Dimethyl sulfate

98%

Reagent Code: #170053
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Alias Dimethyl sulfate
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CAS Number 77-78-1
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Properties liquid

science Other reagents with same CAS 77-78-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 126.13 g/mol
Formula C₂H₆O₄S
badge Registry Numbers
EC Number 201-058-1
MDL Number MFCD00008416
thermostat Physical Properties
Melting Point -32 °C
Boiling Point 76 °C/15 mmHg(lit.)
inventory_2 Storage & Handling
Density 1.333 g/mL
Storage Room temperature, dry, sealed

description Product Description

Dimethyl sulfate is primarily used as a methylating agent in organic synthesis. It transfers methyl groups to nucleophiles such as amines, phenols, and thiols, making it valuable in the production of pharmaceuticals, dyes, and agrochemicals. It is especially effective in the methylation of aromatic hydroxyl groups in phenolic compounds, which is a key step in synthesizing certain drugs and antioxidants. Due to its high reactivity, it is also employed in the preparation of quaternary ammonium compounds and in modifying natural products. However, because of its toxicity and carcinogenic nature, its use is often limited to controlled industrial settings with strict safety protocols.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿430.00
inventory 100g
10-20 days ฿740.00
inventory 500g
10-20 days ฿1,890.00
inventory 2.5kg
10-20 days ฿8,550.00
inventory 12X500g
10-20 days ฿22,500.00

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Dimethyl sulfate
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Dimethyl sulfate is primarily used as a methylating agent in organic synthesis. It transfers methyl groups to nucleophiles such as amines, phenols, and thiols, making it valuable in the production of pharmaceuticals, dyes, and agrochemicals. It is especially effective in the methylation of aromatic hydroxyl groups in phenolic compounds, which is a key step in synthesizing certain drugs and antioxidants. Due to its high reactivity, it is also employed in the preparation of quaternary ammonium compounds an

Dimethyl sulfate is primarily used as a methylating agent in organic synthesis. It transfers methyl groups to nucleophiles such as amines, phenols, and thiols, making it valuable in the production of pharmaceuticals, dyes, and agrochemicals. It is especially effective in the methylation of aromatic hydroxyl groups in phenolic compounds, which is a key step in synthesizing certain drugs and antioxidants. Due to its high reactivity, it is also employed in the preparation of quaternary ammonium compounds and in modifying natural products. However, because of its toxicity and carcinogenic nature, its use is often limited to controlled industrial settings with strict safety protocols.

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