Mustard gas

Chemical compound once used in warfare

Mustard gas  File:Sulfur-mustard-2D-skeletal.svg

File:Sulfur-mustard-3D-balls.png
File:Sulfur-mustard-3D-vdW.png
Names
Preferred IUPAC name

1-Chloro-2-[(2-chloroethyl)sulfanyl]ethane

Other names

Bis(2-chloroethyl) sulfide

Iprit
Schwefel-LOST
Lost
Sulfur mustard
Senfgas
Yellow cross liquid
Yperite
Distilled mustard
Mustard T- mixture
1,1'-thiobis[2-chloroethane]
Dichlorodiethyl sulfide

Identifiers

CAS Number

* 505-60-2 File:Yes check.svgY

3D model (JSmol)

* Interactive image

ChEBI |

* CHEBI:25434 File:Yes check.svgY

ChEMBL |

* ChEMBL455341 File:Yes check.svgY

ChemSpider |

* 21106142 File:Yes check.svgY

ECHA InfoCard | Script error: No such module "Wikidata". Script error: No such module "Wikidata".
E number | Script error: No such module "Wikidata".
KEGG |

* C19164 File:Yes check.svgY

PubChem CID

* 10461

UNII |

* T8KEC9FH9P File:Yes check.svgY

InChI

* InChI=1S/C4H8Cl2S/c5-1-3-7-4-2-6/h1-4H2 File:Yes check.svgY

Key: QKSKPIVNLNLAAV-UHFFFAOYSA-N File:Yes check.svgY

* InChI=1/C4H8Cl2S/c5-1-3-7-4-2-6/h1-4H2

Key: QKSKPIVNLNLAAV-UHFFFAOYAK

SMILES

* ClCCSCCCl

Properties

Chemical formula

| C4H8Cl2S
Molar mass | 159.07 g·mol−1
Appearance  | Colorless if pure. Normally ranges from pale yellow to dark brown. Slight garlic or horseradish type odor.[1]
Density | 1.27 g/mL, liquid
Melting point | 14.4 °C (57.9 °F; 287.5 K)
Boiling point | 217 °C (423 °F; 490 K) begins to decompose at 217 °C (423 °F) and boils at 218 °C (424 °F)

Solubility in water

| 7.6 mg/L at 20°C[2]
Solubility | Alcohols, ethers, hydrocarbons, lipids, THF
Hazards
Occupational safety and health (OHS/OSH):

Main hazards

| Flammable, toxic, vesicant, carcinogenic, mutagenic
GHS labelling:[3]

Pictograms

| GHS06: ToxicGHS07: Exclamation mark

Signal word

| Danger

Hazard statements

| H300, H310, H315, H319, H330, H335

Precautionary statements

| P260, P261, P262, P264, P270, P271, P280, P284, P301+P310, P302+P350, P302+P352, P304+P340, P305+P351+P338, P310, P312, P320, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, P501
NFPA 704 (fire diamond)  |

Flash point | 105 °C (221 °F; 378 K)
Safety data sheet (SDS)  | External MSDS
Related compounds

Related compounds

| Nitrogen mustard, Bis(chloroethyl) ether

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

File:X mark.svgN verify (what is File:Yes check.svgYFile:X mark.svgN ?)

Infobox references

Chemical compound

Mustard gas or sulfur mustard is a chemical compound belonging to a family of cytotoxic and blister agents known as mustard agents. The name mustard gas is widely used, but it is technically incorrect: the substance, when dispersed, is often not actually a gas, but is instead in the form of a fine mist of liquid droplets.[4]

Dichlorodiethyl sulfide is a symmetric, short chain molecule, with a sulfur atom in the middle and chlorine atom at both ends, chemical formula C4H8Cl2S. In the wider sense, compounds with the structural element BC2H4X, where X is any leaving group and B is a Lewis base, are known as mustards. Such compounds can form cyclic -onium ions (sulfonium, ammonium, etc.) that are potent alkylating agents of nucleotides in DNA strands, which prevents cellular division, leading to programmed cell death.[2] Alternatively, if cell death is not immediate, the damaged DNA can lead to the development of cancer.[2] Oxidative stress is another pathology involved in mustard gas toxicity.

Mustard gas has a long history of being used as a blister agent in warfare and is one of the most well-studied of such agents. It can form large blisters on exposed skin and in the lungs, often resulting in prolonged illness ending in death.[5] Sulfur mustards are viscous liquids at room temperature and have an odor resembling mustard plants, garlic, or horseradish, hence the name.[4] When pure, they are colorless, but when used in impure forms, such as in warfare, they are usually yellow-brown.

As a chemical weapon, mustard gas was first used in World War I, and has been used in several armed conflicts since then, including the Iran–Iraq War, resulting in more than 100,000 casualties.[6][7] Today, sulfur-based and nitrogen-based mustard agents are regulated under Schedule 1 of the 1993 Chemical Weapons Convention, as substances with few uses other than in chemical warfare (though since then, mustard gas has been found to be useful in cancer chemotherapy[8]). Mustard agents could be deployed by means of artillery shells, aerial bombs, rockets, or by spraying from aircraft.

## Contents

* 1 Synthesis and reactions
* 2 Mechanism of cellular toxicity
* 3 Physiological effects
* 4 Formulations
* 5 Commonly-stockpiled mustard agents (class)
* 6 History
* 6.1 Development
* 6.2 Use
* 6.2.1 Development of the first chemotherapy drug
* 6.2.2 Disposal
* 6.2.3 Post-war accidental exposure
* 6.3 WWII-era tests on men
* 6.4 Detection in biological fluids
* 7 See also
* 8 References
* 9 External links

## Synthesis and reactions[edit | edit source]

Mustard gas can be synthesized in a variety of different ways.

In the Depretz method, sulfur dichloride is treated with ethylene:

SCl2 \+ 2 C2H4 → (ClC2H4)2S

In the Levinstein process, disulfur dichloride is used instead:[9][10]

S2Cl2 \+ 2 C2H4 → (ClC2H4)2S \+ 1⁄8 S8

In the Meyer method, thiodiglycol is produced from chloroethanol and potassium sulfide and chlorinated with phosphorus trichloride:[11]

3 (HOC2H4)2S + 2 PCl3 → 3 (ClC2H4)2S + 2 P(OH)3

In the Meyer-Clarke method, concentrated hydrochloric acid (HCl) is used instead of PCl3:

(HOC2H4)2S + 2 HCl → (ClC2H4)2S + 2 H2O

Thionyl chloride and phosgene, the latter of which is also a choking agent, have also been used as chlorinating agents. These compounds have the added advantage in that if they are used in excess, they remain as impurities in the finished product and can therefore produce additional mechanisms of toxicity.

