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A82605

11-Aminoundecanoic acid

Name: 11-Aminoundecanoic acid
Brand: ALDRICH

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

UNSPSC Code:

12352106

NACRES:

NA.22

PubChem Substance ID:

24891324

EC Number:

219-417-6

Beilstein/REAXYS Number:

1767291

MDL number:

MFCD00008150

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Properties

Quality Level

200

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

Description

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.

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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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Development of Minimal Diguanosinyl Motif toward RNA G-Quadruplex-Like Structures in Solution

Chembiochem, 21, 1837-1842 (2020)

Syntheses of 12-aminododecanoic and 11-aminoundecanoic acids from vernolic acid

Journal of the American Oil Chemists' Society, 74, 531-538 (1997)

Design of dimeric peptides obtained from a subdominant Epstein-Barr virus LMP2-derived epitope.

M Marastoni et al.

European journal of medicinal chemistry, 35(6), 593-598 (2000-07-25)

The latent membrane protein 2 (LMP2) is expressed in EBV-associated tumours. LMP2 is a target of HLA-A2 restricted EBV-specific CTL responses and consequently it may represent a good target for specific CTL-based immunotherapies. However, the efficacy of such therapy is

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Global Trade Item Number

SKU	GTIN
A82605-500G	04061832596914
A82605-100G	04061833391365