N-(3-Aminopropyl)-2-pipecoline

98%

Reagent Code: #216597
label
Alias 1-(3-aminopropyl)-2-methylpiperidine
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CAS Number 25560-00-3

science Other reagents with same CAS 25560-00-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 156.27 g/mol
Formula C₉H₂₀N₂
badge Registry Numbers
EC Number 247-102-3
MDL Number MFCD00006517
thermostat Physical Properties
Boiling Point 96-97 °C15 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.889 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a building block for pharmaceuticals and biologically active molecules. Its structure contains both primary amine and tertiary amine functionalities, making it valuable in the design of ligands for catalysis and in the development of novel drug candidates. It is also employed in the preparation of specialty polymers and surfactants due to its amphoteric nature and ability to form stable complexes with metal ions. Additionally, it finds use in research settings for modifying peptides and creating custom amino-functionalized compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿1,290.00
inventory 25ml
10-20 days ฿4,470.00
inventory 100ml
10-20 days ฿14,250.00

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N-(3-Aminopropyl)-2-pipecoline
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Used primarily in organic synthesis, this compound serves as a building block for pharmaceuticals and biologically active molecules. Its structure contains both primary amine and tertiary amine functionalities, making it valuable in the design of ligands for catalysis and in the development of novel drug candidates. It is also employed in the preparation of specialty polymers and surfactants due to its amphoteric nature and ability to form stable complexes with metal ions. Additionally, it finds use in r

Used primarily in organic synthesis, this compound serves as a building block for pharmaceuticals and biologically active molecules. Its structure contains both primary amine and tertiary amine functionalities, making it valuable in the design of ligands for catalysis and in the development of novel drug candidates. It is also employed in the preparation of specialty polymers and surfactants due to its amphoteric nature and ability to form stable complexes with metal ions. Additionally, it finds use in research settings for modifying peptides and creating custom amino-functionalized compounds.

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