A82605
11-Aminoundecanoic acid
97%
Synonym(s):
Aminoundecanoic acid
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About This Item
Linear Formula:
NH2(CH2)10CO2H
CAS Number:
Molecular Weight:
201.31
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-417-6
Beilstein/REAXYS Number:
1767291
MDL number:
Product Name
11-Aminoundecanoic acid, 97%
InChI key
GUOSQNAUYHMCRU-UHFFFAOYSA-N
InChI
1S/C11H23NO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10,12H2,(H,13,14)
SMILES string
NCCCCCCCCCCC(O)=O
assay
97%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
color
white
mp
188-191 °C (lit.)
application(s)
peptide synthesis
Quality Level
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Application
11-Aminoundecanoic acid can be used as a linker to synthesize amide-linked linear guanosine dimer.
General description
11-Aminoundecanoic acid also known as aminoundecanoic acid, is utilized in solution phase peptide synthesis. It is also a monomer precursor for nylon-11.
Storage Class
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Syntheses of 12-aminododecanoic and 11-aminoundecanoic acids from vernolic acid
Journal of the American Oil Chemists' Society, 74, 531-538 (1997)
Development of Minimal Diguanosinyl Motif toward RNA G-Quadruplex-Like Structures in Solution
Chembiochem, 21, 1837-1842 (2020)
Zhiyong Qian et al.
Biomaterials, 25(11), 1975-1981 (2004-01-27)
In this paper, a new kind of aliphatic biodegradable polyesteramide copolymers P(CL/AU)x/y based on epsilon-caprolactone and 11-aminoundecanoic acid were synthesized by the melt polycondensation method. Hydrolytic degradation behavior of P(CL/AU) copolymers were studied by using FTIR, 1H-NMR and DSC. Chemical
11-Aminoundecanoic acid.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 39, 239-245 (1986-01-01)
[Antibacterial effect of an ammonium salt of 11-aminoundecanoic acid. 5. Organic ammonium salts].
F Devínsky et al.
Die Pharmazie, 34(9), 574-574 (1979-01-01)
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