Skip to Content
Merck
All Photos(1)

Documents

17758

Sigma-Aldrich

11-Azido-3,6,9-trioxaundecan-1-amine

technical, ≥90% (GC)

Synonym(s):

1-Amino-11-azido-3,6,9-trioxaundecane, 2-{2-[2-(2-Azidoethoxy)ethoxy]ethoxy}ethylamine, O-(2-Aminoethyl)-O′-(2-azidoethyl)diethylene glycol

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C8H18N4O3
CAS Number:
Molecular Weight:
218.25
Beilstein:
4745506
MDL number:
UNSPSC Code:
12352125
PubChem Substance ID:
NACRES:
NA.22

grade

technical

Assay

≥90% (GC)

form

liquid

reaction suitability

reaction type: click chemistry
reagent type: cross-linking reagent

refractive index

n20/D 1.470

density

1.10 g/mL at 20 °C (lit.)

functional group

amine
azide

SMILES string

NCCOCCOCCOCCN=[N+]=[N-]

InChI

1S/C8H18N4O3/c9-1-3-13-5-7-15-8-6-14-4-2-11-12-10/h1-9H2

InChI key

FPVCVHVTMPCZTH-UHFFFAOYSA-N

Application

11-Azido-3,6,9-trioxaundecan-1-amine is an azide with polyethylene glycol-like characteristics that can be used to prepare azide-functionalized polymers via click reaction.

Other Notes

Bifunctional, hydrophilic linker

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis of an O-alkynyl-chitosan and its chemoselective conjugation with a PEG-like amino-azide through click chemistry.
Oliveira JR
Carbohydrate Polymers, 87(1), 240-249 (2012)
Claudia Arndt et al.
Oncoimmunology, 8(11), 1659095-1659095 (2019-10-28)
Chimeric antigen receptor (CAR) T cells have shown impressive therapeutic potential. Due to the lack of direct control mechanisms, therapy-related adverse reactions including cytokine release- and tumor lysis syndrome can even become life-threatening. In case of target antigen expression on
Shigehito Osawa et al.
Biomacromolecules, 17(1), 354-361 (2015-12-20)
Improving the stability of polyplex micelles under physiological conditions is a critical issue for promoting gene transfection efficiencies. To this end, hydrophobic palisade was installed between the inner core of packaged plasmid DNA (pDNA) and the hydrophilic shell of polyplex
C.R. Bertozzi et al.
The Journal of Organic Chemistry, 56, 4326-4326 (1991)
Brittany L Hartwell et al.
Journal of autoimmunity, 93, 76-88 (2018-07-17)
Autoreactive lymphocytes that escape central immune tolerance may be silenced via an endogenous peripheral tolerance mechanism known as anergy. Antigen-specific therapies capable of inducing anergy may restore patients with autoimmune diseases to a healthy phenotype while avoiding deleterious side effects

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service