Mustard gas is a viscous liquid at normal temperatures. The pure compound has a melting point of 14 °C (57 °F) and decomposes before boiling at 218 °C (424 °F).

The idealized combustion of mustard gas in oxygen produces hydrochloric acid and sulfuric acid, in addition to carbon dioxide and water:

(ClC2H4)2S + 7 O2 → 4 CO2 \+ 2 H2O + 2 HCl + H2SO4

Phosgene, sulfur oxides, and chlorine are also produced in this process.

Decontamination of mustard gas can be achieved with sodium hydroxide, giving divinyl sulfide:

(ClC2H4)2S + 2 NaOH → (CH2=CH)2S + 2 H2O + 2 NaCl

Other compounds that have been used for decontamination include sodium ethoxide, which gives ethanol instead of water.

## Mechanism of cellular toxicity[edit | edit source]

File:Mustard-dna.svg

Mustard gas alkylating an amino group via conversion to a sulfonium ion (2-chloroethylthiiranium)

Sulfur mustards readily eliminate chloride ions by intramolecular nucleophilic substitution to form cyclic sulfonium ions. These very reactive intermediates tend to permanently alkylate nucleotides in DNA strands, which can prevent cellular division, leading to programmed cell death.[2] Alternatively, if cell death is not immediate, the damaged DNA can lead to the development of cancer.[2] Oxidative stress would be another pathology involved in mustard gas toxicity.

In the wider sense, compounds with the structural element BC2H4X, where X is any leaving group and B is a Lewis base, are known as mustards. Such compounds can form cyclic "onium" ions (sulfonium, ammonium, etc.) that are good alkylating agents. Other such compounds are bis(2-haloethyl)ethers (oxygen mustards), the (2-haloethyl)amines (nitrogen mustards), and sesquimustard, which has two α-chloroethyl thioether groups (ClC2H4S−) connected by an ethylene bridge (−C2H4−).[citation needed] These compounds have a similar ability to alkylate DNA, but their physical properties vary.

## Physiological effects[edit | edit source]

File:Mustard gas burns.jpg

Soldier with moderate mustard agent burns sustained during World War I showing characteristic bullae on the neck, armpit, and hands

Mustard gases are extremely toxic and have powerful blistering effects on victims. Their alkylating capabilities make them strongly carcinogenic and mutagenic. Furthermore, they are highly lipophilic, which accelerates their absorption into the body.[2] Because people exposed to mustard agents rarely suffer immediate symptoms, and contaminated areas may appear completely normal, victims can unknowingly receive high doses. Within 24 hours of exposure, victims experience intense itching and skin irritation. If this irritation goes untreated, blisters filled with yellow fluid (pus) can start to form wherever the agent contacted the skin. These are chemical burns and are very debilitating. Mustard gases easily penetrate clothing fabrics such as wool or cotton, so it is not only exposed skin that gets burned. If the victim's eyes were exposed, then they become sore, starting with conjunctivitis (also known as pink eye), after which the eyelids swell, resulting in temporary blindness. Extreme ocular exposure to mustard gas vapors may result in corneal ulceration, anterior chamber scarring, and neovascularization.[12][13][14][15] In these severe and infrequent cases, corneal transplantation has been used as a treatment option.[16] Miosis, when the pupil constricts more than usual, may also occur, which is probably the result of the cholinomimetic activity of mustard.[17] At very high concentrations, if inhaled, mustard agents cause bleeding and blistering within the respiratory system, damaging mucous membranes and causing pulmonary edema. Depending on the level of contamination, mustard agent burns can vary between first and second degree burns, though they can also be every bit as severe, disfiguring, and dangerous as third degree burns.[18] Burns that are severe (i.e. covering more than 50% of the victim's skin) are often fatal, with death occurring after only days or weeks. Mild or moderate exposure to mustard gases is unlikely to kill, though victims still require lengthy periods of medical treatment and convalescence before recovery is complete.

Mustard gases' carcinogenic and mutagenic effects mean that victims, even if they fully recover, have an increased risk of developing cancer later in life. In a study of patients 25 years after wartime exposure to chemical weaponry, c-DNA microarray profiling indicated that 122 genes were significantly mutated in the lungs and airways of mustard gas victims. Those genes all correspond to functions commonly affected by mustard gas exposure, including apoptosis, inflammation, and stress responses.[19] The long-term ocular complications include burning, tearing, itching, photophobia, presbyopia, pain, and foreign-body sensations.[20][21]

File:Blister-arm.jpg

Typical appearance of bullae on an arm caused by vesicant burns

Mustard gases' blistering effects can be neutralized by oxidation or chlorination, using household bleach (sodium hypochlorite), or by nucleophilic attack using decontamination solutions such as "DS2" (2% NaOH, 70% diethylenetriamine, 28% 2-methoxyethanol). After initial decontamination of the victim's wounds is complete, medical treatment is similar to that required by any conventional burn. The degree of pain and discomfort suffered by the victim is also comparable. Mustard agent burns do not heal quickly, and (as with other types of burns) present a risk of sepsis caused by pathogens such as Staphylococcus aureus and Pseudomonas aeruginosa. The mechanisms behind mustard gas's effect on endothelial cells are still being studied, but recent studies have shown that high levels of exposure can induce high rates of both necrosis and apoptosis. In vitro tests have shown that at low concentrations of mustard gas, where apoptosis is the predominant result of exposure, pretreatment with 50 mM N-acetyl-L-cysteine (NAC) was able to decrease the rate of apoptosis. NAC protects actin filaments from reorganization by mustard gas, demonstrating that actin filaments play a large role in the severe burns observed in victims.[22]

A British nurse treating soldiers with mustard agent burns during World War I commented:[23]

> They cannot be bandaged or touched. We cover them with a tent of propped-up sheets. Gas burns must be agonizing because usually the other cases do not complain, even with the worst wounds, but gas cases are invariably beyond endurance and they cannot help crying out.

