Record Information |
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Version | 5.0 |
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Status | Expected but not Quantified |
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Creation Date | 2012-09-11 20:41:03 UTC |
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Update Date | 2022-03-07 02:54:35 UTC |
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HMDB ID | HMDB0035675 |
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Secondary Accession Numbers | |
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Metabolite Identification |
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Common Name | 6-Hydroxy-4-nonadecanone |
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Description | 6-Hydroxy-4-nonadecanone belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. Based on a literature review a small amount of articles have been published on 6-Hydroxy-4-nonadecanone. |
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Structure | CCCCCCCCCCCCCC(O)CC(=O)CCC InChI=1S/C19H38O2/c1-3-5-6-7-8-9-10-11-12-13-14-16-19(21)17-18(20)15-4-2/h19,21H,3-17H2,1-2H3 |
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Synonyms | Not Available |
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Chemical Formula | C19H38O2 |
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Average Molecular Weight | 298.5038 |
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Monoisotopic Molecular Weight | 298.28718046 |
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IUPAC Name | 6-hydroxynonadecan-4-one |
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Traditional Name | 6-hydroxynonadecan-4-one |
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CAS Registry Number | Not Available |
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SMILES | CCCCCCCCCCCCCC(O)CC(=O)CCC |
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InChI Identifier | InChI=1S/C19H38O2/c1-3-5-6-7-8-9-10-11-12-13-14-16-19(21)17-18(20)15-4-2/h19,21H,3-17H2,1-2H3 |
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InChI Key | FQXHGCYDYNKFFF-UHFFFAOYSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. |
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Kingdom | Organic compounds |
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Super Class | Lipids and lipid-like molecules |
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Class | Fatty Acyls |
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Sub Class | Fatty alcohols |
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Direct Parent | Long-chain fatty alcohols |
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Alternative Parents | |
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Substituents | - Long chain fatty alcohol
- Beta-hydroxy ketone
- Secondary alcohol
- Ketone
- Organic oxygen compound
- Organic oxide
- Hydrocarbon derivative
- Organooxygen compound
- Carbonyl group
- Alcohol
- Aliphatic acyclic compound
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Molecular Framework | Aliphatic acyclic compounds |
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External Descriptors | Not Available |
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Ontology |
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Physiological effect | Not Available |
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Disposition | |
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Process | |
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Role | |
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Physical Properties |
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State | Not Available |
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Experimental Molecular Properties | Property | Value | Reference |
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Melting Point | Not Available | Not Available | Boiling Point | Not Available | Not Available | Water Solubility | Not Available | Not Available | LogP | Not Available | Not Available |
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Experimental Chromatographic Properties | Not Available |
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Predicted Molecular Properties | |
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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6-Hydroxy-4-nonadecanone,1TMS,isomer #1 | CCCCCCCCCCCCCC(CC(=O)CCC)O[Si](C)(C)C | 2234.8 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,1TMS,isomer #2 | CCC=C(CC(O)CCCCCCCCCCCCC)O[Si](C)(C)C | 2373.2 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,1TMS,isomer #3 | CCCCCCCCCCCCCC(O)C=C(CCC)O[Si](C)(C)C | 2305.3 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,2TMS,isomer #1 | CCC=C(CC(CCCCCCCCCCCCC)O[Si](C)(C)C)O[Si](C)(C)C | 2383.8 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,2TMS,isomer #1 | CCC=C(CC(CCCCCCCCCCCCC)O[Si](C)(C)C)O[Si](C)(C)C | 2396.0 | Standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,2TMS,isomer #2 | CCCCCCCCCCCCCC(C=C(CCC)O[Si](C)(C)C)O[Si](C)(C)C | 2372.7 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,2TMS,isomer #2 | CCCCCCCCCCCCCC(C=C(CCC)O[Si](C)(C)C)O[Si](C)(C)C | 2333.4 | Standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,1TBDMS,isomer #1 | CCCCCCCCCCCCCC(CC(=O)CCC)O[Si](C)(C)C(C)(C)C | 2494.1 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,1TBDMS,isomer #2 | CCC=C(CC(O)CCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C | 2606.6 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,1TBDMS,isomer #3 | CCCCCCCCCCCCCC(O)C=C(CCC)O[Si](C)(C)C(C)(C)C | 2560.0 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,2TBDMS,isomer #1 | CCC=C(CC(CCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C | 2849.3 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,2TBDMS,isomer #1 | CCC=C(CC(CCCCCCCCCCCCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C | 2732.2 | Standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,2TBDMS,isomer #2 | CCCCCCCCCCCCCC(C=C(CCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C | 2860.7 | Semi standard non polar | 33892256 | 6-Hydroxy-4-nonadecanone,2TBDMS,isomer #2 | CCCCCCCCCCCCCC(C=C(CCC)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C | 2665.4 | Standard non polar | 33892256 |
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| GC-MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted GC-MS | Predicted GC-MS Spectrum - 6-Hydroxy-4-nonadecanone GC-MS (Non-derivatized) - 70eV, Positive | splash10-00di-9340000000-547bdfc615141c68d52d | 2017-09-01 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - 6-Hydroxy-4-nonadecanone GC-MS (1 TMS) - 70eV, Positive | splash10-00g0-9243000000-e81d426ff870f5a377d4 | 2017-10-06 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - 6-Hydroxy-4-nonadecanone GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum | Predicted GC-MS | Predicted GC-MS Spectrum - 6-Hydroxy-4-nonadecanone GC-MS (Non-derivatized) - 70eV, Positive | Not Available | 2021-10-12 | Wishart Lab | View Spectrum |
MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 10V, Positive-QTOF | splash10-001j-1090000000-44a6dd1f7d789efa4d22 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 20V, Positive-QTOF | splash10-00ea-9560000000-d8586c33aa67bba7e34a | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 40V, Positive-QTOF | splash10-0596-9610000000-af0490a4cf1bff911c86 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 10V, Negative-QTOF | splash10-0002-1090000000-91b5f31055d4c519a9f5 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 20V, Negative-QTOF | splash10-01rj-6190000000-e73a661302e12d4f0cb7 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 40V, Negative-QTOF | splash10-0apu-9120000000-044be3d273e487825339 | 2016-08-03 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 10V, Positive-QTOF | splash10-000t-2090000000-bb98d7b8f1d3f084a295 | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 20V, Positive-QTOF | splash10-07bu-9130000000-50de2b412fdbeafc0c25 | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 40V, Positive-QTOF | splash10-052f-9000000000-283fa07046f0e4ba5087 | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 10V, Negative-QTOF | splash10-0002-2090000000-92ed921ebe0757b047fb | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 20V, Negative-QTOF | splash10-06s2-9050000000-2e2f464cf3fdeaf343f8 | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 6-Hydroxy-4-nonadecanone 40V, Negative-QTOF | splash10-0ap0-9010000000-d7a8790d4d00708e8a15 | 2021-09-25 | Wishart Lab | View Spectrum |
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General References | - Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
- Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
- Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
- Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
- (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
- Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.
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