ConXport Tablet Disintegration Double Test Apparatus

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ConXport Tablet Disintegration Double Test Apparatus

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ConXport Tablet Disintegration Double Test Apparatus Specification

Dimension (L*W*H)
370 mm x 320 mm x 210 mm

Application
Pharmaceutical Laboratory

Frequency
50 Hz

Shape
Rectangular

Material
Stainless Steel

Properties
Programmable digital timer, double basket operation

Humidity Range
Up to 80% RH

Color Code
White and Blue

Accuracy
1 Second

Phase
Single Phase

Function
Automatic disintegration test

Automation Grade
Semi-Automatic

Suitable For
Tablet Quality Testing

Display Type
LCD

Use
To determine disintegration time of tablets

Height
210 mm

Treatment Type
Tablet disintegration

Temperature Range
Ambient to 45C

Power
40 Watt

Product Type
Tablet Disintegration Double Test Apparatus

Weight
Approx. 12 kg

Voltage
230 V AC

Display
Digital

Power Source
Electric

Heating Arrangement
Built-in water bath heater

Beaker Size
100 mm

Basket Material
Transparent Acrylic

Thermostatic Control
Digital thermostatic control

Bath Capacity
1 litre

Test Standard
Conforms to IP/USP Standards

Timer Range
Programmable up to 99 minutes

Number of Baskets
2 (Double Test)

Safety Features
Overheating protection

Stirring Function
Integrated

Control Type
Microprocessor based

ConXport Tablet Disintegration Double Test Apparatus Trade Information

FOB Port
Delhi

Payment Terms
Letter of Credit (L/C), Telegraphic Transfer (T/T), Paypal

Supply Ability
15 Per Week

Delivery Time
6-7 Days

Sample Available
Yes

Sample Policy
If order is confirmed we will reimburse the sample cost

Main Export Market(s)
South America, Western Europe, Middle East, Central America, Asia, Eastern Europe, North America, Australia, Africa

Main Domestic Market
All India

Certifications
ISO,FDA,CE,WHO-GMP

About ConXport Tablet Disintegration Double Test Apparatus

Voltage	220/230 V
Phase	Single Phase
Frequency	50 Hz
Automation Grade	Semi-Automatic
Power Source	Electric

Product Details:

It is designed for accurateestimation of disintegration time of tablets as per IP/USP standards.

The instrument is designed to testtwo batches of six tablets, simultaneously.

The unit consists of two beakershaving the capacity of 1000 cc each.

In these beakers, suitabledisintegration media can be taken.

These can be temperature controlledusing an inbuilt heater and a high thermostat fitted inside the instrument.

Microprocessor based time totalizeris provided for accurate time readout.

Features:

Baskets move up & down as perIP/USP test specifications

Temperature Controlled by sensitivethermostats

Advanced Double Basket Efficiency

This apparatus features two transparent acrylic baskets, allowing simultaneous testing of multiple tablet batches. Its double test capability significantly increases laboratory throughput and ensures consistent quality results. The programmable timer and microprocessor-based controls provide unmatched precision, making it ideal for extensive pharmaceutical lab routines.

User-Friendly Digital Operation

Equipped with a large LCD display, intuitive programming, and integrated stirring function, the apparatus simplifies operation. Digital thermostatic control and overheating protection maintain optimal and safe working conditions for precise disintegration analysis. The convenient 1-litre bath and programmable timing ensure reproducibility and ease for routine or research tasks.

Reliable and Compliant Design

Manufactured with durable stainless steel and finished in a stylish white and blue color code, the apparatus meets stringent IP/USP testing standards. Its built-in safety features, semi-automatic operation, and clear digital controls make it a dependable choice for tablet quality assessment, supporting pharmaceutical exporters, manufacturers, and laboratories across India.

FAQs of ConXport Tablet Disintegration Double Test Apparatus:

Q: How is the ConXport Tablet Disintegration Double Test Apparatus used in a pharmaceutical laboratory?

A: The apparatus is used to measure the disintegration time of tablets by immersing them in its dual acrylic baskets within the controlled water bath. The user sets parameters like temperature (up to 45C) and timing (up to 99 minutes) using the digital interface, ensuring conformity to IP/USP standards during routine quality testing.

Q: What are the key benefits of using the double basket design?

A: The double basket allows simultaneous testing of two sets of tablets, increasing efficiency and enabling comparative analysis. This dual test capability can help optimize batch approval processes and improve throughput in quality control environments.

Q: When should the programmable digital timer be utilized during the disintegration test?

A: The programmable timer should be set prior to starting the test to ensure accurate tracking of disintegration intervals. Its precision (1 second) is critical for compliance with IP/USP test standards and for comparison across multiple batches.

Q: Where is the apparatus best installed within a laboratory setting?

A: Due to its compact rectangular dimensions (370 mm x 320 mm x 210 mm) and moderate weight (12 kg), the apparatus fits well on benchtops in controlled environments. It should be positioned near a suitable power outlet (230 V AC) and water source for easy operation and maintenance.

Q: What is the process workflow for conducting a tablet disintegration test with this device?

A: First, tablets are placed in each acrylic basket. Fill the water bath (1-litre capacity) and set the desired temperature and time. Activate the test; the microprocessor will control timing, temperature, and stirring. Once complete, the display shows the disintegration time for analysis and recording.

Q: How does its built-in safety system enhance laboratory usage?

A: The apparatus features digital thermostatic control with an overheating protection mechanism, ensuring safety for users and preventing accidental equipment damage. This is especially important during prolonged or repeated testing at higher temperatures.

Q: What makes this apparatus suitable for tablet quality testing?

A: Its automation grade, precise digital controls, compliance with international standards, and reliable construction in stainless steel make it highly suitable for routine quality assurance of pharmaceutical tablets, delivering repeatable and trustworthy results for manufacturers and exporters.

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