Boc-Hyp-OH
98%
- Product Code: 104789
Alias:
BOC-L-Hydroxyproline ; N-tert-Butoxycarbonyl-4-Hydroxy-L-Proline
CAS:
13726-69-7
Molecular Weight: | 231.25 g./mol | Molecular Formula: | C₁₀H₁₇NO₅ |
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EC Number: | MDL Number: | MFCD00053370 | |
Melting Point: | 123-127 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | -20°C |
Product Description:
Used primarily in peptide synthesis, it serves as a protecting group for hydroxyproline, ensuring selective reactions during the formation of peptide bonds. It is particularly valuable in the production of complex peptides and proteins, where precise control over amino acid reactivity is essential. Additionally, it finds application in the development of pharmaceuticals, especially in the synthesis of peptide-based drugs, where it aids in maintaining the structural integrity and functionality of the peptide chain. Its use is also extended to research in biochemistry and molecular biology, where it helps in studying peptide interactions and properties.
Product Specification:
Test | Specification |
---|---|
Appearance | White To Almost White Powder To Crystal |
Purity (%) | 97.5-100 |
Specific Rotation [α]20/D(c=1, MeOH) | -69.0--67.0 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿330.00 |
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5.000 | 10-20 days | ฿380.00 |
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25.000 | 10-20 days | ฿720.00 |
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100.000 | 10-20 days | ฿2,300.00 |
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500.000 | 10-20 days | ฿9,690.00 |
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Boc-Hyp-OH
Used primarily in peptide synthesis, it serves as a protecting group for hydroxyproline, ensuring selective reactions during the formation of peptide bonds. It is particularly valuable in the production of complex peptides and proteins, where precise control over amino acid reactivity is essential. Additionally, it finds application in the development of pharmaceuticals, especially in the synthesis of peptide-based drugs, where it aids in maintaining the structural integrity and functionality of the peptide chain. Its use is also extended to research in biochemistry and molecular biology, where it helps in studying peptide interactions and properties.
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