH)2 + 2 HCl This reaction is accelerated in alkaline solutions, and forms acetylene and trisodium arsenate. Lewisite reacts with metals to form hydrog ...
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Methyldichloroarsine
Methyldichloroarsine, sometimes abbreviated "MD" and also known as methyl Dick, is an organoarsenic compound with the formula CH3AsCl2. This colourless volatile liquid is a highly toxic vesicant that has been used in chemical warfare. History German chemists weaponized methyldichloroarsine during World War I, between 1917 and 1918. It was the first organoarsenic compound to be weaponized. Structure, synthesis, reactivity Focusing on the arsenic center, the molecule geometry is trigonal pyramidal with the Cl-As-Cl and C-As-Cl angles approaching 90° (see image). Virtually all related arsenic(III) compounds adopt similar structures. Methyldichloroarsine is produced by the reaction of methylmagnesium chloride and arsenic trichloride: :AsCl3 + CH3MgCl → CH3AsCl2 + MgCl2 Typically such syntheses are conducted in ether or THF solutions and typically the product is isolated by distillation. Use of larger amounts of the magnesium reagent affords greater amounts of dimethylc ...
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Tetrachlorodinitroethane
Tetrachlorodinitroethane is a chlorinated nitroalkane produced by nitration of tetrachloroethylene with dinitrogen tetroxide or fuming nitric acid. It's a powerful lachrymatory agent and pulmonary agent that is six times more toxic than chloropicrin. Tetrachlorodinitroethane may be used as a fumigant. See also *Chloropicrin * Trifluoronitrosomethane *Trichloronitrosomethane Trichloronitrosomethane is a chlorinated nitrosoalkane. It is a deep blue liquid with powerful lachrymatory effects. Synthesis Trichloronitrosomethane can be produced with following methods: * Oxidation of trichloromethylsulfinic acid with nitri ... References Nitro compounds Organochlorides Lachrymatory agents Pulmonary agents Fumigants {{Organohalide-stub ...
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Arsenical Vesicants
Arsenicals are chemical compounds that contain arsenic. In a military context, the term arsenical refer to toxic arsenic compounds that are used as chemical warfare agents. This include blister agents, blood agents and vomiting agents. Examples Blister agents *Ethyldichloroarsine *Lewisite *Methyldichloroarsine *Phenyldichloroarsine Blood agents *Arsine Vomiting agents *Adamsite *Diphenylchlorarsine *Diphenylcyanoarsine *Phenyldichloroarsine Phenyldichloroarsine, also known by its wartime name phenyl Dick and its NATO abbreviation PD, is an organic arsenical vesicant and vomiting agent developed by Germany and France for use as a chemical warfare agent during World War I. The agent i ... References Arsenic compounds Chemical weapons Poisons {{Chem-stub ...
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Arsenic(III) Compounds
Arsenic is a chemical element with the symbol As and atomic number 33. Arsenic occurs in many minerals, usually in combination with sulfur and metals, but also as a pure elemental crystal. Arsenic is a metalloid. It has various allotropes, but only the gray form, which has a metallic appearance, is important to industry. The primary use of arsenic is in alloys of lead (for example, in car batteries and ammunition). Arsenic is a common n-type dopant in semiconductor electronic devices. It is also a component of the III-V compound semiconductor gallium arsenide. Arsenic and its compounds, especially the trioxide, are used in the production of pesticides, treated wood products, herbicides, and insecticides. These applications are declining with the increasing recognition of the toxicity of arsenic and its compounds. A few species of bacteria are able to use arsenic compounds as respiratory metabolites. Trace quantities of arsenic are an essential dietary element in rats, hamsters, ...
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Vomiting Agents
Vomiting (also known as emesis and throwing up) is the involuntary, forceful expulsion of the contents of one's stomach through the mouth and sometimes the nose. Vomiting can be the result of ailments like food poisoning, gastroenteritis, pregnancy, motion sickness, or hangover; or it can be an after effect of diseases such as brain tumors, elevated intracranial pressure, or overexposure to ionizing radiation. The feeling that one is about to vomit is called nausea; it often precedes, but does not always lead to vomiting. Impairment due to alcohol or anesthesia can cause inhalation of vomit, leading to suffocation. In severe cases, where dehydration develops, intravenous fluid may be required. Antiemetics are sometimes necessary to suppress nausea and vomiting. Self-induced vomiting can be a component of an eating disorder such as bulimia, and is itself now classified as an eating disorder on its own, purging disorder. Complications Aspiration Vomiting is dangerous if g ...
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