Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More

Ethoxyacetylene, ca 50% w/w in hexanes, Thermo Scientific Chemicals

Catalog Number AAA1424506
Click to view available options
Quantity:
1 g
5 g
25 g
927-80-0
C4H6O
70.091
MFCD00009247
WMYNMYVRWWCRPS-UHFFFAOYSA-N
ethoxyacetylene, ethoxyethyne, ethyl ethynyl ether, ethyne, ethoxy, ether, ethyl ethynyl, ethoxy-ethyne, ethyne, ethoxy-9ci, 1-ethoxyacetylene, ethoxyacetylene w/w solution in hexanes, ethoxy acetylene
61239
ethynoxyethane
CCOC#C
927-80-0
C4H6O
70.091
MFCD00009247
WMYNMYVRWWCRPS-UHFFFAOYSA-N
ethoxyacetylene, ethoxyethyne, ethyl ethynyl ether, ethyne, ethoxy, ether, ethyl ethynyl, ethoxy-ethyne, ethyne, ethoxy-9ci, 1-ethoxyacetylene, ethoxyacetylene w/w solution in hexanes, ethoxy acetylene
61239
ethynoxyethane
CCOC#C

Ethoxyacetylene is used in Arens-van Dorp synthesis to prepare propargyl alcohol via reaction with ketone. In organic synthesis, it undergoes [2+2] cycloaddition reactions with ketenes to give cyclobutenone derivatives. It is also used to prepare alpha, beta-unsaturated esters from ketones by following Meyer-Schuster rearrangement.Used with N-vinylamides and triflic anhydride in a direct, three-component synthesis of pyridines. Also used to prepare α, β-unsaturated esters from ketones via a Meyer-Schuster rearrangement.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Ethoxyacetylene is used in Arens-van Dorp synthesis to prepare propargyl alcohol via reaction with ketone. In organic synthesis, it undergoes [2+2] cycloaddition reactions with ketenes to give cyclobutenone derivatives. It is also used to prepare alpha, beta-unsaturated esters from ketones by following Meyer-Schuster rearrangement.Used with N-vinylamides and triflic anhydride in a direct, three-component synthesis of pyridines. Also used to prepare α, β-unsaturated esters from ketones via a Meyer-Schuster rearrangement.

Solubility
Slightly miscible with water.

Notes
Incompatible with strong oxidizing agents and strong acids.
TRUSTED_SUSTAINABILITY
Density 0.718
Boiling Point 55°C to 56°C
Flash Point −28°C (−18°F)
Odor Recognizable
Refractive Index 1.38
Linear Formula CH3CH2OC≡CH
Quantity 5 g
UN Number UN1993
Beilstein 741882
Solubility Information Slightly miscible with water.
Formula Weight 70.09
Concentration or Composition (by Analyte or Components) ≈50% w/w in hexanes
Chemical Name or Material Ethoxyacetylene
Show More Show Less
Hazard Category H225-H304-H312+H332-H315-H319-H336-H351-H361f-H373
Hazard Statement GHS H Statement
H225-H304-H361-H373-H315
Highly flammable liquid and vapour.
May be fatal if swallowed and enters airways.
Suspected of damaging fertility or the unborn child.
May cause damage to organs through prolonged or repeated exposure.
Causes skin irritation.
Precautionary Statement P201-P202-P210-P233-P235-P240-P241-P242-P243-P260-P264b-P271-P280i-P281-P301+P310-P303+P361+P353-P304+P340-P305+P351+P338-P308+P313-P312-P331-P332+P313-P363-P370+P378q-P501c
DOTInformation Transport Hazard Class: 3; Packing Group: II; Proper Shipping Name: FLAMMABLE LIQUIDS, N.O.S.
EINECSNumber 213-164-5
RTECSNumber KN9900000
TSCA No
Recommended Storage Keep cold

RUO – Research Use Only

Provide Content Correction

We continue to work to improve your shopping experience and your feedback regarding this content is very important to us. Please use the form below to provide feedback related to the content on this product.

Product Title

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.

Cancel Submit