Boc-beta-alanine
98%
- Product Code: 76360
CAS:
3033-84-2
| Molecular Weight: | 189.21 g./mol | Molecular Formula: | C₈H₁₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, airtight |
Product Description:
Boc-beta-alanine is widely used in peptide synthesis as a protecting group for the amino acid beta-alanine. The Boc (tert-butoxycarbonyl) group shields the amine functionality during the synthesis process, preventing unwanted reactions and ensuring the correct sequence of amino acids in the peptide chain. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise addition of amino acids to build complex peptides and proteins. After the synthesis is complete, the Boc group can be easily removed under mild acidic conditions, revealing the free amine for further reactions. Additionally, Boc-beta-alanine is utilized in the preparation of various bioactive molecules and pharmaceutical intermediates, contributing to the development of drugs and therapeutic agents. Its stability and ease of deprotection make it a preferred choice in organic and medicinal chemistry research.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Crystalline Powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿2,410.00 |
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| 25.000 | 10-20 days | ฿5,220.00 |
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Boc-beta-alanine
Boc-beta-alanine is widely used in peptide synthesis as a protecting group for the amino acid beta-alanine. The Boc (tert-butoxycarbonyl) group shields the amine functionality during the synthesis process, preventing unwanted reactions and ensuring the correct sequence of amino acids in the peptide chain. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise addition of amino acids to build complex peptides and proteins. After the synthesis is complete, the Boc group can be easily removed under mild acidic conditions, revealing the free amine for further reactions. Additionally, Boc-beta-alanine is utilized in the preparation of various bioactive molecules and pharmaceutical intermediates, contributing to the development of drugs and therapeutic agents. Its stability and ease of deprotection make it a preferred choice in organic and medicinal chemistry research.
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