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Chem Impex
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Product Information

Product Name
(-)-O,O'-Di-p-toluoyl-L-tartaric acid
Brand Name
Chem Impex
Product Number
24596
CAS
32634-66-5
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
3037000
IUPAC Name
(2R,3R)-2,3-bis(4-methylbenzoyl)oxybutanedioic acid
InChI Key
CMIBUZBMZCBCAT-HZPDHXFCSA-N
SMILES
CC1=CC=C(C=C1)C(=O)OC@H(C@H(C(=O)O)OC(=O)C2=CC=C(C=C2)C)C(=O)O

Application

(-)-O,O'-Di-p-toluoyl-L-tartaric acid is widely utilized in research focused on:

Chiral Resolution: This compound is effective in separating enantiomers, making it valuable in pharmaceutical development where the purity of chiral drugs is crucial.

Asymmetric Synthesis: It serves as a chiral auxiliary in asymmetric synthesis, enhancing the efficiency of producing specific stereoisomers in organic chemistry.

Food Industry: Used as a food additive, it helps in stabilizing emulsions and improving the texture of various food products, ensuring quality and consistency.

Analytical Chemistry: It plays a role in chromatography techniques, aiding in the separation and analysis of complex mixtures, which is essential for quality control in manufacturing.

Biotechnology: This compound is utilized in biocatalysis, facilitating reactions that are environmentally friendly and cost-effective, thus supporting sustainable practices in the industry.

References

Avacopan

Publication Name: Pharmaceutical Substances
Publication Date: 2022

Valbenazine

Publication Name: Pharmaceutical Substances
Publication Date: 2020

Esketamine

Publication Name: Pharmaceutical Substances
Publication Date: 2019

Determination of the Enantiomeric Purity of the Antiasthmatic Drug Montelukast by Means of 1H NMR Spectroscopy

Publication Name: Chirality
Publication Date: 2013-07-29
DOI: 10.1002/chir.22213

Application of mixtures of tartaric acid derivatives in resolution via supercritical fluid extraction

Publication Name: Chirality
Publication Date: 2007-03-07
DOI: 10.1002/chir.20362