## Formulations[edit | edit source]

File:TestYperite4030618980 242ab5c81d b.jpg

Lewisite (top row) and mustard gas (bottom row) test with concentrations from 0.01% to 0.06%

In its history, various types and mixtures of mustard gas have been employed. These include:

* H – Also known as HS ("Hun Stuff") or Levinstein mustard. This is named after the inventor of the "quick but dirty" Levinstein Process for manufacture,[9][10] reacting dry ethylene with disulfur dichloride under controlled conditions. Undistilled mustard gas contains 20–30% impurities, which means it does not store as well as HD. Also, as it decomposes, it increases in vapor pressure, making the munition it is contained in likely to split, especially along a seam, releasing the agent to the atmosphere.[1]
* HD – Codenamed Pyro by the British, and Distilled Mustard by the US.[1] Distilled mustard of 95% or higher purity. The term "mustard gas" usually refers to this variety of mustard.
* HT – Codenamed Runcol by the British, and Mustard T- mixture by the US.[1] A mixture of 60% mustard and 40% O-mustard, a related vesicant with lower freezing point, lower volatility and similar vesicant characteristics.
* HL – A blend of distilled mustard (HD) and lewisite (L), originally intended for use in winter conditions due to its lower freezing point compared to the pure substances. The lewisite component of HL was used as a form of antifreeze.[24]
* HQ – A blend of distilled mustard (HD) and sesquimustard (Q) (Gates and Moore 1946).

## Commonly-stockpiled mustard agents (class)[edit | edit source]

Chemical  | Code  | Trivial name  | CAS number  | PubChem  | Structure

|
|
|
|
|

Bis(2-chloroethyl) sulfide  | H, HD  | Mustard  | 505-60-2  | CID 10461 from PubChemTemplate:WikidataCheck | File:Sulfur mustard.svg
1,2-Bis(2-chloroethylsulfanyl) ethane  | Q  | Sesquimustard | 3563-36-8  | CID 19092 from PubChemTemplate:WikidataCheck | File:Sesquimustard.svg
2-Chloroethyl ethyl sulfide  |  | Half mustard | 693-07-2  | CID 12733 from PubChemTemplate:WikidataCheck | File:Chloroethyl ethyl sulfide.svg
Bis(2-(2-chloroethylsulfanyl)ethyl) ether  | T  | O-Mustard | 63918-89-8  | CID 45452 from PubChemTemplate:WikidataCheck | File:O-Mustard.svg
2-Chloroethyl chloromethyl sulfide  |  |  | 2625-76-5  |  | File:2-Chlorethylchlormethylsulfid.svg
Bis(2-chloroethylsulfanyl) methane  | HK  |  | 63869-13-6  |  | File:Bis(2-chlorethylthio)methan.svg
1,3-Bis(2-chloroethylsulfanyl) propane  |  |  | 63905-10-2  |  | File:Bis-1,3-(2-chlorethylthio)-n-propan.svg
1,4-Bis(2-chloroethylsulfanyl) butane  |  |  | 142868-93-7  |  | File:Bis-1,4-(2-chlorethylthio)-n-butan.svg
1,5-Bis(2-chloroethylsulfanyl) pentane  |  |  | 142868-94-8  |  | File:Bis-1,5-(2-chlorethylthio)-n-pentan.svg
Bis((2-chloroethylsulfanyl)methyl) ether  |  |  | 63918-90-1  |  | File:Bis(2-chlorethylthiomethyl)ether.svg

## History[edit | edit source]

### Development[edit | edit source]

Mustard gases were possibly developed as early as 1822 by César-Mansuète Despretz (1798–1863).[25] Despretz described the reaction of sulfur dichloride and ethylene but never made mention of any irritating properties of the reaction product. In 1854, another French chemist, Alfred Riche (1829–1908), repeated this procedure, also without describing any adverse physiological properties. In 1860, the British scientist Frederick Guthrie synthesized and characterized the mustard agent compound and noted its irritating properties, especially in tasting.[26] Also in 1860, chemist Albert Niemann, known as a pioneer in cocaine chemistry, repeated the reaction, and recorded blister-forming properties. In 1886, Viktor Meyer published a paper describing a synthesis that produced good yields. He combined 2-chloroethanol with aqueous potassium sulfide, and then treated the resulting thiodiglycol with phosphorus trichloride. The purity of this compound was much higher and consequently the adverse health effects upon exposure were much more severe. These symptoms presented themselves in his assistant, and in order to rule out the possibility that his assistant was suffering from a mental illness (psychosomatic symptoms), Meyer had this compound tested on laboratory rabbits, most of which died. In 1913, the English chemist Hans Thacher Clarke (known for the Eschweiler-Clarke reaction) replaced the phosphorus trichloride with hydrochloric acid in Meyer's formulation while working with Emil Fischer in Berlin. Clarke was hospitalized for two months for burns after one of his flasks broke. According to Meyer, Fischer's report on this accident to the German Chemical Society sent the German Empire on the road to chemical weapons.[27]

Mustard gas can have the effect of turning a patient's skin different colors, including shades of red, orange, pink, and in unusual cases, blue. The German Empire during World War I relied on the Meyer-Clarke method because 2-chloroethanol was readily available from the German dye industry of that time.

### Use[edit | edit source]

File:155mmMustardGasShells.jpg

Pallets of 155 mm artillery shells containing "HD" (distilled mustard gas agent) at the Pueblo Chemical Depot. The distinctive color-coding scheme on each shell is visible

Mustard gas was first used in World War I by the German army against British and Canadian soldiers near Ypres, Belgium, "on the night of July 12, 1917."[28] Later also against the French Second Army. Yperite is "a name used by the French, because the compound was first used at Ypres."[29] The Allies did not use mustard gas until November 1917 at Cambrai, France, after the armies had captured a stockpile of German mustard shells. It took the British more than a year to develop their own mustard agent weapon, with production of the chemicals centred on Avonmouth Docks (the only option available to the British was the Despretz–Niemann–Guthrie process).[30][31] This was used first in September 1918 during the breaking of the Hindenburg Line.

