Myristic Anhydride (TCI M0484), with CAS number 626-29-9, is a chemical compound widely used in laboratory settings for organic synthesis. As an anhydride, it plays a crucial role in chemical reactions by forming esters and amides when reacting with alcohols and amines. This versatility makes it a valuable reagent in the development of complex organic molecules. Its application spans various fields, including pharmaceutical and cosmetic research, where it contributes to the creation of surfactants, drugs, and industrial chemicals.
The chemical properties of Myristic Anhydride make it a preferred choice in laboratory environments. It is stable under specific conditions but highly reactive towards water and polar compounds. This reactivity necessitates careful handling to prevent unwanted degradation or side reactions. Its solid form and solubility in organic solvents enhance its usability in diverse experimental setups. These characteristics ensure that it remains a reliable and effective reagent for chemical synthesis.
In Indonesian laboratories, Myristic Anhydride is commonly used in organic chemistry research, particularly in the pharmaceutical and cosmetic industries. Its availability and consistent quality make it a top choice for researchers. It supports the development of new compounds and formulations, contributing to both academic and industrial advancements in chemical sciences.
- Organic synthesis is a key application where Myristic Anhydride is used to produce esters and amides, essential for drug and cosmetic development.
- Pharmaceutical research benefits from its ability to form amides, aiding in the creation of complex molecular structures required for new drug compounds.
- Cosmetic formulation relies on Myristic Anhydride for producing surfactants and emulsifiers, enhancing product stability and effectiveness.
- Industrial chemical production utilizes this compound for synthesizing various organic compounds with specific functional groups.
- Academic research in chemistry laboratories employs Myristic Anhydride for teaching and experimental purposes, demonstrating its role in esterification and amidation reactions.
| Brand | TCI |
|---|---|
| CAS number | 626-29-9 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | — |
| Physical form | Solid |
| Storage | Requires protection from moisture and polar substances |
Myristic Anhydride should be stored in a cool, dry place away from moisture and polar substances to maintain its chemical integrity. It is recommended to use airtight containers made of glass or polyethylene to prevent exposure to air and humidity. Due to its reactivity with water, it should be handled in a fume hood to minimize the risk of unintended reactions. Proper labeling and storage in a designated chemical cabinet are essential for safety. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound to ensure safe and effective use.
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