1-Propanamine, 3-(triethoxysilyl)-N-[3-(triethoxysilyl)propyl]-|13497-18-2,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)-

1-Propanamine, 3-(triethoxysilyl)-N-[3-(triethoxysilyl)propyl]-

CCO[Si](OCC)(OCC)CCCNCCC[Si](OCC)(OCC)OCC

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Chemical Name:	1-Propanamine, 3-(triethoxysilyl)-N-[3-(triethoxysilyl)propyl]-
CAS Number:	13497-18-2
Product Number:	AG007LOF(AGN-PC-0JLULF)
Synonyms:
MDL No:
Molecular Formula:	C18H43NO6Si2
Molecular Weight:	425.7081

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

Computed Properties

Molecular Weight:

425.713g/mol

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

425.263g/mol

Monoisotopic Mass:

425.263g/mol

Topological Polar Surface Area:

67.4A^2

Heavy Atom Count:

Formal Charge:

Complexity:

275

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:

Danger

UN#:

2735

Hazard Statements:

H314

Precautionary Statements:

P280-P305+P351+P338-P310

Class:

Packing Group:

Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure

1-Propanamine, 3-(triethoxysilyl)-N-[3-(triethoxysilyl)propyl] is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable coupling agent in the process of functionalizing surfaces with silane chemistry. Its dual triethoxysilyl groups allow for efficient binding to various substrates, making it an essential component in surface modification processes. Additionally, 1-Propanamine, 3-(triethoxysilyl)-N-[3-(triethoxysilyl)propyl] is commonly employed in the synthesis of silane-modified materials for applications such as coatings, adhesives, sealants, and composite materials. Its ability to enhance adhesion and compatibility makes it a key ingredient in formulating high-performance products with improved durability and quality.