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  2. Methylphosphonyl dichloride - Wikipedia

    en.wikipedia.org/wiki/Methylphosphonyl_dichloride

    Methylphosphonyl dichloride (DC) or dichloro is an organophosphorus compound. It has commercial application in oligonucleotide synthesis, [1] but is most notable as being a precursor to several chemical weapons agents. It is a white crystalline solid that melts slightly above room temperature. [2]

  3. Methyldichlorophosphine - Wikipedia

    en.wikipedia.org/wiki/Methyldichlorophosphine

    Methyldichlorophosphine belongs to the group of halophosphines, some of which are used as intermediates in the production of plant protection agents, stabilizers for plastics, and catalysts.

  4. Dimethyl methylphosphonate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_methylphosphonate

    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.

  5. The best muscle pain relief creams of 2025, according to ...

    www.aol.com/lifestyle/best-muscle-pain-relief...

    Cost: $7 | Active ingredients: Lidocaine | Type: Cream | Amount: 4.3 ounces. Lidocaine is another popular ingredient found in pain relief creams. It's a topical anesthetic that's often used to ...

  6. Tolperisone - Wikipedia

    en.wikipedia.org/wiki/Tolperisone

    Tolperisone (trade name Mydocalm among others) is a centrally acting skeletal muscle relaxant used for the treatment of increased muscle tone associated with neurological diseases. It has been used since the 1960s. [1] [2]

  7. QL (chemical) - Wikipedia

    en.wikipedia.org/wiki/QL_(chemical)

    It, along with methylphosphonyl difluoride (DF), was developed during the 1980s in order to replace an aging stockpile of unitary chemical weapons. [3] QL is listed as a Schedule 1 chemical by the Chemical Weapons Convention .

  8. C01-A035 - Wikipedia

    en.wikipedia.org/wiki/C01-A035

    57 °C (135 °F; 330 K) [1] at 2 mmHg Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

  9. Dichlorophenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Dichlorophenylphosphine

    [1] [2] However, aluminum chloride often induces diarylation; a cleaner catalyst for monoarylation is stannic chloride. [2] The compound is an intermediate for the synthesis of other chemicals for instance dimethylphenylphosphine: C 6 H 5 PCl 2 + 2 CH 3 MgI → C 6 H 5 P(CH 3) 2 + 2 MgICl. Many tertiary phosphines can be prepared by this route. [3]

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