Mustard gas was originally assigned the name LOST, after the scientists Wilhelm Lommel and Wilhelm Steinkopf, who developed a method of large-scale production for the Imperial German Army in 1916.[32]

Mustard gas was dispersed as an aerosol in a mixture with other chemicals, giving it a yellow-brown color. Mustard agent has also been dispersed in such munitions as aerial bombs, land mines, mortar rounds, artillery shells, and rockets.[1] Exposure to mustard agent was lethal in about 1% of cases. Its effectiveness was as an incapacitating agent. The early countermeasures against mustard agent were relatively ineffective, since a soldier wearing a gas mask was not protected against absorbing it through his skin and being blistered. A common countermeasure was using a urine-soaked mask or facecloth to prevent or reduce injury, a readily available remedy attested by soldiers in documentaries (e.g. They Shall Not Grow Old in 2018) and others (such as forward aid nurses) interviewed between 1947 and 1981 by the British Broadcasting Corporation for various World War One history programs; however, the effectiveness of this measure is unclear.

Mustard gas can remain in the ground for weeks, and it continues to cause ill effects. If mustard agent contaminates one's clothing and equipment while cold, then other people with whom they share an enclosed space could become poisoned as contaminated items warm up enough material to become an airborne toxic agent. An example of this was depicted in a British and Canadian documentary about life in the trenches, particularly once the "sousterrain" (subways and berthing areas underground) were completed in Belgium and France. Towards the end of World War I, mustard agent was used in high concentrations as an area-denial weapon that forced troops to abandon heavily contaminated areas.

File:Mustard gas ww2 poster.jpg

US Army World War II gas identification poster, c. 1941–1945

Since World War I, mustard gas has been used in several wars and other conflicts, usually against people who cannot retaliate in kind:[33]

* United Kingdom against the Red Army in 1919[34]
* Alleged British use in Mesopotamia in 1920[35]
* Spain and France against the Rifian resistance in Morocco during the Rif War of 1921–27 (see also: Spanish use of chemical weapons in the Rif War)[33][36]
* Italy in Libya in 1930[33]
* The Soviet Union in Xinjiang, Republic of China, during the Soviet Invasion of Xinjiang against the 36th Division (National Revolutionary Army) in 1934, and also in the Xinjiang War (1937) in 1936–37[34][36]
* Italy against Abyssinia (now Ethiopia) in 1935-1936[33]
* The Japanese Empire against China in 1937–1945[34]
* The United States Government tested effectiveness on US Naval recruits in a laboratory setting at The Great Lakes Naval Base, June 3, 1945.[37]
* The 2 December 1943 air raid on Bari destroyed an Allied stockpile of mustard gas on the SS John Harvey.[38]
* Egypt against North Yemen in 1963–1967[33]
* Iraq against Kurds in the town of Halabja during the Halabja chemical attack[34][39]
* Iraq against Iranians in 1983–1988[40]
* Possibly in Sudan against insurgents in the civil war, in 1995 and 1997.[33]
* In the Iraq War, abandoned stockpiles of mustard gas shells were destroyed in the open air,[41] and were used against Coalition forces in roadside bombs.[42]
* By ISIS forces against Kurdish forces in Iraq in August 2015.[43]
* By ISIS against another rebel group in the town of Mare' in 2015.[44]
* According to Syrian State media, by ISIS against Syrian Army during the battle in Deir ez-Zor in 2016.[45]

In 1943, during World War II, a shipment of mustard gas from the US exploded aboard SS John Harvey that was bombed during an air raid in the harbor of Bari, Italy. Eighty-three of the 628 hospitalized victims who had been exposed to the mustard agent died.[46]

After WWII, stockpiled mustard gas was dumped by the British in the sea near Port Elizabeth, South Africa, resulting in many cases of burns among trawler crews.[47]

The use of toxic gases or other chemicals, including mustard gas, during warfare is known as chemical warfare, and this kind of warfare was prohibited by the Geneva Protocol of 1925, and also by the later Chemical Weapons Convention of 1993. The latter agreement also prohibits the development, production, stockpiling, and sale of such weapons.

In September 2012, a US official stated that the rebel militant group ISIS was manufacturing and using mustard gas in Syria and Iraq, which was allegedly confirmed by the group's head of chemical weapons development, Sleiman Daoud al-Afari, who has since been captured.[48][49][50]

#### Development of the first chemotherapy drug[edit | edit source]

As early as 1919 it was known that mustard agent was a suppressor of hematopoiesis.[51] In addition, autopsies performed on 75 soldiers who had died of mustard agent during World War I were done by researchers from the University of Pennsylvania who reported decreased counts of white blood cells.[46] This led the American Office of Scientific Research and Development (OSRD) to finance the biology and chemistry departments at Yale University to conduct research on the use of chemical warfare during World War II.[46][52]

As a part of this effort, the group investigated nitrogen mustard as a therapy for Hodgkin's lymphoma and other types of lymphoma and leukemia, and this compound was tried out on its first human patient in December 1942. The results of this study were not published until 1946, when they were declassified.[52] In a parallel track, after the air raid on Bari in December 1943, the doctors of the U.S. Army noted that white blood cell counts were reduced in their patients. Some years after World War II was over, the incident in Bari and the work of the Yale University group with nitrogen mustard converged, and this prompted a search for other similar chemical compounds. Due to its use in previous studies, the nitrogen mustard called "HN2" became the first cancer chemotherapy drug, mustine (also called chlormethine), to be used.

#### Disposal[edit | edit source]

File:Ambox current red Asia Australia.svg

This section needs to be updated. Please help update this article to reflect recent events or newly available information. (February 2022)

|

In the United States, storage and incineration of mustard gas and other chemical weapons were carried out by the U.S. Army Chemical Materials Agency.[53] Disposal projects at the two remaining American chemical weapons sites were carried out near Richmond, Kentucky, and Pueblo, Colorado. Although not yet declassified,[specify] toxicology specialists who dealt with the accidental puncturing of World War I gas stockpiles add that Air Force bases in Colorado have been made available to assist veterans of the 2003 American war with Iraq in which many Marines were exposed to gas as caches of up to 25,000 lb (11,000 kg).[citation needed] The United Nations definition of a weapon of mass destruction for mustard gas is 30,000 lb (14,000 kg), typically the Marines and other coalition allies discovered caches of 25,000 pounds (11,000 kg) located across a road from 5,000 pounds (2,300 kg) caches as multiple memoirs attest. These were discovered by the assistance of host country allies, or through leaks affecting personnel in an area with a weapon and gas cache called an ASP.

