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Brc1cnc(nc1)C
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CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
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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
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Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

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

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Chemical Name: Ethanol, 2-[2-[2-(dodecyloxy)ethoxy]ethoxy]-
CAS Number: 3055-94-5
Product Number: AG0030J3(AGN-PC-0JLQ1O)
Synonyms:
MDL No:
Molecular Formula: C18H38O4
Molecular Weight: 318.4919

Identification/Properties

Properties
MP:
16.5-17.0℃
Storage:
Room Temperature;
Form:
Liquid
Refractive Index:
n20/D 1.451
Computed Properties
Molecular Weight:
318.498g/mol
XLogP3:
4.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
19
Exact Mass:
318.277g/mol
Monoisotopic Mass:
318.277g/mol
Topological Polar Surface Area:
47.9A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
188
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Triethyleneglycolmono-n-dodecylether, also known as TEGMDoE, is a versatile compound widely used in chemical synthesis. Its unique properties make it a valuable tool in various reactions and processes. TEGMDoE serves as an excellent surfactant and emulsifier, aiding in the dispersion of reactants and facilitating the formation of stable emulsions in organic solvents. This characteristic is particularly beneficial in polymerization reactions, where TEGMDoE can help control the size and distribution of particles.Additionally, TEGMDoE is a valuable solvent in organic synthesis, especially in reactions that require both hydrophilic and hydrophobic components. Its ability to solubilize a wide range of compounds makes it a popular choice in the production of specialty chemicals and pharmaceutical intermediates.Furthermore, TEGMDoE can act as a phase transfer catalyst, enhancing the transfer of reactants between immiscible phases and promoting efficient reactions. This property is particularly advantageous in processes such as nucleophilic substitution and catalysis.In conclusion, Triethyleneglycolmono-n-dodecylether plays a crucial role in chemical synthesis by serving as a surfactant, solvent, and phase transfer catalyst. Its versatility and unique properties make it a valuable asset in various industries, including pharmaceuticals, polymers, and specialty chemicals.