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A82605

Sigma-Aldrich

11-Aminoundecanoic acid

97%

Synonym(s):

Aminoundecanoic acid

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About This Item

Linear Formula:
NH2(CH2)10CO2H
CAS Number:
2432-99-7
Molecular Weight:
201.31
Beilstein:
1767291
EC Number:
219-417-6
MDL number:
MFCD00008150
UNSPSC Code:
12352106
PubChem Substance ID:
24891324
NACRES:
NA.22

Assay

97%

form

powder

reaction suitability

reaction type: solution phase peptide synthesis

color

white

mp

188-191 °C (lit.)

application(s)

peptide synthesis

SMILES string

NCCCCCCCCCCC(O)=O

InChI

1S/C11H23NO2/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h1-10,12H2,(H,13,14)

InChI key

GUOSQNAUYHMCRU-UHFFFAOYSA-N

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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 Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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
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)
Development of Minimal Diguanosinyl Motif toward RNA G-Quadruplex-Like Structures in Solution
Chembiochem, 21, 1837-1842 (2020)
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