• 1. A triple-triangle cluster derived from a simple tridentate ligand
  Takuya Shiga,Natsumi Okawa,Hiroki Oshio Dalton Trans. 2019 48 17437

• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives 2-pyridylmethylamines

Comprehensive Overview of 2-(Pyridin-2-ylmethyl)-amino-ethanol (CAS No. 6636-71-1): Properties, Applications, and Industry Insights

2-(Pyridin-2-ylmethyl)-amino-ethanol (CAS No. 6636-71-1) is a versatile organic compound with a pyridine-based structure, widely recognized for its role in pharmaceutical intermediates, agrochemical synthesis, and specialty chemical formulations. This compound, often referred to by its systematic name or CAS number, has garnered significant attention due to its unique molecular properties, including a balanced hydrophilic-lipophilic character and reactive amino-alcohol functionality. Researchers and industry professionals frequently search for "6636-71-1 synthesis," "2-(Pyridin-2-ylmethyl)-amino-ethanol applications," and "pyridine derivative uses," reflecting its broad utility across scientific disciplines.

The molecular structure of 2-(Pyridin-2-ylmethyl)-amino-ethanol combines a pyridine ring with an ethanolamine side chain, enabling dual reactivity as both a hydrogen bond donor and acceptor. This feature makes it valuable in catalysis, where queries like "pyridine-ethanolamine catalyst" trend in scientific databases. Recent studies highlight its potential in green chemistry applications, aligning with the global focus on sustainable synthesis methods. The compound's solubility profile—miscible in polar solvents like water and ethanol—also supports its use in formulations where "solubility enhancement strategies" are critical, a hot topic in drug delivery system research.

In pharmaceutical contexts, CAS 6636-71-1 serves as a key intermediate for bioactive molecules, particularly those targeting neurological pathways. Online searches for "pyridine derivatives in CNS drugs" correlate with this application. Its structural similarity to neurotransmitter modulators has spurred interest in medicinal chemistry, though rigorous safety assessments are always recommended. The compound's stability under physiological pH ranges (investigated via "6636-71-1 stability studies") further enhances its appeal for biomedical uses.

Industrial applications of 2-(Pyridin-2-ylmethyl)-amino-ethanol extend to corrosion inhibition, where its nitrogen-rich structure forms protective metal chelates—a subject explored in queries like "pyridine-based corrosion inhibitors." Additionally, its role in polymer modification (search term: "amino-ethanol polymer additives") contributes to materials with improved thermal resistance, addressing industry demands for high-performance composites. Analytical methods for this compound, including HPLC and GC-MS protocols (often searched as "6636-71-1 analysis methods"), ensure quality control in these applications.

Environmental and handling considerations for 6636-71-1 follow standard laboratory safety protocols, with particular attention to its amine functionality. While not classified as high-risk, proper storage conditions (searched as "pyridine-ethanolamine storage guidelines") are essential to maintain stability. The compound's biodegradability profile, a growing concern in chemical manufacturing, has been investigated through "ecological impact of pyridine derivatives" studies, showing moderate environmental persistence under aerobic conditions.

Market trends indicate rising demand for 2-(Pyridin-2-ylmethyl)-amino-ethanol, driven by expanding pharmaceutical R&D in Asia-Pacific regions. Patent analysis (search term: "6636-71-1 patent applications") reveals innovative uses in electronic materials and asymmetric synthesis. As regulatory landscapes evolve, documentation of "pyridine-ethanolamine regulatory status" remains crucial for global compliance. Future research directions may explore its potential in energy storage systems, responding to queries about "nitrogen-containing compounds for batteries."

For synthetic chemists, optimization of 6636-71-1 production routes continues to be refined, with microwave-assisted and flow chemistry approaches gaining traction (searched as "green synthesis of pyridine ethanolamines"). The compound's cost-effectiveness compared to similar heterocyclic amines contributes to its commercial viability. Analytical challenges, such as distinguishing stereoisomers (studied via "chiral separation of 2-(Pyridin-2-ylmethyl)-amino-ethanol"), represent active areas of methodological development.

In conclusion, 2-(Pyridin-2-ylmethyl)-amino-ethanol (CAS No. 6636-71-1) exemplifies the importance of multifunctional pyridine derivatives in modern chemistry. Its diverse applications—from life sciences to industrial processes—are reflected in trending search terms like "multipurpose pyridine compounds" and "specialty chemical innovations." As interdisciplinary research progresses, this compound will likely find new roles in emerging technologies, maintaining its relevance across scientific and industrial communities.

• 109746-53-4(6,9-dioxa-3,12,18-triazabicyclo[12.3.1]octadeca-1(18),14,16-triene)
• 62402-15-7(Ethanol, 2-[[2-[(2-pyridinylmethyl)amino]ethyl]amino]-)
• 1539-42-0(Bis(2-pyridylmethyl)amine)
• 149860-22-0(2-(Bis-(2-pyridyl-methyl)-amino)-ethanol)
• 62402-29-3(Ethanol, 2-[[2-[[2-[(2-pyridinylmethyl)amino]ethyl]amino]ethyl]amino]-)
• 29227-68-7(Pyridinemethanamine, N-(pyridinylmethyl)-)
• 62402-19-1((2-methoxyethyl)(pyridin-2-ylmethyl)amine)
• 302542-43-4(Ethanol,2-[[2-[bis(2-pyridinylmethyl)amino]ethyl](2-pyridinylmethyl)amino]-)
• 2444-13-5(2-{(pyridin-2-yl)methylamino}acetic acid)
• 51639-58-8(N-Ethyl-N-(2-pyridylmethyl)amine)