Bocaminooxyacetamide-PEG2-Azido

Bocaminooxyacetamide-PEG2-Azido Catalog number: BADC-01234

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Bocaminooxyacetamide-PEG2-Azido is a cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Category
ADCs Linker
Product Name
Bocaminooxyacetamide-PEG2-Azido
Catalog Number
BADC-01234
Molecular Formula
C13H25N5O6
Molecular Weight
347.37
Purity
98.0%

Ordering Information

Catalog Number Size Price Quantity
BADC-01234 -- $-- Inquiry
Description
Bocaminooxyacetamide-PEG2-Azido is a cleavable 2 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
Solubility
10 mm in DMSO
Shelf Life
0-4°C for short term (days to weeks), or -20°C for long term (months).
Shipping
Room temperature
Storage
Store at -5°C,keep in dry and avoid sunlight.

Bocaminooxyacetamide-PEG2-Azido, a multifunctional chemical compound, finds its first key application in the field of bioconjugation. This compound is designed with reactive azide and oxyacetamide groups which facilitate the formation of stable conjugates with various biomolecules, such as proteins, peptides, and antibodies. The presence of polyethylene glycol (PEG) enhances the solubility and stability of the conjugates, making it ideal for developing bioconjugated molecules that can be used in a multitude of biological assays and therapeutic applications. The controlled and specific attachment of these biomolecules via Bocaminooxyacetamide-PEG2-Azido allows researchers to create more effective targeted drug delivery systems and diagnostic tools, leading to advancements in personalized medicine.

Another critical application of Bocaminooxyacetamide-PEG2-Azido is in click chemistry, a class of biocompatible small molecule reactions commonly used to quickly join substrates of interest. The azido group in Bocaminooxyacetamide-PEG2-Azido makes it an excellent candidate for copper-catalyzed azide-alkyne cycloaddition (CuAAC), one of the most popular click reactions. This reaction strategy is widely utilized in the synthesis of complex molecules, drug development, and the creation of functionalized polymers and materials. The high efficiency, specificity, and bio-orthogonality of the click reaction ensure that it can proceed without interfering with other bioactive molecules, underlining its importance in chemical biology and materials science.

In the realm of imaging and diagnostic techniques, Bocaminooxyacetamide-PEG2-Azido holds significant promise due to its modularity and versatility. The compound’s ability to covalently attach to various imaging agents, such as fluorescent dyes or radionuclides, enables the creation of highly specific imaging probes. These probes can be used for in vivo imaging to monitor biological processes, track disease progression, or evaluate the efficacy of therapeutic interventions. Furthermore, the PEGylation minimizes non-specific interactions and enhances the bioavailability and circulation time of the probes, thereby improving the sensitivity and specificity of the diagnostic assays. Such advancements in imaging techniques contribute to better disease diagnosis and monitoring.

Lastly, Bocaminooxyacetamide-PEG2-Azido is pivotal in the development of advanced biomaterials. The functionality provided by the azido and oxyacetamide groups allows for the straightforward modification of surfaces and the creation of multifunctional materials. For example, in tissue engineering and regenerative medicine, Bocaminooxyacetamide-PEG2-Azido can be utilized to functionalize scaffolds with bioactive molecules such as growth factors or cell adhesion peptides, promoting cell growth and differentiation. Similarly, it can be employed to coat medical devices and implants with antimicrobial peptides or other therapeutic agents, reducing the risk of infection and improving the integration of implants with the surrounding tissues. These applications are instrumental in the advancement of biomaterial science and the improvement of patient outcomes in various medical treatments.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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