3,4-Dimethoxyphenethylamine

97%

Reagent Code: #72090
label
Alias 3,4-Dimethoxyphenethylamine ; Hoveratramine
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CAS Number 120-20-7

science Other reagents with same CAS 120-20-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.23 g/mol
Formula C₁₀H₁₅NO₂
badge Registry Numbers
EC Number 204-376-9
MDL Number MFCD00008188
thermostat Physical Properties
Melting Point 12-15 °C
Boiling Point 188 °C15 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.074 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used in research settings to study its effects on the central nervous system, particularly in relation to neurotransmitter activity. It has been explored for its potential psychoactive properties, often in the context of understanding its interaction with serotonin receptors. Additionally, it serves as a precursor in the synthesis of more complex compounds for pharmacological studies. Its applications are primarily confined to laboratory environments, where it aids in the investigation of neurochemical processes and drug development.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 97-100
Refractive Index (n20D) 1.543-1.549
Specific Gravity (20°C) 1.087-1.104
Appearance Colorless to yellow to brown viscous liquid
Infrared Spectrometry Conforms to Structure
Note Low melting point solid; may change state in different environments (solid, liquid, or semi-solid)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿520.00
inventory 100g
10-20 days ฿1,590.00
inventory 500g
10-20 days ฿6,990.00

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3,4-Dimethoxyphenethylamine
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Used in research settings to study its effects on the central nervous system, particularly in relation to neurotransmitter activity. It has been explored for its potential psychoactive properties, often in the context of understanding its interaction with serotonin receptors. Additionally, it serves as a precursor in the synthesis of more complex compounds for pharmacological studies. Its applications are primarily confined to laboratory environments, where it aids in the investigation of neurochemical processes and drug development.
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