534641
Amano Lipase PS, from Burkholderia cepacia
≥23,000 U/g, pH 7.0, 50 °C (Optimum pH and temperature)
Sinonimo/i:
APS-BCL, Pseudomonas cepacia (APS-PCL)
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About This Item
Prodotti consigliati
Livello qualitativo
Attività specifica
≥23,000 U/g, pH 7.0, 50 °C (Optimum pH and temperature)
Applicazioni
Amano Lipase PS is generally used in the enantioselective transesterification and hydrolysis. Applications include:
- Lipase catalyzed transesterification of prochiral pyrimidine acyclonucleoside.
- Lipase catalyzed hydrolysis of diacetylated pyrimidine acyclonucleosides.
- Enantiomer selective acylation of racemic alcohols in continuous-flow bioreactors.
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Resp. Sens. 1
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 1
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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I clienti hanno visto anche
Enantiomer selective acylation of racemic alcohols by lipases in continuous-flow bioreactors.
Tetrahedron Asymmetry, 19(2), 237-246 (2008)
Reverse Stereoselectivity in the Lipase-Catalyzed Hydrolysis of Diacetylated Pyrimidine Acyclonucleosides.
ChemCatChem, 8(23), 3644-3649 (2016)
Lipase-catalyzed enantioselective transesterification of prochiral 1-((1, 3-dihydroxypropan-2-yloxy) methyl)-5, 6, 7, 8-tetrahydroquinazoline-2, 4 (1H, 3H)-dione in ionic liquids.
Chirality, 30(2), 206-214 (2018)
Immobilization of lipase from Burkholderia cepacia into calcium carbonate microcapsule and its use for enzymatic reactions in organic and aqueous media.
Journal of Molecular Catalysis. B, Enzymatic, 109, 94-100 (2014)
Chemistry (Weinheim an der Bergstrasse, Germany), 25(43), 10156-10164 (2019-05-29)
A new protocol based on lipase-catalyzed tandem reaction toward α,β-enones/enoesters is presented. For the synthesis of the desired products the tandem process based on enzyme-catalyzed hydrolysis and Knoevenagel reaction starting from enol acetates and aldehyde is developed. The relevant impact
Articoli
SHVO’S CATALYST: EFFICIENT EPIMERIZATION CATALYST FOR ENZYME MEDIATED DYNAMIC KINETIC RESOLUTION (DKR).
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