(S)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid hydrate
95%
- Product Code: 97297
CAS:
200936-87-4
| Molecular Weight: | 249.3 g./mol | Molecular Formula: | C₁₁H₂₃NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 84-87°C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. This protection is crucial in multi-step organic synthesis, particularly in peptide coupling reactions, where selective deprotection and coupling are required. It is often employed in the production of bioactive peptides, enzyme inhibitors, and other therapeutic agents. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure compounds, which are essential in drug development to ensure specificity and efficacy. The hydrate form ensures stability and ease of handling during storage and use in laboratory settings.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 94.5-100 |
| WATER | 6 % 8 % |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 10.000 | 10-20 days | ฿350.00 |
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| 25.000 | 10-20 days | ฿450.00 |
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| 100.000 | 10-20 days | ฿1,740.00 |
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(S)-2-((tert-Butoxycarbonyl)amino)-4-methylpentanoic acid hydrate
This chemical is primarily used in the synthesis of peptides and pharmaceutical compounds. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during chemical reactions. This protection is crucial in multi-step organic synthesis, particularly in peptide coupling reactions, where selective deprotection and coupling are required. It is often employed in the production of bioactive peptides, enzyme inhibitors, and other therapeutic agents. Additionally, its chiral nature makes it valuable in the synthesis of enantiomerically pure compounds, which are essential in drug development to ensure specificity and efficacy. The hydrate form ensures stability and ease of handling during storage and use in laboratory settings.
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