2-Propynal
- Formula: C3H2O
- Molecular weight: 54.0474
- IUPAC Standard InChI: InChI=1S/C3H2O/c1-2-3-4/h1,3H
- IUPAC Standard InChIKey: IJNJLGFTSIAHEA-UHFFFAOYSA-N
- CAS Registry Number: 624-67-9
- Chemical structure:
This structure is also available as a 2d Mol file - Other names: Propyn-3-al; Propiolaldehye; Propargylaldehyde; Propioaldehyde; Propynal; Propiolaldehyde; 2-Propyn-1-one; Formylacetylene; Acetylenecarboxaldehyde
- Permanent link for this species. Use this link for bookmarking this species for future reference.
- Information on this page:
- Other data available:
- Data at other public NIST sites:
- Options:
Phase change data
Go To: Top, Gas phase ion energetics data, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Robert L. Brown and Stephen E. Stein
| Quantity | Value | Units | Method | Reference | Comment |
|---|---|---|---|---|---|
| Tboil | 333.2 | K | N/A | Weast and Grasselli, 1989 |
Gas phase ion energetics data
Go To: Top, Phase change data, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
LL - Sharon G. Lias and Joel F. Liebman
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
Ionization energy determinations
| IE (eV) | Method | Reference | Comment |
|---|---|---|---|
| 10.62 ± 0.15 | EI | Opitz, 1991 | LL |
| 10.8 | PE | Von Niessen, Bieri, et al., 1980 | LLK |
| 10.70 | PE | Carlier and Mouvier, 1979 | Vertical value; LLK |
Appearance energy determinations
| Ion | AE (eV) | Other Products | Method | Reference | Comment |
|---|---|---|---|---|---|
| CO+ | 12.6 ± 0.2 | C2H | EI | Opitz, 1991 | LL |
| C2+ | 19.7 ± 0.2 | ? | EI | Opitz, 1991 | LL |
| C2H2+ | 11.49 ± 0.15 | ? | EI | Opitz, 1991 | LL |
| C3HO+ | 11.38 ± 0.15 | H | EI | Opitz, 1991 | LL |
References
Go To: Top, Phase change data, Gas phase ion energetics data, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]
Opitz, 1991
Opitz, J.,
Photoionization of propynal in the gas phase,
Int. J. Mass Spectrom. Ion Processes, 1991, 107, 503. [all data]
Von Niessen, Bieri, et al., 1980
Von Niessen, W.; Bieri, G.; Asbrink, L.,
30.4 nm He(II) photoelectron spectra of organic molecules. Part III. Oxo-compounds (C,H,O),
J. Electron Spectrosc. Relat. Phenom., 1980, 21, 175. [all data]
Carlier and Mouvier, 1979
Carlier, P.; Mouvier, G.,
Etude par spectrometrie de photoelectrons de la structure electronique des ynals et des ynones conjugues,
J. Electron Spectrosc. Relat. Phenom., 1979, 17, 169. [all data]
Notes
Go To: Top, Phase change data, Gas phase ion energetics data, References
- Symbols used in this document:
AE Appearance energy Tboil Boiling point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
- The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
- Customer support for NIST Standard Reference Data products.