2,4,6-TRIS[BIS(METHOXYMETHYL)AMINO]-1,3,5-TRIAZINE

average Mn~432, 84 wt.% in 1-butanol

Reagent Code: #242367
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CAS Number 68002-20-0

science Other reagents with same CAS 68002-20-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 390.44 g/mol
Formula C₁₅H₃₀N₆O₆
badge Registry Numbers
MDL Number MFCD00197912
thermostat Physical Properties
Boiling Point 118 °C
inventory_2 Storage & Handling
Density 1.2 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a curing agent in epoxy resin systems, particularly in coatings, adhesives, and electrical encapsulation. Offers low-temperature curing with extended pot life due to its latent reactivity. Provides excellent thermal and chemical resistance in the final product. Commonly applied in automotive, electronics, and industrial maintenance industries where durable, high-performance polymer networks are required. Its methoxymethyl groups enable controlled release of active amine during heating, ensuring uniform crosslinking.

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Size Availability Unit Price Quantity
inventory 250 ml
10-20 days ฿5,650.00

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2,4,6-TRIS[BIS(METHOXYMETHYL)AMINO]-1,3,5-TRIAZINE
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Used as a curing agent in epoxy resin systems, particularly in coatings, adhesives, and electrical encapsulation. Offers low-temperature curing with extended pot life due to its latent reactivity. Provides excellent thermal and chemical resistance in the final product. Commonly applied in automotive, electronics, and industrial maintenance industries where durable, high-performance polymer networks are required. Its methoxymethyl groups enable controlled release of active amine during heating, ensuring u

Used as a curing agent in epoxy resin systems, particularly in coatings, adhesives, and electrical encapsulation. Offers low-temperature curing with extended pot life due to its latent reactivity. Provides excellent thermal and chemical resistance in the final product. Commonly applied in automotive, electronics, and industrial maintenance industries where durable, high-performance polymer networks are required. Its methoxymethyl groups enable controlled release of active amine during heating, ensuring uniform crosslinking.

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