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Mustard gas or sulfur mustard are names commonly used for the organosulfur chemical compound bis(2-chloroethyl) sulfide, which has the chemical structure S(CH 2 CH 2 Cl) 2, as well as other species. In the wider sense, compounds with the substituents −SCH 2 CH 2 X or −N(CH 2 CH 2 X) 2 are known as sulfur mustards or nitrogen mustards ...
The idealized combustion of mustard gas in oxygen produces hydrochloric acid and sulfuric acid, in addition to carbon dioxide and water: (ClC 2 H 4) 2 S + 7 O 2 → 4 CO 2 + 2 H 2 O + 2 HCl + H 2 SO 4. Bis(2-chloroethyl)sulfide reacts with sodium hydroxide, giving divinyl sulfide: (ClC 2 H 4) 2 S + 2 NaOH → (CH 2 =CH) 2 S + 2 H 2 O + 2 NaCl ...
Additionally, chemical burns can be caused by biological toxins (such as anthrax toxin) and by some types of cytotoxic chemical weapons, e.g., vesicants such as mustard gas and Lewisite, or urticants such as phosgene oxime. Chemical burns may: need no source of heat; occur immediately on contact; not be immediately evident or noticeable; be ...
Although it is a colorless solid, impure samples are often brown. The compound is a type of mustard gas, a vesicant used as a chemical weapon. From the chemical perspective, the compound is both a thioether and an alkyl chloride. Because sesquimustard is a solid at room temperature, it is not as easily deployed as related liquid mustards.
Beginning in the early 1930s, scientists at Rawalpindi sent British Indian Army soldiers, wearing shorts and cotton shirts, into gas chambers to experience the effects of mustard gas. The scientists hoped to determine the appropriate dosage to use on battlefields. Many of the subjects suffered severe burns from their exposure to the gas. [4]
This chemical is a form of nitrogen mustard gas and a powerful vesicant. Historically, some uses of mechlorethamine have included lymphoid malignancies such as Hodgkin's disease, lymphosarcoma, chronic myelocytic leukemia, polycythemia vera, and bronchogenic carcinoma [ 7 ] Mechlorethamine is often administered intravenously, [ 8 ] but when ...
It was developed in England in the 1930s as a thickener for mustard gas to make it more persistent when used in warm climates. A mixture of 60% sulfur mustard and 40% O-mustard also has a lower freezing point than pure sulfur mustard, and was given the code name HT. O-mustard is a Schedule I substance under the Chemical Weapons Convention.
Mustard compounds can refer to: Sulfur mustard (mustard gas) Nitrogen mustard This page was last edited on 15 January 2021 ...