Chemistry:Bitartrate
From HandWiki
Names | |
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Preferred IUPAC name | |
Other names | |
Identifiers | |
3D model (JSmol)
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3905887[3][2] | |
ChEBI | |
ChemSpider | |
PubChem CID
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Properties | |
C4H5O6− | |
Molar mass | 149.079 g·mol−1 |
Conjugate acid | Tartaric acid |
Conjugate base | Tartrate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Tracking categories (test):
Bitartrate is an anion which is the conjugate base of tartaric acid. It may also refer to any salt or monoester of tartaric acid.
Some examples of bitartrate salts include:
- Choline bitartrate
- Cysteamine bitartrate
- Dihydrocodeine bitartrate
- Dimethylaminoethanol bitartrate
- Hydrocodone bitartrate
- Metaraminol bitartrate
- Norepinephrine bitartrate
- Potassium bitartrate
- Sodium bitartrate
References
- ↑ 1.0 1.1 1.2 1.3 1.4 1.5 "3-Carboxy-2,3-dihydroxypropanoate | C4H5O6 | ChemSpider". http://www.chemspider.com/Chemical-Structure.2900154.html. Retrieved 27 January 2019.
- ↑ 2.0 2.1 2.2 2.3 2.4 2.5 "Hydrogen tartrate". https://pubchem.ncbi.nlm.nih.gov/compound/3667129#section=IUPAC-Name. Retrieved 27 January 2019.
- ↑ 3.0 3.1 3.2 3.3 3.4 "3-carboxy-2,3-dihydroxypropanoate (CHEBI:48929)". 25 June 2014. https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:48929. Retrieved 27 January 2019.
Original source: https://en.wikipedia.org/wiki/Bitartrate.
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