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N-Dodecanoyl-DL-homoserine lactone - ≥97.0% (HPLC), high purity , CAS No.18627-38-8

COA

Grade & Purity:

≥97%

Cas Number: 18627-38-8
Molecular Weight: 283.41
MDL number: MFCD03100412
PubChem CID: 11565426

In stock

Item Number

N464439

Grouped product items
SKU	Size	Availability	Price
N464439-5mg	5mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$69.90
N464439-10mg	10mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$112.90
N464439-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$224.90
N464439-50mg	50mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$359.90
N464439-100mg	100mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$579.90

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Amino Acid Derivatives (349)

Basic Description

Synonyms	N-Lauroyl-DL-homoserine lactone \| C12-homoserine lactone \| CHEBI:182085 \| N-(2-Oxotetrahydrofuran-3-yl)dodecanamide \| SCHEMBL3738642 \| C12-HSL \| N-(2-OXOOXOLAN-3-YL)DODECANAMIDE
Specifications & Purity	≥97%
Biochemical and Physiological Mechanisms	N-Lauroyl- DL-homoserine lactone is a member of N-acyl-homoserine lactone family. N-acylhomoserine lactones (AHL) regulate gene expression in gram-negative bacteria, such asEcherichiaandSalmonellaare involved in quorum sensing, cell to cell commu
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	Description Application test: Induces violacein expression in aChromobacterium violaceummutant usually not able to produce homoserine lactones.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organic acids and derivatives
  - Class Carboxylic acids and derivatives
    - Subclass Amino acids, peptides, and analogues
      - Level5 Amino acids and derivatives
        Level6 Alpha amino acids and derivatives
        Level7 N-acyl-alpha amino acids and derivatives

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 Oxolanes 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 - Oxolane - 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	Not available
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. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

IUPAC Name	N-(2-oxooxolan-3-yl)dodecanamide
INCHI	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)
InChIKey	WILLZMOKUUPJSL-UHFFFAOYSA-N
Smiles	CCCCCCCCCCCC(=O)NC1CCOC1=O
Isomeric SMILES	CCCCCCCCCCCC(=O)NC1CCOC1=O
Molecular Weight	283.41
Reaxy-Rn	1647202
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1647202&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

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10 results found

Lot Number	Certificate Type	Date	Item
L2411381	Certificate of Analysis	Sep 05, 2024	N464439
L2411382	Certificate of Analysis	Sep 05, 2024	N464439
L2411369	Certificate of Analysis	Sep 05, 2024	N464439
L2411385	Certificate of Analysis	Sep 05, 2024	N464439
L2411388	Certificate of Analysis	Sep 05, 2024	N464439
L2411395	Certificate of Analysis	Sep 05, 2024	N464439
L2411406	Certificate of Analysis	Sep 05, 2024	N464439
L2411370	Certificate of Analysis	Sep 05, 2024	N464439
L2411371	Certificate of Analysis	Sep 05, 2024	N464439
L2411372	Certificate of Analysis	Sep 05, 2024	N464439

Chemical and Physical Properties

Flash Point(°F)	Not applicable
Flash Point(°C)	Not applicable
Melt Point(°C)	114-117℃
Molecular Weight	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 Å²
Heavy Atom Count	20
Formal Charge	0
Complexity	291.000
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

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