Disintegration Tester LE-DT101

Lab Expo Disintegration Tester LE-DT101 offers an automatic time range setting from 5 to 120 minutes to allow precise control. It includes an auto-stop function that activates at the preset timing point. Equipped with MPU to automatically control the back-and-forth frequency of the nacelle. Integrated with digital displays for clear visualization of real-time test parameters. Our Disintegration Tester is an essential tool for pharmaceutical quality control.

$3,293.00 $ 2744

Disintegration Tester LE-DT101 - Specifications

Basket assembly 2
Nacelle back and forth frequency (30 to 32)/min
Nacelle back and forth range 55±1 mm
Automatic time range 5 to 120 mm
Accuracy of controlling temperature 37 ± 0.5°C
Power Consumption 600 W
Power Supply 110V/60 Hz or 220V/50Hz
Dimension 400 × 300 × 420 mm
Weight 16 kg

Disintegration Tester LE-DT101 - Key Features

  • Even temperature distribution with 0.5C accuracy
  • Manual control panel with digital LCD display
  • Automated functions via MPU frequency regulation

Disintegration Tester LE-DT101 - Applications

FunctionImplementation
Pharmaceutical QC labs37 ± 0.5°C temperature accuracy ensures precise tablet disintegration testing
Tablet dissolution analysisAutomatic time range from 5 to 120 minutes allows customizable test durations
Dual-basket operationsBasket assembly of 2 enables simultaneous sample processing
High-frequency motion controlNacelle back and forth frequency of (30 to 32)/min provides consistent mechanical action
Benchtop laboratory useDimension of 400 × 300 × 420 mm fits standard lab workspaces

Disintegration Tester LE-DT101 - Catalog


Disintegration Tester LE-DT101

Disintegration Tester LE-DT101

Disintegration Tester

Lab Expo Disintegration Tester units are used to assess tablet and capsule disintegration under controlled motion conditions in pharmaceutical testing workflows. The range includes systems with dual basket assemblies operating at 30 to 32 cycles per minute and a reciprocating range of 55 ±1 mm. Configurations are structured for consistent immersion and movement, supporting evaluation of dosage form breakdown in quality control and formulation testing environments requiring repeatable disintegration analysis.