Fmoc-Tic-OH

97%

  • Product Code: 105440
  Alias:    Fmoc-Tic-OH
  CAS:    136030-33-6
Molecular Weight: 399.44 g./mol Molecular Formula: C₂₅H₂₁NO₄
EC Number: MDL Number: MFCD00144368
Melting Point: 146-149 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Fmoc-Tic-OH is widely used in peptide synthesis as a protecting group for amino acids. It is particularly valuable in solid-phase peptide synthesis (SPPS) for constructing complex peptides and proteins. The Fmoc group provides stability during the synthesis process and can be selectively removed under mild basic conditions, ensuring the integrity of the peptide chain. This compound is also employed in the development of peptide-based drugs, where precise control over amino acid sequences is critical. Additionally, it is utilized in research to study peptide interactions, folding, and biological activity, making it a key reagent in biochemistry and pharmaceutical development.
Product Specification:
Test Specification
Carbon By Elemental Analysis 72.5-75.5
Purity (HPLC) 97-100
Specific Rotation [A]20/D(C = 1% In Methanol) 23 Degree Celsius - 29 Degree Celsius
Appearance White To Yellow To Beige Solid Or Powder
Infrared Spectrometry Conforms To Structure
INFRARED SPECTROMETRY Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿432.00
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-
5.000 10-20 days ฿927.00
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-
25.000 10-20 days ฿2,817.00
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Fmoc-Tic-OH
Fmoc-Tic-OH is widely used in peptide synthesis as a protecting group for amino acids. It is particularly valuable in solid-phase peptide synthesis (SPPS) for constructing complex peptides and proteins. The Fmoc group provides stability during the synthesis process and can be selectively removed under mild basic conditions, ensuring the integrity of the peptide chain. This compound is also employed in the development of peptide-based drugs, where precise control over amino acid sequences is critical. Additionally, it is utilized in research to study peptide interactions, folding, and biological activity, making it a key reagent in biochemistry and pharmaceutical development.
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