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ConXport . Disintegration Single

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ConXport . Disintegration Single Specification

Weight
7 kg (approx)

Application
Pharmaceutical Tablet Disintegration Testing

Material
Stainless Steel and Acrylic

Properties
Transparent acrylic tank, stainless steel construction, motorized mechanism

Phase
Single Phase

Frequency
50 Hz

Temperature Range
Ambient

Height
260 mm

Product Type
Laboratory Disintegration Tester

Treatment Type
Tablet Disintegration

Use
To test tablet/capsule disintegration

Accuracy
±1 sec (Timer)

Dimension (L*W*H)
320 x 260 x 260 mm

Display Type
LED Digital

Power
40 W

Color Code
White/Silver

Suitable For
Pharmaceutical Labs, Research Institutes

Automation Grade
Semi-Automatic

Shape
Rectangular

Function
Disintegration Testing

Storage Capacity
One Basket/Single

Power Source
Electric

Voltage
230 V AC

Display
Digital Timer Display

Motor Specification
Continuous rated motor for basket movement

Safety Feature
Auto stop on completion, overload protection

Heating System
No heating system (external water bath required if heating needed)

Tank Material
Acrylic

Beaker Capacity
1000 ml (Glass Beaker Provided)

Control Type
Touch Keypad

Standards Complied
IP, BP, USP

Operating Temperature
Ambient to 37°C

Basket Material
Stainless Steel Mesh

Timer Range
Up to 99 minutes

ConXport . Disintegration Single 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)
Western Europe, Australia, North America, Eastern Europe, Middle East, Central America, South America, Asia, Africa

Main Domestic Market
All India

Certifications
ISO,CE,FDA,WHO-GMP

About ConXport . Disintegration Single

Product Type Disintegration Single

Weight 10 Kilograms (kg)

Usage For Laboratory Use

Material Stainless Steel

Color Black

ProductDescription

The test equipment work on the up and down movement of the tablet in the medium of water kept at 37C. Built on M.S. Cabinet, which housed a geared motor for the vertical shaft drive the shaft moves up and down by 7.5 cms at speed of 30 per minute. On the upper end of the shaft fitted a horizontal strip with a clamp-on on either side. These clamps hold glass vessels open at both ends and with stainless steel wire gauge with rubber rings at the lower end, which dips in the water. Two independently thermostatically controlled not plates rating 65 watts are fixed on the top of the cabinet upon which beakers of 1000 ml size are net filled with water. Temperature is maintained at 37C with an accuracy of 1 C. Independent switches with neon indicators for motor hot plates are fitted on a panel. Mains fuse with two meters mains cord and plug provided. Work on 220 volts A.C. mains.

HOW TO OPERATE:

2.   Now put the tablet in the basket and fix the basket as the stand.
3.   Inset the socket into the main providers on the left side at the back of the instrument and switch on the set the temperature with digital temperature controller if the green bulb glows it shows the Heater in ON.
4.   Switch the motor up-down movement of the basket will start and adjustable switch of speed control on the right side the instruments.
5.   This instrument will show how much time the table takes to crush in powder.

1. Keep the instrument clean and dry.
2. Do not handle the instrument with wet hands.

Precise Disintegration Testing for Pharmaceuticals

ConXports Disintegration Single is engineered to reliably assess tablet and capsule disintegration. Its stainless steel mesh basket and transparent acrylic tank offer visibility and robust performance. Fully compliant with pharmaceutical standards, its digital display and touch keypad controls simplify testing, making it an essential instrument for research labs and pharmaceutical quality control.

User-Friendly Operation and Construction

Ease of use is paramount with features like a touch keypad, digital timer accuracy to 1 second, and clear LED display. The devices auto-stop function, overload protection, and single-phase operation ensure both user safety and operational consistency, while the stainless steel and acrylic build offers long-lasting reliability.

FAQs of ConXport . Disintegration Single:

Q: How is the ConXport Disintegration Single operated during testing?

A: Operation involves placing tablets or capsules in the stainless steel mesh basket, inserting the provided 1000 ml glass beaker filled with the appropriate medium, and setting the desired time using the LED digital timer. Basket movement is controlled by a continuous-rated motor, and the test process is managed via a responsive touch keypad.

Q: What pharmaceutical standards does this equipment comply with?

A: The instrument is designed in accordance with IP (Indian Pharmacopoeia), BP (British Pharmacopoeia), and USP (United States Pharmacopeia), ensuring reliable results for pharmaceutical quality control purposes.

Q: When should an external water bath be used with this device?

A: An external water bath is required if your testing protocol specifies a temperature-controlled environment above ambient conditions, as the instrument does not include an integrated heating system. This enables testing up to 37C, depending on your labs requirements.

Q: Where is the ConXport Disintegration Single best utilized?

A: Ideal for pharmaceutical laboratories, research institutes, and tablet/capsule production settings, the device supports routine quality control and R&D applications in single or batch testing scenarios.

Q: What are the benefits of using an acrylic tank and stainless steel construction?

A: The transparent acrylic tank allows users to visually monitor the disintegration process, while stainless steel components ensure chemical resistance, easy cleaning, and long-term durability in laboratory environments.

Q: How does the safety system enhance workspace protection?

A: The instrument is equipped with auto-stop functionality upon test completion and overload protection to prevent damage to the motor and internal components, thereby ensuring user and equipment safety during operation.

Q: What processes can be validated using this device?

A: The ConXport Disintegration Single validates the disintegration time of pharmaceutical tablets and capsules, supporting process development, method validation, and ongoing quality assurance for oral dosage forms.

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