Skip to Content
Merck
CN

776130

3-Azido-1-propanol

≥96%

Synonym(s):

1-Azidopropan-3-ol

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

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

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

3-Azido-1-propanol, ≥96%

InChI

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

SMILES string

OCCCN=[N+]=[N-]

InChI key

WHVSIWLMCCGHFW-UHFFFAOYSA-N

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

Quality Level

100

Related Categories

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

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

190.0 °F

flash_point_c

87.77 °C

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000462367
0000462367
0000425008
0000425008
0000417587

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

SPAAC-NAD-seq, a sensitive and accurate method to profile NAD+-capped transcripts
H Hu, et al.
Proceedings of the National Academy of Sciences, 118, e2025595118-e2025595118 (2021)
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
Cetin M, et al.
Polym. Chem., 7(46), 7094-7100 (2016)
View All Related Papers

Articles

What is Click Chemistry? An Introduction

Explore click chemistry: efficient, high-yield reactions for drug discovery, bioconjugation, and green chemistry with simple conditions and wide applications.

Click Chemistry in Drug Discovery

Explore the principles and applications of click chemistry in drug discovery, highlighting efficient reactions that streamline the synthesis of bioactive compounds.

Click Chemistry in Drug Discovery

Explore the principles and applications of click chemistry in drug discovery, highlighting efficient reactions that streamline the synthesis of bioactive compounds.

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