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(+)-Dibenzoyl-D-tartaric acid, anhydrous, 99%
(+)-Dibenzoyl-D-tartaric acid, anhydrous, 99%
(+)-Dibenzoyl-D-tartaric acid, anhydrous, 99%
Thermo Scientific Chemicals

(+)-Dibenzoyl-D-tartaric acid, anhydrous, 99%

CAS: 17026-42-5 | C18H14O8 | 358.30 g/mol
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Catalog number B24754.18
also known as B24754-18
Price (USD)
86.65
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Quantity:
50 g
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Price (USD)
86.65
Online Exclusive
95.60
Save 8.95 (9%)
Each
Chemical Identifiers
CAS17026-42-5
IUPAC Name(2S,3S)-2,3-bis(benzoyloxy)butanedioic acid
Molecular FormulaC18H14O8
InChI KeyYONLFQNRGZXBBF-ZCWZLOQUNA-N
SMILESOC(=O)[C@@H](OC(=O)C1=CC=CC=C1)[C@H](OC(=O)C1=CC=CC=C1)C(O)=O
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SpecificationsSpecification SheetSpecification Sheet
Assay (unspecified)Aqueous acid-base Titration OR HPLC
Assay (HPLC)>98.5%
Optical Rotation+120 ? 3? (c=5 in methanol)
Appearance (Color)White
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For chiral resolution(+)-Dibenzoyl-D-tartaric acid is used as a reagent in the preparation of chiral salts. It also serves as a reagent for chiral resolution of amino compounds.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
For chiral resolution(+)-Dibenzoyl-D-tartaric acid is used as a reagent in the preparation of chiral salts. It also serves as a reagent for chiral resolution of amino compounds.

Solubility
Soluble in ethanol. Insoluble in water.

Notes
Hygroscopic. Store in a cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Kolanos, R.; Partilla, J. S.; Baumann, M. H.; Hutsell, B. A.; Banks, M. L.; Negus, S. S.; Glennon, R. A. Stereoselective Actions of Methylenedioxypyrovalerone (MDPV) To Inhibit Dopamine and Norepinephrine Transporters and Facilitate Intracranial Self-Stimulation in Rats. ACS Chem. Neurosci. 2015, 6 (5), 771-777.
  2. Periasamy, M.; Edukondalu, A.; Reddy, P. O. Synthesis of Chiral 2,3-Disubstituted 1,4-Diazabicyclo[2.2.2]octane Derivatives. J. Org. Chem. 2015, 80 (7), 3651-3655.