1,1',1''-(1,3,5-Triazinane-1,3,5-triyl)tris(2-bromoethan-1-one)

95%

Reagent Code: #129963
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CAS Number 92531-02-7

science Other reagents with same CAS 92531-02-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 449.92 g/mol
Formula C₉H₁₂Br₃N₃O₃
thermostat Physical Properties
Melting Point 191-192 °C(decomp)
Boiling Point 595.7±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.112±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a crosslinking agent in polymer chemistry, this compound enables the formation of stable covalent bonds between polymer chains, enhancing mechanical strength and thermal stability of materials. It is especially effective in modifying resins and functional coatings where high reactivity with nucleophiles such as amines and thiols is required. Its trifunctional structure allows for the creation of three-dimensional networks, making it valuable in the development of specialty adhesives, hydrogels, and functionalized surfaces. Due to the presence of reactive bromo-ketone groups, it also serves as a versatile intermediate in organic synthesis for introducing triazine-based frameworks into complex molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,730.00
inventory 250mg
10-20 days ฿18,230.00

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1,1',1''-(1,3,5-Triazinane-1,3,5-triyl)tris(2-bromoethan-1-one)
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Used primarily as a crosslinking agent in polymer chemistry, this compound enables the formation of stable covalent bonds between polymer chains, enhancing mechanical strength and thermal stability of materials. It is especially effective in modifying resins and functional coatings where high reactivity with nucleophiles such as amines and thiols is required. Its trifunctional structure allows for the creation of three-dimensional networks, making it valuable in the development of specialty adhesives, hy

Used primarily as a crosslinking agent in polymer chemistry, this compound enables the formation of stable covalent bonds between polymer chains, enhancing mechanical strength and thermal stability of materials. It is especially effective in modifying resins and functional coatings where high reactivity with nucleophiles such as amines and thiols is required. Its trifunctional structure allows for the creation of three-dimensional networks, making it valuable in the development of specialty adhesives, hydrogels, and functionalized surfaces. Due to the presence of reactive bromo-ketone groups, it also serves as a versatile intermediate in organic synthesis for introducing triazine-based frameworks into complex molecules.

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