N-Fmoc-D-Valine

98%

  • Product Code: 105050
  Alias:    Fmoc-D-valine ; Fmoc-D-valine
  CAS:    84624-17-9
Molecular Weight: 339.39 g./mol Molecular Formula: C₂₀H₂₁NO₄
EC Number: MDL Number: MFCD00062953
Melting Point: 143-144 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: N-Fmoc-D-Valine is widely used in peptide synthesis as a building block. It serves as a protected form of D-valine, where the Fmoc group acts as a temporary protecting group for the amino group during the synthesis process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the stepwise construction of peptides with high precision. Its application ensures the selective deprotection of the amino group, allowing for the sequential addition of amino acids to form complex peptide chains. Additionally, it is employed in the preparation of chiral compounds and in research involving unnatural amino acids, contributing to advancements in biochemistry, medicinal chemistry, and drug development.
Product Specification:
Test Specification
Melting Point 144-148
Purity (GC) 98-100%
Specific Rotation [A]20/D(C=1, DMF) 15-19
Appearance White To Light Yellow Powder
Infrared Spectrometry Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿270.00
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5.000 10-20 days ฿350.00
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25.000 10-20 days ฿890.00
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100.000 10-20 days ฿3,530.00
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500.000 10-20 days ฿15,460.00
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N-Fmoc-D-Valine
N-Fmoc-D-Valine is widely used in peptide synthesis as a building block. It serves as a protected form of D-valine, where the Fmoc group acts as a temporary protecting group for the amino group during the synthesis process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the stepwise construction of peptides with high precision. Its application ensures the selective deprotection of the amino group, allowing for the sequential addition of amino acids to form complex peptide chains. Additionally, it is employed in the preparation of chiral compounds and in research involving unnatural amino acids, contributing to advancements in biochemistry, medicinal chemistry, and drug development.
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