| Lewisite |
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| | Systematic name | 2-chloroethenyldichloroarsine | | Chemical formula | C2H2AsCl3 | | Molecular mass | 207.32 g/mol | | Density | 1.89 g/cm3 | | Melting point | −18 °C | | Boiling point | 190 °C | | vapour pressure at 20 °C | 0.35 mm Hg (47 Pa) | | CAS number | [xx-xx-xx] | | SMILES | xxxxx | | Disclaimer and references | Lewisite is a chemical compound from a chemical family called arsines. While it is a colorless and odorless liquid when pure it is usually found as an oily, brown liquid with a distinct odor similar to geraniums. It is a chemical weapon, acting as a vesicant (blister agent) and lung irritant, and can be used in combination with mustard gas as mustard-lewisite. IUPAC nomenclature is a system of naming chemical compounds and of describing the science of chemistry in general. ...
This article or section does not cite any references or sources. ...
The molecular mass (abbreviated Mr) of a substance, formerly also called molecular weight and abbreviated as MW, is the mass of one molecule of that substance, relative to the unified atomic mass unit u (equal to 1/12 the mass of one atom of carbon-12). ...
In physics, density is mass m per unit volume V. For the common case of a homogeneous substance, it is expressed as: where, in SI units: Ï (rho) is the density of the substance, measured in kg·m-3 m is the mass of the substance, measured in kg V is...
The melting point of a crystalline solid is the temperature at which it changes state from solid to liquid. ...
The boiling point of a substance is the temperature at which it can change its state from a liquid to a gas throughout the bulk of the liquid at a given pressure. ...
CAS registry numbers are unique numerical identifiers for chemical compounds, polymers, biological sequences, mixtures and alloys. ...
The simplified molecular input line entry specification or SMILES is a specification for unambiguously describing the structure of chemical molecules using short ASCII strings. ...
A chemical compound is a chemical substance of two or more different chemically bonded chemical elements, with a fixed ratio determining the composition. ...
Arsine, the simplest compound of arsenic, is AsH3. ...
Chemical warfare is warfare (and associated military operations) using the toxic properties of chemical substances to kill, injure or incapacitate an enemy. ...
A vesicant (also known as a blister agent) is a chemical agent that causes blistering of the skin. ...
Airborne exposure limit 0. ...
It can easily penetrate ordinary clothing and even rubber; upon skin contact it causes immediate pain and itching with a rash and swelling. Blisters develop after 12 hours, and discomfort lasts for 2 to 3 days. Sufficient absorption can cause systemic poisoning leading to liver necrosis or death. Necrosis (in Greek ÎεκÏÏÏ = Death) is the name given to accidental death of cells and living tissue. ...
Inhalation causes a burning pain, sneezing, coughing, vomiting, and possibly pulmonary edema. Ingestion results in severe pain, nausea, vomiting, and tissue damage. Generalised symptoms also include restlessness, weakness, subnormal temperature and low blood pressure. Pulmonary edema is swelling and/or fluid accumulation in the lungs. ...
Lewisite is usually found as a mixture of isomers, 2-chlorovinylarsonous dichloride should predominate but often bis(2-chloroethenyl)arsinous dichloride and tris(2-chlorovinyl) arsine are present. Lewisite can be given any of the preceding names and is also sometimes described as 2-chlorovinyldichloroarsine, (2-chloroethenyl)arsinous dichloride or dichloro- (2-chlorovinyl) arsine. Lewisite hydrolyses in water to form hydrochloric acid, and in contact with alkaline solutions can form poisonous trisodium arsenate. In chemistry, isomers are molecules with the same chemical formula and often with the same kinds of chemical bonds between atoms, but in which the atoms are arranged differently (analogous to a chemical anagram). ...
