General description
Maltotriose is an oligosaccharide with α-1,4 glycoside linkage. It does not possess any ionic groups, hence is suitable for examining the interaction between molecular motion and water molecules.
Application
Maltotriaose hydrate can be used:
- for sensitive analysis of simple sugars
- to study heat capacities for sugars and sugar alcohols in dilute aqueous solution by calorimetry
- as an internal standard in the analysis of sugar levels, during fermentation process in wort samples using HPLC and spectrophotometry
Molecular Weight: 504.44 (anhydrous basis). Empirical Formula: C
18H
32O
16 · xH
2O. Quality Level: 100. Assay: 95%. form: crystals. optical activity: [α. ]24/D +162°, c : . 2 in H
2O. mp: 132-135 . °C (lit.). SMILES string: [H]O[H].OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O[C@@H]2CO)O[C@H]3[C@H](O)[C@@H](O)C(O)O[C@@H]3CO)[C@H](O)[C@@H](O)[C@@H]1O. InChI: 1S/C18H32O16.H2O/c19-1-4-7(22)8(23)12(27)17(31-4)34-15-6(3-21)32-18(13(28)10(15)25)33-14-5(2-20)30-16(29)11(26)9(14)24. /h4-29H,1-3H2. 1H2/t4-,5-,6-,7-,8+,9-,10-,11-,12-,13-,14-,15-,16?,17-,18-. /m1./s1. InChI key: HNKASWRMLBJLKJ-HNNWOXMSSA-N. Storage Class Code: 11 - Combustible Solids. WGK: WGK 3. Flash Point(F): Not applicable. Flash Point(C): Not applicable. Personal Protective Equipment: Eyeshields, Gloves, type N95 (US).