Di-p-toluoyl-L-tartaric acid monohydrate
99%
- Product Code: 71373
CAS:
71607-32-4
| Molecular Weight: | 404.37 g./mol | Molecular Formula: | C₂₀H₂₀O₉ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00151034 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Di-p-toluoyl-L-tartaric acid monohydrate is widely used as a chiral resolving agent in the pharmaceutical and chemical industries. It is particularly effective in the separation of enantiomers, which is crucial for producing optically pure compounds. This chemical is often employed in the resolution of racemic mixtures of amines, amino acids, and other chiral molecules, ensuring the production of enantiomerically pure substances that are essential for drug development and research. Its ability to form diastereomeric salts with chiral compounds makes it a valuable tool in asymmetric synthesis and purification processes. Additionally, it is utilized in the preparation of chiral catalysts and ligands, further enhancing its role in stereoselective reactions.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Powder |
| PURITY | 98.5-100 |
| WATER | 0 5 % |
| Specific rotation a20D C1MeOH | 140 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $8.40 |
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| 25.000 | 10-20 days | $9.00 |
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| 100.000 | 10-20 days | $13.80 |
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| 500.000 | 10-20 days | $65.11 |
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| 1000.000 | 10-20 days | $122.71 |
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Di-p-toluoyl-L-tartaric acid monohydrate
Di-p-toluoyl-L-tartaric acid monohydrate is widely used as a chiral resolving agent in the pharmaceutical and chemical industries. It is particularly effective in the separation of enantiomers, which is crucial for producing optically pure compounds. This chemical is often employed in the resolution of racemic mixtures of amines, amino acids, and other chiral molecules, ensuring the production of enantiomerically pure substances that are essential for drug development and research. Its ability to form diastereomeric salts with chiral compounds makes it a valuable tool in asymmetric synthesis and purification processes. Additionally, it is utilized in the preparation of chiral catalysts and ligands, further enhancing its role in stereoselective reactions.
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