Fmoc-Tyr(tBu)-OH

98%

  • Product Code: 105137
  Alias:    Fluorenylmethoxycarbonyl-O-tert-butyl-L-tyrosine
  CAS:    71989-38-3
Molecular Weight: 459.53 g./mol Molecular Formula: C₂₈H₂₉NO₅
EC Number: 276-262-7 MDL Number: MFCD00037129
Melting Point: ~150 °C (dec.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for creating peptides, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amino group during the synthesis process. The tert-butyl (tBu) group protects the hydroxyl group of the tyrosine residue, preventing unwanted reactions. It is especially valuable in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and ease of deprotection make it a preferred choice in automated peptide synthesizers. Additionally, it is utilized in the synthesis of peptide-based vaccines, hormones, and other therapeutic agents.
Product Specification:
Test Specification
Appearance White Crystal
Purity (HPLC) 98-100
Specific Rotation [a]20/D(C=1, DMF) -32--28
Infrared Spectrum Conforms To Structure
Melting Point (Degree Celsius) 150-154
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿360.00
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-
5.000 10-20 days ฿700.00
+
-
25.000 10-20 days ฿2,990.00
+
-
100.000 10-20 days ฿8,960.00
+
-
Fmoc-Tyr(tBu)-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a building block for creating peptides, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amino group during the synthesis process. The tert-butyl (tBu) group protects the hydroxyl group of the tyrosine residue, preventing unwanted reactions. It is especially valuable in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies. Its stability and ease of deprotection make it a preferred choice in automated peptide synthesizers. Additionally, it is utilized in the synthesis of peptide-based vaccines, hormones, and other therapeutic agents.
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