Chemodex

3-Hydroxy-butanoyl-DL-homoserine lactone

Product Code:
 
CDX-H0076
Product Group:
 
Other Biochemicals
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
+4°C
1 / 1
Chemical Structure

Chemical Structure

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CDX-H0076-M0055 mg£157.00
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CDX-H0076-M01010 mg£242.00
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
3-Hydroxy-C4-HSL; N-(3-Hydroxybutanoyl)-L-homoserine lactone
Appearance:
White powder.
CAS:
912545-51-8
EClass:
32160000
Form (Short):
liquid
Handling Advice:
Keep cool and dry.Protect from light and moisture.
InChi:
InChI=1S/C8H13NO4/c1-5(10)4-7(11)9-6-2-3-13-8(6)12/h5-6,10H,2-4H2,1H3,(H,9,11)
InChiKey:
FIXDIFPJOFIIEC-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 912545-51-8. Formula: C8H13NO4. MW: 187.19. Synthetic 3-Hydroxy-butanoyl-DL-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:
MFCD24520804
Molecular Formula:
C8H13NO4
Molecular Weight:
187.19
Package Type:
Vial
Product Description:
3-Hydroxy-butanoyl-DL-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:
>98% (HPLC)
SMILES:
CC(O)CC(=O)NC1CCOC1=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) J.H. Kimbrough & E.V. Stabb; J. Bacteriol. 195, 5223 (2013)