N-Cbz-D-aspartic acid

98%

  • Product Code: 105435
  Alias:    N-CBZ-D-Aspartic Acid ; N-Benzyloxycarbonyl-D-Aspartic Acid
  CAS:    78663-07-7
Molecular Weight: 267.23 g./mol Molecular Formula: C₁₂H₁₃NO₆
EC Number: MDL Number: MFCD00063182
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: N-Cbz-D-aspartic acid is widely used in peptide synthesis as a protecting group for the carboxyl function of aspartic acid. Its application is crucial in the preparation of complex peptides and proteins, where selective protection and deprotection of functional groups are necessary. This compound is particularly valuable in the synthesis of biologically active peptides, including those used in pharmaceuticals and research. Additionally, it serves as an intermediate in the production of various fine chemicals and specialty compounds. Its stability and ease of removal under mild conditions make it a preferred choice in organic and medicinal chemistry workflows.
Product Specification:
Test Specification
Appearance White Powder
Purity (GC) 98-100
Melting Point 112-119
Infrared Spectrum Conforms To Structure
Specific Rotation [A]20/D(C=7, ACOH) -8- -11
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days €6.86
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5.000 10-20 days €12.93
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25.000 10-20 days €27.70
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100.000 10-20 days €99.72
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500.000 10-20 days €352.20
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N-Cbz-D-aspartic acid
N-Cbz-D-aspartic acid is widely used in peptide synthesis as a protecting group for the carboxyl function of aspartic acid. Its application is crucial in the preparation of complex peptides and proteins, where selective protection and deprotection of functional groups are necessary. This compound is particularly valuable in the synthesis of biologically active peptides, including those used in pharmaceuticals and research. Additionally, it serves as an intermediate in the production of various fine chemicals and specialty compounds. Its stability and ease of removal under mild conditions make it a preferred choice in organic and medicinal chemistry workflows.
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