Boc-β-homoarginine(Tos)

98%

  • Product Code: 126988
  Alias:    Boc-L-β-homoarginine p-toluenesulfonate; N-Boc-N'-p-toluenesulfonyl-L-beta-homoarginine, N-tert-butoxycarbonyl-N'-p-toluenesulfonate Acyl-L-beta-homoarginine
  CAS:    136271-81-3
Molecular Weight: 442.53 g./mol Molecular Formula: C₁₉H₃₀N₄O₆S
EC Number: MDL Number: MFCD03427576
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: Boc-β-homoarginine(Tos) is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly those requiring homoarginine residues. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Tos (tosyl) group safeguards the guanidine functionality during the synthesis process. This ensures selective reactions and prevents unwanted side reactions. It is especially valuable in research and development of bioactive peptides, pharmaceuticals, and compounds targeting enzyme inhibition or receptor binding. Its stability and compatibility with solid-phase peptide synthesis make it a crucial reagent in medicinal chemistry and biochemistry studies.
Product Specification:
Test Specification
Purity (HPLC) 98-100
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿11,930.00
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-
5.000 10-20 days ฿51,030.00
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-
Boc-β-homoarginine(Tos)
Boc-β-homoarginine(Tos) is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly those requiring homoarginine residues. The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Tos (tosyl) group safeguards the guanidine functionality during the synthesis process. This ensures selective reactions and prevents unwanted side reactions. It is especially valuable in research and development of bioactive peptides, pharmaceuticals, and compounds targeting enzyme inhibition or receptor binding. Its stability and compatibility with solid-phase peptide synthesis make it a crucial reagent in medicinal chemistry and biochemistry studies.
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