Introduction:Basic information about CAS 9024-43-5|(R)-Mandelonitrile lyase, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | (R)-Mandelonitrile lyase |
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| CAS Number | 9024-43-5 | Molecular Weight | / |
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| Density | / | Boiling Point | / |
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| Molecular Formula | / | Melting Point | / |
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| MSDS | USA | Flash Point | / |
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Names
| Name | EC 4.1.1.1 |
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| Synonym | More Synonyms |
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(R)-Mandelonitrile lyase BiologicalActivity
| 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. |
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| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
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Chemical & Physical Properties
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US) |
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| Hazard Codes | Xn |
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| Risk Phrases | 42-42/43 |
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| Safety Phrases | 23-45-36/37-22 |
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| RIDADR | NONH for all modes of transport |
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| WGK Germany | 3 |
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Articles34
More Articles
| 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... | |
Synonyms