Sarin: Difference between revisions
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Sarin, also known | {{Chembox | ||
| Verifiedfields = changed | |||
| Watchedfields = changed | |||
| verifiedrevid = 415149010 | |||
| Name = Sarin | |||
| pronounce = {{IPAc-en|ˈ|s|ɑː|r|ɪ|n}} | |||
| ImageFile = Sarin-2D-by-AHRLS-2011.png | |||
| ImageClass = skin-invert-image | |||
| ImageFile1 = Sarin-3D-balls-by-AHRLS-2012.png | |||
| ImageName1 = ''S''-Sarin | |||
| PIN = Propan-2-yl methylphosphonofluoridate | |||
| SystematicName = | |||
| OtherNames = (''RS'')-''O''-Isopropyl methylphosphonofluoridate; IMPF;<br>GB;<br>2-(Fluoro-methylphosphoryl)oxypropane;<br>Phosphonofluoridic acid, ''P''-methyl-, 1-methylethyl ester<br>EA-1208<br>TL-1618<br>T-144 | |||
| IUPACName = | |||
| Section1 = {{Chembox Identifiers | |||
| ChemSpiderID = 7583 | |||
| InChI1 = 1/C4H10FO2P/c1-4(2)7-8(3,5)6/h4H,1-3H3 | |||
| InChIKey1 = DYAHQFWOVKZOOW-UHFFFAOYAY | |||
| ChEBI = 75701 | |||
| ChEMBL = 509554 | |||
| StdInChI = 1S/C4H10FO2P/c1-4(2)7-8(3,5)6/h4H,1-3H3 | |||
| StdInChIKey = DYAHQFWOVKZOOW-UHFFFAOYSA-N | |||
| CASNo = 107-44-8 | |||
| PubChem = 7871 | |||
| UNII = B4XG72QGFM | |||
| SMILES = FP(=O)(OC(C)C)C | |||
| InChI=1/C4H10FO2P/c1-4(2)7-8(3,5)6/h4H,1-3H3 | |||
}} | |||
| Section2 = {{Chembox Properties | |||
| C=4 | H=10 | F=1 | O=2 | P=1 | |||
| Appearance = Clear colourless liquid, brownish if impure | |||
| Odor = Odourless in pure form. Impure sarin can smell like mustard or burned rubber. | |||
| BoilingPtC = 158 | |||
| MeltingPtC = -56 | |||
| Solubility = Miscible | |||
| Density = 1.0887 g/cm<sup>3</sup> (25 °C)<br>1.102 g/cm<sup>3</sup> (20 °C) | |||
| LogP = 0.30 | |||
}} | |||
| Section3 = {{Chembox Hazards | |||
| ExternalSDS = Lethal Nerve Agent Sarin (GB) | |||
| LD50 = 39 μg/kg (intravenous, rat) | |||
| MainHazards = Extremely lethal [[cholinergic]] agent. | |||
| NFPA-H = 4 | |||
| NFPA-F = 1 | |||
| NFPA-R = 1 | |||
| IDLH = 0.1 mg/m<sup>3</sup> | |||
| TLV-STEL = 0.0001 mg/m<sup>3</sup> | |||
| TLV-TWA = 0.00003 mg/m<sup>3</sup> | |||
| FlashPtC = | |||
| GHSPictograms = {{GHS skull and crossbones}} | |||
| GHSSignalWord = | |||
}} | |||
| Section4 = | |||
| Section5 = | |||
| Section6 = | |||
}} | |||
'''Sarin''' (chemical name: ''propan-2-yl methylphosphonofluoridate''), also known by its NATO designation '''GB''' (denoting the ''G-series'' nerve agents), is a highly toxic, man-made compound classified as a nerve agent. It is considered a weapon of mass destruction (WMD) and is banned under the [[Chemical Weapons Convention]] (CWC) due to its extreme toxicity and lack of any practical civilian applications. Sarin is infamous for its use in warfare and terrorist attacks, posing a severe threat to public health and safety. | |||
== History == | == History == | ||
Sarin was first synthesized in 1938 by German scientists working on [[pesticides]]. Its potential as a chemical weapon was quickly recognized, and it became part of Nazi Germany's chemical weapons program during [[World War II]]. Although not deployed in combat during the war, its production and stockpiling laid the groundwork for its later use. | |||
In the post-war period, sarin became a key component of chemical weapons stockpiles in multiple countries, including the [[United States]] and the [[Soviet Union]]. Its most notorious uses include: | |||
* The [[Iran–Iraq War]] (1980–1988), where it was deployed by Iraqi forces. | |||
* The [[Tokyo subway sarin attack]] (1995), orchestrated by the Japanese doomsday cult [[Aum Shinrikyo]], killing 13 people and injuring thousands. | |||
== Chemical Structure and Mechanism of Action == | == Chemical Structure and Mechanism of Action == | ||
Sarin is a synthetic [[organophosphorus compound]] with the chemical formula (CH<sub>3</sub>)<sub>2</sub>CHOCH<sub>3</sub>P(O)F. It is a colorless, odorless liquid at room temperature that can rapidly vaporize into a gas, enabling it to disperse into the environment. This dual-phase nature makes it highly effective as a chemical weapon. | |||
Sarin | Sarin exerts its effects by inhibiting [[acetylcholinesterase]], an enzyme responsible for breaking down [[acetylcholine]], a neurotransmitter. By blocking this enzyme, sarin causes an accumulation of acetylcholine at neuromuscular junctions, leading to continuous stimulation of muscles and glands. This overstimulation manifests as severe cholinergic symptoms, eventually resulting in [[respiratory failure]] and death if untreated. | ||
