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An ortho­rhom­bic polymorph of 2-(1,3,5-di­thia­zinan-5-yl)ethanol or MEA-di­thia­zine

Substituted triazines are a class of compounds utilized for scavenging and sequestering hydrogen sulfide in oil and gas production operations. The reaction of one of these triazines under field conditions resulted in the formation of the title compound, 2-(1,3,5-di­thia­zinan-5-yl)ethanol, C(5)H(11)...

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Detalles Bibliográficos
Autores principales: Schultheiss, Nate, Holtsclaw, Jeremy, Zeller, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819450/
https://www.ncbi.nlm.nih.gov/pubmed/35145749
http://dx.doi.org/10.1107/S2056989022000342
Descripción
Sumario:Substituted triazines are a class of compounds utilized for scavenging and sequestering hydrogen sulfide in oil and gas production operations. The reaction of one of these triazines under field conditions resulted in the formation of the title compound, 2-(1,3,5-di­thia­zinan-5-yl)ethanol, C(5)H(11)NOS(2), or MEA-di­thia­zine. Polymorphic form I, in space group I4(1)/a, was first reported in 2004 and its extended structure displays one-dimensional, helical strands connected through O—H⋯O hydrogen bonds. We describe here the form II polymorph of the title compound, which crystallizes in the ortho­rhom­bic space group Pbca as centrosymmetric dimers through pairwise O—H⋯N hydrogen bonds from the hydroxyl moiety to the nitro­gen atom of an adjacent mol­ecule.