≥98% 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Dodecanoyl-L-homoserine lactone was confirmed to be an active quorum sensing modulator first recognised in|Sinorhizobium meliloti|. The homoserine lactones are the major chemical modulators of within and between cell communication and regulation. The most significant variable defining the function of the homoserine lactone is the length of the acyl chain, with shorter chains displaying opposing actions to the longer chains.
| Pubchem Sid | 504765338 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504765338 |
| Sonrisas canónicas | CCCCCCCCCCCC(=O)NC1CCOC1=O |
| IUPAC Name | N-[(3S)-2-oxooxolan-3-yl]dodecanamide |
| InChIKey | WILLZMOKUUPJSL-AWEZNQCLSA-N |
| INCHI | 1S/C16H29NO3/c1-2-3-4-5-6-7-8-9-10-11-15(18)17-14-12-13-20-16(14)19/h14H,2-13H2,1H3,(H,17,18)/t14-/m0/s1 |
| Isómeros SMILES | CCCCCCCCCCCC(=O)N[C@H]1CCOC1=O |
| Peso molecular | 283.41 |
| Reaxy-Rn | 1647202 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1647202&ln= |
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 | Organic acids and derivatives |
| Clase | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | N-acyl-alpha amino acids and derivatives |
| Alternative Parents | Alpha amino acid esters Acyl-L-homoserine lactones N-acyl amines Gamma butyrolactones Oxolanes Secondary carboxylic acid amides Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Alpha-amino acid ester - N-acyl-alpha amino acid or derivatives - Acyl-homoserine lactone - Acyl-l-homoserine lactone - Fatty amide - Gamma butyrolactone - N-acyl-amine - Fatty acyl - Oxolane - Secondary carboxylic acid amide - Lactone - Carboxylic acid ester - Carboxamide group - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Aliphatic heteromonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom. |
| External Descriptors | Not available |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 D2620221 | Certificate of Analysis | Mar 20, 2026 | D329450 |
| D2620222 | Certificate of Analysis | Mar 20, 2026 | D329450 |
| D2620225 | Certificate of Analysis | Mar 20, 2026 | D329450 |
| D2315349 | Certificate of Analysis | Jan 21, 2026 | D329450 |
| E2227137 | Certificate of Analysis | Mar 04, 2025 | D329450 |
| J2421523 | Certificate of Analysis | Oct 10, 2024 | D329450 |
| J2421524 | Certificate of Analysis | Oct 10, 2024 | D329450 |
| J2421538 | Certificate of Analysis | Oct 10, 2024 | D329450 |
| J2513054 | Certificate of Analysis | Oct 10, 2024 | D329450 |
| E2227133 | Certificate of Analysis | Feb 24, 2022 | D329450 |
| E2227138 | Certificate of Analysis | Feb 24, 2022 | D329450 |
| G2401067 | Certificate of Analysis | Feb 24, 2022 | D329450 |
| K2330147 | Certificate of Analysis | Feb 24, 2022 | D329450 |
| Solubilidad | Soluble in ethanol, methanol, DMSO, and DMF. |
|---|---|
| Rotación específica [α] | [α]/D -25±5°, c = 0.2 in methanol |
| Punto de ebullición (°C) | ~485.8° C at 760 mmHg (Predicted) |
| Punto de fusión (°C) | 176.84° C (Predicted) |
| Peso molecular | 283.410 g/mol |
| XLogP3 | 4.800 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 11 |
| Exact Mass | 283.215 Da |
| Monoisotopic Mass | 283.215 Da |
| Topological Polar Surface Area | 55.400 Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 291.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
