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
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
5.000 10-20 days ฿360.00
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-
25.000 10-20 days ฿1,260.00
+
-
100.000 10-20 days ฿3,950.00
+
-
500.000 10-20 days ฿14,193.00
+
-
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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