13264-95-4

Basic information

• Product Name: 6-A-D-GLUCOPYRANOSYLMALTOTRIOSE
• Synonyms: 6-A-D-GLUCOPYRANOSYLMALTOTRIOSE;Glc1-a-6Glc1-a-4Glc1-a-4Glc,4-O-[4-O-(6-O-a-D-Glucopyranosyl-a-D-glucopyranosyl)-a-D-glucopyranosyl]-D-glucose;6-O-(a-D-Maltotriosyl)-D-glucopyranose;6-α-D-Glucopyranosylmaltotriose;Glc1-α-6Glc1-α-4Glc1-α-4Glc, 4-O-[4-O-(6-O-α-D-Glucopyranosyl-α-D-glucopyranosyl)-α-D-glucopyranosyl]-D-glucose;4-O-[4-O-(6-O-a-D-Glucopyranosyl-a-D-glucopyranosyl)-a-D-glucopyranosyl]-D-glucose;Glc1-a-6Glc1-a-4Glc1-a-4Glc;6-Alpha-D-GlucopyranosylMaltotriose
• CAS NO: 13264-95-4
• Molecular Formula: C24H42O21
• Molecular Weight: 666.575
• Product Categories: Oligosaccharide Compounds;Carbohydrates & Derivatives;Oligosaccharides
• Mol File: 13264-95-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Refractive Index: 1.687
• CAS DataBase Reference: 6-A-D-GLUCOPYRANOSYLMALTOTRIOSE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-A-D-GLUCOPYRANOSYLMALTOTRIOSE(13264-95-4)
• EPA Substance Registry System: 6-A-D-GLUCOPYRANOSYLMALTOTRIOSE(13264-95-4)

Safety Data

• Hazardous Substances Data: 13264-95-4(Hazardous Substances Data)

Usage

Chemical Properties

Foam-Like White Solid

InChI:InChI=1/C24H42O21/c25-1-5-9(28)12(31)16(35)23(41-5)44-20-7(3-27)43-24(18(37)14(20)33)45-19-6(2-26)42-22(17(36)13(19)32)39-4-8-10(29)11(30)15(34)21(38)40-8/h5-38H,1-4H2/t5?,6?,7?,8?,9-,10-,11?,12?,13?,14?,15+,16+,17+,18+,19-,20-,21-,22+,23-,24-/m1/s1

Relevant articles and documents

Synthesis of Glucose-Containing Linear Oligosaccharides Having α(1->4) and α(1->6) Linkages Using Stereoselective Dehydrative Glycosylation

Glycogen-storage-disease-relating linear tetra-, hexa-, and octasaccharides of D-glucose having α(1->4) and α(1->6) linkages were synthesized using a stereoselective dehydrative glycosylation with a reagent mixture of p-nitrobenzenesulfonyl chloride, silver trifluoromethanesulfonate, N,N-dimethylacetamide, and triethylamine.A cross-condensation of a quasi-stoichiometric amount of a donor and an acceptor of an octasaccheride, followed by deprotection, afforded a glucohexadecasaccharide.