1-(Thiophen-2-yl)ethanamine hydrochloride

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Reagent Code: #242871
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CAS Number 171268-81-8

science Other reagents with same CAS 171268-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.67 g/mol
Formula C₆H₁₀ClNS
badge Registry Numbers
MDL Number MFCD03306021
thermostat Physical Properties
Melting Point 140-142 °C
inventory_2 Storage & Handling
Storage Room temperature, light-proof storage, dry seal

description Product Description

Used primarily as a pharmaceutical intermediate in the synthesis of active drug substances, particularly in the development of central nervous system agents and antipsychotic medications. Its structure serves as a building block for compounds exhibiting dopamine or serotonin receptor activity. Also utilized in research settings for creating novel thiophene-based derivatives with potential biological activity. The hydrochloride salt form improves stability and solubility, making it suitable for use in polar reaction environments and purification processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,760.00
inventory 250mg
10-20 days ฿5,140.00
inventory 1g
10-20 days ฿10,280.00
inventory 5g
10-20 days ฿30,000.00

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1-(Thiophen-2-yl)ethanamine hydrochloride
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Used primarily as a pharmaceutical intermediate in the synthesis of active drug substances, particularly in the development of central nervous system agents and antipsychotic medications. Its structure serves as a building block for compounds exhibiting dopamine or serotonin receptor activity. Also utilized in research settings for creating novel thiophene-based derivatives with potential biological activity. The hydrochloride salt form improves stability and solubility, making it suitable for use in pol

Used primarily as a pharmaceutical intermediate in the synthesis of active drug substances, particularly in the development of central nervous system agents and antipsychotic medications. Its structure serves as a building block for compounds exhibiting dopamine or serotonin receptor activity. Also utilized in research settings for creating novel thiophene-based derivatives with potential biological activity. The hydrochloride salt form improves stability and solubility, making it suitable for use in polar reaction environments and purification processes.

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