Crystallisation From Volatile Deep Eutectic Solvents
Jason Potticary, Charlie Hall, Victoria Hamilton, James F. McCabe,, Simon R. Hall

TL;DR
This paper introduces volatile deep eutectic solvents that enable controlled crystallization and polymorphism, including the spontaneous formation of a more effective acetaminophen form at room temperature.
Contribution
It presents a novel class of volatile deep eutectic solvents with auto-destructive capabilities for controlled crystallization and pharmaceutical polymorphism.
Findings
Successful control of pharmaceutical polymorphism.
First spontaneous formation of a more efficacious acetaminophen form at room temperature.
Demonstration of the solvents' physical characteristics similar to classical deep eutectic solvents.
Abstract
A new class of deep eutectic solvents are presented where one component of the system is inherently volatile, enabling a premeditated, auto-destructive capability which leads inexorably to a series of novel crystal structures. These volatile deep eutectic solvents are easily-formed liquids with a greatly depressed melting point and exhibit all of the physical characteristics of classical deep eutectic solvents, with the exception that the hydrogen-bond donor component is volatile when exposed to the atmosphere at room temperature. We demonstrate the effectiveness of this concept through the exquisite control of pharmaceutical polymorphism, among which is a more efficacious form of acetaminophen, which can be formed spontaneously for the first time at room temperature.
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Taxonomy
TopicsIonic liquids properties and applications · Crystallization and Solubility Studies · Analytical chemistry methods development
