171476
Undecanoic acid
98%
Synonym(s):
Hendecanoic acid
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About This Item
Linear Formula:
CH3(CH2)9COOH
CAS Number:
Molecular Weight:
186.29
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-964-2
Beilstein/REAXYS Number:
1759287
MDL number:
InChI key
ZDPHROOEEOARMN-UHFFFAOYSA-N
InChI
1S/C11H22O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3,(H,12,13)
SMILES string
CCCCCCCCCCC(O)=O
assay
98%
form
solid
bp
228 °C/160 mmHg (lit.), 248-250 °C (lit.)
Quality Level
functional group
carboxylic acid
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Application
Undecanoic acid was used in the formation of cycloamylose crystals.
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
>233.6 °F
flash_point_c
> 112 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Rashanique D Quarels et al.
Beilstein journal of nanotechnology, 8, 1863-1877 (2017-10-20)
Visible-light irradiation of phthalimide esters in the presence of the photosensitizer [Ru(bpy)
Rui Hong et al.
Journal of the American Chemical Society, 126(3), 739-743 (2004-01-22)
Thioalkyl and thioalkylated oligo(ethylene glycol) (OEG) ligands with chain-end functionality were used to fabricate water-soluble CdSe nanoparticle scaffolds. Surface recognition of chymotrypsin (ChT) was achieved using these functionalized nanoparticle scaffolds, with three levels of interaction demonstrated: no interaction (OEG terminated
Fernanda G Paião et al.
FEMS microbiology letters, 271(2), 180-186 (2007-04-12)
Suppressive subtractive hybridization was used to isolate transcripts specifically upregulated during Trichophyton rubrum exposure to acriflavin, fluconazole, griseofulvin, terbinafine or undecanoic acid. Macro-array dot-blot and sequencing of 132 clones, which correspond to genes differentially expressed after exposition of T. rubrum
Margarida M L M Vareiro et al.
Analytical biochemistry, 377(2), 243-250 (2008-04-03)
The development of a single-step, separation-free method for measurement of low concentrations of fatty acid using a surface plasmon resonance-enhanced fluorescence competition assay with a surface-bound antibody is described. The assay behavior was unexpectedly complex. A nonlinear coverage-dependent self-quenching of
Raluca Voicu et al.
Langmuir : the ACS journal of surfaces and colloids, 20(26), 11713-11720 (2004-12-15)
This paper describes a simple strategy for DNA immobilization on chemically modified and patterned silicon surfaces. The photochemical modification of hydrogen-terminated Si(111) with undecylenic acid leads to the formation of an organic monolayer covalently attached to the surface through Si-C
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