It is named after the US chemist and soldier Winford Lee Lewis (1878-1943). In 1918 he found the thesis of Julius Arthur Nieuwland at Maloney Hall, a chemical laboratory part of The Catholic University of America, Washington, D.C. in which Nieuwland detailed the synthesis by the combination of allowing arsenic trichloride to react with acetylene in the presence of a hydrochloric acid solution of mercuric chloride. 1918 (MCMXVIII) was a common year starting on Tuesday of the Gregorian calendar (see link for calendar) or a common year starting on Wednesday of the Julian calendar. ...
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The Martin Maloney Chemical Laboratory of the Catholic University of America was built in November, 1917. ...
The Catholic University of America (abbreviated CUA), located in Washington, D.C., is unique as the national university of the Roman Catholic Church and as the only higher education institution founded by U.S. Roman Catholic bishops. ...
General Name, Symbol, Number arsenic, As, 33 Chemical series metalloids Group, Period, Block 15, 4, p Appearance metallic gray Standard atomic weight 74. ...
Acetylene (systematic name: ethyne) is the simplest alkyne hydrocarbon, consisting of two hydrogen atoms and two carbon atoms connected by a triple bond. ...
The chemical compound hydrochloric acid is the aqueous (water-based) solution of hydrogen chloride gas (HCl). ...
General Name, Symbol, Number mercury, Hg, 80 Chemical series transition metals Group, Period, Block 12, 6, d Appearance silvery white Atomic mass 200. ...
The chloride ion is formed when the element chlorine picks up one electron to form an anion (negatively-charged ion) Clâ. The salts of hydrochloric acid HCl contain chloride ions and can also be called chlorides. ...
It was developed into a secret weapon at Nilo Park, Ohio and given the name "the new G-34" to confuse its development with mustard gas.[citation needed] It was not used in the First World War, but experimented with in the 1920s as the "Dew of Death."[1] Airborne exposure limit 0. ...
After World War I, the US became interested in Lewisite because it was not flammable. It had the military symbol of M1 up into World War II, when it was changed to L. Field trials with Lewisite during the World War II demonstrated that casualty concentrations were not achievable under high humidity due to its rate of hydrolysis and its charactistic odor and lacrymation forced troops to don masks and avoid contaminated areas. The United States produced about 20,000 tons of Lewisite, keeping it on hand primarily as an antifreeze for mustard gas or to penetrate protective clothing in special situations. It was replaced by the mustard gas variant HT (a 60:40 mixture of sulfur mustard and O Mustard), and declared obsolete in the 1950s. It is effectively treated with British anti-Lewisite (dimercaprol). Stockpiles of Lewisite were neutralized with bleach and dumped into the Gulf of Mexico.[citation needed] âThe Great War â redirects here. ...
Combatants Allied powers: China France Great Britain Soviet Union United States and others Axis powers: Germany Italy Japan and others Commanders Chiang Kai-shek Charles de Gaulle Winston Churchill Joseph Stalin Franklin Roosevelt Adolf Hitler Benito Mussolini Hideki TÅjÅ Casualties Military dead: 17,000,000 Civilian dead: 33,000...
Combatants Allied powers: China France Great Britain Soviet Union United States and others Axis powers: Germany Italy Japan and others Commanders Chiang Kai-shek Charles de Gaulle Winston Churchill Joseph Stalin Franklin Roosevelt Adolf Hitler Benito Mussolini Hideki TÅjÅ Casualties Military dead: 17,000,000 Civilian dead: 33,000...
Also see: Tears (song) by X Japan, or Tears (film) by Im Sang-soo. ...
Airborne exposure limit 0. ...
British Anti Lewisite, often referred to by its acronym BAL, is a compound developed by the British biochemists of Oxford University during World War II . ...
Gulf of Mexico in 3D perspective. ...
Recently, mid 2006, it has been revealed in the world news media that China and Japan are still jointly cleaning up Japan's buried World War II stock of Lewisite in northeastern China. Japan is well behind on its commitment to clean up the site. Residents of China have died over the past twenty years from accidental exposure to the toxin. [1]
References
- ^ Domingo Tabangcura, Jr. and G. Patrick Daubert, MD. British anti-Lewisite Development Molecule of the Month, University of Bristol School of Chemistry
External links - Links to external chemical sources
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