ConXport . Dissolution Six Test Apparatus

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ConXport . Dissolution Six Test Apparatus

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ConXport . Dissolution Six Test Apparatus Specification

Application
Pharmaceutical and Quality Control Testing

Product Type
Dissolution Six Test Apparatus

Function
Uniform stirring & temperature control for dissolution tests

Dimension (L*W*H)
Approx. 600 mm x 480 mm x 550 mm

Accuracy
1 RPM

Material
Stainless Steel & Glass

Properties
Digital control, Uniform stirring, Transparent vessel lids

Height
Approx. 550 mm

Shape
Rectangular base with cylindrical glass vessels

Use
Analysis of dissolution rate of drug samples

Treatment Type
Tablet Dissolution

Suitable For
Tablet dissolution testing (six vessels)

Power
75 W

Frequency
50 Hz

Temperature Range
Room temperature to 45C

Phase
Laboratory Equipment

Automation Grade
Semi-Automatic

Color Code
White / Metallic Silver

Storage Capacity
Six test vessels

Weight
Approx. 35 kg

Display Type
LED Digital

Voltage
230 V AC

Power Source
Electric

Display
Digital LED

Stirrer Drive
Stepper motor with microprocessor control

Safety Features
Over-temperature protection, Low-water level cutoff

Stirring Speed
Variable, 25 to 250 RPM

Paddle Shaft Material
Stainless Steel 316

Lid Type
Transparent acrylic lid for each vessel

Operation Mode
Manual and programmable

Drain Valve
Provided for bath water discharge

Number of Vessels
6 positions

Compliance
Conforms to USP/IP specifications

Water Bath Capacity
Approx. 15 liters

Bath Type
Double wall, insulated water bath

Heater Type
SS Immersion heater

Temperature Control
Digital thermostat with auto cut-off

Timer
Programmable digital timer

Vessel Capacity
1000 ml per vessel

Vessel Alignment
Precisely centered & easy access arrangement

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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