2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. SDS of cas: 112-59-4
Surface Activity of Alkoxy Ethoxyethyl β-D-Glucopyranosides was written by Fan, Yulin;Fu, Fang;Chen, Langqiu;Li, Jiping;Zhang, Jing. And the article was included in Journal of Agricultural and Food Chemistry in 2020.SDS of cas: 112-59-4 The following contents are mentioned in the article:
Dioxyethene fragment (-(OCH2CH2)2-) was introduced into traditional alkyl β-D-glucopyranosides to ameliorate the water solubility, and eight nonionic surfactants, i.e., alkoxy ethoxyethyl β-D-glucopyranosides with alkyl chain lengths (n = 6-16), were synthesized and characterized. Their hydrophilic and lipophilic balance number, water solubility, critical micelle concentration (cmc), γcmc, Γmax, and hygroscopic rate decreased with an increase in the alkyl chain length. Hexadecoxy ethoxyethyl β-D-glucopyranoside had no water solubility at 25°C. Decoxy ethoxyethyl β-D-glucopyranoside had the best emulsifying property in the toluene/water and n-octane/water systems and the strongest foaming property, whereas dodecoxy ethoxyethyl β-D-glucopyranoside had the best emulsifying property in the rapeseed oil/water system. Such β-D-glucopyranosides (n = 6-12) exhibited excellent surface activity. In addition, for the binary mixture of alkoxy ethoxyethyl β-D-glucopyranosides (n = 8, 10, 12) and sodium dodecyl sulfate or cetyl tri-Me ammonium chloride, their cmc values were lower than the pure β-D-glucopyranosides, indicating that they had synergistic interactions. The fan focal conic textures of alkoxy ethoxyethyl β-D-glucopyranosides (n = 7-16) were observed during the cooling process under a polarizing optical microscope. Alkoxy ethoxyethyl β-D-glucopyranosides (n = 14, 16) had the related m.ps. and the clear points with differential scanning calorimetry. With β-D-glucopyranosides (n = 6-16) and n-butanol as the surfactant and cosurfactant, resp., and with cyclohexane as the oil phase, the related microemulsion areas in their pseudoternary phase diagram system were investigated with the visual observation at 25°C. Along with the slashing requirements of petroleum consumption, environmental protection, and green and sustainable development, nonionic sugar-based alkoxy ethoxyethyl β-D-glucopyranosides should be expected to have their potential practical application because of their strengthened hydrophilicity, improved water solubility, and enhanced surface activity. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4SDS of cas: 112-59-4).
2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. SDS of cas: 112-59-4
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem