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Sigma-Aldrich

3-Azido-1-propanamine

≥95%

Synonym(e):

3-Azidopropylamine

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About This Item

Empirische Formel (Hill-System):
C3H8N4
CAS-Nummer:
88192-19-2
Molekulargewicht:
100.12
MDL-Nummer:
MFCD11046568
UNSPSC-Code:
12352116
PubChem Substanz-ID:
329766597
NACRES:
NA.22

Qualitätsniveau

100

Assay

≥95%

Form

liquid

Eignung der Reaktion

reaction type: click chemistry

Brechungsindex

n20/D 1.471

Dichte

1.020 g/mL at 25 °C

Lagertemp.

−20°C

SMILES String

NCCCN=[N+]=[N-]

InChI

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

InChIKey

OYBOVXXFJYJYPC-UHFFFAOYSA-N

Allgemeine Beschreibung

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.

Anwendung

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.

Piktogramme

FlameSkull and crossbones
GHS02,GHS06

Signalwort

Danger

H-Sätze

H226,H301

Gefahreneinstufungen

Acute Tox. 3 Oral - Flam. Liq. 3

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

140.0 °F

Flammpunkt (°C)

60 °C

Analysenzertifikate (COA)

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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
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
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)
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)
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