Fmoc-Dab(Mtt)-OH

≥95%

Reagent Code: #38036
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CAS Number 851392-68-2

science Other reagents with same CAS 851392-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 596.71 g/mol
Formula C₃₉H₃₆N₂O₄
badge Registry Numbers
MDL Number MFCD02094096
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the Mtt (4-methyltrityl) group protects the side chain amine of diaminobutyric acid (Dab). This protection strategy allows for selective deprotection during the synthesis process, enabling the stepwise construction of complex peptides. It is especially valuable in synthesizing peptides with multiple functional groups or those requiring precise side-chain modifications. Its application is common in pharmaceutical research, drug development, and the production of biologically active peptides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,091.00
inventory 10g
10-20 days ฿15,300.00
inventory 1g
10-20 days ฿2,151.00
inventory 250mg
10-20 days ฿873.00

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Fmoc-Dab(Mtt)-OH
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This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the Mtt (4-methyltrityl) group protects the side chain amine of diaminobutyric acid (Dab). This protection strategy allows for selective deprotection during the synthesis process, enabling the stepwise construction of complex peptides. It is especially valuable in synthesizin

This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group, and the Mtt (4-methyltrityl) group protects the side chain amine of diaminobutyric acid (Dab). This protection strategy allows for selective deprotection during the synthesis process, enabling the stepwise construction of complex peptides. It is especially valuable in synthesizing peptides with multiple functional groups or those requiring precise side-chain modifications. Its application is common in pharmaceutical research, drug development, and the production of biologically active peptides.

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