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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

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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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
Highly regioselective Vilsmeier-Haack acylation of hexahydropyrroloindolizine.
B Sayah et al.
The Journal of organic chemistry, 66(7), 2522-2525 (2001-04-03)
Hannes Löwe et al.
Biotechnology for biofuels, 10, 190-190 (2017-08-18)
One of the major challenges for the present and future generations is to find suitable substitutes for the fossil resources we rely on today. Cyanobacterial carbohydrates have been discussed as an emerging renewable feedstock in industrial biotechnology for the production
Robert K Ernst et al.
The Journal of infectious diseases, 196(7), 1088-1092 (2007-09-01)
Three structural features of lipid A (addition of palmitate [C16 fatty acid], addition of aminoarabinose [positively charged amino sugar residue], and retention of 3-hydroxydecanoate [3-OH C10 fatty acid]) were determined for Pseudomonas aeruginosa isolates from patients with cystic fibrosis (CF;
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
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