Cas no 15290-93-4 (1-Heptanamine,N,N-dimethyl-, N-oxide)
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 Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHENG KE LU SI SHENG WU JI SHU | sc-228771-1 g |
N,N-Dimethylheptylamine N-oxide hydrate, |
15290-93-4 | 1g |
¥436.00 | 2023-07-10 | ||
| SHENG KE LU SI SHENG WU JI SHU | sc-228771-1g |
N,N-Dimethylheptylamine N-oxide hydrate, |
15290-93-4 | 1g |
¥436.00 | 2023-09-05 | ||
| 1PlusChem | 1P007YWL-100mg |
1-Heptanamine,N,N-dimethyl-, N-oxide |
15290-93-4 | 95% | 100mg |
$185.00 | 2024-06-20 | |
| 1PlusChem | 1P007YWL-250mg |
1-Heptanamine,N,N-dimethyl-, N-oxide |
15290-93-4 | 95% | 250mg |
$335.00 | 2024-06-20 | |
| 1PlusChem | 1P007YWL-1g |
1-Heptanamine,N,N-dimethyl-, N-oxide |
15290-93-4 | 95% | 1g |
$964.00 | 2024-06-20 | |
| 1PlusChem | 1P007YWL-5g |
1-Heptanamine,N,N-dimethyl-, N-oxide |
15290-93-4 | 95% | 5g |
$2818.00 | 2024-06-20 |
1-Heptanamine,N,N-dimethyl-, N-oxide Related Literature
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Tao Wang,Yangyang Liu,Yue Deng,Hongbo Fu,Jianmin Chen Environ. Sci.: Nano, 2018,5, 1821-1833
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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Norihito Fukui,Keisuke Fujimoto,Hideki Yorimitsu,Atsuhiro Osuka Dalton Trans., 2017,46, 13322-13341
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Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
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David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
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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