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Dimethyl methylphosphonate





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Dimethyl methylphosphonate is an organophosphorus compound with the chemical formula CH3PO(OCH3)2. It is a colourless liquid, which is primarily used as a flame retardant.

Dimethyl methylphosphonate
Names
Preferred IUPAC name

Dimethyl methylphosphonate

Other names
  • methylphosphonic acid dimethyl ester
  • dimethoxymethyl phosphine oxide
  • dimethyl methanephosphonate
  • dimethyl methyl phosphonate
  • Fran TF 2000
  • Fyron DMMP
  • Metaran
  • NSC 62240
  • O,O-dimethyl methylphosphonate
  • {[methoxy(methyl)phosphoryl]oxy}methane
  • Reoflam DMMP
  • Identifiers

    CAS Number

    3D model (JSmol)

    ChEMBL
    ChemSpider
    ECHA InfoCard 100.010.957 Edit this at Wikidata
    EC Number
    • 212-052-3

    PubChem CID

    UNII
    UN number 1993

    CompTox Dashboard (EPA)

    • InChI=1S/C3H9O3P/c1-5-7(3,4)6-2/h1-3H3 checkY

      Key: VONWDASPFIQPDY-UHFFFAOYSA-N checkY

    • InChI=1/C3H9O3P/c1-5-7(3,4)6-2/h1-3H3

      Key: VONWDASPFIQPDY-UHFFFAOYAG

    • O=P(OC)(OC)C

    Properties

    Chemical formula

    C3H9O3P
    Molar mass 124.076 g·mol−1
    Appearance colourless liquid
    Density 1.145 g/mL at 25 °C
    Melting point −50 °C (−58 °F; 223 K)
    Boiling point 181 °C (358 °F; 454 K)

    Solubility in water

    slowly hydrolyses
    Hazards[1]
    Occupational safety and health (OHS/OSH):

    Main hazards

    Toxic
    GHS labelling:

    Pictograms

    GHS07: Exclamation markGHS08: Health hazard

    Signal word

    Warning

    Hazard statements

    H319, H340, H361f

    Precautionary statements

    P201, P305+P351+P338, P308+P310
    Flash point 69 °C (156 °F; 342 K) closed cup
    Lethal dose or concentration (LD, LC):

    LD50 (median dose)

    • Oral (rat) 8,210 mg/kg
  • Inhalation (rat) 1h 20.13 mg/L
  • Dermal (rabbit) >2,000 mg/kg
  • Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    checkY verify (what is checkY☒N ?)

    Infobox references

    Synthesis

    edit

    Dimethyl methylphosphonate can be prepared from trimethyl phosphite and a halomethane (e.g. iodomethane) via the Michaelis–Arbuzov reaction.[2]

    Dimethyl methylphosphonate is a schedule 2 chemical as it may be used in the production of chemical weapons. It will react with thionyl chloride to produce methylphosphonic acid dichloride, which is used in the production of sarin and soman nerve agents. Various amines can be used to catalyse this process.[3] It can be used as a sarin-simulant for the calibration of organophosphorus detectors.

    Uses

    edit

    The primary commercial use of dimethyl methylphosphonate is as a flame retardant. Other commercial uses are a preignition additive for gasoline, anti-foaming agent, plasticizer, stabilizer, textile conditioner, antistatic agent, and an additive for solvents and low-temperature hydraulic fluids.[4] It can be used as a catalyst and a reagent in organic synthesis, as it can generate a highly reactive ylide. The yearly production in the United States varies between 100 and 1,000 short tons (91,000 and 907,000 kg).[citation needed]

    About 190 liters of dimethyl methylphosphonate, together with other chemicals, were released during the crash of El Al Flight 1862atBijlmerinAmsterdam in 1992.[5][6]

    References

    edit
    1. ^ "GESTIS-Stoffdatenbank". gestis.dguv.de.
  • ^ Jasiak, Aleksandra; Mielniczak, Grażyna; Owsianik, Krzysztof; Koprowski, Marek; Krasowska, Dorota; Drabowicz, Józef (2019). "Solvent-Free Michaelis–Arbuzov Rearrangement under Flow Conditions". The Journal of Organic Chemistry. 84 (5): 2619–2625. doi:10.1021/acs.joc.8b03053. PMID 30698971. S2CID 73412537.
  • ^ Maier, Ludwig (1990). "Organic Phosphorus Compounds 90.l A Convenient, One-Step Synthesis of Alkyl- and Arylphosphonyl Dichlorides". Phosphorus, Sulfur, and Silicon and the Related Elements. 47 (3–4): 465–470. doi:10.1080/10426509008038002.
  • ^ "Product Stewardship Summary Dimethyl methylphosphonate" (PDF). ashland.com. Ashland Global. Retrieved April 27, 2022.
  • ^ "Israel says El Al crash chemical 'non-toxic'". BBC. 2 October 1998. Archived from the original on 18 August 2003. Retrieved 2 July 2006.
  • ^ Greenberg, Joel (2 October 1998). "Nerve-Gas Element Was in El Al Plane Lost in 1992 Crash". The New York Times. Retrieved 11 October 2007.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Dimethyl_methylphosphonate&oldid=1177302802"
     



    Last edited on 27 September 2023, at 03:11  





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    This page was last edited on 27 September 2023, at 03:11 (UTC).

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