N,N-Diisopropylethylamine solution

~2 M in 1-methyl-2-pyrrolidinone

Reagent Code: #215245
label
Alias N,N-diisopropylethylamine;N-ethyldiisopropylamine,N,N'-diisopropylethylamine
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CAS Number 7087-68-5

science Other reagents with same CAS 7087-68-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.24 g/mol
Formula C₈H₁₉N
badge Registry Numbers
EC Number 230-392-0
MDL Number MFCD00008868
inventory_2 Storage & Handling
Storage Room temperature, avoid light

description Product Description

Widely used as a non-nucleophilic base in organic synthesis, particularly in the formation of sensitive intermediates where strong but sterically hindered bases are required. Commonly employed in peptide coupling reactions to neutralize acids and promote amide bond formation without causing racemization. Also utilized in the preparation of pharmaceuticals, agrochemicals, and fine chemicals where controlled basic conditions are essential. Its low nucleophilicity minimizes unwanted side reactions, making it ideal for deprotonation steps in multi-step syntheses. Frequently chosen in industrial processes due to its effectiveness in aprotic solvents and compatibility with a wide range of functional groups.

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Size Availability Unit Price Quantity
inventory 50ml
10-20 days ฿3,650.00

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N,N-Diisopropylethylamine solution
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Widely used as a non-nucleophilic base in organic synthesis, particularly in the formation of sensitive intermediates where strong but sterically hindered bases are required. Commonly employed in peptide coupling reactions to neutralize acids and promote amide bond formation without causing racemization. Also utilized in the preparation of pharmaceuticals, agrochemicals, and fine chemicals where controlled basic conditions are essential. Its low nucleophilicity minimizes unwanted side reactions, making i

Widely used as a non-nucleophilic base in organic synthesis, particularly in the formation of sensitive intermediates where strong but sterically hindered bases are required. Commonly employed in peptide coupling reactions to neutralize acids and promote amide bond formation without causing racemization. Also utilized in the preparation of pharmaceuticals, agrochemicals, and fine chemicals where controlled basic conditions are essential. Its low nucleophilicity minimizes unwanted side reactions, making it ideal for deprotonation steps in multi-step syntheses. Frequently chosen in industrial processes due to its effectiveness in aprotic solvents and compatibility with a wide range of functional groups.

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