≥98%, solution in ethanol for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
19(R)-HETE is a potent vasodilator of renal preglomerular vessels which completely blocks 20-HETE-induced vasoconstriction of renal arterioles at a concentration of 1 μM.
| Sorrisi canonici | CC(CCCC=CCC=CCC=CCC=CCCCC(=O)O)O |
|---|---|
| IUPAC Name | (5Z,8Z,11Z,14Z,19R)-19-hydroxyicosa-5,8,11,14-tetraenoic acid |
| InChIKey | XFUXZHQUWPFWPR-PCYSVGMOSA-N |
| INCHI | 1S/C20H32O3/c1-19(21)17-15-13-11-9-7-5-3-2-4-6-8-10-12-14-16-18-20(22)23/h3-6,9-12,19,21H,2,7-8,13-18H2,1H3,(H,22,23)/b5-3-,6-4-,11-9-,12-10-/t19-/m1/s1 |
| Isomeri SMILES | C[C@H](CCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O)O |
| PubChem CID | 11244126 |
| Peso molecolare | 320.47 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Classe | Fatty Acyls |
| Subclass | Eicosanoids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Hydroxyeicosatetraenoic acids |
| Alternative Parents | Long-chain fatty acids Hydroxy fatty acids Unsaturated fatty acids Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Hydroxyeicosatetraenoic acid - Long-chain fatty acid - Hydroxy fatty acid - Fatty acid - Unsaturated fatty acid - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxide - Organic oxygen compound - Alcohol - Hydrocarbon derivative - Carbonyl group - Organooxygen compound - Aliphatic acyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as hydroxyeicosatetraenoic acids. These are eicosanoic acids with an attached hydroxyl group and four CC double bonds. |
| External Descriptors | Hydroxy/hydroperoxyeicosatetraenoic acids |
| Punto di ebollizione (°C) | 78° C |
|---|---|
| Peso molecolare | 320.500 g/mol |
| XLogP3 | 4.600 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 14 |
| Exact Mass | 320.235 Da |
| Monoisotopic Mass | 320.235 Da |
| Topological Polar Surface Area | 57.500 Ų |
| Heavy Atom Count | 23 |
| Formal Charge | 0 |
| Complexity | 392.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 4 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 4 |
| Covalently-Bonded Unit Count | 1 |
| 1. Wen Nie, Kezhou Cai, Yuzhu Li, Zehui Tu, Bing Hu, Cunliu Zhou, Conggui Chen, Shaotong Jiang. (2019) Study of polycyclic aromatic hydrocarbons generated from fatty acids by a model system. JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 99 (7): (3548-3554). [PMID:30623971] [10.1002/jsfa.9575] |
