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Description
6,6'-Diazido-6,6'-dideoxytrehalose is a chemical compound widely used in chemical biology, particularly in conjugation and click chemistry applications within laboratory settings. This modified trehalose derivative features two azido groups at the 6 and 6' positions, making it a valuable reagent for molecular conjugation. Its unique structure allows it to participate in highly specific and efficient chemical reactions, enabling the creation of complex molecular structures with precision. As a key component in conjugation chemistry, it plays a crucial role in the development of bioconjugates and functionalized molecules.
The compound's reactivity and selectivity make it a preferred choice for researchers working in molecular modification and drug development. The azido groups are highly reactive and can form covalent bonds with various ligands such as amines or hydroxyl groups, facilitating the synthesis of targeted and functionalized compounds. This reactivity, combined with its stability under specific conditions, ensures reliable performance in a wide range of experimental setups. Its ability to undergo click chemistry reactions further enhances its utility in bioconjugation and molecular labeling.
In Indonesian laboratories, 6,6'-Diazido-6,6'-dideoxytrehalose is commonly used by researchers in biotechnology, biochemistry, and pharmaceutical sciences. It supports the development of advanced molecular tools and therapeutic agents. Its versatility and effectiveness make it an essential reagent for scientists aiming to explore new molecular interactions and applications in both academic and industrial research settings.
Laboratory Applications
Bioconjugation Research: This compound is ideal for creating stable and specific molecular linkages, enabling the development of targeted therapeutics and diagnostic tools.
Molecular Labeling: Its azido groups allow for the precise attachment of fluorescent or functional moieties to biomolecules, enhancing the accuracy of imaging and analytical techniques.
Drug Development: It supports the synthesis of modified carbohydrates that can be used in the design of novel therapeutic agents with improved pharmacological properties.
Click Chemistry Applications: The compound's reactivity makes it a key player in click chemistry protocols, facilitating rapid and efficient molecular assembly in synthetic biology projects.
Biomolecular Modification: It enables the selective modification of proteins, nucleic acids, and other biomolecules, supporting a wide range of biochemical and biotechnological experiments.
Specifications
Brand: TCI
CAS number: 18933-88-5
Category: Chemistry > Chemical Biology > Conjugation Chemistry/Click Chemistry
Pack sizes: Available in various quantities as per supplier specifications
Physical form: Solid (as per standard chemical product description)
Storage note: Store in a cool, dry place away from light and moisture
Handling and Storage
This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. While it is stable under standard storage conditions, it is important to avoid prolonged exposure to extreme temperatures or reactive substances. Proper labeling and storage practices help ensure the compound remains effective for its intended applications in research settings.
