2D Structure
3D Structure
Properties | |
---|---|
PID | PID00087 |
Mol. Weight | 58.08 g/mol |
LogP | 0.59 |
Water solubility | 306000 mg/L at 25 °C |
Hydrogen Bond Donor | 0 |
Hydrogen Bond Acceptor | 1 |
Rotatable Bonds | 1 |
XLogP3 | 0.6 |
Identifiers | |
---|---|
Formula | C3H6O |
PubChem CID | 527 |
FEMA | 2923 |
Flavor Profile | Floral, Pungent, Solvent; Suffocating, Fruity, Characteristic Odor Similar To Acetaldehyde, Pungent, Unpleasant, Choking Odor |
Smiles | CCC=O |
InChl Key | NBBJYMSMWIIQGU-UHFFFAOYSA-N |
InChl | InChI=1S/C3H6O/c1-2-3-4/h3H,2H2,1H3 |
CAS Registry Number | 123-38-6 |
IUPAC Systematic Name | propanal |
Organ Location Map/System Distribution of Pungent Flavor Compounds’ Targets
Note: Known Targets (Gene) from 6952 literatures, DrugBank (http://www.drugbank.ca/), STITCH (http://stitch.embl.de/), ChEMBL (https://www.ebi.ac.uk/chembl/), Therapeutic Target Database (http://bidd.nus.edu.sg/group/ttd/), and Comparative Toxicogenomics Database (CTD, http://ctdbase.org/)
English Name | Pinyin Name (Chinese Name) | Latin Name | Properties in TCM | merdians | View Graph |
---|---|---|---|---|---|
Fresh Common Ginger | Sheng Jiang (生姜) | Zingiber Rhizoma Recens | Warm, Pungent | Lung, Spleen, Stomach | View Graph |
Propionaldehyde is an organic compound,saturated 3-carbon aldehyde,a structural isomer of acetone,colorless liquid ,slightly irritating, fruity odor,
produced industrially through hydroformylation,etc.
It is principally used as a precursor to trimethylolethane (CH3C(CH2OH)3) through a condensation reaction with formaldehyde; this triol is an important
intermediate in the production of alkyd resins. Other applications include reduction to propanol and oxidation to propionic acid.It has the in vitro
inhibition of lipase activity.
Note: Click anywhere in the blank, you can drag the whole dynamic diagram. Click on a node, you can drag his location to see it more clearly. The blue circle represents pharmacology, toxicology, or daily use. Orange hexagon represents the pungent compounds.
1. Ai M, Min S, Grosjean Y,Leblanc, C., Bell, R., Benton, R., & Suh, G. S. Acid sensing by the Drosophila olfactory system[J]. Nature, 2010, 468(7324): 691.
2. Langevin F, Crossan G P, Rosado I V,Arends, M. J., & Patel, K. J. Fancd2 counteracts the toxic effects of naturally produced aldehydes in mice[J]. Nature, 2011, 475(7354): 53.
3. Landsberg J D, Sinnhuber R O. In vitro inhibition of lipase activity by malonaldehyde, formaldehyde and propionaldehyde[J]. Journal of the American Oil Chemists' Society, 1965, 42(10): 821-824.
4. Macpherson L J, Dubin A E, Evans M J,Marr, F., Schultz, P. G., Cravatt, B. F.,atapoutian, A. Noxious compounds activate TRPA1 ion channels through covalent modification of cysteines[J]. Nature, 2007, 445(7127): 541.
5. Denby K J, Iwig J, Bisson C, Westwood, J., Rolfe, M. D., Sedelnikova, S. E., Green, J. The mechanism of a formaldehyde-sensing transcriptional regulator[J]. Scientific reports, 2016, 6: 38879.
6. https://en.wikipedia.org/wiki/Propionaldehyde
7. Anthony J. Papa "Propanal" In Ullmann's Encyclopedia of Industrial Chemistry, 2011, WIley-VCH, Weinheim. doi:10.1002/14356007.a22_157.pub2
8. Dethlefsen J R, Lupp D, Teshome A, et al. Molybdenum-catalyzed conversion of diols and biomass-derived polyols to alkenes using isopropyl alcohol as reductant and solvent[J]. Acs Catalysis, 2015, 5(6): 3638-3647.
9. Goho A. Two newly found space molecules[J]. Science News, 2004, 166(4): 61-61.
10. Bibring J P, Taylor M, Alexander C, et al. Philae's first days on the comet[J]. 2015.