N-(2-AMINOETHYL)-5-((3AS, 4S, 6AR)-2-OXOHEXAHYDRO-1H-THIENO[3, 4-D]IMIDAZOL-4-YL)PENTANAMIDE HYDROCHLORIDE

≥95%

Reagent Code: #219481
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CAS Number 111822-45-8

science Other reagents with same CAS 111822-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.85 g/mol
Formula C₁₂H₂₃ClN₄O₂S
badge Registry Numbers
MDL Number MFCD29916930
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is a biotin derivative with an aminoethylamide linker, utilized in biochemical and molecular biology research for preparing biotinylated conjugates. The biotin moiety enables high-affinity binding to avidin or streptavidin, facilitating detection and purification in techniques such as immunoassays (e.g., ELISA), Western blotting, and fluorescence microscopy. The terminal primary amine allows for covalent attachment to proteins, peptides, antibodies, or other biomolecules, making it ideal for labeling and studying cellular processes, protein-protein interactions, and targeted delivery systems. It exhibits low toxicity and is suitable for in vitro applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,320.00
inventory 250mg
10-20 days ฿5,730.00
inventory 1g
10-20 days ฿19,720.00
N-(2-AMINOETHYL)-5-((3AS, 4S, 6AR)-2-OXOHEXAHYDRO-1H-THIENO[3, 4-D]IMIDAZOL-4-YL)PENTANAMIDE HYDROCHLORIDE
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This compound is a biotin derivative with an aminoethylamide linker, utilized in biochemical and molecular biology research for preparing biotinylated conjugates. The biotin moiety enables high-affinity binding to avidin or streptavidin, facilitating detection and purification in techniques such as immunoassays (e.g., ELISA), Western blotting, and fluorescence microscopy. The terminal primary amine allows for covalent attachment to proteins, peptides, antibodies, or other biomolecules, making it ideal fo

This compound is a biotin derivative with an aminoethylamide linker, utilized in biochemical and molecular biology research for preparing biotinylated conjugates. The biotin moiety enables high-affinity binding to avidin or streptavidin, facilitating detection and purification in techniques such as immunoassays (e.g., ELISA), Western blotting, and fluorescence microscopy. The terminal primary amine allows for covalent attachment to proteins, peptides, antibodies, or other biomolecules, making it ideal for labeling and studying cellular processes, protein-protein interactions, and targeted delivery systems. It exhibits low toxicity and is suitable for in vitro applications.

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