2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)tetradecanoic acid

95%

  • Product Code: 41095
  CAS:    919122-99-9
Molecular Weight: 465.6200 g./mol Molecular Formula: C₂₉H₃₉NO₄
EC Number: MDL Number: MFCD07781258
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the formation of peptide bonds, preventing unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise assembly of peptides on a solid support. The Fmoc group can be selectively removed under mild basic conditions, such as with piperidine, without affecting other functional groups in the peptide. This makes it a versatile tool in the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology applications. Additionally, its hydrophobic nature aids in the purification of intermediates during synthesis.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿4,572.00
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2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)tetradecanoic acid
This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the formation of peptide bonds, preventing unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise assembly of peptides on a solid support. The Fmoc group can be selectively removed under mild basic conditions, such as with piperidine, without affecting other functional groups in the peptide. This makes it a versatile tool in the production of complex peptides and proteins for research, pharmaceuticals, and biotechnology applications. Additionally, its hydrophobic nature aids in the purification of intermediates during synthesis.
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