(S)-3′-Hydroxy-N-methylcoclaurine is a compound that has potential implications in the field of medicine, particularly in the development of new pharmaceutical drugs. Studies have shown that this compound possesses various biological activities, including anti-inflammatory and analgesic properties. As such, further research into (S)-3′-Hydroxy-N-methylcoclaurine could lead to the discovery of new treatments for common ailments such as pain and inflammation. This highlights the significance of this compound in potentially improving everyday life through the advancement of medical science.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
(S)-3′-Hydroxy-N-methylcoclaurine, a natural alkaloid found in plants, has various commercial and industrial applications. It is utilized in the pharmaceutical industry as a building block for the synthesis of complex alkaloids and pharmaceutical compounds. Additionally, this compound has potential uses in the development of new drugs due to its structural properties.
In the realm of drug and medication applications, (S)-3′-Hydroxy-N-methylcoclaurine has shown promise in the treatment of various medical conditions. Its anti-inflammatory and analgesic properties make it a potential candidate for pain management medications. Furthermore, research has suggested that this compound may have neuroprotective effects, making it a target for the development of drugs for neurological disorders.
Furthermore, (S)-3′-Hydroxy-N-methylcoclaurine has been explored for its potential applications in the agricultural industry. It has been studied for its pesticidal properties and potential use in crop protection. Research is ongoing to determine its efficacy and safety as a biopesticide for sustainable agriculture practices.
⚗️ Chemical & Physical Properties
(S)-3′-Hydroxy-N-methylcoclaurine is a white crystalline solid with no distinct odor, making it imperceptible to the human olfactory sense. Its appearance is of utmost importance in chemical identification and characterization.
The molar mass of (S)-3′-Hydroxy-N-methylcoclaurine is approximately 343.4 g/mol, with a density of about 1.17 g/cm3. This places it in the range of molar masses and densities commonly found in various food items such as sugars and amino acids.
(S)-3′-Hydroxy-N-methylcoclaurine has a melting point of around 217-220°C and a boiling point of approximately 480-500°C. These values are markedly higher than those of most common food items, which typically have lower melting and boiling points.
This compound is sparingly soluble in water and exhibits moderate viscosity. Compared to common food items like salt or sugar, (S)-3′-Hydroxy-N-methylcoclaurine has lower solubility in water and higher viscosity, which may impact its culinary applications.
🏭 Production & Procurement
(S)-3′-Hydroxy-N-methylcoclaurine is primarily produced through the isolation and extraction of certain plant species, such as Stephania japonica. This process involves the use of organic solvents to separate and purify the compound from the plant material, followed by further processing to obtain the final product in its pure form.
The procurement of (S)-3′-Hydroxy-N-methylcoclaurine typically involves sourcing the compound from specialized chemical suppliers or manufacturers. Once obtained, the compound can be transported in various forms, such as powders or solutions, depending on the specific requirements of the end user. Transportation methods may include air, sea, or land freight, adhering to strict regulations regarding the handling and storage of chemical substances.
It is important to note that the production and procurement of (S)-3′-Hydroxy-N-methylcoclaurine require compliance with safety measures and regulations set forth by governing bodies, such as the Occupational Safety and Health Administration (OSHA) and the Environmental Protection Agency (EPA). Additionally, proper documentation and labeling are crucial in the handling and transport of the compound to ensure its integrity and safety throughout the supply chain.
⚠️ Safety Considerations
Safety considerations for (S)-3′-Hydroxy-N-methylcoclaurine are of utmost importance due to its potential hazards. This compound should be handled with care and stored in a cool, dry place away from heat and direct sunlight. Lab personnel should wear appropriate personal protective equipment, including goggles, gloves, and lab coats, when working with (S)-3′-Hydroxy-N-methylcoclaurine to prevent potential skin and eye irritation. In case of inhalation or ingestion, immediate medical attention should be sought.
Hazard statements for (S)-3′-Hydroxy-N-methylcoclaurine include the classification of the compound as harmful if swallowed, causing skin and eye irritation, and being potentially harmful if inhaled. It is recommended to avoid contact with skin, eyes, and clothing when handling (S)-3′-Hydroxy-N-methylcoclaurine. In the event of exposure, rinse affected areas with plenty of water and seek medical advice if irritation persists. It is crucial to keep this compound out of reach of children and pets to prevent accidental ingestion or contact.
Precautionary statements for (S)-3′-Hydroxy-N-methylcoclaurine involve handling the compound with caution to avoid any potential risks. It is advised to wash hands thoroughly after handling (S)-3′-Hydroxy-N-methylcoclaurine and before eating, drinking, or smoking. The compound should be stored in a tightly closed container in a cool, well-ventilated area, away from incompatible materials. Proper waste disposal procedures should be followed to prevent environmental contamination, and any spills should be cleaned up immediately with suitable absorbent materials.
🔬 Potential Research Directions
(S)-3′-Hydroxy-N-methylcoclaurine, a chemically modified isoquinoline alkaloid with potential biological activity, presents a promising avenue for future research in the field of medicinal chemistry.
Investigations focusing on the synthesis of (S)-3′-Hydroxy-N-methylcoclaurine derivatives may yield novel compounds with improved pharmacological properties and therapeutic potential.
Exploring the interactions of (S)-3′-Hydroxy-N-methylcoclaurine with specific protein targets could elucidate its mechanism of action and facilitate the development of new drugs for various diseases.
🧪 Related Compounds
One similar compound to (S)-3′-Hydroxy-N-methylcoclaurine based upon molecular structure is (S)-3′-Hydroxycoclaurine, which shares a similar core structure but lacks the methyl group attached to the nitrogen atom. This compound also possesses a hydroxy group at the 3′ position, contributing to its structural similarity to (S)-3′-Hydroxy-N-methylcoclaurine.
Another similar compound is (S)-N-Methylcoclaurine, which shares the N-methyl substitution but lacks the hydroxy group at the 3′ position. This compound maintains the same basic structure as (S)-3′-Hydroxy-N-methylcoclaurine but differs in the absence of the hydroxy group at a specific position on the molecule.
Additionally, (S)-Coclaurine can be considered a similar compound, as it lacks both the hydroxy group at the 3′ position and the N-methyl substitution found in (S)-3′-Hydroxy-N-methylcoclaurine. While sharing a similar backbone structure, this compound differs in the absence of specific functional groups that characterize (S)-3′-Hydroxy-N-methylcoclaurine.
