(S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride
98.0%
- Product Code: 60194
Alias:
(-)-Bis[(S)-1-phenylethyl]amine hydrochloride
(-)-Bis[(S)-α-methylbenzyl]amine hydrochloride
(S,S)-(-)-bis(1-phenylethyl)amine hydrochloride
CAS:
40648-92-8
| Molecular Weight: | 261.79 g./mol | Molecular Formula: | C₁₆H₁₉NHCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00216671 | |
| Melting Point: | 261-263 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
(S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride is primarily used as a chiral auxiliary or resolving agent in asymmetric synthesis. It is particularly valuable in the preparation of enantiomerically pure compounds, aiding in the separation of racemic mixtures. This compound is often employed in the pharmaceutical industry to synthesize chiral drugs, ensuring high enantiomeric purity, which is crucial for drug efficacy and safety. Additionally, it finds application in the development of catalysts for asymmetric hydrogenation and other stereoselective reactions, enhancing the efficiency of producing optically active molecules. Its role in organic synthesis also extends to the creation of complex natural products and fine chemicals, where precise stereochemistry is essential.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿530.00 |
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| 1.000 | 10-20 days | ฿1,770.00 |
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| 5.000 | 10-20 days | ฿6,420.00 |
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| 25.000 | 10-20 days | ฿22,000.00 |
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(S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride
(S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride is primarily used as a chiral auxiliary or resolving agent in asymmetric synthesis. It is particularly valuable in the preparation of enantiomerically pure compounds, aiding in the separation of racemic mixtures. This compound is often employed in the pharmaceutical industry to synthesize chiral drugs, ensuring high enantiomeric purity, which is crucial for drug efficacy and safety. Additionally, it finds application in the development of catalysts for asymmetric hydrogenation and other stereoselective reactions, enhancing the efficiency of producing optically active molecules. Its role in organic synthesis also extends to the creation of complex natural products and fine chemicals, where precise stereochemistry is essential.
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