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ConXport . Dissolution Six Test Apparatus
ConXport . Dissolution Six Test Apparatus

ConXport . Dissolution Six Test Apparatus

ConXport . Dissolution Six Test Apparatus Specification

  • Storage Capacity
  • Six test vessels
  • Treatment Type
  • Tablet Dissolution
  • Use
  • Analysis of dissolution rate of drug samples
  • Shape
  • Rectangular base with cylindrical glass vessels
  • Product Type
  • Dissolution Six Test Apparatus
  • Automation Grade
  • Semi-Automatic
  • Accuracy
  • 1 RPM
  • Frequency
  • 50 Hz
  • Height
  • Approx. 550 mm
  • Suitable For
  • Tablet dissolution testing (six vessels)
  • Temperature Range
  • Room temperature to 45C
  • Application
  • Pharmaceutical and Quality Control Testing
  • Phase
  • Laboratory Equipment
  • Weight
  • Approx. 35 kg
  • Function
  • Uniform stirring & temperature control for dissolution tests
  • Properties
  • Digital control, Uniform stirring, Transparent vessel lids
  • Dimension (L*W*H)
  • Approx. 600 mm x 480 mm x 550 mm
  • Display Type
  • LED Digital
  • Material
  • Stainless Steel & Glass
  • Color Code
  • White / Metallic Silver
  • Power
  • 75 W
  • Display
  • Digital LED
  • Voltage
  • 230 V AC
  • Power Source
  • Electric
 

ConXport . Dissolution Six 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, Australia, North America, Eastern Europe, Middle East, Africa, Central America, Asia
  • Main Domestic Market
  • All India
  • Certifications
  • ISO,FDA,CE,WHO-GMP
 

About ConXport . Dissolution Six Test Apparatus

Voltage

220/230 V

Temperature

37deg +- 0.55deg C

Phase

Single Phase

Frequency

50 Hz

Shaking Speed Rpm

25 to 200 RPM

Automation Grade

Semi-Automatic

Power Source

Electric

 

ProductDescription

 

The apparatus consists of 4 parts. Awater bath with 500 watt heater covered 1000 ml. vessel made from Borosil glassand digital temperature control. Variable speed motor, with 30cms longsstainless steel shaft. A cylindrical stainless steel basket and a membranefixing attachment, water bath is made of imported thick Acrylic sheet withtransparent cover at top. Temperature of the bath is maintained at 37C with anaccuracy of 1 C.A cylindrical glass vessel of 1000 ml. capacity with slightlyconcave bottom has a flanged edge at the top to accept a fitted cover havingfour holes. One hole placed in the centre. The shaft of the motor is fitted onan upright and has an electronic speed regulating device that allows the speedto be varied from 25 to 250 R.P.M. The shaft is 6 mm dia. 30 cms on with basketfitted at end rotates smoothly and without any significant wobble. The basketconsists of two parts one of which is attached to the shaft. It is of solidmetal except for 2 mm vent and is screwed on the main shaft. Lower part of thebasket is held with this part by means of threading and this allows properremoval of lower part for introduction of the test samples. The detachable partof the basket is fabricated of stainless steel mesh formed into cylinder ofsize 36 mm x 25 mm dia. The equipment is workable on 220 volts 50 C/S A.C. butAnalog type single, Double, Three, Six & Eight stage.

 



Precision in Tablet Dissolution Testing

ConXports Six Test Dissolution Apparatus ensures consistent and repeatable results for pharmaceutical and quality control applications. With variable stirring speeds and uniform temperature control, the device is designed to provide precise conditions essential for accurate dissolution rate analysis of drug samples. Digital controls allow effortless configuration, and compliance with USP/IP specifications guarantees standard-compliant results every time.


User-Friendly Design and Operation

Equipped with transparent individual lids and easy vessel access, this apparatus simplifies sample handling and observation. The programmable digital timer, intuitive LED display, and semi-automatic operation enhance usability. Thoughtful features, including a drain valve for water discharge and robust stainless steel construction, add convenience and dependability, making it ideal for daily laboratory use.

FAQs of ConXport . Dissolution Six Test Apparatus:


Q: How does the ConXport Dissolution Six Test Apparatus ensure uniform stirring and temperature control?

A: The apparatus uses a microprocessor-controlled stepper motor to provide accurate and consistent stirring within the range of 25 to 250 RPM. Its double-walled, insulated water bath is equipped with a digital thermostat and SS Immersion heater, maintaining precise temperatures up to 45C with automatic cut-off and over-temperature protection for safety and consistency.

Q: What type of samples can be analyzed with this apparatus?

A: This apparatus is primarily designed for the analysis of dissolution rates in tablet drug samples, making it suitable for pharmaceutical research, quality control, and compliance testing as per USP/IP standards.

Q: When is it appropriate to use the programmable timer feature?

A: The programmable digital timer is best used whenever you need to time dissolution experiments with high accuracy. It enables users to set specific testing durations, ensuring that all samples undergo identical exposure to testing conditions for comparable and reliable results.

Q: Where should the ConXport Dissolution Six Test Apparatus be installed for optimal performance?

A: For optimal performance, the apparatus should be placed in a dedicated laboratory environment on a stable, level surface near a suitable power source (230 V AC, 50 Hz). Ensure adequate space for ventilation, easy access to all vessels, and safe operation of the water bath and electrical controls.

Q: What is the process for conducting a dissolution test on this instrument?

A: To conduct a dissolution test, fill each vessel with 1000 ml of testing medium, set the desired temperature and stirring speed, and insert the tablets. Secure the transparent acrylic lids, set the programmable timer, and monitor the process via the digital display. Samples can be withdrawn at specific intervals for analysis.

Q: How does the apparatus ensure sample and operator safety during operation?

A: The apparatus includes multiple safety features such as over-temperature protection, a low-water level cut-off, and a transparent lid for each vessel. These measures help prevent overheating, damage to sensitive samples, and exposure to hot liquids during operation.

Q: What are the main benefits of using this dissolution apparatus in pharmaceutical testing?

A: Key benefits include precise and uniform dissolution testing, compliance with industry standards, ease of operation, and robust safety mechanisms. Its design supports both manual and programmable modes, ensuring flexibility and reliability for routine quality control and research activities.

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