BRAND / VENDOR: Agilent
Agilent, 12-5000V, EaseAlign Vessel, clear glass, 1000mL, Verified (includes Certificate), for 705-DS, VK7000/7010
CATALOG NUMBER: 12-5000V
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CATALOG NUMBER: 12-5000V
EaseAlign Vessel, clear glass, 1000mL, Verified (includes Certificate), for 705-DS, VK7000/7010
Specifications:
Apparatus Compatibility: Apparatus 1Apparatus 2
Certificate Available: Yes
Glass Type: Clear glass
Instrument Compatibility: 705-DSVK7000
Pharmacopoeia: USP
UNSPSC Code: 41121804
Vessel Family: Easealign
Vessel Form: Standard
Volume: 1000 mL
**********The following product description is generated by AI and is for reference only. If you have any questions, please contact customer service.**********
The EaseAlign Vessel is a high-quality clear glass solution vessel with a 1000mL capacity, designed for use in pharmaceutical dissolution testing. Precision engineered and verified, each unit is supplied with a Certificate of Verification ensuring dimensional accuracy and reliable performance. This vessel is specifically compatible with Agilent 705-DS as well as VK7000 and VK7010 dissolution testing systems, providing seamless integration into existing laboratory workflows.
Its clear glass construction allows unobstructed visual monitoring throughout dissolution testing, aiding in accurate observation and validation of processes. The vessel supports a broad range of routine and advanced research applications, including quality control, formulation development, and regulatory compliance testing in pharmaceutical laboratories. Rigorous verification guarantees compliance with industry standards, making it ideal for laboratories prioritizing data integrity and reproducibility.
This vessel is an essential accessory for dissolution system users seeking consistent, validated performance across multiple testing scenarios. It is compatible with a variety of related lab accessories, such as vessel covers and paddles, further streamlining the setup and operation of dissolution tests. By ensuring reliability and precision, it supports the accurate assessment of pharmaceutical dosage forms and active ingredient release characteristics.
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