== Symptoms of Exposure == | |||
Exposure to sarin, even in minute amounts, can cause a range of symptoms depending on the dose and method of exposure (inhalation, dermal contact, or ingestion). Symptoms progress rapidly and may include: | |||
== Symptoms | === Mild Symptoms === | ||
* Runny nose and watery eyes | |||
* Constriction of [[pupils]] ([[miosis]]) | |||
* Eye pain and blurred vision | |||
* Drooling and excessive [[sweating]] | |||
* [[Chest tightness]] and coughing | |||
* Nausea, vomiting, diarrhea, and abdominal pain | |||
Symptoms of | === Severe Symptoms === | ||
* [[Seizures]] | |||
* Loss of consciousness | |||
* Muscular [[paralysis]] | |||
* Respiratory failure due to paralysis of the [[diaphragm]] and other respiratory muscles | |||
* Death within minutes to hours if untreated | |||
== Treatment and Management == | == Treatment and Management == | ||
Immediate action is critical following sarin exposure to prevent death or permanent damage. Treatment involves: | |||
1. **Decontamination**: | |||
* Removing contaminated clothing. | |||
* Washing the skin thoroughly with soap and water to reduce absorption. | |||
* Using chemical decontaminants where available. | |||
2. **Medical Intervention**: | |||
* **[[Atropine]]**: Blocks the effects of excess acetylcholine at muscarinic receptors, alleviating many cholinergic symptoms. | |||
* **[[Pralidoxime]] (2-PAM)**: Reactivates acetylcholinesterase by cleaving the sarin-enzyme bond, especially if administered early. | |||
* **[[Benzodiazepines]]**: Used to control seizures and prevent brain damage. | |||
== Detection and Protection == | == Detection and Protection == | ||
Sarin detection requires specialized equipment capable of identifying trace levels of the agent in the environment. Military and emergency response units often use portable detectors or chemical sensors. | |||
**Personal Protection**: | |||
* [[Hazmat suits]] and [[gas masks]] are essential for individuals at risk of exposure, such as first responders and military personnel. | |||
* Protective measures must also be taken to prevent secondary contamination from exposed individuals or objects. | |||
== Impact on Public Health == | == Impact on Public Health == | ||
Sarin is a significant threat in scenarios of warfare or terrorism due to its rapid action and lethality. Even small amounts can cause mass casualties, overwhelming healthcare systems and creating long-lasting psychological and environmental impacts. Its use has spurred international treaties, such as the [[Chemical Weapons Convention]], which prohibits the production, stockpiling, and use of sarin and other chemical weapons. | |||
The | == Legacy and International Regulation == | ||
The [[Organisation for the Prohibition of Chemical Weapons]] (OPCW) oversees compliance with the Chemical Weapons Convention, working to eliminate stockpiles of sarin and similar agents. Despite these efforts, sarin remains a weapon of choice for rogue states and terrorist groups, necessitating ongoing vigilance and preparedness. | |||
== See Also == | == See Also == | ||
* [[Nerve agent]] | |||
* [[Nerve | |||
* [[Chemical warfare]] | * [[Chemical warfare]] | ||
* [[Organophosphates]] | |||
* [[Tokyo subway sarin attack]] | * [[Tokyo subway sarin attack]] | ||
* [[Chemical Weapons Convention]] | * [[Chemical Weapons Convention]] | ||
Revision as of 05:54, 19 January 2025
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| GHS Pictograms | [[File:|50px]] |
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| NFPA 704 | [[File:|50px]] |
| References | |
Sarin (chemical name: propan-2-yl methylphosphonofluoridate), also known by its NATO designation GB (denoting the G-series nerve agents), is a highly toxic, man-made compound classified as a nerve agent. It is considered a weapon of mass destruction (WMD) and is banned under the Chemical Weapons Convention (CWC) due to its extreme toxicity and lack of any practical civilian applications. Sarin is infamous for its use in warfare and terrorist attacks, posing a severe threat to public health and safety.
