Orotic acid (TCI O0633, CAS 65-86-1) is a chemical compound widely used in various chemical and biochemical experiments conducted in laboratories. As a heterocyclic building block, it plays a crucial role in the synthesis of organic compounds, particularly in the development of nucleotides. These nucleotides are fundamental components of DNA and RNA, making orotic acid an essential reagent for molecular biology and biochemistry research. Its presence in laboratory workflows supports the study of metabolic pathways and the creation of complex organic molecules.
Orotic acid is valued for its chemical stability and predictable behavior under different conditions. It is a colorless crystalline substance, which simplifies identification and handling in laboratory settings. Its neutral chemical properties make it less reactive with other reagents, ensuring consistency in experimental outcomes. This stability and predictability make it a reliable choice for researchers seeking reproducible results in their experiments.
In Indonesian laboratories, orotic acid is commonly used in biochemical, pharmaceutical, and organic chemistry research. Its availability and consistent chemical properties make it a preferred choice for scientists working on nucleotide synthesis and metabolic studies. Researchers in Indonesia rely on orotic acid for its reliability and versatility in supporting a wide range of experimental applications.
- Biochemical research utilizes orotic acid for studying nucleotide synthesis and metabolic pathways due to its role in DNA and RNA formation.
- Organic chemistry experiments benefit from orotic acid as a heterocyclic building block for the synthesis of complex organic compounds.
- Pharmaceutical research employs orotic acid in the development of nucleotide-based drugs, leveraging its structural properties.
- Metabolic studies rely on orotic acid to investigate the biochemical processes involved in nucleotide metabolism.
- Laboratory teaching uses orotic acid as an educational tool to demonstrate heterocyclic compound behavior and synthesis techniques.
| Brand | TCI |
|---|---|
| CAS number | 65-86-1 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Heterocyclic Building Blocks |
| Pack sizes | Available in standard laboratory quantities |
| Physical form | Colorless crystalline solid |
| Storage | Store in a cool, dry place away from direct sunlight |
Orotic acid should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in a sealed container to avoid moisture exposure, which could affect its crystalline structure. Due to its neutral chemical properties, orotic acid does not react readily with other substances, but it should still be handled with care in a well-ventilated laboratory setting. Avoid direct contact with skin and eyes, and ensure proper disposal according to local regulations. Regular monitoring of storage conditions ensures the compound remains suitable for use in experimental applications.
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