New detection techniques are being developed in order to detect the presence of mustard gas and its metabolites. The technology is portable and detects small quantities of the hazardous waste and its oxidized products, which are notorious for harming unsuspecting civilians. The immunochromatographic assay would eliminate the need for expensive, time-consuming lab tests and enable easy-to-read tests to protect civilians from sulfur-mustard dumping sites.[54]

In 1946, 10,000 drums of mustard gas (2,800 tonnes) stored at the production facility of Stormont Chemicals in Cornwall, Ontario, Canada, were loaded onto 187 boxcars for the 900 miles (1,400 km) journey to be buried at sea on board a 400 foot (120 m) long barge 40 miles (64 km) south of Sable Island, southeast of Halifax, at a depth of 600 fathoms (1,100 m). The dump location is 42 degrees, 50 minutes north by 60 degrees, 12 minutes west.[55]

A large British stockpile of old mustard agent that had been made and stored since World War I at M. S. Factory, Valley near Rhydymwyn in Flintshire, Wales, was destroyed in 1958.[56]

Most of the mustard gas found in Germany after World War II was dumped into the Baltic Sea. Between 1966 and 2002, fishermen have found about 700 chemical weapons in the region of Bornholm, most of which contain mustard gas. One of the more frequently dumped weapons was "Sprühbüchse 37" (SprüBü37, Spray Can 37, 1937 being the year of its fielding with the German Army). These weapons contain mustard gas mixed with a thickener, which gives it a tar-like viscosity. When the content of the SprüBü37 comes in contact with water, only the mustard gas in the outer layers of the lumps of viscous mustard hydrolyzes, leaving behind amber-colored residues that still contain most of the active mustard gas. On mechanically breaking these lumps (e.g., with the drag board of a fishing net or by the human hand) the enclosed mustard gas is still as active as it had been at the time the weapon was dumped. These lumps, when washed ashore, can be mistaken for amber, which can lead to severe health problems. Artillery shells containing mustard gas and other toxic ammunition from World War I (as well as conventional explosives) can still be found in France and Belgium. These were formerly disposed of by explosion undersea, but since the current environmental regulations prohibit this, the French government is building an automated factory to dispose of the accumulation of chemical shells.

In 1972, the U.S. Congress banned the practice of disposing of chemical weapons into the ocean by the United States. 29,000 tons of nerve and mustard agents had already been dumped into the ocean off the United States by the U.S. Army. According to a report created in 1998 by William Brankowitz, a deputy project manager in the U.S. Army Chemical Materials Agency, the army created at least 26 chemical weapons dumping sites in the ocean offshore from at least 11 states on both the East Coast and the West Coast (in Operation CHASE, Operation Geranium, etc.). In addition, due to poor recordkeeping, about one-half of the sites have only their rough locations known.[57]

In June 1997, India declared its stock of chemical weapons of 1,044 tonnes (1,151 short tons) of mustard gas.[58][59] By the end of 2006, India had destroyed more than 75 percent of its chemical weapons/material stockpile and was granted extension for destroying the remaining stocks by April 2009 and was expected to achieve 100 percent destruction within that time frame.[58] India informed the United Nations in May 2009 that it had destroyed its stockpile of chemical weapons in compliance with the international Chemical Weapons Convention. With this India has become the third country after South Korea and Albania to do so.[60][61] This was cross-checked by inspectors of the United Nations.

Producing or stockpiling mustard gas is prohibited by the Chemical Weapons Convention. When the convention entered force in 1997, the parties declared worldwide stockpiles of 17,440 tonnes of mustard gas. As of December 2015, 86% of these stockpiles had been destroyed.[62]

A significant portion of the United States' mustard agent stockpile was stored at the Edgewood Area of Aberdeen Proving Ground in Maryland. Approximately 1,621 tons of mustard agents were stored in one-ton containers on the base under heavy guard. A chemical neutralization plant was built on the proving ground and neutralized the last of this stockpile in February 2005. This stockpile had priority because of the potential for quick reduction of risk to the community. The nearest schools were fitted with overpressurization machinery to protect the students and faculty in the event of a catastrophic explosion and fire at the site. These projects, as well as planning, equipment, and training assistance, were provided to the surrounding community as a part of the Chemical Stockpile Emergency Preparedness Program (CSEPP), a joint program of the Army and the Federal Emergency Management Agency (FEMA).[63] Unexploded shells containing mustard gases and other chemical agents are still present in several test ranges in proximity to schools in the Edgewood area, but the smaller amounts of poison gas (4 to 14 pounds (1.8 to 6.4 kg)) present considerably lower risks. These remnants are being detected and excavated systematically for disposal. The U.S. Army Chemical Materials Agency oversaw disposal of several other chemical weapons stockpiles located across the United States in compliance with international chemical weapons treaties. These include the complete incineration of the chemical weapons stockpiled in Alabama, Arkansas, Indiana, and Oregon. Earlier, this agency had also completed destruction of the chemical weapons stockpile located on Johnston Atoll located south of Hawaii in the Pacific Ocean.[64] The largest mustard agent stockpile, at approximately 6,200 short tons, was stored at the Deseret Chemical Depot in northern Utah. The incineration of this stockpile began in 2006. In May 2011, the last of the mustard agents in the stockpile were incinerated at the Deseret Chemical Depot, and the last artillery shells containing mustard gas were incinerated in January 2012.

In 2008, many empty aerial bombs that contained mustard gas were found in an excavation at the Marrangaroo Army Base just west of Sydney, Australia.[65][66] In 2009, a mining survey near Chinchilla, Queensland, uncovered 144 105-millimeter howitzer shells, some containing "Mustard H", that had been buried by the U.S. Army during World War II.[66][67]

In 2014, a collection of 200 bombs was found near the Flemish villages of Passendale and Moorslede. The majority of the bombs were filled with mustard agents. The bombs were left over from the German army and were meant to be used in the Battle of Passchendale in World War I. It was the largest collection of chemical weapons ever found in Belgium.[68]

A large amount of chemical weapons, including mustard gas, was found in a neighborhood of Washington DC. The cleanup was completed in 2021.[69]

#### Post-war accidental exposure[edit | edit source]

In 2002, an archaeologist at the Presidio Trust archaeology lab in San Francisco was exposed to mustard gas, which had been dug up at the Presidio of San Francisco, a former military base.[70]

