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Home > products > Chemical Intermediates > 11-Azido-3,6,9-trioxaundecan-1-amine CAS 134179-38-7

11-Azido-3,6,9-trioxaundecan-1-amine CAS 134179-38-7

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 134179-38-7

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Price: Negotiation

Packaging Details: Plastic bottles, Plastic buckets

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CAS 134179-38-7 11-Azido-3

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6

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9-trioxaundecan-1-amine

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CAS 134179-38-7

CAS NO::
134179-38-7
Appearance::
Very Pale Yellow Oil
Molecular Formula::
C8H18N4O3
Molecular Weight::
218.25400
EINECS NO::
629-285-5
MDL NO::
MFCD00269874
CAS NO::
134179-38-7
Appearance::
Very Pale Yellow Oil
Molecular Formula::
C8H18N4O3
Molecular Weight::
218.25400
EINECS NO::
629-285-5
MDL NO::
MFCD00269874
11-Azido-3,6,9-trioxaundecan-1-amine CAS 134179-38-7

Product Description:

Product Name: 11-Azido-3,6,9-trioxaundecan-1-amine CAS NO: 134179-38-7

 

 

Synonyms:

1-Amino-11-azido-3,6,9-trioxaundecane;

2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethanamine;

Amino-PEG3-Azide;

 

 

Chemical & Physical Properties:

Appearance: Very pale yellow oil

Assay :≥98.0%

Density: 1.1

Boiling Point: 198-202℃

Refractive Index: 1.47

Storage Temp.: Amber Vial, Refrigerator, Under Inert Atmosphere

 

 

Safety Information:

Symbol: GHS05

Signal Word: Danger

Safety Statements: S26-S36/37/39-S45

RIDADR: UN 2735

Risk Statement: R34

Packing Group: III

Hazard Codes: C,Xi

Hazard Class: 8

HS Code: 2929909090

Hazard Statement: H314

Precautionary Statements: P280-P305 + P351 + P338-P310

 

 

A PEG derivative, which contains a free amine that can be conjugated to biological molecules directly by an amide linkage (or via the corresponding isothiocyanate) 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.

 

 

 

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