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Merck

480983

Sigma-Aldrich

Propyne

≥97%

Sinónimos:

Allylene, Methylacetylene

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About This Item

Fórmula lineal:
CH3C≡CH
Número de CAS:
Peso molecular:
40.06
EC Number:
MDL number:
UNSPSC Code:
12142100
PubChem Substance ID:
NACRES:
NA.22

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:

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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signalword

Danger

Hazard Classifications

Flam. Gas 1A - Press. Gas Compr. Gas - STOT SE 3

target_organs

Respiratory system

Storage Class

2A - Gases

wgk_germany

nwg

ppe

Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)


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Propyne hydrogenation over alumina-supported palladium and platinum catalysts
Kennedy DR, et al.
Applied Catalysis A: General, 259(1), 109-120 (2004)
Ying Guo et al.
Physical chemistry chemical physics : PCCP, 9(16), 1972-1979 (2007-04-14)
Crossed molecular beams experiments have been utilized to investigate the reaction dynamics between two closed shell species, i.e. the reactions of tricarbon molecules, C(3)(X(1)Sigma(g)(+)), with allene (H(2)CCCH(2); X(1)A(1)), and with methylacetylene (CH(3)CCH; X(1)A(1)). Our investigations indicated that both these reactions
Lourdes Gracia et al.
The journal of physical chemistry. A, 112(8), 1808-1816 (2008-02-07)
Possible molecular mechanisms of the gas-phase ion/molecule reaction of VO2+ in its lowest singlet and triplet states (1A1/3A' ') with propyne have been investigated theoretically by density functional theory (DFT) methods. The geometries, energetic values, and bonding features of all
In situ generation of 1-propyne: A useful introduction of 1-propyne on unsaturated halogenated compounds through the Sonogashira reaction
Abraham E and Suffert J
Synlett, 2002(02), 0328-0330 (2002)
Yongping Zhang et al.
Langmuir : the ACS journal of surfaces and colloids, 29(6), 1868-1874 (2013-01-19)
To achieve silicon functionalization for the development of hybrid devices, multifunctional molecules may be employed to attach to the silicon surfaces. It is important to get a fundamental understanding about the molecule/silicon interface chemistry and the binding configuration. The surface

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