In 2010, a clamming boat pulled up some old artillery shells of World War I from the Atlantic Ocean south of Long Island, New York. Multiple fishermen suffered from blistering and respiratory irritation severe enough to require hospitalization.[71]

### WWII-era tests on men[edit | edit source]

File:Edgewood Arsenal - Mustard Gas Test Subjects March 1945.jpg

Mustard gas test subjects enter gas chamber, Edgewood Arsenal, March 1945

From 1943 to 1944, mustard agent experiments were performed on Australian service volunteers in tropical Queensland, Australia, by British Army and American experimenters, resulting in some severe injuries. One test site, the Brook Islands National Park, was chosen to simulate Pacific islands held by the Imperial Japanese Army.[72][73]

The United States tested sulfur mustards and other chemical agents including nitrogen mustards and lewisite on up to 60,000 servicemen during and after WWII. The experiments were classified secret and as with Agent Orange, claims for medical care and compensation were routinely denied, even after the WWII-era tests were declassified in 1993. The Department of Veterans Affairs stated that it would contact 4,000 surviving test subjects but failed to do so, eventually only contacting 600. Skin cancer, severe eczema, leukemia, and chronic breathing problems plagued the test subjects, some of whom were as young as 19 at the time of the tests, until their deaths, but even those who had previously filed claims with the VA went without compensation.[74]

File:Mustard gas four test subjects NRL.jpg

Arms of four test subjects after exposure to nitrogen mustard and lewisite agents.

African-American servicemen were tested alongside white men in separate trials to determine whether their skin color would afford them a degree of immunity to the agents, and Nisei servicemen, some of whom had joined after their release from Japanese American Internment Camps were tested to determine susceptibility of Japanese military personnel to these agents. These tests also included Puerto-Rican subjects.[75]

### Detection in biological fluids[edit | edit source]

Concentrations of thiodiglycol in urine have been used to confirm a diagnosis of chemical poisoning in hospitalized victims. The presence in urine of 1,1'-sulfonylbismethylthioethane (SBMTE), a conjugation product with glutathione, is considered a more specific marker, since this metabolite is not found in specimens from unexposed persons. In one case, intact mustard gas was detected in postmortem fluids and tissues of a man who died one week post-exposure.[76]

## See also[edit | edit source]

* Bis(chloromethyl) ether
* Blister agent
* Chlorine gas
* Half mustard
* Keen as Mustard
* Lewisite
* Nitrogen mustard
* Phosgene oxime
* Poison gas in World War I
* Rawalpindi experiments
* Selenium mustard
* Yellow Cross (chemical warfare)
* Mustard (condiment)

## References[edit | edit source]

1. ^ a b c d e FM 3–8 Chemical Reference handbook, US Army, 1967
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3. ^ "Pubchem".
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* Mustard gas (Sulphur Mustard) (IARC Summary & Evaluation, Supplement7, 1987). Inchem.org (1998-02-09). Retrieved on 2011-05-29.
* Institute of Medicine (1993). "History and Analysis of Mustard Agent and Lewisite Research Programs in the United States". Veterans at Risk: The Health Effects of Mustard Gas and Lewisite. ISBN 978-0-309-04832-3.
* "CDC - Facts About Sulfur Mustard". cdc.gov. Archived from the original on 2006-08-09.
* "NATO Presses New Libyan Leaders to Eliminate Mustard Agent - Global Security Newswire - NTI". NTI: Nuclear Threat Initiative.
6. ^ Salouti, Ramin; Ghazavi, Roghayeh; Rajabi, Sattar; Zare, Mohammad; Talebnejad, Mohammadreza; Abtahi, Mohammad Bagher; Parvizi, Maryam; Madani, Sedigheh; Asadi-Amoli, Fahimeh; Mirsharif, Ensieh-Sadat; Gharebaghi, Reza (2020). "Sulfur Mustard and Immunology; Trends of 20 Years Research in the Web of Science Core Collection: A Scientometric Review". Iranian Journal of Public Health. 49 (7): 1202–1210. doi:10.18502/ijph.v49i7.3573. ISSN 2251-6085. PMC 7548481. PMID 33083286.
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## External links[edit | edit source]

File:Commons-logo.svg

Wikimedia Commons has media related to Mustard gas.

* Textbook of Military Medicine – Intensive overview of mustard gas Includes many references to scientific literature
* Detailed information on physical effects and suggested treatments
* Iyriboz Y (2004). "A Recent Exposure to Mustard Gas in the United States: Clinical Findings of a Cohort (n = 247) 6 Years After Exposure". MedGenMed. 6 (4): 4. PMC 1480580. PMID 15775831. Shows photographs taken in 1996 showing people with mustard gas burns.
* An overview of the sulfur and nitrogen mustard agents (Caution: contains graphic images)
* Questions and Answers for Mustard Gas
* UMDNJ-Rutgers University CounterACT Research Center of Excellence A research center studying mustard gas, includes searchable reference library with many early references on mustard gas.
* Clayton, William; Howard, Alfred John; Thomson, David (25 May 1946). "Treatment of Mustard Gas Burns". British Medical Journal. 1 (4455): 797–799. doi:10.1136/bmj.1.4455.797. PMC 2058956. PMID 20786722.
* Nightmare in Bari
* surgical treatment of mustard gas burns
* UK Ministry of Defence Report on disposal of weapons at sea and incidents arising
* Rhydymwyn Valley History Society
* The advent of mustard gas in 1917, Simon Jones
* Measures to protect against mustard gas, 1917-1918, Simon Jones

* v
* t
* e

* Agents used in chemical warfare
* incapacitation
* riot control

Blood agents|

* Cyanogen
* Cyanogen bromide
* Cyanogen chloride (CK)
* Hydrogen cyanide (AC)
* Arsine
* Cacodyl cyanide
* Cacodyl oxide
* Hydrogen sulfide
* Phosphine
* Carbon monoxide
* Phosphorus trifluoride
* Methyl cyanoformate
* Iron pentacarbonyl
* Nickel tetracarbonyl
* 2,3,7,8-Tetrachlorodibenzodioxin
* Glycolonitrile
* Lactonitrile
* Acetone cyanohydrin
* Stibine

