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Sigma-Aldrich

3-Azido-1-propanamine

≥95%

Synonym(s):

3-Azidopropylamine

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About This Item

Empirical Formula (Hill Notation):
C3H8N4
CAS Number:
88192-19-2
Molecular Weight:
100.12
MDL number:
MFCD11046568
UNSPSC Code:
12352116
PubChem Substance ID:
329766597
NACRES:
NA.22

Quality Level

100

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

Related Categories

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
GHS02,GHS06

signalword

Danger

hcodes

H226,H301

Hazard Classifications

Acute Tox. 3 Oral - Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

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’.

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Xiaoqiang Chen et al.
Biomaterials, 122, 130-140 (2017-01-24)
The development of multifunctional reagents for simultaneous specific near-infrared (NIR) imaging and phototherapy of tumors is of great significance. This work describes the design of a cathepsin B-activated fluorescent probe (CyA-P-CyB) and its applications as an NIR imaging probe for
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)
Nicolò Mauro et al.
International journal of pharmaceutics, 555, 207-219 (2018-11-21)
The extremely complex tumor microenvironment (TME) in humans is the major responsible for the therapeutic failure in cancer nanomedicine. A new concept of disease-driven nanomedicine, henceforth named "Theranomics", which attempts to target cancer cells and TME on the whole, represents
Anthony Angeli et al.
Chembiochem : a European journal of chemical biology, 18(11), 1036-1047 (2017-03-21)
Lectin A (LecA) from Pseudomonas aeruginosa is an established virulence factor. Glycoclusters that target LecA and are able to compete with human glycoconjugates present on epithelial cells are promising candidates to treat P. aeruginosa infection. A family of 32 glycodendrimers of generation 0
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