H3648
(±)-3-Hydroxydecanoic acid
≥98%
Synonym(s):
DL-β-Hydroxycapric acid
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About This Item
Empirical Formula (Hill Notation):
C10H20O3
CAS Number:
Molecular Weight:
188.26
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352211
MDL number:
Product Name
(±)-3-Hydroxydecanoic acid, ≥98%
assay
≥98%
form
powder
InChI
1S/C10H20O3/c1-2-3-4-5-6-7-9(11)8-10(12)13/h9,11H,2-8H2,1H3,(H,12,13)
SMILES string
CCCCCCCC(O)CC(O)=O
InChI key
FYSSBMZUBSBFJL-UHFFFAOYSA-N
functional group
carboxylic acid
lipid type
saturated FAs
shipped in
ambient
storage temp.
2-8°C
Quality Level
Related Categories
Application
- LORE receptor homomerization is required for 3-hydroxydecanoic acid-induced immune signaling and determines the natural variation of immunosensitivity within the Arabidopsis genus.: This study unveils the crucial role of 3-Hydroxydecanoic acid in mediating immune responses through LORE receptor homomerization in plants, providing insights into the molecular mechanisms of plant defense and potential agricultural applications (Eschrig et al., 2024).
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ahmad Mohammad Abdel-Mawgoud et al.
Applied microbiology and biotechnology, 86(5), 1323-1336 (2010-03-26)
Rhamnolipids are glycolipidic biosurfactants produced by various bacterial species. They were initially found as exoproducts of the opportunistic pathogen Pseudomonas aeruginosa and described as a mixture of four congeners: alpha-L-rhamnopyranosyl-alpha-L-rhamnopyranosyl-beta-hydroxydecanoyl-beta-hydroxydecanoate (Rha-Rha-C(10)-C(10)), alpha-L-rhamnopyranosyl-alpha-L-rhamnopyranosyl-beta-hydroxydecanoate (Rha-Rha-C(10)), as well as their mono-rhamnolipid congeners Rha-C(10)-C(10)
Evrim Acar et al.
Molecular nutrition & food research, 63(1), e1800215-e1800215 (2018-08-11)
Self-reported dietary intake does not represent an objective unbiased assessment. The effect of the new Nordic diet (NND) versus average Danish diet (ADD) on plasma metabolic profiles is investigated to identify biomarkers of compliance and metabolic effects. In a 26-week
Q Qi et al.
Applied microbiology and biotechnology, 54(1), 37-43 (2000-08-22)
For the first time, the purification has been achieved of the type II polyhydroxyalkanoate (PHA) synthases PhaC1 and PhaC2 from Pseudomonas aeruginosa applying N-terminal His6-tag fusions and metal chelate affinity chromatography. In vivo His6-tagged PHA synthase activity was confirmed by
Anders Broberg et al.
Applied and environmental microbiology, 73(17), 5547-5552 (2007-07-10)
The metabolite production of lactic acid bacteria (LAB) on silage was investigated. The aim was to compare the production of antifungal metabolites in silage with the production in liquid cultures previously studied in our laboratory. The following metabolites were found
Florian Bredenbruch et al.
Journal of bacteriology, 187(11), 3630-3635 (2005-05-20)
The role of intercellular communication in the regulation of bacterial multicellular behavior has received widespread attention, and a variety of signal molecules involved in bacterial communication have been discovered. In addition to the N-acyl-homoserine lactones, 4-hydroxy-2-alkylquinolines (HAQs), including the Pseudomonas
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