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
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25
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![Poly[(R)-3-hydroxybutyric acid] natural origin](/deepweb/assets/sigmaaldrich/product/structures/129/476/7d1c924b-f644-4889-a2d6-d7a923ce382c/640/7d1c924b-f644-4889-a2d6-d7a923ce382c.png)
Quality Level
Assay
≥98%
form
powder
functional group
carboxylic acid
lipid type
saturated FAs
shipped in
ambient
storage temp.
2-8°C
SMILES string
CCCCCCCC(O)CC(O)=O
InChI
1S/C10H20O3/c1-2-3-4-5-6-7-9(11)8-10(12)13/h9,11H,2-8H2,1H3,(H,12,13)
InChI key
FYSSBMZUBSBFJL-UHFFFAOYSA-N
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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3-Hydroxydecanoic acid (3HD) was produced in Escherichia coli by mobilizing (R)-3-hydroxydecanoyl-acyl carrier protein-coenzyme A transacylase (PhaG, encoded by the phaG gene). By employing an isogenic tesB (encoding thioesterase II)-negative knockout E. coli strain, CH01, it was found that the expressions
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