4-Aminopentan-1-ol

95%

Reagent Code: #137444
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CAS Number 927-55-9

science Other reagents with same CAS 927-55-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 103.16 g/mol
Formula C₆H₁₃NO
badge Registry Numbers
MDL Number MFCD16251198
thermostat Physical Properties
Melting Point 32 °C (lit.)
Boiling Point 174.7 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows for functionalization in the development of bioactive molecules. Commonly employed in the preparation of heterocyclic compounds and as a building block in medicinal chemistry for designing novel drug candidates. Also finds use in the synthesis of specialty polymers and surfactants due to its amine and hydroxyl groups enabling crosslinking and solubility modifications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿18,340.00
inventory 5g
10-20 days ฿85,000.00

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4-Aminopentan-1-ol
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows for functionalization in the development of bioactive molecules. Commonly employed in the preparation of heterocyclic compounds and as a building block in medicinal chemistry for designing novel drug candidates. Also finds use in the synthesis of specialty polymers and surfactants due to its amine and hydroxyl groups enabling crosslinking and solubility modifications.

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows for functionalization in the development of bioactive molecules. Commonly employed in the preparation of heterocyclic compounds and as a building block in medicinal chemistry for designing novel drug candidates. Also finds use in the synthesis of specialty polymers and surfactants due to its amine and hydroxyl groups enabling crosslinking and solubility modifications.

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