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CAS 91774-25-3

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Ethanaminium,N,N,N-trimethyl-2-[(methylsulfonyl)thio]-, bromide (1:1)

Description:
Ethanaminium, N,N,N-trimethyl-2-[(methylsulfonyl)thio]-, bromide (1:1), with CAS number 91774-25-3, is a quaternary ammonium compound characterized by its cationic nature due to the presence of a positively charged nitrogen atom. This compound features a trimethylated amine structure, which contributes to its solubility in polar solvents, and a methylsulfonylthio group that enhances its reactivity and potential applications in various chemical processes. The bromide ion serves as a counterion, stabilizing the cationic form of the molecule. Typically, quaternary ammonium compounds exhibit surfactant properties, making them useful in formulations for disinfectants, emulsifiers, and phase transfer catalysts. Additionally, the presence of the methylsulfonylthio group may impart unique biological activities, potentially influencing its use in pharmaceuticals or agrochemicals. Overall, this compound's characteristics suggest versatility in both industrial and research applications, particularly in fields requiring cationic agents.
Formula:C6H16NO2S2·Br
Synonyms:
  • (2-Mercaptoethyl)trimethylammoniumbromide, methanesulfonate (7CI)
  • Ethanaminium, N,N,N-trimethyl-2-[(methylsulfonyl)thio]-,bromide (9CI)
  • 2-(Trimethylammonium)ethyl methanethiosulfonate bromide
  • Mtset
  • Methanethiosulfonate ethyltrimethylammonium bromide
  • N,N,N-trimethyl-2-[(methylsulfonyl)thio]-ethanaminium Bromide
  • (2-Mercaptoethyl)trimethylammonium Bromide Methanesulfonate
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Found 2 products.
  • [2-(TRIMETHYLAMMONIUM)ETHYL] METHANETHIOSULFONATE BROMIDE

    CAS:
    Formula:C6H16BrNO2S2
    Purity:%
    Color and Shape:Solid
    Molecular weight:278.2307

    Ref: IN-DA00GW4O

    50mg
    212.00€
  • [2-(Trimethylammonium)ethyl]methanethiosulfonate Bromide

    Controlled Product
    CAS:
    <p>Applications Reacts specifically and rapidly with thiols to form mixed disulfides. Used to probe the structures of the ACh receptor channel of the GABAA receptor channel and of lactose permease.<br>References Duhten, R.L., et al.: Biochemistry, 32, 3139 (1993), Yang, N. et al.: Neuron, 16, 113 (1996), Kuner, T. et al.: Neuron, 17, 343 (1996), Holmgren, M. et al: Neuropharmacology, 35, 797 (1996), Chahine, M. et al.: Biochemical &amp; Biophysical Res. Commun., 233, 606 (1997), Ehrlich, B.E., et al.: J. Gen. Physiol., 109, 255 (1997), Rassendren, F., et al.: The EMBO Journal, 16, 3446 (1997), Vedantham, V. and Cannon, C.C.: J. Gen. Physiol., 111, 83 (1998), Lin, C.-W. and Tsung-Yu, C.: J. Gen. Physiol., 116, 535 (2000), Sullivan, D.A. and cohen, J.B.: J. B.C., 275, 17, 12651 (2000)<br></p>
    Formula:C6H16NO2S2·Br
    Color and Shape:White To Off-White
    Molecular weight:278.23

    Ref: TR-T795900

    250mg
    247.00€
    2500mg
    1,669.00€