Monomers of Chitosan Oligosaccharide are made from crab shell, and obtained by enzymatic hydrolysis, chemical derivatization and column chromatography, the degree of polymerization is from 2 to 10.
Chitosan Oligosaccharide can be developing chitosan oligosaccharide’s applications in pharmaceuticals, foods, modern agriculture, feed, daily chemical industry and biochem ical reagents. They are reference substances in assay, analysis and quality control. They could also be applied in research fields of Carbohydrate Chemistry and Glycobiology, such as preparation of oligosaccharide microarray, the interaction between oligosaccharide and protein, and structure-activity relationship and mechanism of oligosaccharide-derived medicine.
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Chitosan Oligosaccharides
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Products
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Formula
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Cat. No.
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Chitosan Oligosaccharide Monomers
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Chitobiose 2HCl
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C12H24N2O9·2HCl
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DCJ0265A
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Chitotriose 3HCl
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C18H35N3O13·3HCl
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DCJ0267A
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Chitotetraose 4HCl
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C24H46N4O17·4HCl
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DCJ0268A
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Chitopentaose 5HCl
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C30H57N5O21·5HCl
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DCJ0269A
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Chitohexaose 6HCl
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C36H68N6O25·6HCl
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DCJ0266A
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Chitoheptaose 7HCl
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C42H79N7O29·7HCl
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DCJ0261A
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Chitooctaose 8HCl
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C48H90N8O33·8HCl
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DCJ0296A
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Chitononaose 9HCl
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C54H101N9O37·9HCl
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DCJ0297A
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Chitodecaose 10HCl
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C60H112N10O41·10HCl
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DCJ0298A
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Chito-Oligosaccharides(Dp3-7)
Hydrochloride
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(C6H13NO5·HCl)3-7
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DCJ0299A
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Acetylated Chitosan Oligosaccharide
Monomers
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Chitobiose Octaacetate
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C28H40N2O17
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DCJ0270A
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Chitotriose Undecaacetate
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C40H57N3O24
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DCJ0272A
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Chitotetraose Tetradecaacetate
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C52H74N4O31
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DCJ0273A
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Peracetylated Chitopentaose
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C64H91N5O38
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DCJ0274A
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Peracetylated Chitohexaose
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C76H108N6O45
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DCJ0271A
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Peracetylated Chitoheptaose
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C88H125N7O52
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DCJ0300A
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N, N'-Diacetyl Chitobiose
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C16H28N2O11
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DCJ0260A
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N,N',N''-Triacetyl Chitotriose
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C24H41N3O16
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DCJ0262A
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N,N',N'',N'''-Tetraacetyl Chitotetraose
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C32H54N4O21
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DCJ0263A
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N,N',N'',N''',N''''-Pentaacetyl
Chitopentaose
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C40H67N5O26
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DCJ0264A
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N,N',N'',N''',N'''',N'''''-Hexaacetyl
Chitohexaose
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C48H80N6O31
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DCJ0301A
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N,N',N'',N''',N'''',N''''',N''''''-Heptaacetyl
chitoheptaose
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C56H93N7O36
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DCJ0302A
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