3,4,5-Trimethoxytoluene

98%

Reagent Code: #239790
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Alias 3,4,5-Trimethoxytoluene
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CAS Number 6443-69-2

science Other reagents with same CAS 6443-69-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.22 g/mol
Formula C₁₀H₁₄O₃
badge Registry Numbers
EC Number 229-239-0
MDL Number MFCD00008397
thermostat Physical Properties
Melting Point 24-26 °C(lit.)
Boiling Point 117-118 °C5 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.082 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilator drugs like papaverine. It serves as a building block in organic reactions where methoxy-substituted aromatic systems are required. Commonly employed in the preparation of natural product analogs and bioactive molecules due to its electron-rich aromatic ring and stability. Also utilized in research settings for developing compounds with potential neurological or cardiovascular activity.

format_list_bulleted Product Specification

Test Parameter Specification
Freezing Point 34-39°C
Purity (GC) 98-100%
Water (Karl Fischer) 0-0.5%
Appearance Colorless to light yellow liquid or solid
Infrared Spectrum Conforms to Structure
Note This product is 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 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿420.00
inventory 500g
10-20 days ฿5,490.00
inventory 100g
10-20 days ฿1,460.00

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3,4,5-Trimethoxytoluene
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilator drugs like papaverine. It serves as a building block in organic reactions where methoxy-substituted aromatic systems are required. Commonly employed in the preparation of natural product analogs and bioactive molecules due to its electron-rich aromatic ring and stability. Also utilized in research settings for developing compounds with potential neurological or cardiovascular activity.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of vasodilator drugs like papaverine. It serves as a building block in organic reactions where methoxy-substituted aromatic systems are required. Commonly employed in the preparation of natural product analogs and bioactive molecules due to its electron-rich aromatic ring and stability. Also utilized in research settings for developing compounds with potential neurological or cardiovascular activity.

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