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BP11104 PTMC, Poly(trimethylene carbonate), Hydroxyl Terminated, IV: 0.5–1.0 dl/g, Mw: 20–49 kDa

Catalogue Number BP11104
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 exhibits excellent biocompatibility and biodegradability. At body temperature, it remains in a rubbery state, offering 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 guarantees 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

What is the technical significance of the intrinsic viscosity range in this polymer?

The intrinsic viscosity range indicates the average molecular weight and influences processability. A defined IV ensures that the polymer exhibits consistent chain length, which is critical for achieving predictable thermal and mechanical behaviour in biomedical fabrication.

How does the hydroxyl termination affect further chemical modification?

The hydroxyl groups serve as active sites for post-polymerisation reactions, facilitating grafting or crosslinking processes. This modification capability enables fine-tuning of degradation rates and mechanical properties in tissue engineering and drug delivery applications.

How is batch consistency maintained during production?

SAM employs differential scanning calorimetry (DSC) and gel permeation chromatography (GPC) to monitor intrinsic viscosity and molecular weight. These analytical methods verify that each batch meets the defined specifications, ensuring consistent performance for subsequent biomedical processing.

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