1999 Sets Of Data Store Double Pore Drug Pour Point Analyzer USP 40651 - 10℃~+170℃

Brand Name:Shandong Shengtai Instrument
Certification:USP 40 651
Model Number:ST203CS
Minimum Order Quantity:1
Delivery Time:7-15 work days
Payment Terms:T/T
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Location: Jinan Shandong China
Address: Times Headquarters Base, Tianqiao District, Jinan City
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ST203CS Automatic drug pour point analyzer

The ST203CS automatic drug pour point analyzer is designed and manufactured based on USP40 (USP 40 version) USP 40 651 pour point determination and the 2025 Chinese Pharmacopoeia General Rule 0613 pour point determination method. Suitable for determining the pour point of medicinal liquids. Measure the temperature at which a drug remains constant for a short period of time when it solidifies from a liquid to a solid. Some drugs have a certain pour point and purity change, and the pour point also changes accordingly. The determination of pour point can distinguish or check the purity level of drugs, etc. For example, polyethylene glycol, acetic acid, phenol, stearic acid, magnesium, bisphenol A, etc.

Technical parameters:

Working power supplyAC220V ± 10% 50Hz
Working cold bathdouble-layer vacuum glass bath
Cold bath temperature control- 10℃~+170℃
Temperature control accuracy± 0.1 ℃ (customizable to 0.01 ℃).
Number of test holesdouble holes
Cooling methodCompressor cooling
Cooling methodair cooling
Display7-inch touchscreen display
Bath liquid stirringThe stirring motor automatically stirs, with a power of 6W and a speed of 1200r/min.
Refrigeration systemnew type of refrigeration compressor.
Data memory16GB
Sample mixingsynchronous reduction motor, 60 times/minute.
Data storage1999
Result outputUSB flash drive
Output formatCSV or Excel
Standard printingStandard micro printer with automatic measurement and needle printing
Data managementCan connect to LIMS system
Data ExtensionAudit Tracking Function
Instrument size680 * 450 * 580mm
Instrument weight38kg

● Adopting embedded system design, automatic detection and printing throughout the entire testing process

● The test results can be exported through a USB flash drive;

● 7-inch color touch screen; The experimental results can be stored; You can view historical data;

● Print the results on the instrument and use mechanical automatic mixing.

● Account management: Audit tracking function and hierarchical account management, capable of three-level account management.

● Working power supply: AC220V ± 10%; 50Hz.

● Working cold bath: double-layer vacuum glass bath.

● Cold bath temperature control:- 10℃~+170℃

● Temperature control accuracy: ± 0.1 ℃ (customizable to 0.01 ℃).

● Number of test holes: double holes

● Cooling method: Compressor cooling

● Cooling method: air cooling

● Display: 7-inch touchscreen display

● Bath liquid stirring: The stirring motor automatically stirs, with a power of 6W and a speed of 1200r/min.

● Refrigeration system: new type of refrigeration compressor.

Data memory: The memory of the microcomputer instrument can be expanded to 16GB.

● Sample mixing: synchronous reduction motor, 60 times/minute.

● Storage method: The experimental results can store 1999 sets of historical data for easy retrieval;

● Result output: It can also be equipped with a USB drive output function to output to the computer for long-term storage

● Output format: The output format of the result USB drive is CSV or Excel.

● Standard printing: Standard micro printer with automatic measurement and needle printing

● Data management: Can connect to LIMS system

● Data Extension: Audit Tracking Function

● Instrument size: 680 * 450 * 580mm

● Instrument weight: 38kg

Note: The appearance pictures, dimensions, volume, and weight of the instrument are for reference only. If there are any updates to the instrument, there may be slight changes without prior notice.


Shandong Shengtai Instrument Co., Ltd. provides the following quality assurance for the instruments sold to you:

----The provided instrument materials are brand new, meet national quality standards, and have a manufacturer's certificate of conformity;

----The materials and main components provided meet the technical requirements specified in the technical documentation;

----The overall quality assurance period of the equipment is one year (excluding normal wear and tear of vulnerable parts).

----We are responsible for free maintenance of any instrument quality issues that occur during the warranty period. Due to equipment malfunction caused by the user's responsibility, we are responsible for repairing and charging reasonable fees.

----Lifetime discounted supply of parts for equipment, and lifetime maintenance and repair of the entire machine.

----After the expiration of the warranty period, if the user needs maintenance and technical services, we will only charge a cost fee.

Packing list

NumberNameSpecificationsQuantityNote
1Automatic drug freezing point analyzerHost1 unit
2Gel point plug2 piecesComplies with pharmacopoeia regulations
3Condensation test tube2 pieces
4Sensor2 pieces
5Power line1 piece
6Printing paper2 rollsNeedle printing paper
7Certificate of Conformity Warranty Card1 copy
8Instructions1 copy

China 1999 Sets Of Data Store Double Pore Drug Pour Point Analyzer USP 40651 - 10℃~+170℃ supplier

1999 Sets Of Data Store Double Pore Drug Pour Point Analyzer USP 40651 - 10℃~+170℃

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