Z-Tyr-OH

98%

  • Product Code: 105673
  Alias:    N-Benzyloxycarbonyl-L-tyrosine ; CBZ-L-tyrosine
  CAS:    1164-16-5
Molecular Weight: 315.32 g./mol Molecular Formula: C₁₇H₁₇NO₅
EC Number: 214-609-6 MDL Number: MFCD00191899
Melting Point: 57-60 °C(lit.) Boiling Point:
Density: Storage Condition: Room temperature, dry, sealed
Product Description: Z-Tyr-OH is widely used in peptide synthesis as a protecting group for tyrosine. It helps in preventing unwanted side reactions during the formation of peptide bonds, ensuring the integrity and specificity of the final peptide product. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it aids in the stepwise assembly of amino acids. Additionally, Z-Tyr-OH is employed in the development of bioactive peptides and pharmaceutical compounds, where precise control over amino acid reactivity is crucial. Its application extends to research in biochemistry and molecular biology, where it is used to study protein interactions and enzyme mechanisms.
Product Specification:
Test Specification
Melting Point 93-97
Purity (HPLC) 98-100%
Purity (Neutralization Titration) 97.5-102.5%
Specific Rotation [A]20/D(C=1%, Acetic Acid)
Specific Rotation [A]20/D(C=1%, Acetic Acid) 8-12
Appearance Colorless Liquid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿540.00
+
-
25.000 10-20 days ฿1,410.00
+
-
100.000 10-20 days ฿5,680.00
+
-
Z-Tyr-OH
Z-Tyr-OH is widely used in peptide synthesis as a protecting group for tyrosine. It helps in preventing unwanted side reactions during the formation of peptide bonds, ensuring the integrity and specificity of the final peptide product. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), where it aids in the stepwise assembly of amino acids. Additionally, Z-Tyr-OH is employed in the development of bioactive peptides and pharmaceutical compounds, where precise control over amino acid reactivity is crucial. Its application extends to research in biochemistry and molecular biology, where it is used to study protein interactions and enzyme mechanisms.
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