Fmoc-Bpa-OH

≥95%

Reagent Code: #50478
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CAS Number 117666-96-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 491.53 g/mol
Formula C₃₁H₂₅NO₅
badge Registry Numbers
MDL Number MFCD00151937
thermostat Physical Properties
Boiling Point 729°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Fmoc-Bpa-OH is widely used in peptide synthesis, particularly in the preparation of photoactivatable peptides. Its incorporation into peptide chains allows for cross-linking studies, enabling researchers to investigate protein-protein interactions and structural conformations. The compound is also valuable in the development of bioactive peptides, where it serves as a protective group for the amino acid during solid-phase synthesis. Additionally, it is utilized in the study of peptide-based drug delivery systems, where its photoactivatable properties can be leveraged for targeted release mechanisms. Its role in bioconjugation and labeling experiments further highlights its importance in biochemical and pharmaceutical research.

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Test Parameter Specification
Appearance white to off-white powder
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,800.00
inventory 250mg
10-20 days ฿2,250.00
inventory 5g
10-20 days ฿35,250.00
Fmoc-Bpa-OH
Fmoc-Bpa-OH is widely used in peptide synthesis, particularly in the preparation of photoactivatable peptides. Its incorporation into peptide chains allows for cross-linking studies, enabling researchers to investigate protein-protein interactions and structural conformations. The compound is also valuable in the development of bioactive peptides, where it serves as a protective group for the amino acid during solid-phase synthesis. Additionally, it is utilized in the study of peptide-based drug delivery systems, where its photoactivatable properties can be leveraged for targeted release mechanisms. Its role in bioconjugation and labeling experiments further highlights its importance in biochemical and pharmaceutical research.
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