Cas no 89130-62-1 (1-Octanamine, N-[3-(trimethoxysilyl)propyl]-)

1-Octanamine, N-[3-(trimethoxysilyl)propyl]- is a bifunctional organosilane compound featuring both an amine group and a trimethoxysilyl moiety. This structure enables dual reactivity, allowing it to act as a coupling agent between organic and inorganic materials. The primary amine functionality facilitates interactions with polymers, resins, or biological molecules, while the hydrolyzable methoxy groups promote adhesion to silica-based substrates, metals, or glass surfaces. Its compatibility with silanol-rich surfaces enhances interfacial bonding in composites, coatings, and adhesives. The C8 alkyl chain contributes to hydrophobic properties, improving moisture resistance in modified materials. This compound is particularly useful in surface modification, hybrid material synthesis, and corrosion inhibition applications, where strong interfacial bonding and durability are required.
1-Octanamine, N-[3-(trimethoxysilyl)propyl]- structure
89130-62-1 structure
Product Name:1-Octanamine, N-[3-(trimethoxysilyl)propyl]-
CAS No:89130-62-1
MF:C14H33NO3Si
MW:291.502225637436
MDL:MFCD29067128
CID:611370
PubChem ID:20276468
Update Time:2025-05-19

1-Octanamine, N-[3-(trimethoxysilyl)propyl]- Chemical and Physical Properties

Names and Identifiers

    • 1-Octanamine, N-[3-(trimethoxysilyl)propyl]-
    • N-(3-trimethoxysilylpropyl)octan-1-amine
    • MFCD29067128
    • (N-n-Octyl-3-aminopropyl)trimethoxysilane, 95%
    • SCHEMBL3443515
    • N-[3-(Trimethoxysilyl)propyl]octan-1-amine
    • 89130-62-1
    • DTXSID50604532
    • (N-n-Octyl-3-aminopropyl)trimethoxysilane
    • MDL: MFCD29067128
    • Inchi: 1S/C14H33NO3Si/c1-5-6-7-8-9-10-12-15-13-11-14-19(16-2,17-3)18-4/h15H,5-14H2,1-4H3
    • InChI Key: CEZKFSFZWCXHHJ-UHFFFAOYSA-N
    • SMILES: [Si](CCCNCCCCCCCC)(OC)(OC)OC

Computed Properties

  • Exact Mass: 291.22297045g/mol
  • Monoisotopic Mass: 291.22297045g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 14
  • Complexity: 181
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 39.7?2

Experimental Properties

  • PSA: 39.72000
  • LogP: 3.59560

1-Octanamine, N-[3-(trimethoxysilyl)propyl]- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
abcr
AB368677-25 g
(N-n-Octyl-3-aminopropyl)trimethoxysilane, 95%; .
89130-62-1 95%
25g
€224.00 2023-04-26
abcr
AB368677-100 g
(N-n-Octyl-3-aminopropyl)trimethoxysilane, 95%; .
89130-62-1 95%
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€485.00 2022-08-31
abcr
AB368677-25g
(N-n-Octyl-3-aminopropyl)trimethoxysilane, 95%; .
89130-62-1 95%
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€224.00 2025-02-19

Additional information on 1-Octanamine, N-[3-(trimethoxysilyl)propyl]-

Introduction to 1-Octanamine, N-[3-(trimethoxysilyl)propyl]- (CAS No. 89130-62-1) and Its Emerging Applications in Modern Chemistry

1-Octanamine, N-[3-(trimethoxysilyl)propyl]-, identified by the CAS number 89130-62-1, is a specialized organic compound that has garnered significant attention in the field of advanced materials and pharmaceutical chemistry. This compound, characterized by its unique structural features, combines an octylamine moiety with a trimethoxysilyl group, making it a versatile intermediate in the synthesis of various functional materials. The dual functionality of this molecule allows it to serve as a bridge between organic and inorganic domains, facilitating the development of hybrid materials with tailored properties.

The significance of 1-Octanamine, N-[3-(trimethoxysilyl)propyl]- lies in its ability to enhance the adhesion and compatibility between organic polymers and inorganic substrates. This property is particularly valuable in the fabrication of coatings, adhesives, and composite materials where interfacial bonding plays a critical role. The trimethoxysilyl group, in particular, enables hydrolyzable silane coupling, a process that promotes strong chemical bonds between organic and inorganic matrices. Such interactions are essential for improving the mechanical strength, thermal stability, and environmental resistance of material systems.

Recent advancements in nanotechnology have further highlighted the potential of 1-Octanamine, N-[3-(trimethoxysilyl)propyl]- as a modifier for nanomaterials. Researchers have demonstrated its efficacy in stabilizing nanoparticles and enhancing their dispersion in solvents. This improvement in dispersion is crucial for applications such as drug delivery systems, where uniform distribution of active ingredients is necessary for optimal efficacy. The compound’s ability to form stable colloidal solutions makes it an attractive candidate for formulating advanced pharmaceutical formulations.

In the realm of pharmaceutical chemistry, 1-Octanamine, N-[3-(trimethoxysilyl)propyl]- has been explored as a precursor for designing novel therapeutic agents. Its structural motif can be incorporated into drug molecules to improve their pharmacokinetic profiles. For instance, the octylamine part can enhance lipophilicity, while the silane group offers opportunities for targeted delivery systems. Studies have shown promising results in using this compound to develop prodrugs that exhibit controlled release mechanisms. Such innovations are particularly relevant in addressing challenges related to drug bioavailability and therapeutic efficacy.

The compound’s utility extends to the field of catalysis as well. The trimethoxysilyl group can be hydrolyzed to form silanol groups, which can act as anchors for catalysts on solid surfaces. This property has been leveraged in designing heterogeneous catalysts that offer high selectivity and reactivity for various organic transformations. These catalytic systems are integral to green chemistry initiatives, as they enable reactions under milder conditions with reduced waste generation.

From an industrial perspective, 1-Octanamine, N-[3-(trimethoxysilyl)propyl]- plays a pivotal role in the development of specialty chemicals. Its incorporation into polymer matrices enhances flame retardancy and UV resistance, making it valuable for applications in construction materials and automotive components. Additionally, its use as a crosslinking agent in epoxy resins improves material durability under extreme conditions. These applications underscore the compound’s versatility and its importance in advancing high-performance materials.

The synthesis of 1-Octanamine, N-[3-(trimethoxysilyl)propyl]- involves multi-step organic reactions that require precise control over reaction conditions. The introduction of the trimethoxysilyl group necessitates careful handling to prevent unwanted side reactions. Recent methodologies have focused on optimizing synthetic routes to improve yield and purity while minimizing environmental impact. Such efforts align with global trends toward sustainable chemical manufacturing practices.

Future research directions for 1-Octanamine, N-[3-(trimethoxysilyl)propyl]- include exploring its potential in biomedicine and energy storage technologies. For instance, its ability to form stable interfaces could be exploited in designing bio-compatible coatings for medical implants or as an electrolyte additive in lithium-ion batteries. These applications highlight the compound’s broad utility across multiple scientific disciplines.

In conclusion, 1-Octanamine,N-[3-(trimethoxysilyl)propyl]- (CAS No 89130-62-1) is a multifunctional compound with significant implications for modern chemistry Its unique structural features enable diverse applications ranging from advanced materials to pharmaceuticals As research continues to uncover new possibilities this compound is poised to play an even greater role In shaping innovative solutions across scientific industries

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