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Flag Counter
  2. World Encyclopedia
  3. Bitartrate - Wikipedia
Bitartrate - Wikipedia
From Wikipedia, the free encyclopedia
Bitartrate anion
Names
Preferred IUPAC name
3-Carboxy-2,3-dihydroxypropanoate[3][1]
Other names
  • Bitartrate
  • Butanedioic acid, 2,3-dihydroxy-, ion(1−)
  • 3-Carboxylato-2,3-dihydroxypropionic acid
  • Hydrogen tartrate
  • 2,3,4-Trihydroxy-4-oxobutanoate
  • 2,3,4-Trihydroxy-4-oxobutyric acidanion[1][2]
Identifiers
3D model (JSmol)
3905887[3][2]
ChEBI
ChemSpider
  • InChI=1S/C4H6O6/c5-1(3(7)8)2(6)4(9)10/h1-2,5-6H,(H,7,8)(H,9,10)/p-1
    Key: FEWJPZIEWOKRBE-UHFFFAOYSA-M
  • [3]: OC(C(O)C([O-])=O)C(O)=O
  • [1][2]: C(C(C(=O)[O-])O)(C(=O)O)O
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).

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:

References

  1. ^ a b c d e f "3-Carboxy-2,3-dihydroxypropanoate | C4H5O6 | ChemSpider". www.chemspider.com. Retrieved 27 January 2019.
  2. ^ a b c d e f "Hydrogen tartrate". pubchem.ncbi.nlm.nih.gov. Retrieved 27 January 2019.
  3. ^ a b c d e "3-carboxy-2,3-dihydroxypropanoate (CHEBI:48929)". www.ebi.ac.uk. 25 June 2014. Retrieved 27 January 2019.
Sunting pranala
url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url url 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