Ru-MACHO

≥95%

  • Product Code: 57521
  CAS:    1295649-40-9
Molecular Weight: 6073 g./mol Molecular Formula: C₂₉H₃₀ClNOP₂Ru
EC Number: MDL Number: MFCD22377801
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: Ru-MACHO is primarily used as a highly efficient catalyst in hydrogenation reactions, particularly for the reduction of esters to alcohols under mild conditions. Its application is significant in organic synthesis, where it enables the conversion of complex ester-containing molecules into valuable alcohols with high selectivity and yield. This makes it a crucial tool in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additionally, Ru-MACHO is employed in the development of sustainable chemical processes due to its ability to operate at lower temperatures and pressures, reducing energy consumption and environmental impact. Its versatility also extends to asymmetric hydrogenation, contributing to the synthesis of chiral compounds used in drug development and other industries.
Product Specification:
Test Specification
APPEARANCE White to Yellow powder or crystal
PURITY 94.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿5,330.00
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-
1.000 10-20 days ฿23,400.00
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-
Ru-MACHO
Ru-MACHO is primarily used as a highly efficient catalyst in hydrogenation reactions, particularly for the reduction of esters to alcohols under mild conditions. Its application is significant in organic synthesis, where it enables the conversion of complex ester-containing molecules into valuable alcohols with high selectivity and yield. This makes it a crucial tool in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additionally, Ru-MACHO is employed in the development of sustainable chemical processes due to its ability to operate at lower temperatures and pressures, reducing energy consumption and environmental impact. Its versatility also extends to asymmetric hydrogenation, contributing to the synthesis of chiral compounds used in drug development and other industries.
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