Azido beheniko
| Azido beheniko | |
|---|---|
 | |
| Formula kimikoa | C22H44O2 |
| SMILES kanonikoa | 2D eredua |
| MolView | 3D eredua |
| Konposizioa | oxigeno, karbono eta hidrogeno |
| Base konjokatua | behenate (en)  |
| Mota | very long chain fatty acid (en) , gantz-azido ase eta straight chain fatty acids (en) |
| Ezaugarriak | |
| Fusio-puntua | 76 ℃ |
| Masa molekularra | 340,334 Da |
| Identifikatzaileak | |
| InChlKey | UKMSUNONTOPOIO-UHFFFAOYSA-N |
| CAS zenbakia | 112-85-6 |
| ChemSpider | 7923 |
| PubChem | 8215 |
| Reaxys | 1792887 |
| Gmelin | 28941 |
| ChEBI | 351197 |
| ChEMBL | CHEMBL1173474 |
| ZVG | 492792 |
| EC zenbakia | 204-010-8 |
| ECHA | 100.003.646 |
| CosIng | 74584 |
| RxNorm | 1368203 |
| Human Metabolome Database | HMDB0000944 |
| KNApSAcK | C00001211 |
| UNII | H390488X0A |
| KEGG | C08281 |
| PDB Ligand | EO3 |
Azido behenikoa edo azido dokosaonikoa konposatu organikoa da CH3(CH2)20COOH formula duena, azido karboxilikoen eta gantz-azidoen klasekoa. Solidoa da. Uretan eta ohiko disolbatzaile organikoetan disolbagaitza da[1].
Produktu naturala da. Besteak beste, Moringa oleifera zuhaixkaren olioaren, koltza-olioaren eta ugaztunen esnearen osagaia da.
Sintesia
Azido eruzikoaren erredukzio katalitikoz sintetizatzen da[2].
Erabilera
Azido kaprilikoa kosmetikan, argizarietan, plastifikatzaileetan, lubrifikatzaileetan eta egonkortzaileetan usatzen da[2].
Erreferentziak
- ↑ (Ingelesez) PubChem. «Docosanoic Acid» pubchem.ncbi.nlm.nih.gov (kontsulta data: 2026-06-29).
- ↑ a b O'Neil,, M.J. (ed). (2006). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals.. Merck and Co., Inc, 169 or..
| Autoritate kontrola |
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Datuak: Q422590
Multimedia: Behenic acid / Q422590
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Index:
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