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Disintegration Test Apparatus

Price 500.0 INR/ Piece

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MOQ : 1 Piece

Disintegration Test Apparatus Specification

Shape
Rectangular Body

Application
Pharmaceutical Laboratory, Tablet Testing

Material
Stainless Steel, Borosilicate Glass

Height
Approx. 450 mm Millimeter (mm)

Phase
Single Phase

Suitable For
Pharmaceutical R&D, Quality Control

Automation Grade
Semi/fully automatic

Properties
Corrosion-resistant, Chemically inert

Storage Capacity
Holds up to 6 or 12 test tubes (depending on model) Kilogram(Kg)

Function
Automated Disintegration Test

Color Code
White/Silver finish

Power
35 W Watt (w)

Temperature Range
Ambient to 45 C (for water bath) Celsius (oC)

Use
Testing disintegration time of pharmaceutical tablets/capsules

Frequency
50 Hz Hertz (HZ)

Weight
Approx. 15 kg Kilograms (kg)

Product Type
Disintegration Test Apparatus

Humidity Range
Up to 90% RH (non-condensing)

Dimension (L*W*H)
Approx. 400 x 300 x 450 mm Millimeter (mm)

Treatment Type
Tablet/Capsule Disintegration

Accuracy
1 sec (timer) %

Display Type
LED/LCD

Display
Digital

Power Source
Electric

Voltage
230V AC Volt (v)

Disintegration Test Apparatus Trade Information

Minimum Order Quantity
1 Piece

Payment Terms
Cash in Advance (CID), Cheque, Telegraphic Transfer (T/T), Letter of Credit (L/C), Cash Advance (CA)

Sample Available
Yes

Sample Policy
Sample costs shipping and taxes has to be paid by the buyer

Packaging Details
carton box, export quality also available

Main Export Market(s)
Asia, Eastern Europe, Middle East, Western Europe, Africa

Main Domestic Market
All India

Certifications
ISO 9001, 14001 ,CE

About Disintegration Test Apparatus

Disintegration Test Apparatus

Description of Disintegration Test Apparatus:

Disintegration apparatus for solid dosage forms ( Tablets, capsules etc) and Disintegration apparatus for semisolid dosage forms ( Suppositories and pessaries ) The USP device to test for disintegration time consists of six glass tubes each of three inches length, open at the top, and held against a 10 mesh screen at the bottom end of the basket rack assembly. To test for the disintegration time, a single tablet is placed in each tube, and the basket rack is positioned in a 1-L beaker containing water or simulated gastric fluid, or stimulated intestinal fluid.

The temperature of the system is maintained at 37+/-2oc and the tablets remain 2.5 cm below the surface of the liquid on their upward movement and descend not closer than 2.5 cm from the bottom of the beaker.A standard motor-driven device is used to move the basket assembly containing the tablets up and down through a distance of 5 to 6 cm at a frequency of 28 to 32 cycles per minute. Perforated plastic discs may also be used in the test.

Advanced Automation for Accurate Tablet Testing

This apparatus utilizes a basket lift mechanism for precise, automatic up-and-down movement, ensuring consistent test conditions. Its programmable digital timer and continuous or timed operation modes provide flexibility for varying test protocols. The microprocessor-based PID controller maintains accurate temperature, critical for reproducible results in pharmaceutical quality control and research environments.

Robust Construction and User-Centric Design

Crafted with a double-walled stainless steel chamber and chemically inert materials, this disintegration tester is built for durability and resistance to corrosion. The powder-coated housing and use of borosilicate glass beakers enhance lifespan and maintain chemical compatibility. With accessible digital/LED display and included accessories, set-up and daily operation remain efficient and straightforward.

Safety and Standard Compliance Assured

Over-temperature protection, audio alarms, and adherence to major pharmacopoeia standards (IP, USP, BP, Ph.Eur.) guarantee both operational safety and regulatory compliance. The built-in magnetic stirrer and precise PT-100 sensor further ensure uniform temperature throughout the test, reducing chances of error and maximizing reliability for pharmaceutical applications.

FAQs of Disintegration Test Apparatus:

Q: How does the basket lift mechanism improve the disintegration test process?

A: The automatic basket lift mechanism provides consistent, error-free up-and-down motion for 1 or 2 baskets (model dependent), leading to more reliable disintegration time measurements. This automation reduces manual intervention and ensures uniform movement throughout the test cycle.

Q: What standard compliance does this disintegration apparatus meet?

A: This apparatus is compliant with international standards including IP, USP, BP, and Ph.Eur., making it suitable for pharmaceutical quality control and regulatory submissions worldwide.

Q: When should I use the programmable preset timer function?

A: The digital timer with programmable presets should be used to automate test intervals, ensuring accuracy and repeatability. This is particularly useful for batch processing and in high-throughput laboratory environments.

Q: Where can this apparatus be used within the pharmaceutical sector?

A: The device is ideal for pharmaceutical laboratories, both for R&D and quality control environments, where testing the disintegration time of tablets and capsules is essential for product development and lot release testing.

Q: What is the process for maintaining uniform temperature during testing?

A: A microprocessor-based PID controller, assisted by a built-in magnetic stirrer and PT-100 sensor, manages the water bath temperature (ambient to 45C), ensuring consistent thermal conditions across beakers and accurate disintegration results.

Q: How is user safety ensured during operation?

A: User safety is prioritized through over-temperature protection and an audible alarm system. The corrosion-resistant, double-walled construction and powder-coated body further amplify safety and longevity in daily use.

Q: What are the benefits of using this automatic disintegration test apparatus?

A: This device offers automated operations, high measurement accuracy (1 sec timer), robust construction, regulatory compliance, and ease of use, making it a valuable asset for pharmaceutical tablet/capsule disintegration studies.

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