TETRAETHYLENE GLYCOL DI-P-TOSYLATE

97%

Reagent Code: #240378
label
Alias Tetraethylene glycol diptoluenesulfonate; Tetraethylene glycol diptoluenesulfonate
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CAS Number 37860-51-8

science Other reagents with same CAS 37860-51-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 502.59 g/mol
Formula C₂₂H₃₀O₉S₂
badge Registry Numbers
MDL Number MFCD00075239
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a cross-linking agent in polymer synthesis, particularly in the production of specialty resins and polyurethanes. It functions as a bifunctional alkylating agent, enabling the introduction of tosyl groups to modify reactivity in organic intermediates. Commonly employed in pharmaceutical synthesis to build molecular frameworks where controlled spacer length and solubility are required. Also utilized in the preparation of crown ether analogs and as a derivatizing agent in analytical chemistry for enhancing detection of polar compounds. Its liquid form and stability make it suitable for solution-phase reactions in fine chemical manufacturing.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿520.00
inventory 25g
10-20 days ฿2,560.00
inventory 100g
10-20 days ฿6,430.00

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TETRAETHYLENE GLYCOL DI-P-TOSYLATE
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Used as a cross-linking agent in polymer synthesis, particularly in the production of specialty resins and polyurethanes. It functions as a bifunctional alkylating agent, enabling the introduction of tosyl groups to modify reactivity in organic intermediates. Commonly employed in pharmaceutical synthesis to build molecular frameworks where controlled spacer length and solubility are required. Also utilized in the preparation of crown ether analogs and as a derivatizing agent in analytical chemistry for e

Used as a cross-linking agent in polymer synthesis, particularly in the production of specialty resins and polyurethanes. It functions as a bifunctional alkylating agent, enabling the introduction of tosyl groups to modify reactivity in organic intermediates. Commonly employed in pharmaceutical synthesis to build molecular frameworks where controlled spacer length and solubility are required. Also utilized in the preparation of crown ether analogs and as a derivatizing agent in analytical chemistry for enhancing detection of polar compounds. Its liquid form and stability make it suitable for solution-phase reactions in fine chemical manufacturing.

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