Ethyl 2-Hydroxyethyl Sulfide

≥98%

Reagent Code: #182992
label
Alias 2-(ethylthio)ethanol,
fingerprint
CAS Number 110-77-0

science Other reagents with same CAS 110-77-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 106.19 g/mol
Formula C₄H₁₀OS
badge Registry Numbers
MDL Number MFCD00002909
thermostat Physical Properties
Melting Point -100°C
Boiling Point 180-184°C
inventory_2 Storage & Handling
Density 1.02g/mL
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for sulfide-containing compounds due to its reactive thioether and hydroxyl functional groups. Commonly employed in the development of specialty chemicals, including surfactants and lubricant additives, where sulfur functionality enhances performance under extreme conditions. Also utilized in the preparation of certain polymer modifiers to improve flexibility and chemical resistance. Its bifunctional nature allows for cross-linking or chain extension in polymer chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿370.00
inventory 25mL
10-20 days ฿1,000.00
inventory 100ml
10-20 days ฿3,300.00
inventory 500ml
10-20 days ฿13,970.00
inventory 2.5L
10-20 days ฿62,000.00
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Ethyl 2-Hydroxyethyl Sulfide
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for sulfide-containing compounds due to its reactive thioether and hydroxyl functional groups. Commonly employed in the development of specialty chemicals, including surfactants and lubricant additives, where sulfur functionality enhances performance under extreme conditions. Also utilized in the preparation of certain polymer modifiers to improve flexibility an

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a building block for sulfide-containing compounds due to its reactive thioether and hydroxyl functional groups. Commonly employed in the development of specialty chemicals, including surfactants and lubricant additives, where sulfur functionality enhances performance under extreme conditions. Also utilized in the preparation of certain polymer modifiers to improve flexibility and chemical resistance. Its bifunctional nature allows for cross-linking or chain extension in polymer chemistry.

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