09926

N-Hexanoyl-DL-homoserine lactone

≥97.0% (HPLC)

• Synonyme(s) : N-Caproyl-DL-homoserine lactone
• Formule empirique (notation de Hill) : C₁₀H₁₇NO₃
• CAS Number: 106983-28-2
• Poids moléculaire : 199.25
• Beilstein: 1640340
• Numéro MDL: MFCD01862908
• Code UNSPSC : 12352209
• eCl@ss : 32160406
• ID de substance PubChem : 329748862
• Nomenclature NACRES : NA.26

Propriétés

• Niveau de qualité: 100
• Essai: ≥97.0% (HPLC)
• Forme: powder or crystals
• Technique(s): LC/MS: suitable
• Couleur: white to faint beige
• Pf: 101-106 °C
• Température de stockage: 2-8°C
• Chaîne SMILES: CCCCCC(=O)NC1CCOC1=O; CCCCCC(=O)NC1CCOC1=O
• InChI: 1S/C10H17NO3/c1-2-3-4-5-9(12)11-8-6-7-14-10(8)13/h8H,2-7H2,1H3,(H,11,12)
• Clé InChI: ZJFKKPDLNLCPNP-UHFFFAOYSA-N

Description

Application

Induces violacein expression in a Chromobacterium violaceum mutant usually not able to produce homoserine lactones.

Actions biochimiques/physiologiques

N-Hexanoyl-DL-homoserine lactone is a member of N-acyl-homoserine lactone family. N-acylhomoserine lactones (AHL) regulate gene expression in gram-negative bacteria, such as Echerichia and Salmonella and are involved in quorum sensing, cell to cell communication among bacteria. Some AHLs are potent chemoattractants for human immune cells such as neutrophils.

Quorum-sensing signal generation

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 3
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable
• Équipement de protection individuelle: Eyeshields, Gloves, type N95 (US)