N,N-Diisopropylethylamine

Redistilled, 99.5%

Reagent Code: #126791
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
thermostat Physical Properties
Melting Point −50 °C(lit.)
Boiling Point 127 °C
inventory_2 Storage & Handling
Density 0.742 g/mL at 25 °C(lit.)
Storage room temperature, away from light

description 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.

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Test Parameter Specification
Refractive Index (20°C) 1.412-1.415
Assay (GC) 99.5-100
Specific Gravity (20/20°C) 0.754-0.758
Water (Karl Fischer) 0.05
Appearance Clear colourless to pale yellow liquid
Infrared Spectrometry Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500ml
10-20 days ฿5,120.00
inventory 100ml
10-20 days ฿1,390.00
inventory 2.5L
10-20 days ฿17,980.00
inventory 25ml
10-20 days ฿570.00

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N,N-Diisopropylethylamine
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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

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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