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Comprehensive Overview of 2-Propanol, 1-(diethylamino)-2-methyl- (CAS No. 36293-04-6): Properties, Applications, and Industry Insights

2-Propanol, 1-(diethylamino)-2-methyl- (CAS No. 36293-04-6) is a specialized organic compound with a unique molecular structure that combines an isopropanol backbone with diethylamino and methyl functional groups. This configuration grants the molecule distinct physicochemical properties, making it valuable in various industrial and research applications. The compound is also referred to by its systematic IUPAC name, 1-(diethylamino)-2-methylpropan-2-ol, which precisely describes its chemical architecture.

In recent years, the demand for functionalized alcohols like 2-Propanol, 1-(diethylamino)-2-methyl- has surged due to their versatility in pharmaceutical intermediates, agrochemical formulations, and specialty solvents. Researchers and manufacturers frequently search for "CAS 36293-04-6 solubility" or "1-(diethylamino)-2-methyl-2-propanol synthesis," reflecting the compound's technical relevance. Its balanced polarity and amine-alcohol synergy enable applications in catalysis and surface modification, aligning with trends in green chemistry and sustainable material design.

The compound's physicochemical profile includes a moderate boiling point (typically 180–190°C) and good miscibility with polar organic solvents, which users often inquire about when optimizing reaction conditions. Analytical techniques like GC-MS and NMR spectroscopy are commonly employed for its characterization, as noted in queries such as "36293-04-6 spectroscopic data." These properties make it a candidate for high-performance liquid chromatography (HPLC) mobile phase adjustments and polymer additive formulations.

From an industrial perspective, 2-Propanol, 1-(diethylamino)-2-methyl- plays a role in corrosion inhibition systems, particularly in metalworking fluids where its amine group contributes to pH stabilization. This aligns with growing interest in "environmentally friendly corrosion inhibitors"—a hot topic in material science forums. Additionally, its derivatization potential supports fine chemical synthesis, answering frequent searches for "CAS 36293-04-6 reactivity" and "amine-alcohol cross-coupling."

Quality control protocols for this compound emphasize purity verification (often ≥98% by GC) and moisture content management, critical for sensitive applications like electronic-grade chemicals. The rise of battery technology and semiconductor manufacturing has further driven interest in its electrochemical properties, with researchers exploring its utility in electrolyte formulations and dielectric layers.

In conclusion, 2-Propanol, 1-(diethylamino)-2-methyl- (CAS No. 36293-04-6) represents a multifaceted compound bridging traditional chemistry and emerging technologies. Its dual functional groups respond to contemporary needs for multifunctional additives and tailored molecular architectures, while analytical queries around "36293-04-6 safety data" and "biodegradability of amino alcohols" reflect evolving regulatory and sustainability considerations in chemical development.

• 138001-48-6(2-methyl-1-[(2-methylpropyl)amino]propan-2-ol)
• 391689-42-2(Ethoxy, 2-(ethylmethylamino)-1,1-dimethyl-)
• 391689-44-4(Ethoxy, 1,1-dimethyl-2-[methyl(1-methylethyl)amino]-)
• 14123-48-9(1-(Dimethylamino)-2-methylpropan-2-OL)
• 156339-46-7(2-methyl-1-(piperazin-1-yl)propan-2-ol)
• 51387-97-4(2-Propanol, 1-[(2-aminoethyl)ethylamino]-2-methyl-)
• 73825-96-4(1-(ethylamino)-2-methylpropan-2-ol)
• 79365-81-4(1-(2-hydroxy-2-methylpropyl)amino-2-methylpropan-2-ol)
• 60278-96-8(1,2-Propanediol,3-[bis(2-methylpropyl)amino]-)
• 921752-39-8(2-Propanol, 1,1'-[[3-(dimethylamino)-2,2-dimethylpropyl]imino]bis-)