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Merck
CN

851493

Maltotriose hydrate

95%

Synonym(s):

O-α-D-Glucopyranosyl-(1→4)-O-α-D-glucopyranosyl-(1→4)-O-α-D-glucose

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About This Item

Empirical Formula (Hill Notation):
C18H32O16 · xH2O
CAS Number:
Molecular Weight:
504.44 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352201
EC Number:
214-174-2
MDL number:
Technical Service
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Quality Segment

assay

95%

form

crystals

optical activity

[α]24/D +162°, c = 2 in H2O

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

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


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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