N-Cbz-L-4-Hydroxyproline methyl ester
95%
- Product Code: 105437
Alias:
N-CBZ-Hydroxyproline methyl ester
CAS:
64187-48-0
Molecular Weight: | 279.29 g./mol | Molecular Formula: | C₁₄H₁₇NO₅ |
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EC Number: | MDL Number: | MFCD00055851 | |
Melting Point: | Boiling Point: | ||
Density: | 1.313 | Storage Condition: | -20°C |
Product Description:
Used in peptide synthesis as a protected amino acid derivative, it helps in the construction of complex peptides by providing stability to the hydroxyproline residue during reactions. It is particularly valuable in the production of collagen-like peptides and other bioactive molecules where hydroxyproline plays a critical role. The N-Cbz protecting group ensures selective deprotection, allowing for controlled and efficient synthesis. Additionally, it is employed in the development of pharmaceuticals targeting connective tissue disorders and wound healing due to its structural similarity to natural collagen components. Its methyl ester form enhances solubility, making it easier to handle in organic solvents during synthesis.
Product Specification:
Test | Specification |
---|---|
Carbon By Elemental Analysis | 43.9-45.2 |
Nitrogen | 4.4-5.1 |
Purity (HPLC) | 95-100 |
Specific Rotation (23 Degree Celsius, 589 NM) (C=0.1, H2O) | |
Proton NMR Spectrum | Conforms To Structure |
Solubility | Clear Colorless Solution (50mg/ml, Water) |
Appearance | Light Yellow Liquid |
APPEARANCE | Light yellow liquid |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿360.00 |
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25.000 | 10-20 days | ฿1,260.00 |
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100.000 | 10-20 days | ฿3,950.00 |
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500.000 | 10-20 days | ฿14,193.00 |
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N-Cbz-L-4-Hydroxyproline methyl ester
Used in peptide synthesis as a protected amino acid derivative, it helps in the construction of complex peptides by providing stability to the hydroxyproline residue during reactions. It is particularly valuable in the production of collagen-like peptides and other bioactive molecules where hydroxyproline plays a critical role. The N-Cbz protecting group ensures selective deprotection, allowing for controlled and efficient synthesis. Additionally, it is employed in the development of pharmaceuticals targeting connective tissue disorders and wound healing due to its structural similarity to natural collagen components. Its methyl ester form enhances solubility, making it easier to handle in organic solvents during synthesis.
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