Cas no 1687-68-9 (Benzyl(dodecyl)amine)

Benzyl(dodecyl)amine is a secondary amine featuring both a benzyl and a dodecyl (lauryl) group attached to the nitrogen atom. This compound is characterized by its amphiphilic nature, combining hydrophobic and hydrophilic properties, making it useful in surfactant and corrosion inhibitor applications. Its structure allows for effective interfacial activity, facilitating emulsification and dispersion processes. The long alkyl chain enhances solubility in organic solvents, while the aromatic benzyl group contributes to stability and reactivity in chemical synthesis. Benzyl(dodecyl)amine is also employed as an intermediate in the production of quaternary ammonium compounds. Its balanced properties make it suitable for industrial formulations requiring tailored surface-active performance.
Benzyl(dodecyl)amine structure
Benzyl(dodecyl)amine structure
Product Name:Benzyl(dodecyl)amine
CAS No:1687-68-9
MF:C19H33N
MW:275.472025632858
CID:236729
PubChem ID:232909
Update Time:2025-06-27

Benzyl(dodecyl)amine Chemical and Physical Properties

Names and Identifiers

    • Benzenemethanamine,N-dodecyl-
    • N-benzyldodecan-1-amine
    • 1687-68-9
    • NSC-30887
    • N-benzyl-n-dodecylamine
    • SCHEMBL1683345
    • EN300-124772
    • SB82014
    • dodecylbenzylamine
    • NSC30887
    • CS-0225736
    • Z90531597
    • DTXSID20937521
    • TWOFDIYIPNBWBG-UHFFFAOYSA-N
    • AKOS009009723
    • benzyl(dodecyl)amine
    • G63465
    • DS-010159
    • Benzyl(dodecyl)amine
    • Inchi: 1S/C19H33N/c1-2-3-4-5-6-7-8-9-10-14-17-20-18-19-15-12-11-13-16-19/h11-13,15-16,20H,2-10,14,17-18H2,1H3
    • InChI Key: TWOFDIYIPNBWBG-UHFFFAOYSA-N
    • SMILES: N(CC1C=CC=CC=1)CCCCCCCCCCCC

Computed Properties

  • Exact Mass: 275.26149
  • Monoisotopic Mass: 275.261
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 13
  • Complexity: 184
  • 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
  • XLogP3: 6.9
  • Topological Polar Surface Area: 12?2

Experimental Properties

  • Density: 0.881
  • Boiling Point: 369.3°Cat760mmHg
  • Flash Point: 146.3°C
  • Refractive Index: 1.489
  • PSA: 12.03
  • LogP: 6.08800
  • Vapor Pressure: 0.0±0.8 mmHg at 25°C

Benzyl(dodecyl)amine Security Information

Benzyl(dodecyl)amine Pricemore >>

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Additional information on Benzyl(dodecyl)amine

Benzyl(dodecyl)amine: A Versatile Compound with CAS No. 1687-68-9 in Modern Biomedical Applications

Benzyl(dodecyl)amine (CAS No. 1687-68-9) is a key organic compound characterized by its unique molecular structure, which combines a benzyl group with a dodecyl chain. This chemical entity has garnered significant attention in biomedical research due to its dual functionality as both a surfactant and a potential candidate for drug delivery systems. Recent studies have highlighted its role in enhancing the solubility of hydrophobic drugs and its potential applications in nanotechnology. The CAS No. 1687-68-9 identifier ensures precise identification of this compound, which is critical for reproducibility in scientific experiments.

Benzyl(dodecyl)amine is a secondary amine with a molecular formula of C19H33NO. Its structure consists of a benzene ring connected to a dodecyl chain, which is further attached to an amino group. This combination of aromatic and aliphatic moieties imparts unique physicochemical properties, including hydrophobicity and amphiphilic behavior. These characteristics make it particularly suitable for applications in lipid-based drug delivery systems and surface modification of biomaterials. The CAS No. 1687-68-9 designation is essential for distinguishing it from structurally similar compounds, ensuring accurate reporting in scientific literature.

Recent advancements in biomedical research have demonstrated the potential of Benzyl(dodecyl)amine in enhancing the bioavailability of poorly soluble drugs. A 2023 study published in Advanced Drug Delivery Reviews highlighted its ability to form self-assembled micelles in aqueous solutions, which can encapsulate hydrophobic therapeutic agents. This property is particularly valuable in the development of oral drug formulations, where solubility limitations often hinder therapeutic efficacy. The CAS No. 1687-68-9 compound has also been explored for its role in stabilizing nanoparticles, a critical factor in the delivery of biopharmaceuticals.

Another notable application of Benzyl(dodecyl)amine is its use in the synthesis of functionalized surfaces for biomedical devices. Research published in Biomaterials in 2022 demonstrated its effectiveness in modifying polymer surfaces to enhance cell adhesion and reduce bacterial adhesion. This property is particularly relevant for the development of implantable medical devices and tissue engineering scaffolds. The CAS No. 1687-68-9 compound's amphiphilic nature allows it to act as a bridge between hydrophilic and hydrophobic materials, optimizing surface interactions for biomedical applications.

Recent studies have also explored the potential of Benzyl(dodecyl)amine in the field of nanotechnology. A 2023 paper in Nano Letters reported its use as a surfactant in the synthesis of metal-organic frameworks (MOFs), which are being investigated for their applications in drug delivery and sensing. The CAS No. 1687-68-9 compound's ability to stabilize nanoparticles and control their morphology has opened new avenues for its use in advanced materials science. This highlights the versatility of Benzyl(dodecyl)amine beyond traditional applications in pharmaceuticals.

The environmental impact of Benzyl(dodecyl)amine is another area of active research. A 2022 study in Environmental Science & Technology examined its biodegradation pathways and ecological effects. While the compound is not classified as a hazardous substance, its persistence in aquatic environments has raised concerns about its long-term ecological impact. Researchers are now focusing on developing sustainable synthesis methods to minimize its environmental footprint, aligning with global efforts to promote green chemistry practices.

Despite its promising applications, the use of Benzyl(dodecyl)amine requires careful consideration of its physicochemical properties. Its low polarity and high hydrophobicity necessitate specific formulation strategies to ensure optimal performance in different environments. For instance, in drug delivery systems, the compound must be combined with other excipients to achieve the desired release kinetics. The CAS No. 1687-68-9 compound's behavior in different solvents and its interaction with biological membranes are critical factors that influence its efficacy in biomedical applications.

Industrial applications of Benzyl(dodecyl)amine extend beyond the biomedical field. It is used as a component in the production of certain types of lubricants and coatings, where its hydrophobic properties provide functional advantages. However, the primary focus of current research remains on its biomedical potential, driven by the increasing demand for innovative therapeutic solutions. The CAS No. 1687-68-9 compound's role in these applications underscores its importance in both academic and industrial settings.

As research into Benzyl(dodecyl)amine continues to expand, new applications are being discovered that leverage its unique properties. For example, its ability to form stable emulsions has led to its exploration in the development of topical pharmaceutical formulations. The CAS No. 1687-68-9 compound's potential in these areas highlights its adaptability to meet the evolving needs of the biomedical industry. Ongoing studies are expected to further elucidate its mechanisms of action and optimize its use in various therapeutic contexts.

In conclusion, Benzyl(dodecyl)amine (CAS No. 1687-68-9) is a multifunctional compound with significant potential in biomedical research. Its unique molecular structure and physicochemical properties make it a valuable tool for advancing drug delivery systems, surface modification of biomaterials, and nanotechnology. As new studies continue to uncover its capabilities, the compound is likely to play an increasingly important role in the development of innovative therapeutic solutions.

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