Soman.

Soman. Struktur
96-64-0
CAS-Nr.
96-64-0
Englisch Name:
Soman.
Synonyma:
Soman.;AGENTGD;GRXKLBBBQUKJJZ-UHFFFAOYSA-N;PINACOLYLMETHYLPHOSPHONOFLUORIDATE;O-PINACOLYLMETHYLPHOSPHONOFLUORIDATE;PINACOLYHEXYLMETHYLPHOSPHONOFLURIDATE;1,2,2-TRIMETHYLPROPYLESTER,PHOSPHONOFLUORIDATE;[fluoro(1,2,2-trimethylpropoxy)phosphoryl]methane;O-(1,2,2-TRIMETHYLPROPYL)-METHYLPHOSPHONOFLUORIDATE;3-(fluoro-methyl-phosphoryl)oxy-2,2-dimethyl-butane
CBNumber:
CB91252616
Summenformel:
C7H16FO2P
Molgewicht:
182.17
MOL-Datei:
96-64-0.mol

Soman. Eigenschaften

Schmelzpunkt:
-41.9°C
Siedepunkt:
182.5°C
Dichte
1.0222 g/cm3(Temp: 25 °C)
Aggregatzustand
liquid
EPA chemische Informationen
Phosphonofluoridic acid, methyl-, 1,2,2-trimethylpropyl ester (96-64-0)

Sicherheit

RIDADR  2810
HazardClass  6.1(a)
PackingGroup  I
Giftige Stoffe Daten 96-64-0(Hazardous Substances Data)
Toxizität LD50 in mice (mg/100 g): 0.062 i.p.; 0.78 dermally (Loomis, Salafsky)

Soman. Chemische Eigenschaften,Einsatz,Produktion Methoden

Beschreibung

Soman was first synthesized in 1944 by the German chemist Richard Kuhn. It was the third of a family of related organophosphate or organophosphorus (OP) compounds that were developed for use as chemical warfare agents during World War II (tabun (GA) and sarin (GB) were developed several years earlier). Unlike tabun and sarin, soman was not produced in large quantities or loaded into munitions during World War II due to its late discovery and difficulties associated with scaling up the manufacturing process. After the war, other nations including the United States, United Kingdom, and former Soviet Union were also quick to realize the weaponization potential of OP nerve agents and establish research and development programs of their own. Soman was never mass produced by the United States due to the difficulty and cost of large-scale production as well as concerns over the lack of effective antidotes (compared to tabun and sarin). However, it was manufactured in large quantities and loaded into munitions by the former Soviet Union beginning in the 1960s. In the 1990s, the production, stockpiling, and use of chemical weapons (including soman) by nations were banned by the Chemical Weapons Convention (CWC), an international agreement that entered into force in 1997. The CWC is implemented by the Organisation for the Prohibition of Chemical Weapons (OPCW) and requires the destruction of existing chemical weapons stockpiles. Nearly all of the nations in the world are members of the OPCW, and destruction of existing chemical weapons stockpiles was ongoing at the time of this writing in 2012.

Chemische Eigenschaften

Colorless liquid. Evolves odorless gas.

Verwenden

Chemical warfare agent.

Allgemeine Beschreibung

Colorless liquid, odorless to fruity.

Air & Water Reaktionen

Hydrolyzed by water, rapidly hydrolyzed by dilute aqueous sodium hydroxide. Water alone removes Fluoride atom producing nontoxic acid.

Reaktivität anzeigen

Acidic conditions produce hydrogen fluoride; alkaline conditions produce isopropyl alcohol and polymers. When heated to decomposition or reacted with steam, Soman. emits very toxic fumes of fluorides and oxides of phosphorus. Slightly corrosive to steel. Hydrolyzed by water.

Hazard

Highly toxic by ingestion, inhalation, and skin absorption; may be fatal on short exposure; cholinesterase inhibitor; military nerve gas; fatal dose (man) 0.01 mg/kg.

Health Hazard

Median lethal dose (mg-min/m3): 2500 by skin (vapor) or 350 (liquid); 35 inhaled. Median incapacitating dose: 25 inhaled. Eye/skin toxicity: Very high. Rate of action: Very rapid. Physiological action: Cessation of breath-death may follow. Detoxification rate: Low, essentially cumulative. (ANSER)

mögliche Exposition

Agent GD, an organic fluoride compound, is a quick-acting chemical warfare nerve agent (nerve gas). Medical treatment of soman is difficult because it permanently binds to receptors in the body in minutes. Large amounts of the vapor or liquid can hurt you in minutes, and can quickly lead to death.

Versand/Shipping

UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poison Inhalation Hazard, Technical Name Required. Military driver shall be given full and complete information regarding shipment and conditions in case of emergency. AR 50-6 deals specifically with the shipment of chemical agents. Shipments of agent will be escorted in accordance with AR 740-32

Inkompatibilitäten

Hydrolyzed by water to form hydrogen fluoride and the nontoxic phosphonic acid derivative. It is rapidly hydrolyzed by dilute aqueous NaOH Stable after storage in steel for 3 months @ 65 C. Raising the pH increases the rate of decomposition significantly. GD decomposes slowly in water; will hydrolyze to form HF-H-H-O-CH3 and (CH3)3-C-C-O-P-OH. GD reacts readily with bases and weak acids. Under acid conditions, GD hydrolyzes, forming hydrofluoric acid (HF). Flammable hydrogen gas produced by the corrosive vapors reacting with metals, concrete, etc., may be present. Corrosive to steel and possibly other ferrous metals. GD corrodes steel at the rate of 1×10-5 in/month. When heated to decomposition or on contact with steam, it emits very toxic fumes of fluorides and oxides of phosphorus.

Soman. Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

96-64-0()Verwandte Suche:


  • Soman.
  • 3-(fluoro-methyl-phosphoryl)oxy-2,2-dimethyl-butane
  • PINACOLYLMETHYLPHOSPHONOFLUORIDATE
  • 1,2,2-TRIMETHYLPROPYLESTER,PHOSPHONOFLUORIDATE
  • PINACOLYHEXYLMETHYLPHOSPHONOFLURIDATE
  • O-(1,2,2-TRIMETHYLPROPYL)-METHYLPHOSPHONOFLUORIDATE
  • AGENTGD
  • Soman: (3,3-Dimethyl-2-butanol methylphosphonofluoridate, GD)
  • Methyl(fluoro)phosphinic acid 1,2,2-trimethylpropyl ester
  • Methylfluoridophosphonic acid 1,2,2-trimethylpropyl ester
  • Methylfluorophosphinic acid (1,2,2-trimethylpropyl) ester
  • Methylfluorophosphinic acid 1,2,2-trimethylpropyl ester
  • Methylphosphonofluoridic acid 1,2,2-trimethylpropyl
  • O-PINACOLYLMETHYLPHOSPHONOFLUORIDATE
  • [fluoro(1,2,2-trimethylpropoxy)phosphoryl]methane
  • GRXKLBBBQUKJJZ-UHFFFAOYSA-N
  • Phosphonofluoridic acid, P-methyl-, 1,2,2-trimethylpropyl ester
  • 96-64-0
  • C7H16FO2P
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