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CHEBI:16125 - hexadecan-1-ol
| Formula | C16H34O |
| Net Charge | 0 |
| Average Mass | 242.447 |
| Monoisotopic Mass | 242.26097 |
| SMILES | CCCCCCCCCCCCCCCCO |
| InChI | InChI=1S/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H3 |
| InChIKey | BXWNKGSJHAJOGX-UHFFFAOYSA-N |
| Wikipedia |
|---|
| Species of Metabolite | Component | Source | Comments |
|---|---|---|---|
| Chlamydomonas reinhardtii (ncbitaxon:3055) | |||
| - | PubMed (25515814) | ||
| - | MetaboLights (MTBLS208) | ||
| Homo sapiens (ncbitaxon:9606) | faeces (UBERON:0001988) | PubMed (24029555) | |
| Lotus japonicus (ncbitaxon:34305) | |||
| - | MetaboLights (MTBLS43) | ||
| - | MetaboLights (MTBLS54) | ||
| - | MetaboLights (MTBLS44) | ||
| Mus musculus (ncbitaxon:10090) | - | MetaboLights (MTBLS345) |
| Roles Classification |
|---|
| Biological Roles: | flavouring agent A food additive that is used to added improve the taste or odour of a food. human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. algal metabolite Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae. |
| Application: | flavouring agent A food additive that is used to added improve the taste or odour of a food. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| hexadecan-1-ol (CHEBI:16125) has role algal metabolite (CHEBI:84735) |
| hexadecan-1-ol (CHEBI:16125) has role flavouring agent (CHEBI:35617) |
| hexadecan-1-ol (CHEBI:16125) has role human metabolite (CHEBI:77746) |
| hexadecan-1-ol (CHEBI:16125) has role plant metabolite (CHEBI:76924) |
| hexadecan-1-ol (CHEBI:16125) is a hexadecanol (CHEBI:197387) |
| hexadecan-1-ol (CHEBI:16125) is a long-chain primary fatty alcohol (CHEBI:77396) |
| Incoming Relation(s) |
| 1-O-hexadecyl-2-(5-hydroxyvaleroyl)-sn-glycero-3-phosphocholine (CHEBI:142765) has functional parent hexadecan-1-ol (CHEBI:16125) |
| 1-O-hexadecyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphocholine (CHEBI:142764) has functional parent hexadecan-1-ol (CHEBI:16125) |
| 1-palmityl-2-acetyl-sn-glycero-3-phosphate(2−) (CHEBI:78385) has functional parent hexadecan-1-ol (CHEBI:16125) |
| 14-methylhexadecan-1-ol (CHEBI:84920) has functional parent hexadecan-1-ol (CHEBI:16125) |
| hexadecyl benzoate (CHEBI:145972) has functional parent hexadecan-1-ol (CHEBI:16125) |
| hexadecyl elaidate (CHEBI:84072) has functional parent hexadecan-1-ol (CHEBI:16125) |
| palmityl acetate (CHEBI:146185) has functional parent hexadecan-1-ol (CHEBI:16125) |
| palmityl heptadecanoate (CHEBI:84079) has functional parent hexadecan-1-ol (CHEBI:16125) |
| palmityl laurate (CHEBI:84080) has functional parent hexadecan-1-ol (CHEBI:16125) |
| palmityl oleate (CHEBI:75622) has functional parent hexadecan-1-ol (CHEBI:16125) |
| palmityl palmitate (CHEBI:75584) has functional parent hexadecan-1-ol (CHEBI:16125) |
| palmityl palmitoleate (CHEBI:75629) has functional parent hexadecan-1-ol (CHEBI:16125) |
| palmityl stearate (CHEBI:75631) has functional parent hexadecan-1-ol (CHEBI:16125) |
| IUPAC Name |
|---|
| hexadecan-1-ol |
| Synonyms | Source |
|---|---|
| Hexadecanol | KEGG COMPOUND |
| 1-Hexadecanol | KEGG COMPOUND |
| Cetyl alcohol | KEGG COMPOUND |
| Palmityl alcohol | KEGG COMPOUND |
| 16-Hexadecanol | KEGG COMPOUND |
| n-hexadecyl alcohol | ChemIDplus |
| UniProt Name | Source |
|---|---|
| hexadecan-1-ol | UniProt |
| Manual Xrefs | Databases |
|---|---|
| C00823 | KEGG COMPOUND |
| PL3 | PDBeChem |
| LMFA05000061 | LIPID MAPS |
| Cetyl_Alcohol | Wikipedia |
| CPD-348 | MetaCyc |
| HMDB0003424 | HMDB |
| D00099 | KEGG DRUG |
| FDB003051 | FooDB |
| 4750 | DrugCentral |
| DB09494 | DrugBank |
| C00052572 | KNApSAcK |
| Registry Numbers | Sources |
|---|---|
| Reaxys:1748475 | Reaxys |
| CAS:36653-82-4 | KEGG COMPOUND |
| CAS:36653-82-4 | ChemIDplus |
| CAS:36653-82-4 | NIST Chemistry WebBook |
| Citations |
|---|