Skip to Content
Merck

17758

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 In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C8H18N4O3
CAS Number:
134179-38-7
Molecular Weight:
218.25
UNSPSC Code:
12352125
NACRES:
NA.22
PubChem Substance ID:
57647613
MDL number:
MFCD00269874
Beilstein/REAXYS Number:
4745506
Assay:
≥90% (GC)
Form:
liquid

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

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

SMILES string

NCCOCCOCCOCCN=[N+]=[N-]

InChI key

FPVCVHVTMPCZTH-UHFFFAOYSA-N

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

Quality Level

200

Related Categories

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

signalword

Danger

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

ppe

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

pictograms

CorrosionExclamation mark
GHS05,GHS07

hcodes

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

flash_point_f

No data available

flash_point_c

No data available

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

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)
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
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)
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