4-(Hydroxymethyl)piperidin-4-ol

≥95%

Reagent Code: #195625
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CAS Number 89584-31-6

science Other reagents with same CAS 89584-31-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 131.17 g/mol
Formula C₆H₁₃NO₂
badge Registry Numbers
MDL Number MFCD13176333
thermostat Physical Properties
Boiling Point 263.0±15.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and analgesics. Its structure supports the creation of bioactive molecules due to the presence of two hydroxyl groups and a secondary amine, enabling hydrogen bonding and improved solubility. Commonly employed in the preparation of opioid receptor modulators and kinase inhibitors. Also utilized in medicinal chemistry for scaffold modification to enhance metabolic stability and target selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,090.00
inventory 100mg
10-20 days ฿3,060.00
inventory 250mg
10-20 days ฿7,330.00
inventory 1g
10-20 days ฿25,180.00

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4-(Hydroxymethyl)piperidin-4-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and analgesics. Its structure supports the creation of bioactive molecules due to the presence of two hydroxyl groups and a secondary amine, enabling hydrogen bonding and improved solubility. Commonly employed in the preparation of opioid receptor modulators and kinase inhibitors. Also utilized in medicinal chemistry for scaffold modification to enhance metabolic stabilit

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and analgesics. Its structure supports the creation of bioactive molecules due to the presence of two hydroxyl groups and a secondary amine, enabling hydrogen bonding and improved solubility. Commonly employed in the preparation of opioid receptor modulators and kinase inhibitors. Also utilized in medicinal chemistry for scaffold modification to enhance metabolic stability and target selectivity.

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