1-(2-Hydroxyethyl)-4-(3-hydroxypropyl)piperidine

≥98%(GC)(T)

Reagent Code: #195116
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CAS Number 19780-85-9

science Other reagents with same CAS 19780-85-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.28 g/mol
Formula C₁₀H₂₁NO₂
badge Registry Numbers
MDL Number MFCD00047481
thermostat Physical Properties
Melting Point 49°C
inventory_2 Storage & Handling
Storage Room temperature, dryness, inert gas storage

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with central nervous system activity. Its structure supports the creation of compounds with potential antipsychotic, antidepressant, or analgesic effects. Also employed in the preparation of functionalized piperidine derivatives for research in medicinal chemistry. The presence of two hydroxyl groups allows for further chemical modifications, making it valuable in designing drug candidates with improved solubility and binding properties.

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inventory 5g
10-20 days ฿1,160.00

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1-(2-Hydroxyethyl)-4-(3-hydroxypropyl)piperidine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with central nervous system activity. Its structure supports the creation of compounds with potential antipsychotic, antidepressant, or analgesic effects. Also employed in the preparation of functionalized piperidine derivatives for research in medicinal chemistry. The presence of two hydroxyl groups allows for further chemical modifications, making it valuable in designing drug candidates

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with central nervous system activity. Its structure supports the creation of compounds with potential antipsychotic, antidepressant, or analgesic effects. Also employed in the preparation of functionalized piperidine derivatives for research in medicinal chemistry. The presence of two hydroxyl groups allows for further chemical modifications, making it valuable in designing drug candidates with improved solubility and binding properties.

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