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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:
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
Application
Undecanoic acid was used in the formation of cycloamylose crystals.
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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)
Olaf Nimz et al.
Carbohydrate research, 339(8), 1427-1437 (2004-06-05)
Crystal structures are reported of cycloamylose containing 26 D-glucose residues (CA26, cyclohexaicosaose, C156H260O130) in complexes with undecanoic acid (CA26 x 2C10H21COOH x 34.95 H2O, orthorhombic P2(1)2(1)2(1), one CA26 and two bound undecanoic acids F1 and F2 in the asymmetric unit
Dorit Avrahami et al.
Biochemistry, 42(50), 14946-14956 (2003-12-17)
The dramatically increased frequency of opportunistic fungal infections has prompted research to diversify the arsenal of antifungal agents. Antimicrobial peptides constitute a promising family for future antibiotics with a new mode of action. However, only a few are effective against
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 171476-100G | 04061838750969 |
| 171476-25G | 04061838750976 |