4-(4-Chlorophenoxy)butanoic acid

95%

Reagent Code: #161879
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CAS Number 3547-07-7

science Other reagents with same CAS 3547-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.65 g/mol
Formula C₁₀H₁₁ClO₃
badge Registry Numbers
MDL Number MFCD00040911
thermostat Physical Properties
Boiling Point 383.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a selective herbicide, particularly in aquatic environments and non-crop areas to control broadleaf weeds and brush. It is effective in managing invasive plant species in lakes, ponds, and irrigation channels due to its ability to disrupt plant growth hormones. Commonly applied in formulations for aquatic weed control where minimal impact on grasses and monocots is desired. Also utilized in some industrial settings for vegetation management along roadsides and in forestry. Its phenoxy structure allows it to mimic auxins, leading to uncontrolled growth and eventual death in susceptible plants.

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Test Parameter Specification
Appearance White to off-white solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿170.50
inventory 1g
10-20 days ฿253.00

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4-(4-Chlorophenoxy)butanoic acid
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Used as a selective herbicide, particularly in aquatic environments and non-crop areas to control broadleaf weeds and brush. It is effective in managing invasive plant species in lakes, ponds, and irrigation channels due to its ability to disrupt plant growth hormones. Commonly applied in formulations for aquatic weed control where minimal impact on grasses and monocots is desired. Also utilized in some industrial settings for vegetation management along roadsides and in forestry. Its phenoxy structure a

Used as a selective herbicide, particularly in aquatic environments and non-crop areas to control broadleaf weeds and brush. It is effective in managing invasive plant species in lakes, ponds, and irrigation channels due to its ability to disrupt plant growth hormones. Commonly applied in formulations for aquatic weed control where minimal impact on grasses and monocots is desired. Also utilized in some industrial settings for vegetation management along roadsides and in forestry. Its phenoxy structure allows it to mimic auxins, leading to uncontrolled growth and eventual death in susceptible plants.

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