2-Aminooctane

≥98%(GC)(T)

Reagent Code: #136287
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CAS Number 693-16-3

science Other reagents with same CAS 693-16-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.25 g/mol
Formula C₈H₁₉N
badge Registry Numbers
MDL Number MFCD00008103
thermostat Physical Properties
Boiling Point 165°C(lit.)
inventory_2 Storage & Handling
Density 0.77
Storage Room temperature, dryness, inert gas storage

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its chiral amine functionality makes it valuable in the development of bioactive molecules. It can also serve as a building block in the preparation of specialty amines and catalysts for asymmetric reactions. Due to its lipophilic nature, it finds use in the design of compounds requiring membrane permeability, such as certain central nervous system agents. Additionally, it may be employed in research settings for structure-activity relationship studies involving amine-containing compounds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,250.00
inventory 5g
10-20 days ฿15,270.00
inventory 25g
10-20 days ฿24,070.00
inventory 100g
10-20 days ฿68,070.00

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2-Aminooctane
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Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its chiral amine functionality makes it valuable in the development of bioactive molecules. It can also serve as a building block in the preparation of specialty amines and catalysts for asymmetric reactions. Due to its lipophilic nature, it finds use in the design of compounds requiring membrane permeability, such as certain central nervous system agents. Additionally, it may be e

Used primarily as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its chiral amine functionality makes it valuable in the development of bioactive molecules. It can also serve as a building block in the preparation of specialty amines and catalysts for asymmetric reactions. Due to its lipophilic nature, it finds use in the design of compounds requiring membrane permeability, such as certain central nervous system agents. Additionally, it may be employed in research settings for structure-activity relationship studies involving amine-containing compounds.

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