Compound Profile

Harmaline

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Harmaline, a psychoactive alkaloid derived from certain plants such as the Syrian rue, holds significance in everyday life due to its potential therapeutic and recreational uses. With its reported ability to induce altered states of consciousness and potentially enhance mood and cognitive function, harmaline has drawn the interest of researchers and individuals seeking alternative treatments for mental health conditions or recreational experiences. Despite regulatory restrictions on its use, harmaline continues to be explored for its potential benefits and its impact on human behavior and consciousness.

Table of Contents:

💡  Commercial Applications

Harmaline, a natural psychoactive alkaloid extracted from plants of the genus Peganum, has limited commercial and industrial applications. One potential use is as a chemical intermediate in the synthesis of other compounds. Additionally, harmaline has been studied for its potential insecticidal properties.

In terms of drug and medication applications, harmaline has been investigated for its potential use in treating neurological disorders such as Parkinson’s disease. Studies have shown that harmaline has the ability to improve motor coordination in animal models of the disease. It is believed that harmaline’s effects on the brain’s neurotransmitter systems may hold promise for future therapeutic interventions.

Despite its limited commercial and industrial uses, harmaline remains a subject of ongoing research in the fields of pharmacology and neurology. Its potential as a drug target for certain neurological disorders continues to be explored, offering hope for new treatment options in the future. Additionally, its natural origins and psychoactive properties make harmaline a compound of interest for further investigation and potential application.

⚗️  Chemical & Physical Properties

Harmaline is a white crystalline powder with a bitter taste and a faint odor resembling that of violets. It is commonly found in seeds of the Peganum harmala plant, also known as Syrian rue.

Harmaline has a molar mass of 212.28 g/mol and a density of 1.12 g/cm³. In comparison to common food items, harmaline has a higher molar mass and density. For example, the molar mass of table sugar is 342.30 g/mol, while the density of water is 1 g/cm³.

The melting point of harmaline is around 235-237°C, while the boiling point is approximately 294-295°C. In comparison to common food items, harmaline has a higher melting point and boiling point. For example, the melting point of butter is around 32-35°C, while the boiling point of water is 100°C.

Harmaline is sparingly soluble in water and has a low viscosity. In comparison to common food items, harmaline has lower solubility in water and viscosity. For example, table salt is highly soluble in water, while honey has a higher viscosity than harmaline.

🏭  Production & Procurement

Harmaline, a psychoactive alkaloid found in certain plants such as Peganum harmala, is primarily produced through a process of extraction and isolation. The plants containing Harmaline are typically harvested and the alkaloid is extracted using solvents such as ethanol or acetone. The extracted alkaloid is then isolated through various purification techniques to obtain pure Harmaline.

Harmaline can be procured through various means, including cultivation of plants containing the alkaloid or through purchase from suppliers. Cultivation of plants such as Peganum harmala requires suitable growing conditions and knowledge of harvesting practices. Alternatively, Harmaline can be purchased from chemical suppliers who specialize in providing research chemicals to academic institutions and pharmaceutical companies.

Once procured, Harmaline can be transported through various methods depending on the quantity and regulatory restrictions. Small quantities of Harmaline can be shipped via postal services or courier companies, while larger quantities may require specialized shipping arrangements. It is important to adhere to regulations governing the transportation of psychoactive substances to ensure legal compliance and safety.

⚠️  Safety Considerations

Safety considerations for Harmaline entail the recognition of its potential hazards to human health and the environment. Harmaline is a known neurotoxin which may cause central nervous system depression, respiratory issues, and gastrointestinal distress if ingested or inhaled. Prolonged or repeated exposure to Harmaline may also lead to organ damage, including liver and kidney toxicity. Careful handling and storage of Harmaline are essential to prevent accidental exposure, and appropriate personal protective equipment should be worn when working with this compound.

Hazard statements for Harmaline indicate its potential risks to human health and the environment. These include phrases such as “toxic if swallowed, inhaled, or in contact with skin” and “causes skin and eye irritation.” Harmaline is also labeled as a possible carcinogen and mutagen, with specific precautionary measures recommended to minimize exposure and protect against its hazardous effects. It is crucial to adhere to safety guidelines and regulations when working with Harmaline to prevent harm to individuals and the surrounding environment.

Precautionary statements for Harmaline emphasize the importance of protective measures to minimize risks associated with its handling and use. These statements include instructions such as “wear protective gloves/eye protection/face protection” and “use only outdoors or in a well-ventilated area.” It is advised to store Harmaline in a secure location away from incompatible materials and to avoid direct contact with skin, eyes, and clothing. Proper disposal methods should be followed to prevent environmental contamination and potential harm to living organisms. Adherence to precautionary statements is essential to ensure the safe handling and use of Harmaline in various settings.

🔬  Potential Research Directions

One potential research direction of Harmaline is its therapeutic potential in the treatment of neurological disorders, such as Parkinson’s disease. Studies have shown that Harmaline may have neuroprotective effects and could potentially help alleviate symptoms associated with movement disorders.

Another area of research interest is the investigation of Harmaline’s effects on mood and behavior. Preclinical studies have suggested that Harmaline may have antidepressant and anxiolytic properties, which could have implications for the treatment of mood disorders.

Furthermore, researchers are exploring the potential of Harmaline as a tool for studying the neural circuits involved in motor control and coordination. By understanding how Harmaline disrupts motor function, scientists can gain insights into the underlying mechanisms of movement disorders and potentially develop new therapeutic strategies.

One compound with a molecular structure similar to harmaline is harmine. Harmine, also known as telepathine, is a fluorescent harmala alkaloid which has been found in a number of different plant species. It is a reversible inhibitor of monoamine oxidase A (MAO-A) and a competitive antagonist of the serotonin receptor.

Another compound related to harmaline in terms of molecular structure is tetrahydroharmine. Tetrahydroharmine is a naturally-occurring β-carboline alkaloid found in various plant species. It is structurally related to harmaline and harmine, sharing a similar core structure and certain pharmacological properties.

A further compound in the same structural family as harmaline is harmol. Harmol is a metabolite of harmaline, arising from the reduction of the carbonyl group in harmaline. Like harmaline, harmol has been shown to exhibit hallucinogenic effects and to have affinity for serotonin receptors. It is closely related to other harmala alkaloids and shares similarities in its biological activity.

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