Blister agents|

| Arsenicals|

* Ethyldichloroarsine (ED)
* Methyldichloroarsine (MD)
* Phenyldichloroarsine (PD)
* Lewisite (L)
* Lewisite 2 (L2)
* Lewisite 3 (L3)

|

Sulfur mustards|

* Levinstein mustard (EA-229)
* T
* Q
* CEES

Nitrogen mustards|

* HN1
* HN2
* HN3

Other|

* KB-16
* Dibutylchloromethyltin chloride
* Selenium oxychloride

Nerve agents|

| G-agents|

* Tabun (GA)
* Sarin (GB)
* Chlorosarin (ClGB)
* Thiosarin (SGB)
* Soman (GD)
* Chlorosoman (ClGD)
* Ethylsarin (GE)
* GH
* Cyclosarin (GF)
* GP
* Fluorotabun
* EA-1356
* EA-4352
* Crotylsarin

|

V-agents|

* EA-2192
* EA-3148
* VE
* VG
* VM
* VP
* VR
* VS
* VX
* EA-1763
* Chinese VX
* V-sub x (GD-7)

GV agents|

* GV (EA-5365)

Novichok agents|

* A-208
* A-232
* A-234
* A-242
* A-262
* C01-A035
* C01-A039
* C01-A042

Carbamates|

* Dimethylcarbamoyl fluoride
* EA-3966
* EA-3990
* EA-4056
* T-1123
* T-1152
* Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide)
* TL-599
* TL-1238
* TL-1299
* TL-1317
* Miotine (AR-28/T-1843)

Other|

* Diisopropyl fluorophosphate
* EA-2012
* EA-2054
* EA-2098
* EA-2613
* 2-Ethoxycarbonyl-1-methylvinyl cyclohexyl methylphosphonate
* Neopentylene fluorophosphate
* Selenophos
* Phospholine
* R-16661
* Ro 3-0422
* Methanesulfonyl fluoride
* Dimefox (TL-792)

Precursors|

* Acetonitrile
* AT
* ATO
* A.P.C. complex
* Chlorosarin
* Chlorosoman
* Cyclohexanol
* 1,8-Dibromooctane
* N,N-Diisopropylaminoethanol (KB)
* EA-1250
* DIHP
* ZS
* DEHP
* EA-1224
* Dimethylamidophosphoric dichloride
* Dimethylamidophosphoric dicyanide
* DMHP
* Formaldoxime
* Nital
* 4-Hydroxycoumarin
* Isopropyl alcohol (TB)
* Methyldichlorophosphine (SW)
* Methylphosphonyl difluoride (difluoro) (DF)
* Methylphosphonyl dichloride (dichloro)
* Nitromethane
* OPA mixture
* Phosphoryl chloride
* Phosphorus pentachloride
* Phosphorus trichloride (TH)
* Pinacolone
* Pinacolyl alcohol
* Phenacyl chloride
* QL
* 2,4,5-Trichlorophenol
* 3,3,5-Trimethylcyclohexanol
* Triethyl phosphite
* Trimethyl phosphite
* TC
* TG

Neurotoxins|

* Anatoxin-a
* Saxitoxin (TZ)
* Bungarotoxin
* Botulinum toxin (BTX)
* Tetanospasmin (TeNT)
* Ryanodine
* Ciguatoxin (CTX)
* Guanitoxin (GTX)
* Chlorophenylsilatrane
* Palytoxin (PTX)
* Maitotoxin (MTX)
* Tetrodotoxin
* Aconitine
* Brevetoxin (PbTX)
* Strychnine
* Antillatoxin (ATX)
* Tetraethyllead
* Dimethylmercury
* HN1 hydrochloride
* HN2 hydrochloride
* HN3 hydrochloride
* A-8564
* Sulfuryl fluoride
* Tremorine
* Oxotremorine
* Batrachotoxin
* Tetramethylenedisulfotetramine (TETS)
* Bicyclic phosphates
* IPTBO
* TBPO
* TBPS
* Cloflubicyne
* Trimethylolpropane phosphite
* Domoic acid

Nettle agents|

* Phosgene oxime (CX)

Pulmonary/
choking agents|

* Chlorine
* Bromine
* Phosgene (CG)
* Fluorine
* Perfluoroisobutene
* Chloropicrin (PS)
* Dimethyl(trifluoromethylthio)arsine
* Diphosgene (DP)
* Disulfur decafluoride (Z)
* Acrolein
* Ethyl bromoacetate
* Perchloromethyl mercaptan
* Phenylcarbylamine chloride
* Tetranitromethane
* Tetrachlorodinitroethane
* Chlorine trifluoride
* Perchloryl fluoride
* Cadmium oxide
* Cadmium chloride
* Mercuric chloride
* Selenium dioxide
* Selenoyl fluoride
* Trifluoronitrosomethane
* Trichloronitrosomethane
* Nitric oxide
* Nitrogen dioxide
* Dinitrogen tetroxide
* Sulfur dioxide
* Phosphorus trichloride
* Methyl isocyanate
* Ethenone
* Methyl vinyl ketone
* Trifluoroacetyl chloride
* Salcomine
* Fluomine
* Uranium hexafluoride
* Diborane
* Green Cross

Vomiting agents|

* Adamsite (DM)
* Chloropicrin
* Diphenylchlorarsine
* Diphenylcyanoarsine
* Cacodyl cyanide
* o-Dianisidine

Incapacitating
agents|

* BZ (CS-4030)
* Apomorphine
* Butyrophenone
* EA-4941 (CS-4640)
* Etorphine
* EA-2092
* CS-4297
* Etoxadrol
* Dimethylheptylpyran (DMHP)
* EA-2148
* EA-3167
* EA-3443
* Pethidine
* EA-3580
* EA-3834
* Kolokol-1
* LSD-25
* PAVA spray
* Psilocybin
* Sleeping gas
* Carfentanil
* JB-318
* JB-336
* CS-27349
* CAR-226,086
* CAR-301,060
* CAR-302,196
* CAR-302,282
* CAR-302,668
* Benperidol
* Desflurane
* Enflurane
* Isoflurane
* Halothane
* Sevoflurane
* Pentazocine
* Procarbazine
* Fluphenazine
* Chlorpromazine

Lachrymatory
agents|

* Xylyl bromide
* Pepper spray (OC)
* Mace (spray)
* CN
* CS
* CR
* CNS
* Benzyl chloride
* Benzyl bromide
* Benzyl iodide
* Bromobenzyl cyanide
* Thiophosgene
* Chloroacetone
* Bromoacetone
* Bromomethyl ethyl ketone
* Acrolein
* Phenacyl bromide
* Chloroacetophenone oxime
* Ethyl bromoacetate
* Ethyl iodoacetate
* Iodoacetone
* Allyl isothiocyanate
* Hexamethylene diisocyanate
* Crotonaldehyde

