(N,N-Diethyl-3-aminopropyl)trimethoxysilane

Base Information

• Chemical Name: (N,N-Diethyl-3-aminopropyl)trimethoxysilane
• CAS No.: 41051-80-3
• Molecular Formula: C₁₀H₂₅NO₃Si
• Molecular Weight: 235.399
• Hs Code.: 29319090
• European Community (EC) Number: 255-192-0
• UNII: 8EE2ARR677
• DSSTox Substance ID: DTXSID1068275
• Nikkaji Number: J294.818D
• Wikidata: Q72469172
• Mol file: 41051-80-3.mol

Synonyms:41051-80-3;N,N-Diethyl-3-(trimethoxysilyl)propan-1-amine;(N,N-Diethyl-3-aminopropyl)trimethoxysilane;[3-(Diethylamino)propyl]trimethoxysilane;N,N-Diethyl-3-(trimethoxysilyl)propylamine;N,N-diethyl-3-trimethoxysilylpropan-1-amine;1-Propanamine, N,N-diethyl-3-(trimethoxysilyl)-;EINECS 255-192-0;3-(n,n-diethylamino)propyltrimethoxysilane;8EE2ARR677;(3-Diethylaminopropyl)trimethoxysilane;N,N-Diethyl-3-(trimethoxysilyl)-1-propanamine;UNII-8EE2ARR677;SCHEMBL302546;BARIUMHYDROXIDEMONOHYDRATE;DTXSID1068275;MFCD00039882;3-(diethylamino)propyltrimethoxysilane;AKOS015894845;FS-5216;N,N-Diethyl Aminopropyltrimethoxysilane;diethyl[3-(trimethoxysilyl)propyl]amine;n,n-diethyl-3-aminopropyltrimethoxysilane;Trimethoxy[3-(diethylamino)propyl]silane;BP-30145;D4362;FT-0639692;N,N-diethyl-3-trimethoxysilyl-1-propanamine;N,N-diethyl-3-trimethoxysilyl-propan-1-amine;[3-(Diethylamino)propyl]trimethoxysilane, 96%;D90279;S06300;3-(N,N-Diethylamino)propyltrimethoxysilane (95%);A825416;N,N-Diethyl-3-(trimethoxysilyl)-1-propanamine #;Propyl]Trimethoxysilane;N,N-Diethyl-3-(Trimethoxysilyl;[3-(Diethylamino)propyl]trimethoxysilane, deposition grade, >=98%

Chemical Property of (N,N-Diethyl-3-aminopropyl)trimethoxysilane

Chemical Property:

• Appearance/Colour: Yellowish clear liquid with amine odor
• Vapor Pressure: 0.0717mmHg at 25°C
• Refractive Index: n20/D 1.423(lit.)
• Boiling Point: 228.9 °C at 760 mmHg
• PKA: 10.56±0.25(Predicted)
• Flash Point: 92.2 °C
• PSA: 30.93000
• Density: 0.92 g/cm³
• LogP: 1.59640
• Storage Temp.: 2-8°C
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 9
• Exact Mass: 235.16037019
• Heavy Atom Count: 15
• Complexity: 141

Purity/Quality:

97% ^*data from raw suppliers

[3-(Diethylamino)propyl]trimethoxysilane >97.0%(GC)(T) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 37/38-41
• Safety Statements: 26-39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCN(CC)CCC[Si](OC)(OC)OC
• Uses: [3-(Diethylamino)propyl]trimethoxysilane was covalently bonded to mesoporous titania–silica mixed oxides to act as epoxidation catalysts.{55} [3-(Diethylamino)propyl]trimethoxysilane, immobilized on mesoporous silicas (SBA-15) may be used as adsorbents to capture CO2. {56}

Technology Process of (N,N-Diethyl-3-aminopropyl)trimethoxysilane

There total 1 articles about (N,N-Diethyl-3-aminopropyl)trimethoxysilane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 64.0%

diethylamine (109-89-7) + 3-Chloropropyltrimethoxysilan (2530-87-2) → 3-diethylaminopropyltrimethoxysilane (41051-80-3)

Guidance literature:

In N,N-dimethyl-formamide; at 120 ℃; for 4h; Solvent; Reagent/catalyst; Temperature; Reflux;

upstream raw materials:

diethylamine

3-Chloropropyltrimethoxysilan

Refernces

Cooperative catalysis of primary and tertiary amines immobilized on oxide surfaces for one-pot C-C bond forming reactions

10.1002/anie.200802515

The research investigates the cooperative catalysis of primary and tertiary amines immobilized on oxide surfaces for one-pot carbon-carbon bond-forming reactions. The purpose is to develop an efficient heterogeneous catalyst for organic C-C bond-forming reactions by combining both primary and tertiary amines on the same solid surface to activate both nucleophiles and electrophiles. The key chemicals used include benzaldehyde, nitromethane, silica-alumina (SA), 3-aminopropyltriethoxysilane, and 3-(diethylamino)propyltrimethoxysilane. The study found that the double-amine catalysts immobilized on silica-alumina (SA–NH2–NEt2) showed high initial conversion rates and selectivity for the synthesis of 1,3-dinitroalkanes compared to other amine catalysts and homogeneous mixtures. The presence of surface acid sites on the silica-alumina support enhanced the cooperative catalysis, and the catalyst was effective for one-pot reaction sequences. The research concludes that the SA–NH2–NEt2 catalyst is highly active for the production of 1,3-dinitroalkanes due to its multifunctional surface, which enables both acceleration of single reactions and promotion of one-pot reaction sequences.

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