4-Acetyl-3-methylpyridine
- Formula: C8H9NO
- Molecular weight: 135.1632
- IUPAC Standard InChI: InChI=1S/C8H9NO/c1-6-5-9-4-3-8(6)7(2)10/h3-5H,1-2H3
- IUPAC Standard InChIKey: MWTAIRKNMHLZBS-UHFFFAOYSA-N
- Chemical structure:
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Normal alkane RI, polar column, custom temperature program
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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
| Column type | Capillary | Capillary | Capillary | Capillary |
|---|---|---|---|---|
| Active phase | Carbowax | Carbowax | Carbowax | Carbowax |
| Column length (m) | ||||
| Carrier gas | ||||
| Substrate | ||||
| Column diameter (mm) | ||||
| Phase thickness (μm) | ||||
| Program | not specified | not specified | not specified | not specified |
| I | 1848. | 1848. | 1849. | 1849. |
| Reference | Baltes and Bochmann, 1987 | Baltes and Bochmann, 1987 | Baltes and Bochmann, 1987 | Baltes and Bochmann, 1987 |
| Comment | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI |
References
Go To: Top, Normal alkane RI, polar column, custom temperature program, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Baltes and Bochmann, 1987
Baltes, W.; Bochmann, G.,
Model reactions on roast aroma formations, V. Mass spectrometric identification of pyrifines, oxazoles, and carbocyclic compounds from the reaction of serine and threonine with sucrose under the conditions of coffee roasting,
Z. Lebensm. Unters. Forsch., 1987, 185, 1, 5-9, https://doi.org/10.1007/BF01083331
. [all data]
Notes
Go To: Top, Normal alkane RI, polar column, custom temperature program, References
- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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