Yang, Fei published the artcilePerformances comparison of enantiomeric separation materials prepared from shrimp and crab shells, Quality Control of 161796-78-7, the publication is Carbohydrate Polymers (2019), 238-246, database is CAplus and MEDLINE.
Previously reported studies demonstrate that many chitin/chitosan derivatives are promising for enantioseparation of chiral compounds The aim of the present study is to study influence of the chitin sources on performances of the chitosan type enantiomeric separation materials. Therefore, the chitosans were prepared from crab and shrimp shells, from which two sets of chiral selector, i.e. chitosan bis(3,5-dimethylphenylcarbamate)-(octanamide)s and chitosan bis(3,5-dichlorophenylcarbamate)-(octanamide)s were synthesized. The chitosan bis(3,5-dimethylphenylcarbamate)-(octanamide)s, resp., derived from crab and shrimp shells were close in swelling capacity and enantioseparation capability, and the same feature was found for the other two chiral selectors of chitosan bis(3,5-dichlorophenylcarbamate)-(octanamide). However, although most of the chiral analytes were eluted out in the same elution order, there were two analytes were in reversed elution orders when separated by the two chiral stationary phases of chitosan bis(3,5-dichlorophenylcarbamate)-(octanamide). Based on the observed results, enantiomeric separation materials may be developed either with shrimp chitin or crab chitin, depending on the source accessibility.
Carbohydrate Polymers published new progress about 161796-78-7. 161796-78-7 belongs to imidazoles-derivatives, auxiliary class Membrane Transporter/Ion Channel,Proton Pump, name is Sodium (S)-6-methoxy-2-(((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)sulfinyl)benzo[d]imidazol-1-ide, and the molecular formula is C8H11NO, Quality Control of 161796-78-7.
Referemce:
https://en.wikipedia.org/wiki/Imidazole,
Imidazole | C3H4N2 – PubChem