171476
Undecanoic acid
98%
Synonym(s):
Hendecanoic acid
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25 G
R$296.00
100 G
R$420.00
About This Item
Linear Formula:
CH3(CH2)9COOH
CAS Number:
Molecular Weight:
186.29
Beilstein:
1759287
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
bp
228 °C/160 mmHg (lit.)
248-250 °C (lit.)
mp
28-31 °C (lit.)
functional group
carboxylic acid
SMILES string
CCCCCCCCCCC(O)=O
InChI
1S/C11H22O2/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2-10H2,1H3,(H,12,13)
InChI key
ZDPHROOEEOARMN-UHFFFAOYSA-N
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Application
Undecanoic acid was used in the formation of cycloamylose crystals[1].
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
>233.6 °F
Flash Point(C)
> 112 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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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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Fatty-acid binding proteins (FABPs) are abundantly expressed proteins that bind a range of lipophilic molecules. They have been implicated in the import and intracellular distribution of their ligands and have been linked with metabolic and inflammatory responses in the cells
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