Malodorant agents|

* Thioacetone
* Allicin
* Skatole
* Cadaverine
* Putrescine

Biological toxins|

* Abrin
* Aconitine
* Aflatoxins
* Anatoxin-a
* Batrachotoxin
* Botulinum toxin
* Brevetoxin
* Ciguatoxin
* Domoic acid
* Enterotoxin type B
* Guanitoxin
* Maitotoxin
* Modeccin
* Palytoxin
* Ricin
* Saxitoxin
* Shiga toxin
* T-2 mycotoxin
* Tetanospasmin
* Tetrodotoxin
* Volkensin

Other|

* Methyl fluoroacetate
* Napalm (variants and mixtures)
* Fluoroethyl fluoroacetate
* Depleted uranium
* post-combustion uranium oxides
* Plutonium and its compounds
* Polonium
* White phosphorus

* List of chemical warfare agents
* CB military symbol

* v
* t
* e

Sulfur mustards

Vesicants|

* Bromlost
* EA-5983
* Mustard gas
* O-Mustard
* p-(2-Chloroethylthio)phenyldichloroarsine
* Sesquimustard
* TL-258
* TL-293
* TL-767

Antineoplastic agents|

* S-46
* S-112
* S-150
* S-163
* S-169
* S-170
* S-172
* S-173
* S-179
* S-180
* S-182
* TL-1002

Other|

* 2-Chloroethyl ethyl sulfide
* Mustard chlorohydrin

* v
* t
* e

United States chemical weapons program

Units, formations,
centers and institutes|

* 2nd Chemical Battalion
* U.S. Army Chemical Corps
* U.S. Army Edgewood Chemical Biological Center
* U.S. Army Medical Research Institute of Chemical Defense (USAMRICD)
* U.S. Army Chemical Materials Activity
* Program Executive Office, Assembled Chemical Weapons Alternatives
* Chemical mortar battalion

Industrial facilities|

* Anniston Army Depot
* Anniston Chemical Activity
* Blue Grass Army Depot
* Deseret Chemical Depot
* Edgewood Chemical Activity
* Hawthorne Army Depot
* Johnston Atoll Chemical Agent Disposal System
* Newport Chemical Depot
* Pine Bluff Chemical Activity
* Pueblo Chemical Depot
* Tooele Chemical Agent Disposal Facility
* Umatilla Chemical Depot

Operations
and projects|

| Research|

* Edgewood Arsenal human experiments
* Operation Top Hat
* Project 112
* Project SHAD
* Operation LAC

|

Operational|

* Operation Ranch Hand

Disposal|

* Operation CHASE
* Operation Davy Jones' Locker
* Operation Geranium
* Operation Steel Box
* Operation Red Hat

Agents|

* 3-Quinuclidinyl benzilate (BZ)
* Chlorine
* Methylphosphonyl difluoride (DF)
* Phosgene
* QL
* Sarin (GB)
* Mustard gas (HD)
* VX

Munitions|

* BLU-80/B Bigeye bomb
* M1 chemical mine
* M104 155 mm projectile
* M110 155 mm projectile
* M121 155 mm projectile
* M125 bomblet
* M134 bomblet
* M138 bomblet
* M139 bomblet
* M2 mortar
* M23 chemical mine
* M34 cluster bomb
* M360 105 mm projectile
* M426 8-inch shell
* M43 BZ cluster bomb
* M44 generator cluster
* M55 rocket
* M60 105 mm projectile
* M687 155 mm projectile
* XM736 8-inch projectile
* MC-1 bomb
* M47 bomb
* Weteye bomb

Protective equipment|

* CAIS
* M93 Fox
* MOPP
* People sniffer
* M1135 NBCRV

Related topics|

* CB military symbol
* Dugway sheep incident
* Unethical human experimentation in the United States
* MKULTRA

*[CID]: Compound ID
*[H300]: H300: Fatal if swallowed
*[H310]: H310: Fatal in contact with skin
*[H315]: H315: Causes skin irritation
*[H319]: H319: Causes serious eye irritation
*[H330]: H330: Fatal if inhaled
*[H335]: H335: May cause respiratory irritation
*[P260]: P260: Do not breathe dust/fume/gas/mist/vapours/spray.
*[P261]: P261: Avoid breathing dust/fume/gas/mist/vapours/spray.
*[P262]: P262: Do not get in eyes, on skin, or on clothing.
*[P264]: P264: Wash ... thoroughly after handling.
*[P270]: P270: Do not eat, drink or smoke when using this product.
*[P271]: P271: Use only outdoors or in a well-ventilated area.
*[P280]: P280: Wear protective gloves/protective clothing/eye protection/face protection.
*[P284]: P284: Wear respiratory protection.
*[P301+P310]: P301+P310: IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
*[P302+P350]: P302+P350: IF ON SKIN: Gently wash with soap and water.
*[P302+P352]: P302+P352: IF ON SKIN: Wash with soap and water.
*[P304+P340]: P304+P340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
*[P305+P351+P338]: P305+P351+P338: IF IN EYES: Rinse continuously with water for several minutes. Remove contact lenses if present and easy to do. Continue rinsing.
*[P310]: P310: Immediately call a POISON CENTER or doctor/physician.
*[P312]: P312: Call a POISON CENTER or doctor/physician if you feel unwell.
*[P320]: P320: Specific treatment is urgent (see ... on this label).
*[P321]: P321: Specific treatment (see ... on this label).
*[P322]: P322: Specific measures (see ... on this label).
*[P330]: P330: Rinse mouth.
*[P332+P313]: P332+P313: If skin irritation occurs: Get medical advice/attention.
*[P337+P313]: P337+P313: Get medical advice/attention.
*[P361]: P361: Remove/Take off immediately all contaminated clothing.
*[P362]: P362: Take off contaminated clothing.
*[P363]: P363: Wash contaminated clothing before reuse.
*[P403+P233]: P403+P233: Store in a well ventilated place. Keep container tightly closed.
*[P405]: P405: Store locked up.
*[P501]: P501: Dispose of contents/container to ...
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