| -bitartrate.png.webp) | |
| Names | |
|---|---|
| IUPAC name N,N-Dimethylethanolamine (2R,3R)-bitartrate | |
| Systematic IUPAC name Dimethyl(2-hydroxyethyl)ammonium hydrogen 1,4-butanedioate | |
| Other names 
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| Identifiers | |
| 3D model (JSmol) | 
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| ChemSpider | |
| ECHA InfoCard | 100.025.281 | 
| EC Number | 
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| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
| 
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| 
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| Properties | |
| C8H17NO7 | |
| Molar mass | 239.224 g·mol−1 | 
| Appearance | White powder[4][2] or white crystals[5] | 
| Melting point | 111–113 °C (232–235 °F; 384–386 K)[4] | 
| Slightly[4] | |
| Solubility | Methanol (slightly, heated)[4] | 
| Structure | |
| Tetrahedral at the nitrogen atom | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
| Main hazards | Serious eye damage[1] | 
| GHS labelling: | |
|  | |
| Warning | |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P332, P337, P362+P364, P403+P233, P405, P501 | |
| Lethal dose or concentration (LD, LC): | |
| LD50 (median dose) | 
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| Related compounds | |
| Other cations | |
| Related compounds | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
N,N-Dimethylethanolamine bitartrate or deanol bitartrate is an organic compound with the chemical formula [HN(CH3)2CH2CH2OH]+HOOC−CH(OH)−CH(OH)−COO−. It is a white powder. Modern texts refer to the N,N-dimethylethanolamine salt of the natural form of tartaric acid, that is, the salt called N,N-dimethylethanolamine dextrobitartrate, N,N-dimethylethanolamine (2R,3R)-bitartrate or N,N-dimethylethanolamine L-(+)-bitartrate.
Chemistry
N,N-Dimethylethanolamine bitartrate is a N,N-dimethylethanolamine salt of tartaric acid. N,N-Dimethylethanolamine bitartrate contains tertiary ammonium cations (dimethyl(2-hydroxyethyl)ammonium [HN(CH3)2CH2CH2OH]+) and bitartrate anions (HOOC−CH(OH)−CH(OH)−COO−). Tertiary ammonium cation is a cation in which three hydrogen atoms of ammonium are replaced with organyl groups. In this compound, the three substituents of ammonium are two methyl groups (−CH3) and one 2-hydroxyethyl group (−CH2CH2OH). The bitartrate anion is chiral (there are left, right and meso forms of bitartrate, see tartaric acid).
Uses
N,N-Dimethylethanolamine bitartrate is used in biological studies to evaluate motor activity in response to the injection of N,N-dimethylethanolamine.[4]
