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BP11112 PTMC, Poly(trimethylene carbonate), Carboxyl-Terminated, IV: 0.5–1.0 dl/g, Mw: 20–49 kDa

Catalogue Number BP11112
Composition HO-PTMC-COOH
Form Granule

This product is a hydroxyl-carboxyl heterotelechelic poly(trimethylene carbonate) (HO-PTMC-COOH), a biocompatible polymer synthesised with controlled intrinsic viscosity and molecular weight. It is an amorphous polymer that exhibits excellent biocompatibility and biodegradability. At body temperature, it remains in a rubbery state, offering inherent elasticity. During production, quantitative spectroscopic analysis (e.g., NMR for end-group quantification) and Ubbelohde viscometer testing are employed to ensure consistent product performance and the defined heterobifunctional end-group structure. The systematic quality control process guarantees its reliable integration into medical-grade prototypes and other advanced applications where material performance, reproducibility, and predictable dual reactivity are critical.

The presence of two distinct terminal functional groups enables sophisticated and directional chemical modification. The hydroxyl and carboxyl ends allow for sequential, orthogonal reactions—such as chain extension from the hydroxyl end or conjugation via the carboxyl group—facilitating the precise synthesis of block copolymers, cross-linked networks, or surface-functionalised materials. Binary or multi-component copolymers or conjugates of PTMC with other polymers (such as PLA, PLGA, PCL, PEG, MPEG, etc.) in various architectures can be customised according to customer requirements. Products with other specific molecular weight ranges or alternative end-group functionalities are also available upon request.

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FAQ

What is the role of carboxyl termination in this polymer?

Carboxyl termination enhances reactivity for subsequent conjugation or cross-linking reactions. This feature allows the polymer to form stable interfaces in biomedical devices, potentially facilitating efficient integration with biological tissues. The controlled termination also assists in fine-tuning the polymer's mechanical and degradation properties.

How does the intrinsic viscosity range affect product performance?

The specified intrinsic viscosity range correlates with polymer chain length and impacts both processability and mechanical behaviour. A controlled IV ensures predictable flow properties during moulding and contributes to the material’s consistency in applications such as implantable devices, where mechanical stability is critical.

Can this material be processed using standard polymer fabrication equipment?

 Yes. The material is supplied in granule form and features well-defined molecular weight and viscosity characteristics, making it compatible with a range of standard processing methods, including melt processing (e.g., injection moulding, extrusion) and solution-based processing (e.g., solvent casting). This broad processability facilitates integration into existing production lines and ensures consistent, reproducible performance across various biomedical manufacturing processes. For detailed guidance on specific processing conditions, please contact our technical support team.

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