Skip to Content
Merck
CN

50062

Glycidyl propargyl ether

technical, ≥90% (GC)

Synonym(s):

2,3-Epoxypropyl propargyl ether

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C6H8O2
CAS Number:
18180-30-8
Molecular Weight:
112.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
57651238
MDL number:
MFCD00099300
Beilstein/REAXYS Number:
1098793

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

Glycidyl propargyl ether, technical, ≥90% (GC)

InChI

1S/C6H8O2/c1-2-3-7-4-6-5-8-6/h1,6H,3-5H2

SMILES string

C#CCOCC1CO1

InChI key

SYFZCLMMUNCHNH-UHFFFAOYSA-N

grade

technical

assay

≥90% (GC)

refractive index

n20/D 1.448

density

1.040 g/mL at 20 °C (lit.)

functional group

ether

Related Categories

Application

Glycidyl propargyl ether may be used in the synthesis of:
  • propargyl-functional poly(carbonate)s
  • hyperbranched polyglycerol (hbPG)
  • alkyne-functionalized polytetrahydrofuran (PTHF) diols
  • dextran-based cyclodextrin polymers

General description

Glycidyl propargyl ether (GPE) is a glycidyl ether containing a terminal alkyne group.

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Carc. 1B - Resp. Sens. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

156.2 °F - closed cup

flash_point_c

69 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
WXBF4257V
WXBF4075V
WXBF2713V
WXBD9814V
WXBD7825V

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

Combining cationic ring-opening polymerization and click chemistry for the design of functionalized polyurethanes.
Basko M, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 49(7), 1597-1604 (2011)
One-step synthesis of multi-alkyne functional hyperbranched polyglycerols by copolymerization of glycidyl propargyl ether and glycidol.
Schull C, et al.
Polym. Chem., 4(17), 4730-4736 (2013)
Zoltán Fülöp et al.
Carbohydrate polymers, 97(2), 635-642 (2013-08-06)
Cyclodextrins and their water-soluble derivatives are excellent solubilizers and stabilizers and widely used as enabling pharmaceutical excipients. However, still new cyclodextrin derivatives are being designed and synthesized in an effort to improve their physicochemical properties. In this study physicochemical and
Propargyl-Functional Aliphatic Polycarbonate Obtained from Carbon Dioxide and Glycidyl Propargyl Ether.
Hilf J and Frey H.
Macromolecular Rapid Communications, 34(17), 1395-1400 (2013)

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