3-Hydroxymyristic Acid (3-HM) is a key organic compound used in various chemical reactions for the synthesis of complex molecules. It serves as a fundamental building block in chemical laboratories, playing a crucial role in the formation of molecular structures. This compound is widely utilized in chemical research for constructing molecules with long carbon chains and hydroxyl groups, which have broad applications in pharmaceutical, industrial chemical, and biochemical research. Its chemical stability allows it to participate in a variety of reactions such as esterification, reduction, and substitution reactions.
The structural characteristics of 3-Hydroxymyristic Acid make it a preferred choice for synthetic chemists. It consists of a 14-atom carbon chain with a hydroxyl group at the third position, offering both stability and reactivity. These properties enable it to be a versatile reagent in controlled chemical environments. Its ability to maintain chemical integrity during synthesis processes makes it an essential component in the development of new compounds. This compound is particularly valuable in applications requiring precise molecular manipulation.
In Indonesian laboratories, 3-Hydroxymyristic Acid is commonly used in organic chemistry research, especially in the synthesis of compounds with pharmacological and industrial applications. It is highly relevant to ongoing research in pure and applied chemistry, particularly in higher education institutions and research centers. Its availability and reliability make it a standard material for chemical experimentation and innovation.
- Organic synthesis of long-chain compounds due to its stable carbon chain and hydroxyl group.
- Pharmaceutical research for the development of drug molecules with hydroxyl functionalities.
- Industrial chemical production as a building block for specialty chemicals and polymers.
- Biochemical studies involving hydroxylated molecules in enzyme reactions and metabolic pathways.
- Educational purposes in teaching organic chemistry and synthetic reaction mechanisms.
| Brand | TCI |
|---|---|
| CAS number | 1961-72-4 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Solid, white to off-white crystalline powder |
| Storage | Store in a cool, dry place away from light and moisture |
3-Hydroxymyristic Acid should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to humidity and air. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid contamination. In a laboratory setting, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. The compound is non-hazardous under normal conditions but should be treated with care during chemical reactions to maintain its integrity and safety.
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