2D Structure
3D Structure
| Properties | |
|---|---|
| PID | PID00176 |
| Mol. Weight | 72.107 g/mol |
| LogP | 0.76 |
| Water solubility | In water, 71000 mg/L |
| Hydrogen Bond Donor | 0 |
| Hydrogen Bond Acceptor | 1 |
| Rotatable Bonds | 2 |
| XLogP3 | 0.9 |
| Identifiers | |
|---|---|
| Formula | C4H8O |
| PubChem CID | 261 |
| FEMA | 2219 |
| Flavor Profile | Characteristic, Pungent, Aldehyde Odor; Banana, Green |
| Smiles | CCCC=O |
| InChl Key | ZTQSAGDEMFDKMZ-UHFFFAOYSA-N |
| InChl | InChI=1S/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3 |
| CAS Registry Number | 123-72-8 |
| IUPAC Systematic Name | butanal |
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 |
|---|---|---|---|---|---|
| Chinese Angelica Equivalent plant: Phlojodicarpus | Dang Gui (当归) | Angelicae Sinensis Radix | Warm,Pungent,Sweet | Spleen,Liver,Heart | View Graph |
| Bush Redpepper | La Jiao (辣椒) | Capsici Fructus | Hot, Pungent | Lung, Spleen, Stomach, Heart, Kidney | View Graph |
| Cacumen Tamaricis | Xi He Liu(西河柳) | Chinese Tamarisk Twig | Mild,Pungent,Sweet | Lung,Stomach,Heart | View Graph |
| Virgate Wormwood Herb | Yin Chen(茵陈) | Artemisiae Scopariae Herba | Cold, Bitter, pungent | Bladder, Spleen, Liver，Stomach | View Graph |
Butyraldehyde is noble metal catalysts,Reductive amination with ammonia and hydrogen,The pathway of amination is different from that of liquid amination,reduction of butyraldehyde with hydrogen can complete decomposition occurre,an organic compound of low molecular weight,oxidiz in the electrochemical oxidation,destroy by nitric acid directly,distill on a column in an atmosphere of nitrogen,the aldehyde derivative of butane,a colourless flammable liquid with an acrid smell ,miscible with most organic solvents,produced almost exclusively by the hydroformylation of propylene,can be produced by the catalytic dehydrogenation of n-butano,can oxidize to form?butyric acid,etc.
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.Bdis J, Lefferts L, Mller T E, et al. Activity and selectivity control in reductive amination of butyraldehyde over noble metal catalysts[J]. Catalysis letters, 2005, 104(1-2): 23-28.
2.Popov M A, Shuikin N I. Catalytic reductive amination of butyraldehyde[J]. Russian Chemical Bulletin, 1962, 11(6): 1014-1017.
3.Uchiyama G, Fujine S. Destruction of butyraldehyde isomers using silver catalyzed electrochemical oxidation[J]. Journal of radioanalytical and nuclear chemistry, 1998, 230(1-2): 105-109.
4.Zhulin V M, Gonikberg M G, Zagorbinina V N. Investigation of the influence of pressure on the radical polymerization of styrene in solution Communication 1. Polymerization in benzene, butyraldehyde, and their mixtures[J]. Bulletin of the Academy of Sciences of the USSR, Division of chemical science, 1966, 15(5): 791-795.
MLA
5.Jiang B S, Chang R, Hou Y C, et al. Kinetics of n-Butanol Partial Oxidation to Butyraldehyde over LanthanumCTransition Metal Perovskites[J]. Industrial & Engineering Chemistry Research, 2012, 51(43): 13993-13998.