N -methyl- D -glucamine
Structural formula | |||||||||||||||||||
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Structural formula in the Fischer projection | |||||||||||||||||||
General | |||||||||||||||||||
Surname | N -methyl- D -glucamine | ||||||||||||||||||
other names |
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Molecular formula | C 7 H 17 NO 5 | ||||||||||||||||||
Brief description |
white, odorless solid |
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External identifiers / databases | |||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 195.22 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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Melting point |
128-131 ° C |
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boiling point |
210 ° C (decomposition) |
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solubility |
easily soluble in water: 1000 g l −1 (25 ° C) |
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safety instructions | |||||||||||||||||||
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Toxicological data | |||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
N -methyl- D -glucamine (abbreviation NMDG or NMG , also meglumine ) is a chemical compound thatis derivedfrom D - glucose . Instead of the aldehyde oxygen in glucose, it carries a methylamino group. The amine has a basic reaction, so the nitrogen is able to take up a proton . As a result, N -methyl- D -glucamine is partially positively charged in aqueous solution.
In electrophysiology , N -methyl- D -glucamine is used as a substitute for sodium ions (Na + ). NMDG is characterized by osmotic activity that is similar to that of sodium ions. Cell membranes are impermeable to NMDG. NMDG is also used as a sodium substitute in culture media , for example when the cultured cells are sensitive to Na + ions.
Individual evidence
- ↑ Entry on METHYLGLUCAMINE in the CosIng database of the EU Commission, accessed on May 19, 2020.
- ↑ a b c d e f g Data sheet N-Methyl-D-glucamine (PDF) from Merck , accessed on December 25, 2019.