2-Propenamide
- Formula: C3H5NO
- Molecular weight: 71.0779
- IUPAC Standard InChIKey: HRPVXLWXLXDGHG-UHFFFAOYSA-N
- CAS Registry Number: 79-06-1
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Acrylamide; Ethylenecarboxamide; Propenamide; CH2CHCONH2; Acrylic amide; Akrylamid; Amid kyseliny akrylove; Rcra waste number U007; UN 2074; Vinyl amide; 2-Propeneamide; Propenoic acid, amide; NSC 7785
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Phase change data
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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:
BS - Robert L. Brown and Stephen E. Stein
AC - William E. Acree, Jr., James S. Chickos
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing
Reduced pressure boiling point
Tboil (K) | Pressure (bar) | Reference | Comment |
---|---|---|---|
398.2 | 0.033 | Weast and Grasselli, 1989 | BS |
Enthalpy of vaporization
ΔvapH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
61.5 | 372. | A | Stephenson and Malanowski, 1987 | Based on data from 357. to 413. K.; AC |
76.5 | 388. | A | Stephenson and Malanowski, 1987 | Based on data from 373. to 413. K.; AC |
Enthalpy of sublimation
ΔsubH (kJ/mol) | Temperature (K) | Method | Reference | Comment |
---|---|---|---|---|
81.8 | 330. | N/A | Carpenter and Davis, 2007 | Based on data from 303. to 358. K.; AC |
81.81 | 330. | V | Steele, Chirico, et al., 1989 | Hfusion=15.33 kJ/mol at 358K; ALS |
Enthalpy of fusion
ΔfusH (kJ/mol) | Temperature (K) | Reference | Comment |
---|---|---|---|
15.330 | 358. | Steele, Chirico, et al., 1989 | DH |
15.33 | 358. | Domalski and Hearing, 1996 | AC |
References
Go To: Top, Phase change 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]
Stephenson and Malanowski, 1987
Stephenson, Richard M.; Malanowski, Stanislaw,
Handbook of the Thermodynamics of Organic Compounds, 1987, https://doi.org/10.1007/978-94-009-3173-2
. [all data]
Carpenter and Davis, 2007
Carpenter, E.L.; Davis, H.S.,
Acrylamide. Its preparation and properties,
J. Appl. Chem., 2007, 7, 12, 671-676, https://doi.org/10.1002/jctb.5010071206
. [all data]
Steele, Chirico, et al., 1989
Steele, W.V.; Chirico, R.D.; Nguyen, A.; Hossenlopp, I.A.; Smith, N.K.,
Determination of some pure compound ideal-gas enthalpies of formation,
AIChE Symp. Ser., 1989, 85, 140-162. [all data]
Domalski and Hearing, 1996
Domalski, Eugene S.; Hearing, Elizabeth D.,
Heat Capacities and Entropies of Organic Compounds in the Condensed Phase. Volume III,
J. Phys. Chem. Ref. Data, 1996, 25, 1, 1, https://doi.org/10.1063/1.555985
. [all data]
Notes
Go To: Top, Phase change data, References
- Symbols used in this document:
Tboil Boiling point ΔfusH Enthalpy of fusion ΔsubH Enthalpy of sublimation ΔvapH Enthalpy of vaporization - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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