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· · COA & SDS available for every product · Same-day shipping on in-stock items N-3-oxo-octanoyl-L-Homoserine lactone - ≥97% , CAS No.147795-39-9
Synonyms
N-(beta-Oxooctan-1-oyl)-L-homoserine lactone | OOHL | SW222225-1 | AAI-1 | Conjugation factor 1, agrobacterium | N-beta-oxo-octanoyl-L-Homoserine lactone | 3-Oxo-N-[(3S)-tetrahydro-2-oxo-3-furanyl]octanamide | PD004806 | Spectrum4_000781 | 3-OXO-OCTANOIC
Shipped In
Ice chest + Ice pads
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview N-3-oxo-octanoyl-L-Homoserine lactone promotes the expression of the transcriptional activator (and LuxR homolog) TraR.
Specifications Synonyms
N-(beta-Oxooctan-1-oyl)-L-homoserine lactone | OOHL | SW222225-1 | AAI-1 | Conjugation factor 1, agrobacterium | N-beta-oxo-octanoyl-L-Homoserine lactone | 3-Oxo-N-[(3S)-tetrahydro-2-oxo-3-furanyl]octanamide | PD004806 | Spectrum4_000781 | 3-OXO-OCTANOIC
Specifications & Purity
≥97%
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Properties pKa pKa: 11.09 (Predicted)
Names and Identifiers Pubchem Sid 488187796 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488187796 Canonical Smiles CCCCCC(=O)CC(=O)NC1CCOC1=O IUPAC Name 3-oxo-N-[(3S)-2-oxooxolan-3-yl]octanamide InChIKey FXCMGCFNLNFLSH-JTQLQIEISA-N INCHI 1S/C12H19NO4/c1-2-3-4-5-9(14)8-11(15)13-10-6-7-17-12(10)16/h10H,2-8H2,1H3,(H,13,15)/t10-/m0/s1 Isomeric SMILES CCCCCC(=O)CC(=O)N[C@H]1CCOC1=O WGK Germany 3 Molecular Weight 241.28 Reaxy-Rn 18369654 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=18369654&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification 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-L-homoserine lactones N-acyl amines Gamma butyrolactones 1,3-dicarbonyl compounds Tetrahydrofurans Secondary carboxylic acid amides Ketones Carboxylic acid esters Oxacyclic compounds Monocarboxylic acids and derivatives Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives 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 - Fatty acyl - 1,3-dicarbonyl compound - N-acyl-amine - Tetrahydrofuran - Carboxamide group - Carboxylic acid ester - Ketone - Secondary carboxylic acid amide - Lactone - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Carbonyl group - Organooxygen compound - Organic oxygen 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 Fatty acyl homoserine lactones Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Soluble in ethanol (~10 mg/ml), DMSO (~30 mg/ml), DMF (~30 mg/ml), and chloroform (50 mg/ml, clear, colorless). Refractive Index n20D1.49 (Predicted) Boil Point(°C) ~490.1° C at 760 mmHg (Predicted) Melt Point(°C) 166.72° C (Predicted) Molecular Weight 241.280 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 7 Exact Mass 241.131 Da Monoisotopic Mass 241.131 Da Topological Polar Surface Area 72.500 Ų Heavy Atom Count 17 Formal Charge 0 Complexity 301.000 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
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