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H3648

Sigma-Aldrich

(±)-3-Hydroxydecanoic acid

≥98%

Synonym(s):

DL-β-Hydroxycapric acid

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About This Item

Empirical Formula (Hill Notation):
C10H20O3
CAS Number:
5561-87-5
Molecular Weight:
188.26
MDL number:
MFCD00133275
UNSPSC Code:
12352211
PubChem Substance ID:
24895586
NACRES:
NA.25

Quality Level

200

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

Certificates of Analysis (COA)

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B Füchtenbusch et al.
Applied microbiology and biotechnology, 53(2), 167-172 (2000-03-10)
Screening experiments identified several bacteria which were able to use residual oil from biotechnological rhamnose production as a carbon source for growth. Ralstonia eutropha H16 and Pseudomonas oleovorans were able to use this waste material as the sole carbon source
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
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)
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
A Hiraishi et al.
Antonie van Leeuwenhoek, 61(3), 231-236 (1992-04-01)
Nine Zoogloea strains including the type strain of Z. ramigera (IAM 12136 = ATCC 19544 = N.C. Dondero 106) and newly isolated strains were investigated for isoprenoid quinone composition and whole-cell fatty acid profiles. Seven of the tested strains, having
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