Fmoc-Dab(Fmoc)-OH

97%

Reagent Code: #38010
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CAS Number 201473-83-8

science Other reagents with same CAS 201473-83-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 562.61 g/mol
Formula C₃₄H₃₀N₂O₆
badge Registry Numbers
MDL Number MFCD00237004
thermostat Physical Properties
Boiling Point 824.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used primarily in peptide synthesis, this compound serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to its dual Fmoc protection, which allows for selective deprotection during the stepwise assembly of peptides. The presence of Fmoc groups ensures the stability of the amino acid during the synthesis process, preventing unwanted side reactions. It is commonly employed in the production of complex peptides for research, pharmaceuticals, and biotechnology applications, where precise control over peptide sequence and structure is critical. Its use is especially prevalent in the development of therapeutic peptides and peptidomimetics.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,293.00
inventory 1g
10-20 days ฿1,080.00
inventory 10g
10-20 days ฿7,074.00
inventory 25g
10-20 days ฿14,166.00

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Fmoc-Dab(Fmoc)-OH
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Used primarily in peptide synthesis, this compound serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to its dual Fmoc protection, which allows for selective deprotection during the stepwise assembly of peptides. The presence of Fmoc groups ensures the stability of the amino acid during the synthesis process, preventing unwanted side reactions. It is commonly employed in the production of complex peptides for research, pharmaceuticals, and

Used primarily in peptide synthesis, this compound serves as a protected amino acid derivative. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to its dual Fmoc protection, which allows for selective deprotection during the stepwise assembly of peptides. The presence of Fmoc groups ensures the stability of the amino acid during the synthesis process, preventing unwanted side reactions. It is commonly employed in the production of complex peptides for research, pharmaceuticals, and biotechnology applications, where precise control over peptide sequence and structure is critical. Its use is especially prevalent in the development of therapeutic peptides and peptidomimetics.

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