N-Carbobenzyloxy-L-aspartic acid

99%

  • Product Code: 105553
  Alias:    N-Benzyloxycarbonyl-L-Aspartic Acid ; N-CBZ-L-Aspartic Acid
  CAS:    1152-61-0
Molecular Weight: 267.23 g./mol Molecular Formula: C₁₂H₁₃NO₆
EC Number: 214-568-4 MDL Number: MFCD00002719
Melting Point: 117-119 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: N-Carbobenzyloxy-L-aspartic acid is primarily used in peptide synthesis as a protecting group for the carboxyl function of aspartic acid. This compound helps to prevent unwanted side reactions during the formation of peptide bonds, ensuring the correct sequence and structure of the synthesized peptide. It is particularly valuable in the production of complex peptides and proteins, where selective protection and deprotection of functional groups are crucial. Additionally, it finds application in the preparation of aspartic acid derivatives for research and pharmaceutical development, contributing to the study of enzyme mechanisms and drug design. Its role in organic synthesis also extends to the creation of specialized amino acid analogs for biochemical studies.
Product Specification:
Test Specification
Purity (Neutralization Titration) 98.5-101.5
Specific Rotation [A]23/D(C=1,ACOH) 8.5-10.5
Water By Karl Fischer 0-0.5
Appearance White To Light Yellow Powder
Infrared Spectrum Conforms To Structure
Solubility In Methanol Almost Transparency
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿290.00
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25.000 10-20 days ฿960.00
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100.000 10-20 days ฿3,080.00
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500.000 10-20 days ฿14,120.00
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N-Carbobenzyloxy-L-aspartic acid
N-Carbobenzyloxy-L-aspartic acid is primarily used in peptide synthesis as a protecting group for the carboxyl function of aspartic acid. This compound helps to prevent unwanted side reactions during the formation of peptide bonds, ensuring the correct sequence and structure of the synthesized peptide. It is particularly valuable in the production of complex peptides and proteins, where selective protection and deprotection of functional groups are crucial. Additionally, it finds application in the preparation of aspartic acid derivatives for research and pharmaceutical development, contributing to the study of enzyme mechanisms and drug design. Its role in organic synthesis also extends to the creation of specialized amino acid analogs for biochemical studies.
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