Pentaacetyl-α- D -glucose
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Pentaacetyl-α- D -glucose | |||||||||||||||
other names |
1,2,3,4,6- penta- O- acetyl-α- D -glucopyranose |
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Molecular formula | C 16 H 22 O 11 | |||||||||||||||
External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 390.34 g mol −1 | |||||||||||||||
Melting point |
109-111 ° C |
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Refractive index |
≥ + 98 ° (c = 1 in ethanol) |
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safety instructions | ||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
Pentaacetyl-α- D -glucose (also α- D - (+) - glucose pentaacetate ) is a chemical compound from the group of monosaccharides . It is produced from anhydrous α- D - (+) - glucose in acetic anhydride in the presence of zinc chloride . On the human tongue, α- D - (+) - glucose pentaacetate produces a bitter taste . α- D - (+) - glucose pentaacetate increases the secretion of insulin in beta cells .
literature
- WJ Malaisse: Insulin release: the receptor hypothesis. In: Diabetologia . Volume 57, Number 7, July 2014, pp. 1287-1290, doi: 10.1007 / s00125-014-3221-0 . PMID 24700279 .
Individual evidence
- ↑ a b c Data sheet α-D (+) - Glucose pentaacetate, 99% from Sigma-Aldrich , accessed on July 4, 2019 ( PDF ).
- ^ Addison Ault: Techniques and Experiments For Organic Chemistry. 1998, ISBN 0-935702-76-8 , p. 433.
- ↑ a b Itaru Kojima: Glucose-sensing Receptor in Pancreatic Beta-Cells. 2018, ISBN 978-981-1300-01-1 , p. 14.