Boc-Tyr(Bzl)-OH

98%

  • Product Code: 104836
  Alias:    BOC-O-Benzyl-L-Tyrosine ; N-tert-Butyloxycarbonyl-O-Benzyl-L-Tyrosine
  CAS:    2130-96-3
Molecular Weight: 371.43 g./mol Molecular Formula: C₂₁H₂₅NO₅
EC Number: 218-349-4 MDL Number: MFCD00065597
Melting Point: 110-112 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: This chemical is widely used in peptide synthesis as a protected tyrosine derivative. It serves as a key building block in the production of peptides, ensuring the tyrosine residue remains intact during the synthesis process. Its application is particularly important in the pharmaceutical and biotechnology industries, where it aids in the development of peptide-based drugs, hormones, and other bioactive molecules. The Boc (tert-butoxycarbonyl) group provides temporary protection for the amino group, while the Bzl (benzyl) group protects the hydroxyl group of tyrosine, allowing selective reactions to occur at other sites. This compound is essential in creating complex peptide structures with high precision and efficiency.
Product Specification:
Test Specification
Melting Point 110-115
Specific Rotation [A]20/D(C=2 In Ethoh) 25.5-28.5
Appearance White To Light Yellow Powder
Infrared Spectrum Conforms To Structure
TLC Analysis One Spot
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿320.00
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-
5.000 10-20 days ฿700.00
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-
25.000 10-20 days ฿2,700.00
+
-
Boc-Tyr(Bzl)-OH
This chemical is widely used in peptide synthesis as a protected tyrosine derivative. It serves as a key building block in the production of peptides, ensuring the tyrosine residue remains intact during the synthesis process. Its application is particularly important in the pharmaceutical and biotechnology industries, where it aids in the development of peptide-based drugs, hormones, and other bioactive molecules. The Boc (tert-butoxycarbonyl) group provides temporary protection for the amino group, while the Bzl (benzyl) group protects the hydroxyl group of tyrosine, allowing selective reactions to occur at other sites. This compound is essential in creating complex peptide structures with high precision and efficiency.
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