480983
Propyne
≥97%
Synonym(s):
Allylene, Methylacetylene
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About This Item
Recommended Products
vapor pressure
204.6 mmHg ( −49.5 °C)
Quality Level
Assay
≥97%
form
gas
bp
−23.2 °C (lit.)
mp
−102.7 °C (lit.)
SMILES string
CC#C
InChI
1S/C3H4/c1-3-2/h1H,2H3
InChI key
MWWATHDPGQKSAR-UHFFFAOYSA-N
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General description
Propyne (methylacetylene) is commonly used in gas welding.
Application
Propyne (CH3C≡CH) can be used:
- As a fuel for stoichiometric low-pressure flat-flames in isomer-specific combustion studies.
- In the synthesis of polycyclic aromatic hydrocarbons under various reaction conditions.
- In the synthesis of phenylacetylenes.
- In the selective synthesis of propene by catalytic hydrogenation using Pt/Al2O3 catalyst.
Packaging
Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.
Compatible with the following:
Compatible with the following:
Legal Information
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Gas 1A - Press. Gas Compr. Gas - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
2A - Gases
WGK
nwg
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Isomer-specific combustion chemistry in allene and propyne flames
Combustion and Flame, 156(11), 2153-2164 (2009)
Reaction of phenyl radicals with propyne
Journal of the American Chemical Society, 124(11), 2781-2789 (2002)
In situ generation of 1-propyne: A useful introduction of 1-propyne on unsaturated halogenated compounds through the Sonogashira reaction
Synlett, 2002(02), 0328-0330 (2002)
Propyne hydrogenation over alumina-supported palladium and platinum catalysts
Applied Catalysis A: General, 259(1), 109-120 (2004)
Magnetic resonance in chemistry : MRC, 45(8), 661-666 (2007-06-15)
Configurational assignment of five carbon, silicon and germanium containing propynal oximes has been carried out by means of experimental measurements and high-level ab initio calculations of their 13C-1H, 13C-13C and 15N-1H spin-spin coupling constants. The title compounds were shown to
Protocols
Separation of Acetylene; Propyne; Propylene; Propane
2-Butene; 2-Methylbutane; 1,3-Butadiene; Propyne
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