N,N-Diisopropylethylamine

99%

  • Product Code: 126790
  Alias:    N,N-Diisopropylethylamine ; N-Ethyldiisopropylamine, N,N'-Diisopropylethylamine
  CAS:    7087-68-5
Molecular Weight: 129.24 g./mol Molecular Formula: C₈H₁₉N
EC Number: 230-392-0 MDL Number: MFCD00008868
Melting Point: −50 °C(lit.) Boiling Point: 127 °C
Density: 0.742 g/mL at 25 °C(lit.) Storage Condition: room temperature, away from light
Product Description:

Widely used as a base in organic synthesis, it facilitates reactions such as peptide coupling, where it helps in the formation of amide bonds. It is also employed in the production of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs), due to its ability to neutralize acids and stabilize intermediates. In polymer chemistry, it acts as a catalyst or neutralizing agent in the production of polyurethanes and other polymers. Additionally, it is utilized in the manufacture of agrochemicals, aiding in the synthesis of herbicides and pesticides. Its non-nucleophilic nature makes it suitable for reactions where strong, sterically hindered bases are required.

Product Specification:
Test Specification
Purity (GC) 99-100
Refractive Index N20/D 1.412-1.415
Water By Karl Fischer 0-1
Appearance Colorless Liquid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
25.000 10-20 days $12.46
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100.000 10-20 days $20.76
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250.000 10-20 days $37.38
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500.000 10-20 days $65.62
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5000.000 10-20 days $622.52
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N,N-Diisopropylethylamine

Widely used as a base in organic synthesis, it facilitates reactions such as peptide coupling, where it helps in the formation of amide bonds. It is also employed in the production of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs), due to its ability to neutralize acids and stabilize intermediates. In polymer chemistry, it acts as a catalyst or neutralizing agent in the production of polyurethanes and other polymers. Additionally, it is utilized in the manufacture of agrochemicals, aiding in the synthesis of herbicides and pesticides. Its non-nucleophilic nature makes it suitable for reactions where strong, sterically hindered bases are required.

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