Hyaluronic Acid 2-(2-Methyl-1-oxo-2-propen-1-yl)hydrazide (degree of substitution 20%) TCI H1826

Hyaluronic Acid 2-(2-Methyl-1-oxo-2-propen-1-yl)hydrazide is a specialized chemical compound used in various laboratory experiments, particularly in organic and biochemical research. This compound is a derivative of hyaluronic acid, which is known for its unique ability to bind water and its presence in connective tissues. The modification of hyaluronic acid with a hydrazide group makes it a versatile reagent for chemical synthesis and molecular modification. Its structural complexity allows it to participate in high-reactivity and specificity-driven chemical reactions, making it a valuable tool for researchers.

The compound's key feature is its 20% degree of substitution, meaning that 20% of the hydroxyl groups in the original hyaluronic acid molecule have been replaced by hydrazide groups. This substitution significantly enhances its reactivity, enabling it to engage in reactions such as reduction or oxidation. Its stability combined with reactivity ensures consistent performance in laboratory settings, making it a preferred choice for scientists requiring reliable chemical intermediates.

In Indonesian laboratories, this compound is commonly used in biomedical, pharmaceutical, and biodegradable material research. Its unique chemical properties make it ideal for applications where molecular modification and reactivity are essential. Researchers in these fields rely on its predictable behavior and compatibility with various synthetic processes to advance their studies and develop new products.

• Biomedical research utilizes this compound for synthesizing biomaterials due to its ability to modify molecular structures and enhance reactivity.
• Pharmaceutical development benefits from its role in creating drug delivery systems by enabling controlled molecular interactions and chemical modifications.
• Biodegradable material research leverages its chemical structure to design sustainable polymers with tailored degradation properties.
• Organic synthesis applications take advantage of its hydrazide functionality for efficient coupling reactions and functional group transformations.
• Biochemical studies use it as a reagent for modifying hyaluronic acid derivatives, supporting research in tissue engineering and regenerative medicine.

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption, which could affect its chemical stability. Due to its reactivity, it should be handled in a well-ventilated laboratory setting, preferably under a fume hood. Avoid contact with incompatible substances, such as strong oxidizing agents, to ensure safety. Always wear appropriate personal protective equipment, including gloves and safety goggles, when handling this material. Proper storage and handling practices help maintain its chemical integrity and ensure safe laboratory operations.

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