Skip to Content
Merck
All Photos(1)

Key Documents

543128

Sigma-Aldrich

Propargyl acetate

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CO2CH2C≡CH
CAS Number:
Molecular Weight:
98.10
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

refractive index

n20/D 1.417 (lit.)

bp

27-28 °C/8 mmHg (lit.)

density

0.989 g/mL at 25 °C (lit.)

functional group

ester

SMILES string

CC(=O)OCC#C

InChI

1S/C5H6O2/c1-3-4-7-5(2)6/h1H,4H2,2H3

InChI key

RIZZXCJMFIGMON-UHFFFAOYSA-N

Application

Propargyl acetate may be used to synthesize:
  • optically active γ-hydroxy α,β-unsaturated aldehydes
  • homopropargyl alcohols
  • poly(propargyl acetate)

Pictograms

FlameSkull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

91.0 °F - closed cup

Flash Point(C)

32.8 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

Investigations on the ion transport mechanism in conducting polymer films
Casalbore-Miceli G, et al.
Solid State Ionics, 131.3, 311-321 (2000)
Asymmetric synthesis of ?-hydroxy a, ?-unsaturated aldehydes via enantioselective direct addition of propargyl acetate to aldehydes
El-Sayed E, et al.
Organic Letters, 3.19, 3017-3020 (2001)
Nucleophilic reactions of propargyl acetates mediated by titanocene dichloride and magnesium
Yang F, et al.
Tetrahedron Letters, 42.15, 2839- 2841 (2001)

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