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(+)-Dibenzoyl-D-tartaric acid monohydrate, 99%, Thermo Scientific Chemicals
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Catalog number A16503.14
also known as A16503-14
Price (USD)/ Each
53.10
-
Quantity:
25 g
Price (USD)/ Each
53.10
(+)-Dibenzoyl-D-tartaric acid monohydrate, 99%, Thermo Scientific Chemicals
Catalog numberA16503.14
Price (USD)/ Each
53.10
-
Chemical Identifiers
CAS80822-15-7
IUPAC Name(2S,3S)-2,3-bis(benzoyloxy)butanedioic acid hydrate
Molecular FormulaC18H16O9
InChI KeyDXDIHODZARUBLA-DZWQFRRJNA-N
SMILESO.OC(=O)[C@@H](OC(=O)C1=CC=CC=C1)[C@H](OC(=O)C1=CC=CC=C1)C(O)=O
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White
Assay (Aqueous acid-base Titration)≥98.5 to ≤101.5%
Melting Point (clear melt)86.0-92.0?C
Water Content (Karl Fischer Titration)2.45-7.01% (0.5-1.5 waters)
Optical Rotation109.5 ± 0.1? (c=2 in EtOH)
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(+)-Dibenzoyl-D-tartaric acid monohydrate is used as a chiral separation and racemization agent for amines. It is also used as a pharmaceutical raw material.
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
(+)-Dibenzoyl-D-tartaric acid monohydrate is used as a chiral separation and racemization agent for amines. It is also used as a pharmaceutical raw material.
Solubility
Soluble in methanol. Slightly soluble in water.
Notes
Incompatible with strong oxidizing agents, strong acids and bases.
(+)-Dibenzoyl-D-tartaric acid monohydrate is used as a chiral separation and racemization agent for amines. It is also used as a pharmaceutical raw material.
Solubility
Soluble in methanol. Slightly soluble in water.
Notes
Incompatible with strong oxidizing agents, strong acids and bases.
RUO – Research Use Only
General References:
- Chavakula, R.; Mutyala, N. R.; Chennupati, S. R. Industrially Viable Preparation of (R)-3-Quinuclidinol, a Key Building Block of Muscarine M1, M3 Agonists and M3 Antagonists. Org. Prep. Proced. Int. 2013, 45 (6), 507-509.
- Gizur, T.; Fogassy, E.; Balint, J.; Egri, G.; Törley, J.; Demeter, A.; Greiner, I. New practical synthesis of Tamsulosin. Chirality 2008, 20 (6), 790-795.