Struggling with inconsistent tablet breakdown times, complex compliance reporting, or sudden equipment downtime? Pharmaceutical quality control laboratories frequently face the challenge of accurately evaluating capsule degradation under strictly prescribed conditions. Implementing an advanced Disintegration Tester for pharmaceutical compliance directly resolves these workflow hurdles by combining automated diagnostics with an exceptionally stable thermodynamic environment.

Technical Specifications

• Model Number: MSBKBJ2SWISS

• Product Part Number: BKBJ2-SWISS

• Basket Configuration: 2 independent pieces

• Beaker Fluid Capacity: 1000 ml per vessel

• Basket Lifting Frequency: 30 to 31 times per minute

• Vertical Stroke Height: 55 ± 1 mm ensuring exact mechanical repetition

• Minimum Spacing Dimension: 25 ± 2 mm

• Standard Mesh Size: 2 mm pharmaceutical grade

• Thermodynamic Temperature Range: Room temperature to 50 °C

• Temperature Control Precision: ± 0.3 °C for absolute thermal stability

• Operational Timing Range: 1 to 900 minutes

• Timing Control Precision: ± 0.5 minutes

• Continuous Working Time: Greater than 24 hours

• Power Consumption Rating: 600 W

• Power Supply Requirements: AC 220V ± 10 percent at 50 or 60Hz

• External Physical Dimensions: 400 by 320 by 440 millimeters

• Total Gross Weight: 18.5 kilograms

Key Benefits and Solving Lab Challenges

Quality assurance facilities often lose critical time dealing with fluctuating water bath temperatures or recording manual times, leading to high human error rates and compromised batch releases. This equipment completely eliminates these operational pain points. By utilizing a reliable Disintegration Tester independent beaker system, operators can seamlessly run separate testing protocols simultaneously without cross-interference. This guarantees faster, much more accurate measurements and drastically improves overall laboratory throughput without requiring additional bench space.

Equipment failures during extended testing periods are a major vulnerability for any facility aiming for strict pharmacopeia compliance. This instrument actively prevents these mechanical issues through its advanced auto-diagnose and auto-alarm systems. The comprehensive capabilities of the Disintegration Tester allow users to rely on an internal microprocessor that continuously monitors operational health, instantly alerting technicians to any parameter deviations before sample integrity is compromised.

Core Operational Features

Every unit is engineered to maximize testing throughput while minimizing the need for constant manual observation.

• Intelligent Thermal Management: A precision Disintegration Tester water circulating pump utilizes magnetic drive technology to perfectly maintain uniform heat distribution across all test vessels.

• Intuitive Digital Interface: The high-contrast LCD screen provides a crystal-clear readout of both target and real-time parameters, significantly reducing operator eye strain during high-volume testing.

• Durable Construction Materials: Features a high-quality stainless steel basket and paddle assembly that is heavily resistant to chemical corrosion and exceptionally easy to sanitize between test batches.

• Continuous Operation Capability: Engineered to run flawlessly for over 24 continuous hours, supporting demanding high-volume manufacturing environments effortlessly.

Upgrade Your Quality Control Workflow

Modern pharmaceutical manufacturing demands instruments that deliver uncompromising accuracy, rapid sample processing, and absolute regulatory compliance. Integrating a standardized Disintegration Tester into your quality control regimen ensures your facility remains highly efficient and your final dosage forms are perfectly safe for consumer use. Invest in state-of-the-art solid dosage analysis technology today to streamline your complex evaluation protocols, eliminate costly operational downtime, and achieve absolute confidence in every single batch release.