N-(17-Amino-3,6,9,12,15-pentaoxaheptadecyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide

97%

Reagent Code: #109003
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CAS Number 113072-75-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 506.66 g/mol
Formula C₂₂H₄₂N₄O₇S
badge Registry Numbers
MDL Number MFCD22574819
inventory_2 Storage & Handling
Storage -20°C, sealed, dry, away from light

description Product Description

This chemical is primarily utilized in the field of biotechnology and molecular biology, where it serves as a crucial component in the modification and functionalization of biomolecules. Its structure, featuring a biotin moiety and a hydrophilic spacer, makes it highly effective for conjugation with proteins, peptides, or other biomolecules. This conjugation enhances the binding affinity to avidin or streptavidin, which is essential in applications such as immunoassays, histochemistry, and biosensors. Additionally, it is employed in the development of targeted drug delivery systems, where it aids in the precise attachment of therapeutic agents to specific cellular targets. Its water-soluble nature ensures compatibility with aqueous biological environments, facilitating its use in various diagnostic and therapeutic platforms.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days Ft957,301.77
N-(17-Amino-3,6,9,12,15-pentaoxaheptadecyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide
This chemical is primarily utilized in the field of biotechnology and molecular biology, where it serves as a crucial component in the modification and functionalization of biomolecules. Its structure, featuring a biotin moiety and a hydrophilic spacer, makes it highly effective for conjugation with proteins, peptides, or other biomolecules. This conjugation enhances the binding affinity to avidin or streptavidin, which is essential in applications such as immunoassays, histochemistry, and biosensors. Additionally, it is employed in the development of targeted drug delivery systems, where it aids in the precise attachment of therapeutic agents to specific cellular targets. Its water-soluble nature ensures compatibility with aqueous biological environments, facilitating its use in various diagnostic and therapeutic platforms.
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