Sodium ethylate

96%

  • Product Code: 78394
  Alias:    Sodium Ethoxide; Sodium Ethoxide, Sodium Ethoxide, Sodium Ethoxide
  CAS:    141-52-6
Molecular Weight: 68.05 g./mol Molecular Formula: C₂H₅NaO
EC Number: 205-487-5 MDL Number: MFCD00012417
Melting Point: 260 °C Boiling Point: 91°C
Density: 0.868 g/mL at 25 °C Storage Condition: Room temperature, flammable area, dry, sealed
Product Description: Sodium ethylate is widely used as a strong base in organic synthesis, particularly in the production of esters, which are essential in the manufacture of flavors, fragrances, and pharmaceuticals. It is also employed as a catalyst in the transesterification process to produce biodiesel from vegetable oils or animal fats. In the pharmaceutical industry, it plays a crucial role in the synthesis of active pharmaceutical ingredients (APIs) and intermediates. Additionally, it is utilized in the production of dyes, pigments, and other specialty chemicals. Its strong alkalinity makes it effective in deprotonation reactions, facilitating the formation of carbon-carbon bonds in various organic compounds.
Product Specification:
Test Specification
Purity 95.5-104.5
NAOH NA2CO3 AS NAOH 2
TOTAL ALKALINITY AS NAOC2H5 98-100
APPEARANCE White to Yellow powder
INFRARED SPECTRUM Conforms to structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
100.000 10-20 days $22.60
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-
500.000 10-20 days $83.38
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-
2500.000 10-20 days $294.83
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-
10000.000 10-20 days $898.04
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Sodium ethylate
Sodium ethylate is widely used as a strong base in organic synthesis, particularly in the production of esters, which are essential in the manufacture of flavors, fragrances, and pharmaceuticals. It is also employed as a catalyst in the transesterification process to produce biodiesel from vegetable oils or animal fats. In the pharmaceutical industry, it plays a crucial role in the synthesis of active pharmaceutical ingredients (APIs) and intermediates. Additionally, it is utilized in the production of dyes, pigments, and other specialty chemicals. Its strong alkalinity makes it effective in deprotonation reactions, facilitating the formation of carbon-carbon bonds in various organic compounds.
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