Propane-1,3-diyl dipropiolate

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Reagent Code: #227839
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CAS Number 85974-75-0

science Other reagents with same CAS 85974-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.16 g/mol
Formula C₉H₈O₄
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a crosslinking agent in polymer chemistry, enabling the formation of highly rigid and thermally stable networks. Its activated alkyne groups readily participate in click chemistry reactions, especially in thiol-yne and azide-yne couplings, making it valuable in material science for creating functional coatings, photoresists, and 3D-printed structures. Also employed in the synthesis of specialty monomers for high-performance resins and in biomedical applications where controlled, rapid curing is required. Its reactivity allows for efficient UV-initiated curing without the need for photoinitiators in some systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,060.00
inventory 250mg
10-20 days ฿6,880.00
inventory 1g
10-20 days ฿22,780.00

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Propane-1,3-diyl dipropiolate
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Used primarily as a crosslinking agent in polymer chemistry, enabling the formation of highly rigid and thermally stable networks. Its activated alkyne groups readily participate in click chemistry reactions, especially in thiol-yne and azide-yne couplings, making it valuable in material science for creating functional coatings, photoresists, and 3D-printed structures. Also employed in the synthesis of specialty monomers for high-performance resins and in biomedical applications where controlled, rapid c

Used primarily as a crosslinking agent in polymer chemistry, enabling the formation of highly rigid and thermally stable networks. Its activated alkyne groups readily participate in click chemistry reactions, especially in thiol-yne and azide-yne couplings, making it valuable in material science for creating functional coatings, photoresists, and 3D-printed structures. Also employed in the synthesis of specialty monomers for high-performance resins and in biomedical applications where controlled, rapid curing is required. Its reactivity allows for efficient UV-initiated curing without the need for photoinitiators in some systems.

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