N-Boc-L-Tert-Leucine

98%

  • Product Code: 58033
  Alias:    N-Boc-L-tert-leucine
  CAS:    62965-35-9
Molecular Weight: 231.29 g./mol Molecular Formula: C₁₁H₂₁NO₄
EC Number: MDL Number: MFCD00065574
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: N-Boc-L-Tert-Leucine is widely used in peptide synthesis as a protecting group for the amino acid L-tert-leucine. It helps prevent unwanted reactions during the formation of peptide bonds, ensuring the synthesis proceeds efficiently. This compound is particularly valuable in the production of complex peptides and proteins, where selective protection and deprotection of functional groups are critical. Additionally, it finds applications in medicinal chemistry for the development of peptide-based drugs, where it aids in improving the stability and bioavailability of the final products. Its use extends to the synthesis of chiral compounds and as a building block in organic synthesis, contributing to the creation of various biologically active molecules.
Product Specification:
Test Specification
APPEARANCE WHITE TO OFF-WHITE POWDER OR SOLID OR CHUNKS
PURITY 97.5
MELTING POINT 115-125
SPECIFIC ROTATION A20DC1ACOH -6--3
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿410.00
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-
25.000 10-20 days ฿1,260.00
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-
100.000 10-20 days ฿3,880.00
+
-
500.000 10-20 days ฿8,960.00
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-
N-Boc-L-Tert-Leucine
N-Boc-L-Tert-Leucine is widely used in peptide synthesis as a protecting group for the amino acid L-tert-leucine. It helps prevent unwanted reactions during the formation of peptide bonds, ensuring the synthesis proceeds efficiently. This compound is particularly valuable in the production of complex peptides and proteins, where selective protection and deprotection of functional groups are critical. Additionally, it finds applications in medicinal chemistry for the development of peptide-based drugs, where it aids in improving the stability and bioavailability of the final products. Its use extends to the synthesis of chiral compounds and as a building block in organic synthesis, contributing to the creation of various biologically active molecules.
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