Supply solids levels and monohydrate dextrose productivity was written by Rahman, A. F. M. Mahbubar;Schenck, Fred W.. And the article was included in International Sugar Journal in 1999.Name: (2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate This article mentions the following:
Previously it was shown how the reconversion of the mother liquor stream from a monohydrate dextrose (I) crystallization process results in the nearly complete conversion of starch to crystalline I. To increase crystallizer productivity, the solids content of the crystallizer supply was increased from 76 to 79%, resulting in a 35% increase in crystallizer productivity with no noticeable change in product characteristics. While raising crystallizer productivity, the increase in solids also results in an increase in massecuite viscosity. Any increase in solids level must be done with caution to avoid crystallizer damage. In the experiment, the researchers used many compounds, for example, (2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate (cas: 14431-43-7Name: (2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate).
(2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate (cas: 14431-43-7) belongs to tetrahydropyran derivatives. Numerous natural products have tetrahydropyran skeleton as the building block for designing new natural products and their derivatives e.g. aplysiatoxins, avermectins, oscillatoxins, talaromycins, latrunculins and acutiphycins. The reaction of tertiary 1,4- and 1,5-diols with cerium ammonium nitrate at room temperature gives tetrahydrofuran and tetrahydropyran derivatives in high yield and stereoselectivity. Various fragrant compounds have been synthesized using this method.Name: (2S,3R,4S,5S,6R)-6-(Hydroxymethyl)tetrahydro-2H-pyran-2,3,4,5-tetraol hydrate
Referemce:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics