(R)-Mandelonitrile lyase
Modify Date: 2024-01-11 21:22:52
(R)-Mandelonitrile lyase structure
|
Common Name | (R)-Mandelonitrile lyase | ||
|---|---|---|---|---|
| CAS Number | 9024-43-5 | Molecular Weight | N/A | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | N/A | Melting Point | N/A | |
| MSDS | USA | Flash Point | N/A | |
Use of (R)-Mandelonitrile lyase(R)-Mandelonitrile lyase (Mandelonitrile Lyase) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
| Name | EC 4.1.1.1 |
|---|---|
| Synonym | More Synonyms |
| Description | (R)-Mandelonitrile lyase (Mandelonitrile Lyase) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
|---|---|
| Related Catalog |
| Storage condition | 2-8°C |
|---|
| Personal Protective Equipment | Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US) |
|---|---|
| Hazard Codes | Xn |
| Risk Phrases | 42-42/43 |
| Safety Phrases | 23-45-36/37-22 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
|
Investigation of the microheterogeneity and aglycone specificity-conferring residues of black cherry prunasin hydrolases.
Plant Physiol. 129(3) , 1252-64, (2002) In black cherry (Prunus serotina Ehrh.) seed homogenates, (R)-amygdalin is degraded to HCN, benzaldehyde, and glucose by the sequential action of amygdalin hydrolase (AH), prunasin hydrolase (PH), and... |
|
|
Catalytic mechanism of hydroxynitrile lyase from Hevea brasiliensis: a theoretical investigation.
J. Phys. Chem. B 114(29) , 9622-8, (2010) Density functional theory (DFT) calculations using the hybrid functional B3LYP have been performed to investigate the catalytic mechanism of hydroxynitrile lyase from Hevea brasiliensis (Hb-HNL). This... |
|
|
(R)-oxynitrilase-catalysed synthesis of chiral silicon-containing aliphatic (R)-ketone-cyanohydrins.
Biotechnol. Lett. 25(3) , 219-22, (2003) Optically active 2-trimethylsilyl-2-hydroxyl-ethylcyanide was prepared by enzymatic enantioselective transcyanation of acetyltrimethylsilane with acetone cyanohydrin in a biphasic system at 35 degrees... |
| EINECS 232-780-5 |