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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:
Molecular Weight:
201.31
Beilstein:
1767291
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

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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
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
11-Aminoundecanoic acid.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 39, 239-245 (1986-01-01)

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