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Merck

56395

Sigma-Aldrich

N-Hexanoyl-L-homoserin-lacton

≥96% (HPLC)

Synonym(e):

N-Caproyl-L-homoserin-lacton, N-[(3S)-Tetrahydro-2-oxo-3-furanyl]-hexanamid, HHL

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About This Item

Empirische Formel (Hill-System):
C10H17NO3
CAS-Nummer:
Molekulargewicht:
199.25
Beilstein:
8143287
MDL-Nummer:
UNSPSC-Code:
12352211
PubChem Substanz-ID:
NACRES:
NA.28

product name

N-Hexanoyl-L-homoserin-lacton, ≥96% (HPLC)

Qualitätsniveau

Assay

≥96% (HPLC)

Form

powder or crystals

Optische Aktivität

[α]/D -32±3°, c = 0.2 in methanol

Farbe

white to off-white

Eignung

conforms to structure for Proton NMR spectrum

Lagertemp.

−20°C

SMILES String

O=C1OCC[C@@H]1NC(CCCCC)=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)/t8-/m0/s1

InChIKey

ZJFKKPDLNLCPNP-QMMMGPOBSA-N

Biochem./physiol. Wirkung

N-Hexanoyl-L-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; for reviews see. Bacterial intercellular communication has become a target for the development of new anti-virulence drugs, and a research focus for the prevention of biofilm formation.
Quorum-sensing signal generation

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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