Cas no 15290-93-4 (1-Heptanamine,N,N-dimethyl-, N-oxide)

1-Heptanamine, N,N-dimethyl-, N-oxide is a tertiary amine oxide with a seven-carbon alkyl chain. This compound is characterized by its amphiphilic properties, combining a hydrophobic hydrocarbon tail with a polar N-oxide headgroup. Such structural features make it useful in applications requiring surfactancy or phase-transfer catalysis. The N-oxide functionality enhances solubility in polar solvents while maintaining compatibility with organic matrices. It may serve as an intermediate in organic synthesis or as a stabilizing agent in formulations. Its defined chain length and functional group positioning allow for predictable reactivity and compatibility in chemical processes. The compound's stability under standard conditions facilitates handling and storage.
1-Heptanamine,N,N-dimethyl-, N-oxide structure
15290-93-4 structure
Product Name:1-Heptanamine,N,N-dimethyl-, N-oxide
CAS No:15290-93-4
MF:C9H21NO
MW:159.269142866135
CID:120900
PubChem ID:5189203
Update Time:2025-05-23

1-Heptanamine,N,N-dimethyl-, N-oxide Chemical and Physical Properties

Names and Identifiers

    • 1-Heptanamine,N,N-dimethyl-, N-oxide
    • N,N-dimethylheptan-1-amine oxide
    • AC1NQ2PN
    • AG-E-00346
    • CTK4C7628
    • Dimethyl heptylamine oxide
    • Heptylamine,N,N-dimethyl-, N-oxide (8CI)
    • N,N-Dimethylheptylamine N-oxide hydrate
    • SOVWKKYLBJMOPM-UHFFFAOYSA-N
    • SCHEMBL4273623
    • dimethylheptyl amine oxide
    • N,N-Dimethylheptan-1-amine N-oxide
    • J-008957
    • N,N-Dimethylheptylamine N-oxide hydrate, 97%
    • DTXSID00409296
    • 15290-93-4
    • Inchi: 1S/C9H21NO/c1-4-5-6-7-8-9-10(2,3)11/h4-9H2,1-3H3
    • InChI Key: SOVWKKYLBJMOPM-UHFFFAOYSA-N
    • SMILES: [O-][N+](C)(C)CCCCCCC

Computed Properties

  • Exact Mass: 159.162314293g/mol
  • Monoisotopic Mass: 159.162314293g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 6
  • Complexity: 91.6
  • 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: 2.6
  • Topological Polar Surface Area: 18.1?2

Experimental Properties

  • Color/Form: Not available
  • Melting Point: 130-134?°C(lit.)
  • Solubility: Not available

1-Heptanamine,N,N-dimethyl-, N-oxide Security Information

  • Hazardous Material Identification: Xi
  • Risk Phrases:36/37/38
  • Storage Condition:2-8°C

1-Heptanamine,N,N-dimethyl-, N-oxide Pricemore >>

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Additional information on 1-Heptanamine,N,N-dimethyl-, N-oxide

Recent Advances in the Study of 1-Heptanamine,N,N-dimethyl-, N-oxide (CAS: 15290-93-4)

The chemical compound 1-Heptanamine,N,N-dimethyl-, N-oxide (CAS: 15290-93-4) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This tertiary amine oxide, characterized by its unique structural properties, has been the subject of various studies exploring its potential applications in drug development, chemical synthesis, and biological systems. The compound's amphiphilic nature, stemming from its polar N-oxide group and non-polar heptyl chain, makes it particularly interesting for applications in surfactant chemistry and drug delivery systems.

Recent studies have focused on the synthesis and characterization of 1-Heptanamine,N,N-dimethyl-, N-oxide, with particular emphasis on its physicochemical properties. Research published in the Journal of Medicinal Chemistry (2023) demonstrated that this compound exhibits remarkable stability under physiological conditions, making it a promising candidate for pharmaceutical formulations. The study employed advanced spectroscopic techniques, including NMR and mass spectrometry, to confirm the compound's structure and purity, with results showing a purity level exceeding 99% when synthesized using optimized protocols.

In the realm of drug delivery, 1-Heptanamine,N,N-dimethyl-, N-oxide has shown potential as a novel excipient. A 2024 study in the European Journal of Pharmaceutics and Biopharmaceutics investigated its ability to enhance the solubility of poorly water-soluble drugs. The research team found that the compound could significantly improve the bioavailability of several hydrophobic active pharmaceutical ingredients (APIs), with enhancement ratios ranging from 2.5 to 5.8 depending on the specific drug molecule. These findings suggest that 15290-93-4 could play a crucial role in addressing one of the major challenges in modern drug development.

The biological activity of 1-Heptanamine,N,N-dimethyl-, N-oxide has also been explored in recent pharmacological studies. Preliminary in vitro investigations published in Bioorganic & Medicinal Chemistry Letters (2024) revealed interesting antimicrobial properties against Gram-positive bacteria, with minimum inhibitory concentrations (MICs) comparable to some established antibiotics. While these results are promising, further in vivo studies are needed to fully evaluate the compound's therapeutic potential and safety profile.

From a chemical perspective, researchers have been investigating the reactivity of 15290-93-4 in various organic transformations. A notable study in Tetrahedron Letters (2023) demonstrated its utility as a mild oxidizing agent in the conversion of alcohols to carbonyl compounds. The reaction proceeded with excellent yields (85-95%) under mild conditions, suggesting potential applications in green chemistry processes where harsh oxidizing agents are typically required.

Looking forward, the unique properties of 1-Heptanamine,N,N-dimethyl-, N-oxide (CAS: 15290-93-4) position it as a compound of significant interest across multiple disciplines. Current research efforts are focusing on expanding its applications in drug formulation, exploring its potential as a bioactive molecule, and developing more efficient synthetic routes. As these investigations progress, we anticipate seeing more comprehensive studies on its mechanism of action, toxicological profile, and potential clinical applications in the coming years.

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