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:
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
Quality Level
application(s)
peptide synthesis
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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.
Application
11-Aminoundecanoic acid can be used as a linker to synthesize amide-linked linear guanosine dimer.
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)
J K Dunnick et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 3(6), 614-618 (1983-11-01)
11-Aminoundecanoic acid, the monomer of nylon 11, was toxic to the urinary tract of both male and female B6C3F1 mice and Fischer 344 rats, when administered in the diet at 7500 or 15 000 ppm for 103-104 weeks. Dose-related effects
E J Matthews
Environmental health perspectives, 101 Suppl 2, 311-318 (1993-07-01)
A co-culture clonal survival assay was developed to measure the cytotoxicity of test chemical treatments to BALB/c-3T3 cells because the standard clonal survival assay using 200 wild type (WT) cells frequently overestimates chemical cytotoxicity when compared with identical treatment doses
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
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