Butanal (BioCAD00000007700)
feces blood skeletal muscle plant natural products microbial natural products
Metabolite Card
Formula: C4H8O (72.0575)
SMILES: CCCC=O
Synonyms [en]
butanal; butyraldehyde; butan-1-al; n-butyraldehyde; 1-butanal; Butal
Last reviewed on 2024-06-28.
Cite this Page
Butanal. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China.
https://biocad_registry.innovation.ac.cn/s/(-)-arctiin
(retrieved
2026-01-03) (CAD Registry RN: BioCAD00000007700). Licensed
under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).
Note
Butanal, also known as butyral or butyl aldehyde, belongs to the class of organic compounds known as alpha-hydrogen aldehydes. These are aldehydes with the general formula HC(H)(R)C(=O)H, where R is an organyl group. It is miscible with most organic solvents. Butanal exists in all living organisms, ranging from bacteria to humans. Upon prolonged exposure to air, butyraldehyde oxidizes to form butyric acid. Butanal is an apple, bready, and chocolate tasting compound. Outside of the human body, Butanal is found, on average, in the highest concentration within cow milk and carrots. Butanal has also been detected, but not quantified in several different foods, such as hard wheats, borages, ostrich ferns, skunk currants, and fennels. This could make butanal a potential biomarker for the consumption of these foods. The dominant technology involves the use of rhodium catalysts derived from the water-soluble ligand Tppts. Butyraldehyde is produced almost exclusively by the hydroformylation of propylene:CH3CHCH2 + H2 + CO → CH3CH2CH2CHO. Traditionally, hydroformylation was catalyzed by cobalt carbonyl and later rhodium complexes of triphenylphosphine. At one time, it was produced industrially by the catalytic hydrogenation of crotonaldehyde, which is derived from acetaldehyde. Butyraldehyde can be produced by the catalytic dehydrogenation of n-butanol. This compound is the aldehyde derivative of butane. An aqueous solution of the rhodium catalyst converts the propylene to the aldehyde, which forms a lighter immiscible phase. About 6 billion kilograms are produced annually by hydroformylation. It is a colourless flammable liquid with an unpleasant smell.
DBLinks
- CAS Registry Number: 123-72-8
- PubChem CID: 261
- ChEBI: 15743
- HMDB: HMDB0003543
- LipidMaps:
- KEGG: C01412
- BioCyc: BUTANAL
- NCBI MeSH: butyraldehyde
- Wikipedia: Butanal
Other DBLinks
- CAS Registry Number: 123-72-8
- CAS Registry Number: 27789-14-6
- PubChem: 261
- ChEBI: ChEBI:15743
- HMDB: HMDB0003543
- HMDB: HMDB03543
- KEGG: C01412
- BioCyc: BUTANAL
- NCBI MeSH: butyraldehyde
- Wikipedia: Butanal
- Wikipedia: Butyraldehyde
- RefMet: RM0006386
- MoNA: EMBL-MCF_spec196855
- MoNA: EMBL-MCF_spec196860
- MoNA: FiehnLib000094
- MoNA: FiehnLib000095
- MoNA: FiehnLib000096
- MoNA: HMDB0003543_c_ms_99817
- MoNA: HMDB0003543_c_ms_99818
- MoNA: HMDB0003543_c_ms_99819
- MoNA: HMDB0003543_c_ms_99820
- MoNA: HMDB0003543_c_ms_99821
- MoNA: HMDB0003543_ms_ms_2322
- MoNA: HMDB0003543_ms_ms_2323
- MoNA: HMDB0003543_ms_ms_2324
- MoNA: JP001477
- MoNA: JP009320
- MoNA: MoNA002187
- MoNA: MoNA002188
- MoNA: MoNA002189
- Metlin: METLIN_6947
- Coconut NaturalProduct: CNP0518034.0
Class / Ontology
- WishartLab ClassyFire: [Carbonyl compounds] Carbonyl compounds
- RefMet: [Aldehydes] Aldehydes
- ChEBI: [CHEBI:15743] butanal
- Coconut NaturalProduct: [Fatty aldehydes] Fatty aldehydes
| ID | EC Number | Name |
|---|---|---|
| KEGG:R01172 | 1.2.1.10 | butanal:NAD+ oxidoreductase (CoA-acylating) |
| KEGG:R01173 | 1.2.1.57 | butanal:NADP+ oxidoreductase (CoA-acylating) |
| KEGG:R03544 | 1.1.1.- | C01412 + C00004 + C00080<=>C06142 + C00003 |
