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ConXport . Dissolution Single Test Apparatus
ConXport . Dissolution Single Test Apparatus

ConXport . Dissolution Single Test Apparatus

ConXport . Dissolution Single Test Apparatus Specification

  • Product Type
  • Dissolution Single Test Apparatus
  • Temperature Range
  • Ambient to 45C with 0.5C accuracy
  • Dimension (L*W*H)
  • Approx. 40 x 20 x 45 cm
  • Function
  • Dissolution testing
  • Accuracy
  • 1 RPM for paddle/basket speed
  • Phase
  • Single Phase
  • Material
  • Stainless Steel (SS Body with acrylic water bath)
  • Frequency
  • 50 Hz
  • Shape
  • Rectangular base with cylindrical beaker
  • Color Code
  • White/Blue/Silver (as per image aesthetics)
  • Weight
  • Approx. 9-11 kg
  • Properties
  • Robust construction, corrosion resistant, high accuracy control
  • Height
  • Approx. 45 cm
  • Use
  • Testing dissolution rate of pharmaceutical preparations
  • Storage Capacity
  • Single vessel/beaker operation
  • Treatment Type
  • Lab instrument (N/A for medical treatment)
  • Display Type
  • LED/LCD Digital Display
  • Suitable For
  • Tablet/Capsule dissolution testing
  • Automation Grade
  • Manual/Basic Digital
  • Power
  • 40-60 W
  • Application
  • Pharmaceutical and laboratory dissolution testing of tablets and capsules
  • Voltage
  • 220 V AC
  • Display
  • Digital
  • Power Source
  • Electric
 

ConXport . Dissolution Single Test Apparatus Trade Information

  • FOB Port
  • Delhi
  • Payment Terms
  • Paypal, Letter of Credit (L/C), Telegraphic Transfer (T/T)
  • 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)
  • Western Europe, Australia, Eastern Europe, Middle East, Central America, South America, Asia, North America, Africa
  • Main Domestic Market
  • All India
  • Certifications
  • ISO,CE,FDA,WHO-GMP
 

About ConXport . Dissolution Single Test Apparatus

Product Specifications

Color Blue & White

Weight 9 Kilograms (kg)

Material Stainless Steel

Usage For Laboratory Use

Product Type Single Test Apparatus

ProductDescription

With avision to be a pioneer in our domain and establish ourselves as a brand, we areengaged in manufacturing and supplying excellent qualityDissolution Single Test Apparatus. Itconsists of 6 stages water bath with 2kvv heater covered with 1000 ml vesselmade from borosilicate glass. Offered apparatus can be availed from us indifferent models and technical specifications as per requirements.Dissolution Single Test Apparatusisduly checked on well defined quality parameters prior to dispatch.

Features:

Long lastingmaintenance free life

Rugged and sturdyconstruction

Easy operation



Advanced Dissolution Testing Precision

ConXports Dissolution Single Test Apparatus offers granular control and exceptional uniformity for tablet and capsule dissolution studies. The interchangeable paddle and basket system, combined with a microprocessor-controlled heater and digital speed adjustment, guarantees high accuracy for every test cycle. Its transparent acrylic bath, stainless steel framework, and digital display simplify operation and monitoring, ensuring consistency and reliability whether for routine quality checks or in-depth research.


Robust Construction and Safety

Built with corrosion-resistant stainless steel and a durable acrylic bath, this dissolution tester is designed for longevity in demanding laboratory settings. The integrated overheat protection and water level cutoff system safeguard both operator and instrument, letting users focus on reliable data collection. Its compact benchtop design accommodates limited laboratory space, while robust support rods and components ensure stability throughout operation.

FAQs of ConXport . Dissolution Single Test Apparatus:


Q: How does the ConXport Dissolution Single Test Apparatus maintain accurate temperature during tests?

A: The apparatus features a transparent acrylic bath with a water jacket and a microprocessor-controlled heater. Water circulation ensures uniform temperature distribution, while the digital system maintains temperatures from ambient up to 45C with 0.5C accuracy.

Q: What types of samples can be tested with this dissolution apparatus?

A: This unit is suitable for pharmaceutical dissolution testing of tablets and capsules, adhering to USP, BP, and EP compliance standards. The apparatus measures the rate at which these samples dissolve under controlled laboratory conditions.

Q: When is it necessary to use the paddle versus the basket configuration?

A: The interchangeable paddle is generally used for tablets, while the basket is recommended for capsules or samples prone to floating or disintegration. The choice depends on the formulation and standard testing protocols applicable to your sample type.

Q: Where can this dissolution apparatus be installed for optimal use?

A: The benchtop design is ideal for laboratory environments within pharmaceutical companies, research institutes, or any setting requiring controlled dissolution testing. Ensure placement near a stable power supply and with adequate workspace for safe operation.

Q: What process is followed for operating the ConXport Dissolution Single Test Apparatus?

A: Install the dissolution vessel, choose and fix the paddle or basket, fill the beaker with the test medium, and add your sample. Set the desired temperature, RPM, and timer via the digital control panel. Once started, the apparatus maintains set parameters, and safety systems monitor for overheating or low water levels.

Q: How is the programmable digital timer utilized during a dissolution test?

A: The user-friendly digital timer enables precise test durations to be set before starting the dissolution process. Once the test concludes, the system signals completion automatically, promoting consistent and repeatable results.

Q: What are the main benefits of using this single test dissolution apparatus for laboratory work?

A: Key benefits include high accuracy and repeatability, robust and corrosion-resistant construction, ease of operation, compliance with global pharmacopoeia standards, and enhanced safety features. Its design supports precise quality control for tablet and capsule formulations.

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