Isopropylmagnesium chloride

2.0 M solution in THF, MkSeal

Reagent Code: #88884
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Alias Isopropyl magnesium chloride
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CAS Number 1068-55-9

science Other reagents with same CAS 1068-55-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 102.85 g/mol
Formula C₃H₇ClMg
badge Registry Numbers
MDL Number MFCD00000466
thermostat Physical Properties
Boiling Point 256 °C
inventory_2 Storage & Handling
Density 0.98 g/mL at 20 °C
Storage 2~8 ℃

description Product Description

Isopropylmagnesium chloride is widely used as a Grignard reagent in organic synthesis. It plays a crucial role in the formation of carbon-carbon bonds, making it essential for producing complex organic compounds. This reagent is particularly valuable in the pharmaceutical industry for synthesizing active pharmaceutical ingredients (APIs) and intermediates. It is also employed in the production of fine chemicals, agrochemicals, and specialty materials. Additionally, it is used in research laboratories for developing new organic molecules and studying reaction mechanisms. Its ability to react with a variety of electrophiles makes it versatile for creating alcohols, ketones, and other functionalized compounds.

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Test Parameter Specification
Appearance Yellow to dark brown or black liquid
Assay as Sec-Butanol (Titration) 2.0 M

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1L
10-20 days ฿7,980.00
inventory 100ml
10-20 days ฿1,860.00
inventory 500ml
10-20 days ฿5,280.00

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Isopropylmagnesium chloride
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Isopropylmagnesium chloride is widely used as a Grignard reagent in organic synthesis. It plays a crucial role in the formation of carbon-carbon bonds, making it essential for producing complex organic compounds. This reagent is particularly valuable in the pharmaceutical industry for synthesizing active pharmaceutical ingredients (APIs) and intermediates. It is also employed in the production of fine chemicals, agrochemicals, and specialty materials. Additionally, it is used in research laboratories for developing new organic molecules and studying reaction mechanisms. Its ability to react with a variety of electrophiles makes it versatile for creating alcohols, ketones, and other functionalized compounds.
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