N,N-Diisopropylethylamine

Redistilled, 99.5%

  • Product Code: 126791
  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: Used as a base in organic synthesis, particularly in peptide coupling reactions where it facilitates the formation of amide bonds. It is also employed in the production of pharmaceuticals, aiding in the synthesis of active pharmaceutical ingredients (APIs). Additionally, it serves as a catalyst in polymerization processes, helping to control the molecular weight and structure of polymers. Its steric hindrance makes it useful in selective alkylation reactions, ensuring precise chemical transformations. In some cases, it is utilized in the preparation of agrochemicals, contributing to the development of pesticides and herbicides. Its role in deprotonation reactions is valuable in various laboratory and industrial applications.
Product Specification:
Test Specification
Refractive Index (20 Degree Celsius) 1.412-1.415
Assay (GC) 99.5-100
Specific Gravity (20/20 Degree Celsius) 0.754-0.758
Water By Karl Fischer 0.05
Appearance Clear Colourless To Pale Yellow Liquid
Infrared Spectrometry Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
25.000 10-20 days ฿570.00
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100.000 10-20 days ฿1,390.00
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500.000 10-20 days ฿5,120.00
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-
2500.000 10-20 days ฿17,980.00
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N,N-Diisopropylethylamine
Used as a base in organic synthesis, particularly in peptide coupling reactions where it facilitates the formation of amide bonds. It is also employed in the production of pharmaceuticals, aiding in the synthesis of active pharmaceutical ingredients (APIs). Additionally, it serves as a catalyst in polymerization processes, helping to control the molecular weight and structure of polymers. Its steric hindrance makes it useful in selective alkylation reactions, ensuring precise chemical transformations. In some cases, it is utilized in the preparation of agrochemicals, contributing to the development of pesticides and herbicides. Its role in deprotonation reactions is valuable in various laboratory and industrial applications.
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