Metabolomics Structure Database
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MW REGNO: | 50215 |
Common Name: | Meso-tartaric acid |
Systematic Name: | (2R,3S)-2,3-dihydroxybutanedioic acid |
RefMet Name: | Meso-tartaric acid |
Synonyms: | (2R,3S)-2,3-dihydroxysuccinic acid; (2R,3S)-rel-2,3-dihydroxybutanedioic acid; (2R,3S)-tartaric acid; (R*,S*)-2,3-dihydroxybutanedioic acid; Mesoweinsaeure; erythraric acid; internally compensated tartaric acid; meso-tartaric acid; mesotartaric acid; unresolvable tartaric acid [PubChem Synonyms] |
Exact Mass: | |
Formula: | C4H6O6 |
InChIKey: | FEWJPZIEWOKRBE-XIXRPRMCSA-N |
ClassyFire superclass: | Organic oxygen compounds [C0004603] |
ClassyFire class: | Organooxygen compounds [C0000323] |
ClassyFire subclass: | Carbohydrates and carbohydrate conjugates [C0000011] |
ClassyFire direct parent: | Sugar acids and derivatives [C0000215] |
NP-MRD NMR spectra: | View NMR spectra |
SMILES: | [C@H]([C@H](C(=O)O)O)(C(=O)O)O |
Studies: | Available studies (via RefMet name) |
Select appropriate tab below to view additional details:
External database links:
PubChem CID: | 447315 |
CHEBI ID: | 15673 |
NP-MRD ID(NMR): | NP0002638 |
Calculated physicochemical properties (?):
Heavy Atoms: | 10 |
Rings: | 0 |
Aromatic Rings: | 0 |
Rotatable Bonds: | 3 |
van der Waals Molecular volume: | 125.22 Å3 molecule-1 |
Toplogical Polar Sufrace Area: | 115.06 Å2 molecule-1 |
Hydrogen Bond Donors: | 4 |
Hydrogen Bond Acceptors: | 6 |
logP: | -1.55 |
Molar Refractivity: | 28.31 |
Fraction sp3 Carbons: | 0.50 |
sp3 Carbons: | 2 |
References
LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200 ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y