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2,3,3,4-biphenyl tetracarboxylic dianhydride CAS#36978-41-3

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2,3,3,4-biphenyl tetracarboxylic dianhydride CAS#36978-41-3
2,3,3,4-Biphenyl tetracarboxylic dianhydride (a-BPDA) offers excellent heat, chemical and solvent resistance for high-performance polyimide applications.

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Product Description

Excellent Heat Resistance:a-BPDA maintains performance at high temperatures, making it suitable for demanding thermal applications.


Outstanding Chemical and Solvent Resistance:It is highly resistant to solvents and chemical exposure, ensuring durability in harsh environments.


Superior Mechanical and Dielectric Properties:The polymer exhibits impressive strength, rigidity, and dielectric performance, supporting advanced material applications.


Broad Industrial Applicability : With its combination of high-performance properties, a-BPDA is suitable for diverse applications across multiple industries and material fields.


Product Description of 2,3,3,4-biphenyl tetracarboxylic dianhydride CAS#36978-41-3

2,3,3,4-Biphenyl tetracarboxylic dianhydride, commonly known as a-BPDA, is a high-performance polymer renowned for its excellent heat resistance, solvent resistance, radiation resistance, and outstanding mechanical and dielectric properties. It offers significant potential for applications across a wide range of industries and material sectors.


Product Application of 2,3,3,4-biphenyl tetracarboxylic dianhydride CAS#36978-41-3

2,3,3,4-Biphenyl tetracarboxylic dianhydride (a-BPDA) and polyamides (PAA) derived from p-phenylenediamine (PDA) or 4,4'-oxydiphenylamine (ODA) can undergo thermal imidization to produce asymmetric biphenyl-type polyimides (PI). Compared to the semi-rigid s-BPDA/PDA, a-BPDA/PDA polyimides feature a notably bent chain structure. Nonetheless, a-BPDA/PDA films annealed at 350 °C exhibit higher glass transition temperatures (Tg) than s-BPDA/PDA films prepared under similar conditions. The elevated Tg values of a-BPDA-based PIs are likely due to the cranked axial motion that restricts conformational changes. Additionally, the diimide synthesized from a-BPDA and cyclohexylamine demonstrates long-lived luminescence, lasting up to 1.3 seconds following UV irradiation.


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