L-Tyrosine tert-butyl ester

99%

  • Product Code: 105407
  Alias:    L-Tyrosine Tert-Butyl Ester
  CAS:    16874-12-7
Molecular Weight: 237.29 g./mol Molecular Formula: C₁₃H₁₉NO₃
EC Number: 240-902-3 MDL Number: MFCD00042644
Melting Point: 141-144 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: L-Tyrosine tert-butyl ester is widely used in peptide synthesis as a protecting group for the carboxylic acid functionality of tyrosine. This compound helps prevent unwanted side reactions during the formation of peptide bonds, ensuring the integrity and specificity of the peptide chain. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are critical. Additionally, it finds application in the development of pharmaceuticals and bioactive peptides, where tyrosine residues play a key role in biological activity. Its tert-butyl ester group is stable under acidic conditions but can be easily removed under mild acidic conditions, making it a versatile tool in organic and medicinal chemistry.
Product Specification:
Test Specification
Melting Point 140-145
Purity (GC) 99-100%
Specific Rotation [a]20/D(C=2, Ethanol) 23-27
Appearance White To Pale Cream Powder
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿380.00
+
-
5.000 10-20 days ฿1,160.00
+
-
25.000 10-20 days ฿4,900.00
+
-
L-Tyrosine tert-butyl ester
L-Tyrosine tert-butyl ester is widely used in peptide synthesis as a protecting group for the carboxylic acid functionality of tyrosine. This compound helps prevent unwanted side reactions during the formation of peptide bonds, ensuring the integrity and specificity of the peptide chain. It is particularly valuable in solid-phase peptide synthesis (SPPS), where selective deprotection and coupling steps are critical. Additionally, it finds application in the development of pharmaceuticals and bioactive peptides, where tyrosine residues play a key role in biological activity. Its tert-butyl ester group is stable under acidic conditions but can be easily removed under mild acidic conditions, making it a versatile tool in organic and medicinal chemistry.
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