The phrase "alkyl ether" is correct and usable in written English.
It can be used in scientific or chemical contexts to refer to a class of organic compounds derived from alcohols.
Example: "The reaction produced an alkyl ether, which is commonly used as a solvent in various industrial applications."
Alternatives: "alkyl alkylate" or "alkyl ether compound".
A foaming agent (6 mL, EMAL D-3-D, sodium polyoxyethylene alkyl ether sulfate, Kao Corp).
[(EO -3C-im][NTf2] was first synthEO -3C-imrough incorporating alkyl EO -3C-imety into the double imidazolium ring.
These classes also encompass anionic and cationic surfactants such as methylestersulphonate, olefinsulphonate, alkyl benzene sulphonates, alkyl ether sulphates, isotridecanolethoxylates, benzalkonium chloride, n-hexadecyltrimethy, and ammonium chloride.
MFD simulations of the nonionic polyoxyethylene alkyl ether surfactants C6E6, C10E6, C12E6 and C16E6 at the water-air interface are performed to study their nanoscale structures and surface properties.
The simulations of the self-aggregation of the polyoxyethylene alkyl ether surfactants lead to equilibrium nanoscale structures and computationally determined surface tensions which are in agreement with experimental data for different surfactant concentrations [1]. Figure 1.
Aryl ether, alkyl ether, aryl amine, alkyl amine, aryl sulfide, alkyl sulfide, etc., which are all very important structural fragments in many chemical molecules, have an urgent need for better synthetic methods.
The present approach provides a possible route to apply alkyl ethers of aminodeoxyinositols as hexopyranose mimics of biological interest.
Alkyl ethers can be synthesized by the reaction of glycerol with alkenes and preferentially with isobutylene in the presence of an acid catalyst.
The results show relaxation times τ2 in the range of seconds for Triton X-100 to minutes for polyoxyethylene alkyl ethers.
The results showed that the ionic surfactants such as SDS exhibit slow relaxation times in the range from milliseconds to seconds, whereas nonionic surfactants exhibit slow relaxation times in the range from seconds (for Triton X-100) to minutes (for polyoxyethylene alkyl ethers).
PI and PIPx are derivatives of sn-glycero-3-phosphate with (a) an acyl, an alkyl (ether-linked plasmanyl), or an alkenyl (alkyl-1′-enyl, vinyl ether-linked plasmenyl) carbon chain; (b) a fatty acid commonly esterified but also with possible alkyl or alkenyl linkages to the sn-2 position; and (c) a polar headgroup composed of an inositol unit modifying the phosphate group at the sn-3 position.
