≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
Application test: Induces violacein expression in aChromobacterium violaceummutant usually not able to produce homoserine lactones.
| Pubchem Sid | 504758803 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504758803 |
| Canonical Smiles | CCCC(=O)NC1CCOC1=O |
| IUPAC Name | N-(2-oxooxolan-3-yl)butanamide |
| InChIKey | VFFNZZXXTGXBOG-UHFFFAOYSA-N |
| INCHI | 1S/C8H13NO3/c1-2-3-7(10)9-6-4-5-12-8(6)11/h6H,2-5H2,1H3,(H,9,10) |
| Isomeric SMILES | CCCC(=O)NC1CCOC1=O |
| Molecular Weight | 171.19 |
| Beilstein | 6375 |
| Reaxy-Rn | 6375 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=6375&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 |
| Class | 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 homoserine lactones N-acyl amines Gamma butyrolactones Tetrahydrofurans Secondary carboxylic acid amides Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organopnictogen compounds 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 - Fatty amide - Gamma butyrolactone - Fatty acyl - N-acyl-amine - Tetrahydrofuran - Carboxamide group - Carboxylic acid ester - Lactone - Secondary carboxylic acid amide - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Aliphatic heteromonocyclic compound |
| Description | 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 | an acyl-homoserine lactone |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 H2325172 | Certificate of Analysis | Jun 09, 2026 | N464197 |
| H2325173 | Certificate of Analysis | Jun 09, 2026 | N464197 |
| H2325174 | Certificate of Analysis | Jun 09, 2026 | N464197 |
| H2325175 | Certificate of Analysis | Jun 09, 2026 | N464197 |
| H2325176 | Certificate of Analysis | Jun 09, 2026 | N464197 |
| H2325177 | Certificate of Analysis | Jun 09, 2026 | N464197 |
| H2325228 | Certificate of Analysis | Jun 09, 2026 | N464197 |
| H2325315 | Certificate of Analysis | Jun 09, 2026 | N464197 |
| Flash Point(°F) | Not applicable |
|---|---|
| Flash Point(°C) | Not applicable |
| Melt Point(°C) | 89.8 °C |
| Molecular Weight | 171.190 g/mol |
| XLogP3 | 0.500 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 3 |
| Exact Mass | 171.09 Da |
| Monoisotopic Mass | 171.09 Da |
| Topological Polar Surface Area | 55.400 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 191.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Keyang Jiang, Xiao Yang, Qian Gao, Junxia Ni, Jinhu Feng, Di Wu, Xuelian Zou, Li Hu, Xi Liu, Zhaoping Song, Zhiwei Wang. (2024) Exogenous signaling molecules N-acyl-homoserine lactones promotes the reconstruction of sludge particles after impact with highly concentrated urea-formaldehyde resin microplastics. JOURNAL OF ENVIRONMENTAL MANAGEMENT, [PMID:39504669] [10.1016/j.jenvman.2024.123179] |
| 2. Zhiqi Lu, Mengzhe Zhao, Xianglong He, Hongjing Li. (2025) Biochar-Enhanced Nitrogen Removal in SBBR Under PFOA Stress: The Role of Quorum Sensing. Sustainability, 17 (8): (3359). [PMID:] [10.3390/su17083359] |
| 3. Meng Yuan, Guotao Chen, Zhiqi Zhang, Jinghui Wang, Yan Zhao, Guanghong Xie, Yin Jiang, Yuan Ren. (2026) Yarrowia lipolytica extracellular metabolites induce microbial signaling and interactions to enhance chlorinated hydrocarbon degradation in soil. Journal of Environmental Chemical Engineering, 14 (1): (121100). [PMID:] [10.1016/j.jece.2026.121100] |
