Dde-Dab(Fmoc)-OH

97%

Reagent Code: #60726
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CAS Number 1263045-85-7

science Other reagents with same CAS 1263045-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 504.57 g/mol
Formula C₂₉H₃₂N₂O₆
badge Registry Numbers
MDL Number MFCD05663743
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Dde-Dab(Fmoc)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). Its primary application is as a building block for constructing peptides with specific sequences. The Dde (1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl) protecting group is selectively removable under mild conditions, allowing for orthogonal protection strategies. This is especially useful in synthesizing complex peptides where multiple protecting groups are required. The Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group during synthesis and can be removed under basic conditions. Together, these features enable the precise and controlled assembly of peptides, making it a valuable tool in the development of pharmaceuticals, bioactive peptides, and research applications in biochemistry and molecular biology.

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Test Parameter Specification
APPEARANCE White to Off-white Powder
Purity (%) 96.5-100
Water (%) 0-2
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,690.00
100mg
10-20 days ฿810.00
250mg
10-20 days ฿1,440.00
5g
10-20 days ฿16,380.00
Dde-Dab(Fmoc)-OH
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Dde-Dab(Fmoc)-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). Its primary application is as a building block for constructing peptides with specific sequences. The Dde (1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl) protecting group is selectively removable under mild conditions, allowing for orthogonal protection strategies. This is especially useful in synthesizing complex peptides where multiple protecting groups are required. The Fmoc (fluorenylmethyloxycarbonyl) group protects the amino group during synthesis and can be removed under basic conditions. Together, these features enable the precise and controlled assembly of peptides, making it a valuable tool in the development of pharmaceuticals, bioactive peptides, and research applications in biochemistry and molecular biology.
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