Skip to Content
Merck
All Photos(3)

Documents

776130

Sigma-Aldrich

3-Azido-1-propanol

≥96%

Synonym(s):

1-Azidopropan-3-ol

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C3H7N3O
CAS Number:
72320-38-8
Molecular Weight:
101.11
MDL number:
MFCD14652506
UNSPSC Code:
12352125
PubChem Substance ID:
329767811
NACRES:
NA.22

Quality Level

100

Assay

≥96%

form

liquid

reaction suitability

reaction type: click chemistry

refractive index

n20/D 1.461

density

1.095 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

OCCCN=[N+]=[N-]

InChI

1S/C3H7N3O/c4-6-5-2-1-3-7/h7H,1-3H2

InChI key

WHVSIWLMCCGHFW-UHFFFAOYSA-N

General description

3-Azido-1-propanol is an azide-containing reagent utilized in Strain-Promoted Azide-Alkyne Cycloaddition reactions (SPAAC). This enables selective and copper-free click chemistry modifications of biomolecules.

Application

3-Azido-1-propanol is used as a:
  • Precursor in the synthesis of heterocyclic compounds like dihydrooxazines
  • Reagent in the synthesis of heterofunctional polyesters by 1,3-dipolar cycloaddition

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

190.0 °F

Flash Point(C)

87.77 °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

One-step conversion of aldehydes to oxazolines and 5, 6-dihydro-4 H-1, 3-oxazines using 1, 2-and 1, 3-azido alcohols
JG Badiang, et al.
The Journal of Organic Chemistry, 61, 2484-2487 (1996)
Cross-linked polymer-blend gate dielectrics through thermal click chemistry
Li S, et al.
Chemistry?A European Journal , 21(49), 17762-17768 (2015)
Efficient synthesis of linear multifunctional poly (ethylene glycol) by copper (I)-catalyzed Huisgen 1, 3-dipolar cycloaddition
Liu X-M, et al.
Biomacromolecules, 8(9), 2653-2658 (2007)
1, 3-Dipolar and Diels-Alder cycloaddition reactions on polyester backbones possessing internal electron-deficient alkyne moieties
M Cetin
Polym. Chem., 7, 7094-7100 (2016)
1, 3-Dipolar and Diels-Alder cycloaddition reactions on polyester backbones possessing internal electron-deficient alkyne moieties
Cetin M, et al.
Polym. Chem., 7(46), 7094-7100 (2016)
View All Related Papers

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