2,4,6-Trimethoxybenzylamine hydrochloride

≥98%

Reagent Code: #242343
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CAS Number 146548-59-6

science Other reagents with same CAS 146548-59-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.7 g/mol
Formula C₁₀H₁₆ClNO₃
badge Registry Numbers
MDL Number MFCD00012855
thermostat Physical Properties
Melting Point 204-207 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, inert gas, sealed

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. Its structure allows for selective functionalization in multi-step organic reactions, particularly in the development of central nervous system agents and psychoactive substance analogs. Commonly employed in the preparation of amphetamine and cathinone derivatives for research purposes, especially in structure-activity relationship (SAR) studies. Also utilized in the formation of protected amine derivatives due to the stability of its benzylamine core, facilitating peptide coupling and heterocycle formation. Its hydrochloride salt form enhances solubility and handling in aqueous and polar organic solvents, making it suitable for lab-scale synthesis and purification processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,750.00
inventory 250mg
10-20 days ฿3,630.00

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2,4,6-Trimethoxybenzylamine hydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. Its structure allows for selective functionalization in multi-step organic reactions, particularly in the development of central nervous system agents and psychoactive substance analogs. Commonly employed in the preparation of amphetamine and cathinone derivatives for research purposes, especially in structure-activity relationship (SAR) studies. Also utilized in the formation of protected amine derivatives due t

Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. Its structure allows for selective functionalization in multi-step organic reactions, particularly in the development of central nervous system agents and psychoactive substance analogs. Commonly employed in the preparation of amphetamine and cathinone derivatives for research purposes, especially in structure-activity relationship (SAR) studies. Also utilized in the formation of protected amine derivatives due to the stability of its benzylamine core, facilitating peptide coupling and heterocycle formation. Its hydrochloride salt form enhances solubility and handling in aqueous and polar organic solvents, making it suitable for lab-scale synthesis and purification processes.

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