Fmoc-4-tert-butoxy-L-proline

98%

  • Product Code: 105014
  Alias:    Fmoc-4-tert-butoxy-L-proline ; N-fluorenylmethoxycarbonyl-4-tert-butoxy-L-proline
  CAS:    122996-47-8
Molecular Weight: 409.47 g./mol Molecular Formula: C₂₄H₂₇NO₅
EC Number: MDL Number: MFCD00151930
Melting Point: ~63 °C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Fmoc-4-tert-butoxy-L-proline is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of proline, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the tert-butoxy group protects the hydroxyl group. This protection ensures selective reactions during peptide chain assembly, preventing unwanted side reactions. It is especially valuable in synthesizing complex peptides and peptidomimetics, where precise control over amino acid incorporation is critical. Additionally, its stability under standard SPPS conditions makes it a reliable building block for producing peptides used in drug development, biochemical research, and therapeutic applications.
Product Specification:
Test Specification
Appearance White Powder
Purity (%) 97.5-100
Specific Rotation [a]20/D(c = 1% In Methanol) -22.5 Degree Celsius -27.5 Degree Celsius
Infrared Spectrum Conforms To Structure
Proton NMR Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿420.00
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5.000 10-20 days ฿1,260.00
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-
25.000 10-20 days ฿5,680.00
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Fmoc-4-tert-butoxy-L-proline
Fmoc-4-tert-butoxy-L-proline is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected form of proline, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the tert-butoxy group protects the hydroxyl group. This protection ensures selective reactions during peptide chain assembly, preventing unwanted side reactions. It is especially valuable in synthesizing complex peptides and peptidomimetics, where precise control over amino acid incorporation is critical. Additionally, its stability under standard SPPS conditions makes it a reliable building block for producing peptides used in drug development, biochemical research, and therapeutic applications.
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