History
Sarin was first synthesized in 1938 by German scientists working on pesticides. Its potential as a chemical weapon was quickly recognized, and it became part of Nazi Germany's chemical weapons program during World War II. Although not deployed in combat during the war, its production and stockpiling laid the groundwork for its later use.
In the post-war period, sarin became a key component of chemical weapons stockpiles in multiple countries, including the United States and the Soviet Union. Its most notorious uses include:
- The Iran–Iraq War (1980–1988), where it was deployed by Iraqi forces.
- The Tokyo subway sarin attack (1995), orchestrated by the Japanese doomsday cult Aum Shinrikyo, killing 13 people and injuring thousands.
Chemical Structure and Mechanism of Action
Sarin is a synthetic organophosphorus compound with the chemical formula (CH3)2CHOCH3P(O)F. It is a colorless, odorless liquid at room temperature that can rapidly vaporize into a gas, enabling it to disperse into the environment. This dual-phase nature makes it highly effective as a chemical weapon.
Sarin exerts its effects by inhibiting acetylcholinesterase, an enzyme responsible for breaking down acetylcholine, a neurotransmitter. By blocking this enzyme, sarin causes an accumulation of acetylcholine at neuromuscular junctions, leading to continuous stimulation of muscles and glands. This overstimulation manifests as severe cholinergic symptoms, eventually resulting in respiratory failure and death if untreated.
Symptoms of Exposure
Exposure to sarin, even in minute amounts, can cause a range of symptoms depending on the dose and method of exposure (inhalation, dermal contact, or ingestion). Symptoms progress rapidly and may include:
Mild Symptoms
- Runny nose and watery eyes
- Constriction of pupils (miosis)
- Eye pain and blurred vision
- Drooling and excessive sweating
- Chest tightness and coughing
- Nausea, vomiting, diarrhea, and abdominal pain
Severe Symptoms
- Seizures
- Loss of consciousness
- Muscular paralysis
- Respiratory failure due to paralysis of the diaphragm and other respiratory muscles
- Death within minutes to hours if untreated
Treatment and Management
Immediate action is critical following sarin exposure to prevent death or permanent damage. Treatment involves:
1. **Decontamination**:
* Removing contaminated clothing. * Washing the skin thoroughly with soap and water to reduce absorption. * Using chemical decontaminants where available.
2. **Medical Intervention**:
* **Atropine**: Blocks the effects of excess acetylcholine at muscarinic receptors, alleviating many cholinergic symptoms. * **Pralidoxime (2-PAM)**: Reactivates acetylcholinesterase by cleaving the sarin-enzyme bond, especially if administered early. * **Benzodiazepines**: Used to control seizures and prevent brain damage.
Detection and Protection
Sarin detection requires specialized equipment capable of identifying trace levels of the agent in the environment. Military and emergency response units often use portable detectors or chemical sensors.
- Personal Protection**:
- Hazmat suits and gas masks are essential for individuals at risk of exposure, such as first responders and military personnel.
- Protective measures must also be taken to prevent secondary contamination from exposed individuals or objects.
Impact on Public Health
Sarin is a significant threat in scenarios of warfare or terrorism due to its rapid action and lethality. Even small amounts can cause mass casualties, overwhelming healthcare systems and creating long-lasting psychological and environmental impacts. Its use has spurred international treaties, such as the Chemical Weapons Convention, which prohibits the production, stockpiling, and use of sarin and other chemical weapons.
Legacy and International Regulation
The Organisation for the Prohibition of Chemical Weapons (OPCW) oversees compliance with the Chemical Weapons Convention, working to eliminate stockpiles of sarin and similar agents. Despite these efforts, sarin remains a weapon of choice for rogue states and terrorist groups, necessitating ongoing vigilance and preparedness.
See Also
References
<references />
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| Acetylcholine metabolism and transport modulators | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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| Fluorine compounds | ||||||||
|---|---|---|---|---|---|---|---|---|
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- Acetylcholinesterase inhibitors
- Chemical weapons of the United States
- Cold War weapons of the Soviet Union
- G-series nerve agents
- German chemical weapons program
- German inventions of the Nazi period
- Isopropyl esters
- Methylphosphonofluoridates
- Soviet chemical weapons program
- Substances discovered in the 1930s
- Toxicology
- United Kingdom chemical weapons program


