2-propenylpyrazine
- Formula: C7H8N2
- Molecular weight: 120.1518
- IUPAC Standard InChI: InChI=1S/C7H8N2/c1-2-3-7-6-8-4-5-9-7/h2,4-6H,1,3H2
- IUPAC Standard InChIKey: NQRKCUVPFJKKOJ-UHFFFAOYSA-N
- 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: 2-prop-2-enylpyrazine
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Gas Chromatography
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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 by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Van Den Dool and Kratz RI, polar column, temperature ramp
| Column type | Active phase | I | Reference | Comment |
|---|---|---|---|---|
| Capillary | CP-WAX 57CB | 1546. | Salter L.J., Mottram D.S., et al., 1988 | 60. C @ 5. min, 4. K/min; Column length: 50. m; Column diameter: 0.32 mm; Tend: 200. C |
Normal alkane RI, non-polar column, temperature ramp
| Column type | Active phase | I | Reference | Comment |
|---|---|---|---|---|
| Capillary | DB-1 | 1043. | Lambrecht and Kaulen, 1997 | 60. m/0.32 mm/0.25 μm, 4. K/min, 280. C @ 15. min; Tstart: 80. C |
References
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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Salter L.J., Mottram D.S., et al., 1988
Salter L.J.; Mottram D.S.; Whitfield,
Volatile compounds produces in Maillard reactions involving glycine, ribose and phospholid,
J. Sci. Food Agric., 1988, 46, 2, 227-242, https://doi.org/10.1002/jsfa.2740460211
. [all data]
Lambrecht and Kaulen, 1997
Lambrecht, S.; Kaulen, J.,
Synthesis of substituted ethenylpyrazines and dialkylpyridines and their sensory properties,
Flavour Fragr. J., 1997, 12, 439-442. [all data]
Notes
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- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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