2-Ethylbenzenethiol

95%

Reagent Code: #116042
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Alias 2-Ethylthiophenol
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CAS Number 4500-58-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 138.23 g/mol
Formula C₈H₁₀S
badge Registry Numbers
EC Number 224-811-6
MDL Number MFCD00010022
thermostat Physical Properties
Boiling Point 203-205 °C
inventory_2 Storage & Handling
Density 1.025 g/mL at 25 °C
Storage room temperature

description Product Description

Used primarily in the synthesis of organic compounds, 2-Ethylbenzenethiol serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its thiol group makes it valuable for creating sulfur-containing molecules, which are often essential in drug development. Additionally, it is utilized in the manufacture of flavors and fragrances due to its distinct sulfurous aroma. In industrial applications, it acts as a corrosion inhibitor and stabilizer in certain chemical processes. Its reactivity also makes it suitable for research purposes in organic chemistry, particularly in studies involving thiol-ene reactions.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 95-100
Refractive Index (N20/D) 1.568-1.572
Specific Gravity (20/20) 1.035-1.039
Appearance Colorless to Yellow Liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿693.00
inventory 25g
10-20 days ฿7,488.00
inventory 100g
10-20 days ฿23,382.00
inventory 5g
10-20 days ฿2,277.00
2-Ethylbenzenethiol
Used primarily in the synthesis of organic compounds, 2-Ethylbenzenethiol serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its thiol group makes it valuable for creating sulfur-containing molecules, which are often essential in drug development. Additionally, it is utilized in the manufacture of flavors and fragrances due to its distinct sulfurous aroma. In industrial applications, it acts as a corrosion inhibitor and stabilizer in certain chemical processes. Its reactivity also makes it suitable for research purposes in organic chemistry, particularly in studies involving thiol-ene reactions.
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