BSE-0179 Tablet Dissolution

BSE-0179 Tablet Dissolution Specification

Condition
New

Heating Capacity
Multiple beakers (up to 6 vessels)

Control Mode
Digital

Heating Method
Water Bath/Direct Heating

Accuracy
0.5C

Power Source
Electric

Type
Tablet Dissolution Apparatus

Model
BSE-0179

Internal Size
320 x 180 x 30 mm

External Size
420 x 280 x 40 mm

Volume
Each vessel 1000 ml

Temperature Range
Room temp. to 99.9C

Material
Stainless Steel

Dimension (L*W*H)
420 x 280 x 40 mm

Power
1000W

Voltage
220V AC

Surface Finish
Polished

BSE-0179 Tablet Dissolution Trade Information

Minimum Order Quantity
1 Piece

Supply Ability
10 Pieces Per Day

Delivery Time
7-10 Days

About BSE-0179 Tablet Dissolution

Dissolution rate consists of water bath of 30.5cm long 20.5cm wide and 23cm high fitted with a thermostatic control maintains the temperature of water at 47 C with +/-0.5 variation convered vessel 100ml made of coring glass variable speed motor cylinder basket and shaft with blades of stainless steel.

Specification

Cat. No
BSE-179(A)	Single Test	11440.00
BSE-179(B)	Double Test	19800.00
BSE-179(C)	Three Test	36850.00
BSE-179(D)	Six Test with Digital RPM, Timer & Auto Lifting	109450.00

Consistent and Compliant Testing

Experience reliable dissolution testing for tablets and capsules with the BSE-0179. Its six-vessel design ensures uniformity, while adherence to USP and IP standards underlines quality and consistency in every batch, making it suitable for laboratory and quality control environments.

Advanced Controls and Safety

Operate with confidence thanks to a microprocessor-based digital control system. Programmable timers, digital LED displays, and adjustable stirring speeds provide flexibility, while built-in over-temperature protection and audio-visual alarms enhance operational safety.

Flexible Heating and Durable Build

This apparatus offers both water bath and direct heating options for versatility. Its robust stainless steel construction, polished finish, and precise temperature control (room temp to 99.9C, 0.5C accuracy) ensure long-lasting performance in rigorous pharmaceuticals settings.

FAQ's of BSE-0179 Tablet Dissolution:

Q: How does the BSE-0179 Tablet Dissolution Apparatus ensure accurate and reproducible results?

A: The BSE-0179 utilizes digital microprocessor controls, a programmable timer, precise temperature regulation (0.5C), and consistent stirring speeds (20-200 RPM) to maintain standardized testing conditions. Its six vessels allow for simultaneous testing and compliance with USP and IP standards guarantees reliable, reproducible outcomes.

Q: What is the recommended process for performing a dissolution test using this model?

A: Begin by placing tablets or capsules in the individual vessels (each 1000 ml). Set preferred stirring speed and temperature using the digital controls. Choose your heating method (water bath or direct) and program the timer up to 99 minutes. The apparatus maintains accurate, controlled conditions throughout the test.

Q: When should the over-temperature protection and audio-visual alarms be expected to activate?

A: These safety features activate if the device exceeds set temperature limits or encounters operational inconsistencies. They safeguard both samples and users by providing immediate alerts, preventing equipment damage or compromised test results.

Q: Where is the BSE-0179 Tablet Dissolution Apparatus best suited for installation?

A: This apparatus is ideally suited for pharmaceutical QC labs, research facilities, and academic institutions in need of reliable tablet or capsule dissolution analysis. Its compact design (420 x 280 x 40 mm) and electric operation facilitate convenient benchtop installation.

Q: How flexible is the apparatus when it comes to handling different sample types?

A: The BSE-0179 is designed for versatility, accommodating both tablets and capsules with six vessels, each capable of holding 1000 ml. Adjustable stirring speed and temperature settings ensure compatibility with a variety of dissolution testing protocols.

Q: What are the primary benefits of using this apparatus for pharmaceutical testing?

A: Users benefit from fast, accurate, and reproducible dissolution testing in compliance with global standards, enhanced safety via intelligent protection systems, and simplified operation through digital controls. The robust stainless steel build ensures longevity and dependable performance.

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