(R)-(-)-2-Octanol is a chiral organic compound widely used in asymmetric synthesis to create molecules with specific biological activities. Its chiral structure plays a crucial role in laboratory settings, enabling precise control over stereochemistry during chemical reactions. This compound is a key building block in the development of pharmaceuticals and other complex organic molecules. Due to its stability under controlled conditions, it is a reliable reagent in various synthetic processes. Its utility extends to both academic and industrial research, making it an essential component in modern chemical laboratories.
The compound is valued for its chemical stability and solubility in organic solvents, which simplifies its handling and application in laboratory procedures. Its high purity ensures consistent results in experiments, particularly in research requiring precision and reproducibility. The ability to maintain stereochemical integrity makes it ideal for applications where the spatial arrangement of atoms is critical. These properties make (R)-(-)-2-Octanol a preferred choice for chemists working on advanced synthetic pathways.
In Indonesian laboratories, (R)-(-)-2-Octanol is commonly used in organic chemistry and pharmaceutical research. It supports the development of new drugs and the study of molecular interactions. Researchers and educational institutions rely on this compound for its reliability and effectiveness in complex chemical processes. Its presence in laboratory workflows underscores its importance in advancing scientific knowledge and innovation.
- Asymmetric synthesis is a key application where (R)-(-)-2-Octanol is used to produce chiral compounds with specific biological activities.
- Pharmaceutical research benefits from its role in creating enantiomerically pure compounds, essential for drug development.
- Organic chemistry experiments often use this compound as a chiral building block for constructing complex molecular structures.
- It is suitable for stereocontrolled reactions, allowing precise control over the spatial arrangement of atoms in synthesized molecules.
- In academic research, (R)-(-)-2-Octanol supports the study of stereochemistry and its impact on molecular function and activity.
| Brand | TCI |
|---|---|
| CAS number | 5978-70-1 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per standard laboratory requirements |
| Physical form | Liquid |
| Storage | Store in a cool, dry place away from light and incompatible materials |
(R)-(-)-2-Octanol should be stored in a cool, dry environment to maintain its chemical stability. It is best kept in airtight containers to prevent exposure to moisture and air, which could affect its purity. Due to its organic nature, it should be stored away from strong oxidizing agents and incompatible substances. Laboratory personnel should handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation is recommended when working with this compound to minimize inhalation risks. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications.
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