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BP11109 PTMC, Poly(trimethylene carbonate), Hydroxyl Terminated, IV: 5.0–6.0 dl/g, Mw: 378–477 kDa

Catalogue Number BP11109
Composition HO-PTMC-OH
Form Granule

This product is hydroxyl-terminated poly(trimethylene carbonate) (PTMC-OH), a biocompatible polymer with controlled intrinsic viscosity and molecular weight. It is an amorphous polymer that demonstrates excellent biocompatibility and biodegradability. At body temperature, it remains in a rubbery state, providing inherent elasticity. During production, quantitative spectroscopic analysis and Ubbelohde viscometer testing are employed to ensure consistent product performance and hydroxyl functionality. The systematic quality control process ensures its reliable integration into medical-grade prototypes and other advanced applications where material performance, reproducibility, and predictable reactivity are critical.

The presence of terminal hydroxyl groups enables further chemical modification, chain extension, or covalent conjugation with other functional molecules, making it highly versatile for the synthesis of block copolymers, cross-linked networks, or biofunctionalised materials. Binary or multi-component copolymers of PTMC with other polymers (such as PLA, PLGA, PCL, PEG, MPEG, etc.) at various ratios 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

How does the intrinsic viscosity range affect the processing of hydroxyl terminated PTMC?

The specified intrinsic viscosity range indicates the polymer’s chain length and influences melt flow properties during processing. It directly affects processing temperatures and shear conditions for melt extrusion and moulding in biomedical device fabrication.

What processing precautions are advised for hydroxyl terminated polymers such as this PTMC?

It is crucial to control moisture, temperature, and shear forces during processing. Excessive heat or prolonged exposure to humidity may trigger premature degradation or alter end-group functionality, impacting performance in biocompatible applications.

Can the molecular weight parameters be adjusted for specific biomedical formulations?

Yes, modifications in polymerisation conditions can tailor the molecular weight range. Adjustments assist in optimising degradation rates and mechanical properties, ensuring compatibility with diverse biomedical formulations. For detailed customisation, contact us.

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