N,N-Diisopropylethylenediamine

Standard for GC,99.0%

Reagent Code: #216870
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Alias N,N-diisopropylethylenediamine
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CAS Number 121-05-1

science Other reagents with same CAS 121-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.26 g/mol
Formula C₈H₂₀N₂
badge Registry Numbers
EC Number 204-447-4
MDL Number MFCD00015015
thermostat Physical Properties
Boiling Point 169-171 °C(lit.)
inventory_2 Storage & Handling
Density 0.798 g/mL at 25 °C(lit.)
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its ability to act as a ligand or building block in asymmetric synthesis. Its primary and tertiary amine groups enable coordination with metal catalysts, making it valuable in catalytic reactions such as enantioselective hydrogenation. Also employed in the preparation of surfactants and corrosion inhibitors, where its branched alkyl structure enhances solubility and surface activity. In research, it serves as a versatile scaffold for developing novel bioactive molecules and functional materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5ml
10-20 days ฿1,880.00
N,N-Diisopropylethylenediamine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its ability to act as a ligand or building block in asymmetric synthesis. Its primary and tertiary amine groups enable coordination with metal catalysts, making it valuable in catalytic reactions such as enantioselective hydrogenation. Also employed in the preparation of surfactants and corrosion inhibitors, where its branched alkyl structure enhances solubility and surface activity. In research, it serves as a versat

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to its ability to act as a ligand or building block in asymmetric synthesis. Its primary and tertiary amine groups enable coordination with metal catalysts, making it valuable in catalytic reactions such as enantioselective hydrogenation. Also employed in the preparation of surfactants and corrosion inhibitors, where its branched alkyl structure enhances solubility and surface activity. In research, it serves as a versatile scaffold for developing novel bioactive molecules and functional materials.

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