A | B | C | D | E | F | G | H | CH | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z | 0 | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9
Names | |
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IUPAC name
N,N-Dimethylethanolamine (2R,3R)-bitartrate
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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
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UNII | |
CompTox Dashboard (EPA)
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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
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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
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Related compounds
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
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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]
References
- ^ a b c d e f g h i https://pubchem.ncbi.nlm.nih.gov/compound/Deanol-bitartrate
- ^ a b c https://www.sigmaaldrich.com/GB/en/sds/aldrich/39000
- ^ https://commonchemistry.cas.org/detail?cas_rn=5988-51-2
- ^ a b c d e f https://www.trc-canada.com/product-detail/?D471440
- ^ https://cymitquimica.com/cas/29870-28-8/
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