Trimellitic anhydride chloride
98%
- Product Code: 239774
Alias:
Trimellitic anhydride Chloride; 1,2,4-trimellitic anhydride acyl chloride
CAS:
1204-28-0
Molecular Weight: | 210.57 g./mol | Molecular Formula: | C₉H₃ClO₄ |
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EC Number: | 214-874-8 | MDL Number: | MFCD00005924 |
Melting Point: | 66-68 °C(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used primarily as a chemical intermediate in the synthesis of high-performance polymers and resins. It reacts with various alcohols and amines to form esters and amides, which are key building blocks in producing polyimides and polyurethanes. These materials are valued for their thermal stability and mechanical strength, making them suitable for aerospace, electronics, and insulation applications. Also employed in the manufacture of flame-retardant coatings and wire enamels due to its ability to enhance thermal and oxidative resistance. Its reactivity allows for cross-linking in coating formulations, improving durability and chemical resistance.
Product Specification:
Test | Specification |
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Melting point | 66-69 Degree Celsius |
Purity (GC) | 98%-100% |
APPEARANCE | WHITE TO LIGHT YELLOW POWDER |
INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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5.000 | 10-20 days | $15.58 |
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100.000 | 10-20 days | $96.10 |
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500.000 | 10-20 days | $341.82 |
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2500.000 | 10-20 days | $1,462.86 |
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25.000 | 10-20 days | $35.84 |
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Trimellitic anhydride chloride
Used primarily as a chemical intermediate in the synthesis of high-performance polymers and resins. It reacts with various alcohols and amines to form esters and amides, which are key building blocks in producing polyimides and polyurethanes. These materials are valued for their thermal stability and mechanical strength, making them suitable for aerospace, electronics, and insulation applications. Also employed in the manufacture of flame-retardant coatings and wire enamels due to its ability to enhance thermal and oxidative resistance. Its reactivity allows for cross-linking in coating formulations, improving durability and chemical resistance.
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