DODECYL GLYCIDYL ETHER|2461-18-9,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

DODECYL GLYCIDYL ETHER

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Chemical Name:	DODECYL GLYCIDYL ETHER
CAS Number:	2461-18-9
Product Number:	AG002ORB(AGN-PC-0WAK1B)
Synonyms:
MDL No:
Molecular Formula:	C15H30O2
Molecular Weight:	242.3975

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Computed Properties

Molecular Weight:

242.403g/mol

XLogP3:

5.4

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

242.225g/mol

Monoisotopic Mass:

242.225g/mol

Topological Polar Surface Area:

21.8A^2

Heavy Atom Count:

Formal Charge:

Complexity:

159

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

Hazard Statements:

H315-H319-H413

Precautionary Statements:

P501-P273-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

Laurylglycidylether, also known as LGE, plays a crucial role in chemical synthesis as a versatile and highly reactive compound. Its primary application lies in acting as a key building block in the production of various specialty chemicals, resins, and polymers.In chemical synthesis, Laurylglycidylether is often used as a precursor in the synthesis of epoxy resins. Epoxy resins are widely used in various industries such as construction, automotive, and electronics due to their excellent adhesive properties and high chemical resistance. Laurylglycidylether's epoxide group allows for it to undergo reactions with curing agents, resulting in the formation of strong and durable epoxy materials.Furthermore, Laurylglycidylether can also serve as a reactive intermediate in the preparation of surfactants and emulsifiers. Its unique chemical structure makes it suitable for modifying the surface properties of materials and enhancing their stability in emulsion systems. This enables the production of tailored surfactants for use in applications ranging from personal care products to industrial coatings.Overall, Laurylglycidylether's versatility and reactivity make it a valuable component in chemical synthesis, contributing to the creation of a wide range of functional and high-performance materials.