3-(Propylamino)propane-1,2-diol

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Reagent Code: #227629
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CAS Number 70189-88-7

science Other reagents with same CAS 70189-88-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 133.19 g/mol
Formula C₆H₁₅NO₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its structure allows for chiral resolution, making it valuable in creating enantiomerically pure compounds. Also employed in the development of specialty chemicals and fine chemicals where amino diol functionality is required. Shows utility in research settings for building complex organic molecules due to its bifunctional nature, with both amine and hydroxyl groups available for chemical modification.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,610.00
inventory 250mg
10-20 days ฿6,040.00
inventory 1g
10-20 days ฿17,630.00

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3-(Propylamino)propane-1,2-diol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its structure allows for chiral resolution, making it valuable in creating enantiomerically pure compounds. Also employed in the development of specialty chemicals and fine chemicals where amino diol functionality is required. Shows utility in research settings for building complex organic molecules due to its bifunctional nature, with both amine and hydroxyl groups

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its structure allows for chiral resolution, making it valuable in creating enantiomerically pure compounds. Also employed in the development of specialty chemicals and fine chemicals where amino diol functionality is required. Shows utility in research settings for building complex organic molecules due to its bifunctional nature, with both amine and hydroxyl groups available for chemical modification.

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