N-Butanoyl-L-homoserine lactone

Chemodex
Product Code: CDX-B0267
Product Group: Other Biochemicals
Supplier: Chemodex
CodeSizePrice
CDX-B0267-M01010 mg£72.00
Quantity:
CDX-B0267-M05050 mg£194.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Regulatory Status: RUO
Shipping:
AMBIENT
Storage:
-20°C

Images

1 / 1
Chemical Structure

Chemical Structure

Further Information

Alternate Names/Synonyms:
C4-HSL; N-(2-Oxotetrahydro-3-furanyl)butanamide
Appearance:
White solid.
CAS:
67605-85-0
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C8H13NO3/c1-2-3-7(10)9-6-4-5-12-8(6)11/h6H,2-5H2,1H3,(H,9,10)
InChiKey:
VFFNZZXXTGXBOG-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 67605-85-0. Formula: C8H13NO3. MW: 171.2. Synthetic. N-butyryl-L-Homoserine lactone is a small diffusible signaling molecule and is a member of N-acyl-homoserine lactone family. N-acylhomoserine lactones (AHL) are involved in quorum sensing, controlling gene expression, and cellular metabolism. The diverse applications of this kind of molecule include regulation of virulence in general, infection prevention, and formation of biofilms.
MDL:
MFCD12912262
Molecular Formula:
C8H13NO3
Molecular Weight:
171.2
Package Type:
Vial
Product Description:
N-butyryl-L-Homoserine lactone is a small diffusible signaling molecule and is a member of N-acyl-homoserine lactone family. N-acylhomoserine lactones (AHL) are involved in quorum sensing, controlling gene expression, and cellular metabolism. The diverse applications of this kind of molecule include regulation of virulence in general, infection prevention, and formation of biofilms.
Purity:
>97% (GC)
SMILES:
CCCC(=O)N[C@H]1CCOC1=O
Solubility Chemicals:
Soluble in chloroform.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Biochemical Reagents
UNSPSC Number:
12352200
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) T.A. Gould, et al.; J. Bacteriol. 188, 773 (2006) | (2) S.P. Diggle, et al.; J. Bacteriol. 184, 2576 (2002) | (3) G. Pessi, et al.; J. Bacteriol. 183, 6676 (2001) | (4) T.T. Hoang & H.P.Schweizer; J. Bacteriol. 181, 5489 (1999) | (5) T. Morohoshi, et al.; J. Biosci. Bioeng. 98, 274 (2004) | (6) Z.-Q. Luo, et al.; J. Bacteriol. 186, 5665 (2003) | (7) J.M. Henke & B.L. Bassler; Trends Cell Biol. 14, 648 (2004)

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