tert-Butyl 1-amino-3,6,9,12,15,18,21,24,27,30,33,36-dodecaoxanonatriacontan-39-oate

95%

Reagent Code: #106893
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CAS Number 1383814-00-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 673.83 g/mol
Formula C₃₁H₆₃NO₁₄
badge Registry Numbers
MDL Number MFCD11041147
inventory_2 Storage & Handling
Storage -20°C, sealed, dry, away from light

description Product Description

This chemical is primarily used in the field of bioconjugation and drug delivery systems. Its structure, featuring a tert-butyl ester and a polyethyleneglycol (PEG) chain, makes it highly suitable for modifying proteins, peptides, and other biomolecules. The PEG segment enhances solubility, reduces immunogenicity, and extends the circulation time of conjugated drugs in the body. The tert-butyl group serves as a protective moiety that can be selectively removed under mild conditions, allowing for controlled release or activation of the active compound. It is particularly valuable in the development of targeted therapies, such as antibody-drug conjugates (ADCs), where precise delivery of therapeutic agents to specific cells or tissues is critical. Additionally, its application extends to the formulation of hydrogels and other biocompatible materials used in tissue engineering and regenerative medicine.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days Ft71,650.44
inventory 250mg
10-20 days Ft150,392.24
inventory 1g
10-20 days Ft375,934.55
tert-Butyl 1-amino-3,6,9,12,15,18,21,24,27,30,33,36-dodecaoxanonatriacontan-39-oate
This chemical is primarily used in the field of bioconjugation and drug delivery systems. Its structure, featuring a tert-butyl ester and a polyethyleneglycol (PEG) chain, makes it highly suitable for modifying proteins, peptides, and other biomolecules. The PEG segment enhances solubility, reduces immunogenicity, and extends the circulation time of conjugated drugs in the body. The tert-butyl group serves as a protective moiety that can be selectively removed under mild conditions, allowing for controlled release or activation of the active compound. It is particularly valuable in the development of targeted therapies, such as antibody-drug conjugates (ADCs), where precise delivery of therapeutic agents to specific cells or tissues is critical. Additionally, its application extends to the formulation of hydrogels and other biocompatible materials used in tissue engineering and regenerative medicine.
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