CAS 37597-96-9

2-[(methylsulfonyl)sulfanyl]ethanaminium chloride

Description:

2-[(Methylsulfonyl)sulfanyl]ethanaminium chloride, with the CAS number 37597-96-9, is an organic compound characterized by its quaternary ammonium structure. It features a positively charged nitrogen atom bonded to an ethyl chain and a methylsulfonyl group, which contributes to its unique properties. This compound is typically soluble in water due to its ionic nature, making it useful in various applications, including as a surfactant or in biological systems. The presence of the sulfonyl group enhances its reactivity and potential interactions with other molecules. Additionally, the chloride ion serves as a counterion, stabilizing the overall structure. Its properties may include antimicrobial activity, which is common among quaternary ammonium compounds, and it may also exhibit surface-active characteristics. As with many chemical substances, safety data should be consulted to understand its handling and potential hazards. Overall, 2-[(methylsulfonyl)sulfanyl]ethanaminium chloride is a versatile compound with applications in both industrial and research settings.

Formula: C₃H₁₀ClNO₂S₂

InChI: InChI=1/C3H9NO2S2.ClH/c1-8(5,6)7-3-2-4;/h2-4H2,1H3;1H

SMILES: CS(=O)(=O)SCCN.Cl

2-Aminoethyl Methanethiosulfonate Hydrochloride

Controlled Product

CAS: 37597-96-9

Stability Moisture sensitive
Applications Reacts specifically and rapidly with thiols to form mixed disulfides. Used to probe the structures of the ACh receptor channel of the GABA receptor channel and of lactose permease. Useful for mapping the pore-lining regions of the ryanodine receptor.
References Xu, M. & Akabus, M.H.: J. Biol. Chem., 268, 21505 (1993), 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); Frillingos, S., & Kaback, H.R.: Biochem., 35, 3950 - 3956 (1996)

Formula: C₃H₉NO₂S₂·ClH

Color and Shape: Neat

Molecular weight: 191.7

Ref: TR-A609150