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Home > Encyclopedia > 11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE

11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE

11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE structure

11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE 

structure
  • CAS No:

    134179-38-7

  • Formula:

    C8H18N4O3

  • Chemical Name:

    11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE

  • Synonyms:

    1-Amino-11-azido-3,6,9-trioxaundecane,2-{2-[2-(2-Azidoethoxy)ethoxy]ethoxy}ethylamine,O-(2-Aminoethyl)-Oμ-(2-azidoethyl)diethyleneglycol;1-Amino-11-azido-3,6,9-trioxaundecane;11-Azido-3,6,9-trioxaundecane-1-amine;N3-PEG3-CH2CH2NH2;11-Azido-3,6,9-trioxaundecylamine;2-{2-[2-(2-Azidoethoxy)ethoxy]ethoxy}ethylamine, 1-Amino-11-azido-3,6,9-trioxaundecane;1-Amino-11-azido-3,6,9-trioxaundecane11-Amino-3,6,9-trioxaundecanyl Azide;11-Azido-3,6,9-trioxaundecan-1-aMine technical, >=90% (GC)

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

Very Pale Yellow Oil

11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE Basic Attributes

218.25

218.13800

DTXSID60370655

29299090

Characteristics

68.1

0.45826

Yellow to Pale Brown Viscous Liquid

1.10 g/mL at 20 °C(lit.)

198-202°C

n 20/D 1.470

Amber Vial, Refrigerator, Under Inert Atmosphere

Safety Information

III

8

UN 2735 8/PG 3

3

34

26-36/37/39-45

C,Xi

P280-P305 + P351 + P338-P310

H314

|Danger|H314 (97.62%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501|Aggregated GHS information provided by 42 companies from 2 notifications to the ECHA C&L Inventory.

11-AZIDO-3 6 9-TRIOXAUNDECAN-1-AMINE Use and Manufacturing

A PEG derivative, which contains a free amine that can be conjugatedto biological molecules directly by an amide linkage (or via the correspondingisothiocyanate) and an azide that can be reduced to an amine for conjugation to other molecules. PEG derivatives are water soluble. Bifunctional water soluble compounds with flexible dimensions allow for conjugation of small molecules to proteins or molecular probes.1-amino-11-azido-3,6,9-trioxaundecane can be reacted with small organic molecules for the synthesis of heterobifunctional compounds.It has been used to synthesize a mannose-fluorescein conjugate for the study of cell-surface mannose-specific lectins.

Computed Properties

Molecular Weight:218.25
XLogP3:-0.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:11
Exact Mass:218.13789045
Monoisotopic Mass:218.13789045
Topological Polar Surface Area:68.1
Heavy Atom Count:15
Complexity:173
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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