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543128

Sigma-Aldrich

Propargyl acetate

98%

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About This Item

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

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.)

SMILES string

CC(=O)OCC#C

InChI

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

InChI key

RIZZXCJMFIGMON-UHFFFAOYSA-N

Related Categories

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

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’.

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Nucleophilic reactions of propargyl acetates mediated by titanocene dichloride and magnesium
Yang F, et al.
Tetrahedron Letters, 42.15, 2839- 2841 (2001)
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)
Investigations on the ion transport mechanism in conducting polymer films
Casalbore-Miceli G, et al.
Solid State Ionics, 131.3, 311-321 (2000)

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