Skip to Content
Merck
All Photos(3)

Key Documents

762016

Sigma-Aldrich

3-Azido-1-propanamine

≥95%

Synonym(s):

3-Azidopropylamine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C3H8N4
CAS Number:
Molecular Weight:
100.12
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥95%

form

liquid

reaction suitability

reaction type: click chemistry

refractive index

n20/D 1.471

density

1.020 g/mL at 25 °C

storage temp.

−20°C

SMILES string

NCCCN=[N+]=[N-]

InChI

1S/C3H8N4/c4-2-1-3-6-7-5/h1-4H2

InChI key

OYBOVXXFJYJYPC-UHFFFAOYSA-N

General description

3-Azido-1-propanamine can be used to functionalize:
  • Bismethylolpropionic acid (bis-MPA) monomers with azide functional group to generate high-generation dendrimers.,
  • Clickable zinc tetraphenylporphyrin scaffold with an azido group through click chemistry applicable in photodynamic therapy.

Application

Amine modified azide for click chemistry.
3-Azido-1-propanamine may be used in the synthesis of mannopyranoside dendrimers for studying multivalent carbohydrate-protein interactions.

Pictograms

FlameSkull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

140.0 °F

Flash Point(C)

60 °C


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 mono-, di-and triporphyrin building blocks by click chemistry for photodynamic therapy application
Gazzali AM, et al.
Tetrahedron, 73(5), 532-541 (2017)
Synthesis and solvodynamic diameter measurements of closely related mannodendrimers for the study of multivalent carbohydrate?protein interactions.
Chabre YM, et al.
Beilstein Journal of Organic Chemistry, 10, 1524-1524 (2014)
Two-dimensional ultrafast vibrational spectroscopy of azides in ionic liquids reveals solute-specific solvation
Dutta S, et al.
Physical Chemistry Chemical Physics, 17(40), 26575-26579 (2015)
Rapid Synthesis of Functionalized High-Generation Polyester Dendrimers via Strain-Promoted Alkyne-Azide Cycloaddition
McNelles SA and Adronov Al
Macromolecules, 50(20), 7993-8001 (2017)
Mariano Ortega-Muñoz et al.
Nanoscale, 11(16), 7850-7856 (2019-04-10)
Activated carbon nanodots functionalized with acid anhydride groups (AA-CNDs) are prepared by one-pot water-free green thermolysis of citric acid. As a proof of concept of their capabilities as appealing and versatile platforms for accessing engineering nanoconstructs, the as-prepared AA-CNDs have

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