Boc-N-beta-Trityl-L-asparagine
98%
- Product Code: 105730
Alias:
;tert-butoxycarbonyl-N-beta-trityl-L-asparagine
CAS:
132388-68-2
| Molecular Weight: | 474.55 g./mol | Molecular Formula: | C₂₈H₃₀N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00153299 | |
| Melting Point: | ~205 °C (dec.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
Primarily used in peptide synthesis, this compound serves as a protected form of L-asparagine. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, while the trityl (triphenylmethyl) group protects the side chain amide during the synthesis process. This protection is crucial to prevent unwanted reactions at these sites, ensuring the correct sequence and structure of the peptide. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection allows for the stepwise addition of amino acids. Additionally, it finds utility in the preparation of complex peptides and proteins for research in biochemistry and pharmaceutical development.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Crystal |
| Purity (%) | 97.5-100 |
| Specific Rotation [A]20/D(C=1, Methanol) | -22.0--18.0 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿700.00 |
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| 25.000 | 10-20 days | ฿2,260.00 |
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| 100.000 | 10-20 days | ฿8,420.00 |
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Boc-N-beta-Trityl-L-asparagine
Primarily used in peptide synthesis, this compound serves as a protected form of L-asparagine. The Boc (tert-butyloxycarbonyl) group safeguards the amino group, while the trityl (triphenylmethyl) group protects the side chain amide during the synthesis process. This protection is crucial to prevent unwanted reactions at these sites, ensuring the correct sequence and structure of the peptide. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection allows for the stepwise addition of amino acids. Additionally, it finds utility in the preparation of complex peptides and proteins for research in biochemistry and pharmaceutical development.
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