Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

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
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C8H18N4O3
CAS Number:
134179-38-7
Molecular Weight:
218.25
Beilstein/REAXYS Number:
4745506
MDL number:
MFCD00269874
UNSPSC Code:
12352125
PubChem Substance ID:
57647613
NACRES:
NA.22

grade

technical

Quality Level

200

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
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCK0479
BCCB8532
BCBW5737
BCBT5549
BCBR5711V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

C.R. Bertozzi et al.
The Journal of Organic Chemistry, 56, 4326-4326 (1991)
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
Controlled folding of polystyrene single chains: design of asymmetric covalent bridges.
Zamfir M
Polym. Chem., 3(7), 1796-1802 (2012)
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
Hua Wang et al.
Biomaterials science, 8(1), 266-277 (2019-11-07)
Allotransplantation offers the potential to restore the anatomy and function of injured tissues and organs, but typically requires life-long, systemic administration of immunosuppressive drugs to prevent rejection, which can result in serious complications. Targeting the immunosuppressive drug to the graft
View All Related Papers

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