Ether Phase Separation

Ether phase separation is a laboratory extraction technique that separates compounds between an ether-rich organic phase and an aqueous phase according to their solubility and chemical properties. The process relies on the limited miscibility of ether and water: after mixing, centrifugation or settling allows the less-dense ether layer to form above the aqueous layer, while hydrophobic molecules preferentially partition into the organic phase. In biology, this method supports the isolation and purification of lipids, metabolites, and other nonpolar compounds from complex samples. Careful control of pH, solvent ratios, and phase recovery improves selectivity and helps prepare samples for downstream biochemical analysis.

Ether Phase Separation - Related Videos

Research

JoVE EoE - Bacterial Growth and Techniques

Enrichment of Bacterial Lipoproteins Using Non-Ionic Detergent Phase Separation

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2025

Source: Armbruster, K. M., Meredith, T. C. Enrichment of Bacterial Lipoproteins and Preparation of N-terminal Lipopeptides for Structural Determination by Mass Spectrometry. J. Vis. Exp. (2018)This video demonstrates the enrichment of bacterial lipoproteins using a non-ionic detergent that undergoes phase separation upon warming. Through sequential temperature shifts and centrifugation steps, lipoproteins are selectively partitioned into the detergent phase, while non-lipoprotein contaminants...

Protein Phase Separation Assay: An Optogenetic Method for Mutant RNA-Binding Protein Phase Separation in Spinal Motor Neurons of Zebrafish Larvae

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2025

In this video, we describe a phase separation assay, wherein intracellular proteins comprising intrinsically disordered regions fused to a photosensitive oligomerization domain are induced via blue-light exposure to self-associate into membrane-less liquid-like condensates.

Education

JoVE Core - Organic Chemistry

Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis

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2023

Overview Ethers can be prepared from organic compounds by various methods. Some of them are discussed below, Preparation of Ethers by Alcohol Dehydration In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K. This method is a nucleophilic substitution reaction. The two alcohol molecules...

Structure and Nomenclature of Ethers

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2025

Structure and Bonding Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm. Classification of Ethers Based on their attached substituent groups, ethers can be classified into two...

Crown Ethers

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2023

Crown ethers are cyclic polyethers that contain multiple oxygen atoms, usually arranged in a regular pattern. The first crown ether was synthesized by Charles Pederson while working at DuPont in 1967. For this work, Pedersen was co-awarded the 1987 Nobel Prize in Chemistry. Crown ethers are named using the formula x-crown-y, where x is the total number of atoms in the ring and y is the number of ether oxygen atoms. The term 'crown' refers to the crown-like shape that these ether molecules take.

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