1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol is a chemical compound that has several applications in everyday life. This compound is commonly used as a beta-blocker medication in the treatment of cardiovascular conditions such as hypertension and angina. By blocking the action of certain hormones like adrenaline, this compound helps to lower blood pressure and reduce the workload on the heart.
Additionally, 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol has also been found to have potential benefits in treating other conditions such as migraines, anxiety, and tremors. Its ability to regulate heart rate and blood pressure make it a valuable tool in managing these conditions and improving quality of life for many individuals.
In conclusion, 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol plays a crucial role in modern medicine and has a significant impact on everyday life by helping individuals manage various cardiovascular and neurological conditions effectively.
Table of Contents:
- 💡 Commercial Applications
- ⚗️ Chemical & Physical Properties
- 🏭 Production & Procurement
- ⚠️ Safety Considerations
- 🔬 Potential Research Directions
- 🧪 Related Compounds
💡 Commercial Applications
1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol, also known as propranolol, has various commercial and industrial applications. It is commonly used in the pharmaceutical industry as a beta-blocker medication for treating high blood pressure, heart rhythm disorders, and other cardiovascular conditions. Additionally, propranolol is utilized in research laboratories for studying the effects of beta-adrenergic receptor antagonists.
In terms of commercial applications, propranolol has found use in the cosmetic industry as an ingredient in skin creams and ointments due to its beta-blocking properties that can help reduce redness and inflammation. Moreover, this compound is employed in the production of pesticides as an active ingredient in formulations targeting specific pests. Overall, the commercial and industrial applications of propranolol exhibit its versatility and importance in various sectors.
However, when considering its drug and medication applications, propranolol is most notably recognized for its role in treating hypertension, angina, migraines, and tremors. As a non-selective beta-blocker, it works by blocking the action of certain natural chemicals in the body, such as epinephrine, that affect the heart and blood vessels. This mechanism of action makes propranolol an effective medication for managing cardiovascular and neurologic conditions in patients.
Furthermore, propranolol has been studied and used off-label for additional medical purposes, such as reducing stage fright, managing symptoms of anxiety disorders, and preventing severe migraines. Its ability to cross the blood-brain barrier and modulate neurotransmitter levels in the brain has contributed to its efficacy in addressing these conditions. Overall, the drug and medication applications of propranolol highlight its clinical significance and therapeutic benefits in various healthcare settings.
⚗️ Chemical & Physical Properties
1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol is a white crystalline solid with a slight chemical odor. It appears as small crystals and has a faint, but distinct, scent.
The molar mass of 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol is approximately 307.4 g/mol, while its density is around 1.01 g/cm^3. This substance has a higher molar mass and density compared to common food items such as sugar or salt.
The melting point of 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol is approximately 60-63°C, while its boiling point is around 300-305°C. These values are significantly higher than those of common food items like butter or chocolate.
1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol is sparingly soluble in water and has a relatively low viscosity. This substance’s solubility in water and viscosity are notably different from common food items like milk or juice.
🏭 Production & Procurement
1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol, often referred to as t-butylamino cinnanol, is synthesized through a multi-step chemical reaction process. The key starting materials include tert-butylamine, 2-cyclopentylphenol, and propylene oxide. These compounds are reacted under controlled conditions to yield the desired product.
Following the synthesis process, 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol can be procured from chemical suppliers specializing in fine chemicals and intermediates. The compound is typically supplied in liquid form, packaged in suitable containers to ensure safe handling and transportation. It is important to adhere to proper storage and handling procedures to maintain the quality and integrity of the product during transit.
Transportation of 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol is carried out using approved chemical transport vehicles to comply with regulations governing the handling and movement of hazardous materials. Proper labeling and documentation are required to ensure the safe and efficient delivery of the compound to its intended destination. It is recommended to work with experienced logistics providers to facilitate the secure transport of this chemical compound.
⚠️ Safety Considerations
Safety considerations for 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol should be taken seriously due to its potential hazards. The compound may cause skin irritation and eye irritation upon contact. It can also be harmful if swallowed, inhaled, or absorbed through the skin.
It is important to handle 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol with care to avoid any accidents or exposure. When working with this compound, appropriate personal protective equipment such as gloves, goggles, and lab coat should be worn. In case of accidental exposure, it is important to seek medical attention immediately and provide the doctor with the Safety Data Sheet for proper treatment.
Hazard statements for 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol include “Causes skin irritation,” “Causes serious eye irritation,” and “Harmful if swallowed.” These hazard statements indicate the potential risks associated with the compound and emphasize the importance of proper handling and storage to prevent any adverse effects on human health.
Precautionary statements for 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol include “Wear protective gloves/eye protection/face protection,” “IF SWALLOWED: Call a POISON CENTER/doctor if you feel unwell,” and “IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do.” These precautionary statements provide guidance on how to safely handle and respond to exposure to the compound to minimize the risk of harm.
🔬 Potential Research Directions
Potential research directions for 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol may include investigating its pharmacological properties and potential therapeutic applications in the treatment of various medical conditions.
Researchers may also explore its mechanism of action, metabolic pathways, and potential interactions with other drugs or compounds.
Furthermore, studies could be conducted to determine the safety profile, toxicity levels, and potential side effects of 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol to assess its suitability for clinical use.
🧪 Related Compounds
One similar compound to 1-(Tert-butylamino)-3-(2-cyclopentylphenoxy)propan-2-ol based upon molecular structure is 1-(Tert-butylamino)-3-(2-cyclohexylphenoxy)propan-2-ol. This compound has a similar tertiary amine group attached to a cyclohexylphenol moiety, but with a cyclohexyl ring instead of a cyclopentyl ring. The presence of the cyclohexyl ring imparts different steric and electronic properties to the molecule compared to the original compound.
Another similar compound is 1-(Tert-butylamino)-3-(2-phenylphenoxy)propan-2-ol. In this compound, the cyclopentyl ring is replaced by a phenyl ring, leading to a different set of physicochemical properties. The presence of the phenyl ring may influence the compound’s solubility, stability, and biological activity compared to the original compound.
A third similar compound is 1-(Tert-butylamino)-3-(2-methylcyclopentylphenoxy)propan-2-ol. This compound maintains the cyclopentylphenol moiety present in the original compound but introduces a methyl group to the cyclopentyl ring. The addition of the methyl group may impact the compound’s lipophilicity, hydrophobic interactions, and overall pharmacological profile.