| KEGG:R03545 | 1.1.1.- | C01412 + C00005 + C00080<=>C06142 + C00006 |
| KEGG:R11343 | 1.1.2.9 | butan-1-ol:ferricytochrome c oxidoreductase |
| KEGG:R11344 | 1.1.5.11 | butan-1-ol:quinone oxidoreductase |
| BioCyc:RXN0-6973 | 1.14.14.5 | CPD-3744 + OXYGEN-MOLECULE + FMNH2 --> BUTANAL + SO3 + WATER + FMN + 2 PROTON |
| BioCyc:RXN-9562 | CPD-10204 + BUTANAL --> CPD-10208 + WATER | |
| Rhea:RHEA:22969 | 1.2.1.57 | butanal + NAD+ + CoA => butanoyl-CoA + NADH + H+ |
| Rhea:RHEA:22970 | 1.2.1.57 | butanoyl-CoA + NADH + H+ => butanal + NAD+ + CoA |
| Rhea:RHEA:22971 | 1.2.1.57 | butanal + NAD+ + CoA <=> butanoyl-CoA + NADH + H+ |
| Rhea:RHEA:22973 | 1.2.1.57 | butanal + NADP+ + CoA => butanoyl-CoA + NADPH + H+ |
| Rhea:RHEA:22974 | 1.2.1.57 | butanoyl-CoA + NADPH + H+ => butanal + NADP+ + CoA |
| Rhea:RHEA:22975 | 1.2.1.57 | butanal + NADP+ + CoA <=> butanoyl-CoA + NADPH + H+ |
| Rhea:RHEA:29736 | butane-1-sulfonate + FMNH2 + O2 => butanal + FMN + sulfite + H2O + 2 H+ | |
| Rhea:RHEA:29737 | butanal + FMN + sulfite + H2O + 2 H+ => butane-1-sulfonate + FMNH2 + O2 | |
| Rhea:RHEA:29738 | butane-1-sulfonate + FMNH2 + O2 <=> butanal + FMN + sulfite + H2O + 2 H+ | |
| Rhea:RHEA:33200 | butan-1-ol + NAD+ => butanal + NADH + H+ | |
| Rhea:RHEA:33201 | butanal + NADH + H+ => butan-1-ol + NAD+ | |
| Rhea:RHEA:33202 | butan-1-ol + NAD+ <=> butanal + NADH + H+ |
Taxonomy Source
- Aloe africana [ncbi taxid: 1080010]
- Aloe ferox [ncbi taxid: 117798]
- Aloe spicata [ncbi taxid: 992642]
- Aloe vera [ncbi taxid: 34199]
- Angelica acutiloba [ncbi taxid: 55605]
- Angelica gigas [ncbi taxid: 85712]
- Angelica sinensis [ncbi taxid: 165353]
- Artemisia scoparia [ncbi taxid: 72351]
- Butea monosperma [ncbi taxid: 56060]
- Cnidium officinale [ncbi taxid: ]
- Daucus carota [ncbi taxid: 4039]
- Escherichia coli [ncbi taxid: 562]
- Eucalyptus botryoides [ncbi taxid: 33130]
- Homo sapiens [ncbi taxid: 9606]
- Ligusticum chuanxiong [ncbi taxid: 2689076]
- Ligusticum sinense [ncbi taxid: ]
- Mus musculus [ncbi taxid: 10090]
- Radix chuanxiong [ncbi taxid: ]
- Rhizoma chuanxiong [ncbi taxid: ]
- Zingiber officinale [ncbi taxid: 94328]
Pathway Synthetic
| pathway id | name |
|---|---|
| BioCyc:META_PWY-6883 | pyruvate fermentation to butanol II (engineered) |
| BioCyc:META_PWY-6886 | 1-butanol autotrophic biosynthesis (engineered) |
| BioCyc:META_PWY-7780 | butane degradation |
| BioCyc:ARA_PWY-6786 | detoxification of reactive carbonyls in chloroplasts |
| BioCyc:ECOO157_PWY-7003 | glycerol degradation to butanol |
| BioCyc:10403S_RAST_PWY-7003 | glycerol degradation to butanol |
| BioCyc:META_PWY-6604 | superpathway of Clostridium acetobutylicum acidogenic and solventogenic fermentation |
| BioCyc:META_PWY-6594 | superpathway of Clostridium acetobutylicum solventogenic fermentation |
| BioCyc:META_PWY-6786 | detoxification of reactive carbonyls in chloroplasts |
| BioCyc:META_PWY-7396 | butanol and isobutanol biosynthesis (engineered) |
| BioCyc:META_PWY-7003 | glycerol degradation to butanol |
| BioCyc:META_PWY-6583 | pyruvate fermentation to butanol I |
| BioCyc:META_PWY-723 | alkylnitronates degradation |
| BioCyc:CLOSSAC_PWY-7003 | glycerol degradation to butanol |
| PlantCyc:ARA_PWY-6786 | detoxification of reactive carbonyls in chloroplasts |
| PlantCyc:WHEATA_PWY-6786 | detoxification of reactive carbonyls in chloroplasts |
| PlantCyc:WHEATD_PWY-2501 | fatty acid α-oxidation I (plants) |
| PlantCyc:WHEATD_PWY-6786 | detoxification of reactive carbonyls in chloroplasts |
| PlantCyc:BOLERACEA_CAPITATA_PWY-2501 | fatty acid α-oxidation I (plants) |
| PlantCyc:CACUMINATA_PWY-2501 | fatty acid α-oxidation I (plants) |