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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Piperidines Piperidines
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Piperidines

Comprehensive Guide to 3-Piperidine Ethanol (CAS No. 73579-06-3): Properties, Applications, and Market Insights

3-Piperidine ethanol (CAS No. 73579-06-3) is a versatile organic compound with significant applications in pharmaceuticals, agrochemicals, and specialty chemicals. This compound, also known as 3-(2-Hydroxyethyl)piperidine, features a unique molecular structure combining a piperidine ring with an ethanol side chain, making it valuable for synthetic chemistry and industrial applications. Below, we explore its properties, synthesis methods, applications, and market trends.

The chemical structure of 3-Piperidine ethanol consists of a six-membered piperidine ring attached to a two-carbon ethanol group. This structure grants it both basic (due to the nitrogen in the piperidine ring) and hydrophilic (due to the hydroxyl group) properties. Its molecular formula is C7H15NO, and it typically appears as a colorless to pale yellow liquid with a mild amine-like odor. The compound's boiling point ranges between 210–220°C, and it is soluble in water and most organic solvents, enhancing its utility in various formulations.

One of the primary applications of 3-Piperidine ethanol is in the pharmaceutical industry, where it serves as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs). Researchers and manufacturers value it for its role in constructing complex molecules, particularly in central nervous system (CNS) drugs and analgesics. Recent studies highlight its potential in developing novel neuroprotective agents, aligning with the growing demand for treatments targeting neurodegenerative diseases like Alzheimer's and Parkinson's.

Beyond pharmaceuticals, 3-Piperidine ethanol finds use in agrochemical formulations, where it acts as a building block for pesticides and herbicides. Its structural flexibility allows chemists to modify its derivatives for enhanced efficacy and environmental safety—a critical consideration given the increasing regulatory scrutiny on agrochemicals. Additionally, the compound is employed in specialty chemicals, such as corrosion inhibitors and surfactants, due to its amphiphilic nature.

The synthesis of 3-Piperidine ethanol typically involves the reduction of 3-Piperidine acetic acid derivatives or the nucleophilic substitution of piperidine with ethylene oxide. Advances in green chemistry have spurred interest in catalytic methods that minimize waste and improve yield, reflecting broader industry trends toward sustainable production. Researchers are also exploring biocatalytic routes using engineered enzymes, which could further reduce the environmental footprint of its synthesis.

Market demand for 3-Piperidine ethanol is driven by its pharmaceutical and agrochemical applications, with Asia-Pacific emerging as a key production and consumption hub. The compound's versatility and the expanding life sciences sector contribute to its steady growth. Industry reports project a CAGR of 4–6% over the next five years, fueled by R&D investments in drug discovery and precision agriculture.

For researchers and procurement specialists, selecting high-quality 3-Piperidine ethanol requires attention to purity (>98%), supplier reliability, and compliance with regional regulations. Reputable suppliers provide detailed technical data sheets (TDS) and material safety data sheets (MSDS) to ensure safe handling and storage. As the compound is hygroscopic, proper storage in airtight containers under inert conditions is recommended to maintain stability.

In summary, 3-Piperidine ethanol (CAS No. 73579-06-3) is a multifaceted compound with expanding applications in high-growth industries. Its synthesis, properties, and market dynamics underscore its importance in modern chemistry. For further inquiries, consult specialized chemical databases or trusted suppliers to access the latest research and pricing trends.

• 761373-48-2(1-Azabicyclo[2.2.2]octane-3-propanol(9CI))
• 144539-77-5([(3S)-piperidin-3-yl]methanol)
• 7037-49-2(3-(piperidin-4-yl)propan-1-ol)
• 16780-04-4(2-(3-piperidyl)ethanol;hydrochloride)
• 37675-20-0([(3R)-piperidin-3-yl]methanol)
• 25175-58-0(3-(Piperidin-3-yl)propan-1-ol)
• 4606-65-9(piperidin-3-ylmethanol)
• 622-26-4(2-(piperidin-4-yl)ethan-1-ol)
• 51071-76-2(1H-Cyclopenta[c]pyridine-6-methanol,octahydro-,(4a-alpha-,6-bta-,7a-alpha-)-(9CI))
• 920016-99-5(3-azabicyclo[3.2.1]octane-8-methanol hydrochloride)