Metil propionato
| Metil propionato | |
|---|---|
| Formula kimikoa | C4H8O2 |
| SMILES kanonikoa | 2D eredua |
| MolView | 3D eredua |
| Mota | biogenic acyclic ester (en) |
| Ezaugarriak | |
| Fusio-puntua | −88 ℃ −87,5 ℃ |
| Irakite-puntua | 79,8 ℃ (101,325 kPa) |
| Masa molekularra | 88,052 Da |
| Identifikatzaileak | |
| InChlKey | RJUFJBKOKNCXHH-UHFFFAOYSA-N |
| CAS zenbakia | 554-12-1 |
| ChemSpider | 10653 |
| PubChem | 11124 |
| Gmelin | 89873 |
| ChEMBL | CHEMBL3183973 |
| ZVG | 38040 |
| EC zenbakia | 209-060-4 |
| ECHA | 100.008.238 |
| CosIng | 40797 |
| RxNorm | 1435520 |
| Human Metabolome Database | HMDB0030062 |
| KNApSAcK | C00062190 |
| UNII | NB21C0D33W |
Metil propionatoa edo metil propanoatoa konposatu organikoa da CH3CH2COOCH3 formula duena, esterren familiakoa. Hain zuzen ere azido propionikoaren metil esterra da. Likido kolorgea da erronaren antzeko fruta-usaina duena.
Sintesia
Metil propionatoa presta daiteke azido propionikoa metanolez esterifikatzen. Industrian etilenoa, karbono monoxidoa eta metanola erreakzionaraziz katalizatzaile baten laguntzaz prestatzen da. Katalizatzailea normalean nikel eta paladio konplexu bat izaten da[1].
C2H4 + CO + MeOH → MeO2CCH2CH3
Erabilera
Metil metakrilatoa sintetizatzeko usa daiteke. Lehenik formaldehidoz erreakzionarazten da eta, segidan, deshidratatzen da.
- MeO2CCH2CH3 + CH2O → MeO2CCH(CH2OH)CH3
- MeO2CCH(CH2OH)CH3 → MeO2CC(=CH2)CH3
Metil propionatoa disolbatzaile gisa baliatzen da laka eta nitrozelulosen kasuan.
Fruta-usaina duenez aromatizatzaile gisa ere erabiltzen da[2].
Erreferentziak
- ↑ Kent, James Albert; Kent, James Albert. (2012). Handbook of Industrial Chemistry and Biotechnology. (12th ed. 2012. argitaraldia) Springer US Springer e-books Imprint: Springer ISBN 978-1-4614-4259-2. (kontsulta data: 2023-11-21).
- ↑ (Ingelesez) «methyl propionate, 554-12-1» www.thegoodscentscompany.com (kontsulta data: 2023-11-21).
Kanpo estekak
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