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Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Ethanol, 2-[2-[2-(decyloxy)ethoxy]ethoxy]-

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Chemical Name: Ethanol, 2-[2-[2-(decyloxy)ethoxy]ethoxy]-
CAS Number: 4669-23-2
Product Number: AG00721D(AGN-PC-0JSD2F)
Synonyms:
MDL No:
Molecular Formula: C16H34O4
Molecular Weight: 290.4388

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Chemical Structure


Triethylene glycol monodecyl ether, also known as $name$, serves as an effective solvent and surfactant in various chemical synthesis processes. Its unique properties make it a versatile compound widely used in the production of pharmaceuticals, cosmetics, and other specialty chemicals. $name$ facilitates the dissolution of both polar and non-polar substances, making it an excellent choice for extracting or dispersing a wide range of compounds. Additionally, its surfactant properties allow for improved emulsification and dispersion in liquid formulations. In chemical synthesis, $name$ can be utilized as a reaction medium or a stabilizing agent to enhance reaction efficiency and product yield. Its compatibility with various organic solvents and its ability to lower the interfacial tension make it a valuable tool in the development of novel chemical processes. Overall, the application of Triethylene glycol monodecyl ether in chemical synthesis offers numerous advantages and contributes to the advancement of diverse scientific disciplines.