Merck Millipore Lynx ST Connector 1-1/2 in Fractional Triclover

• Used in laboratory and biopharmaceutical settings for secure, sterile fluid transfer.
• Integrated into single-use assemblies for media preparation, cell culture, and purification processes.
• Applied in pilot-scale and manufacturing environments requiring aseptic connections.
• Suitable for connecting various components within a fluid path, such as bags, filters, and bioreactors.

Connection Type

Fractional Triclover, typically 1-1/2 inch for this model.

Material

Commonly made from medical-grade plastics suitable for sterile applications.

Sterilisation Method

Designed for pre-sterilised use, often gamma irradiated.

Flow Path

Typically designed for unidirectional flow, ensuring aseptic integrity.

Compatibility

Engineered to be compatible with other Merck Millipore Lynx components and standard fractional Triclover fittings.

Operating Pressure

Typically rated for pressures common in biopharmaceutical fluid transfer, buyers should verify specific unit ratings.

• What is a Lynx ST Connector?

  The Lynx ST Connector is a sterile connector designed by Merck Millipore for aseptic fluid transfer in biopharmaceutical applications. It allows for quick and secure connections without the need for welding or extensive sterilisation processes on-site.

• What does 'Fractional Triclover' mean in this context?

• Is this connector suitable for high-pressure applications?

• Can this connector be re-used?

• What industries commonly use this type of connector?

Lab organisation and storage equipment is valued for maximising workspace efficiency and protecting sensitive materials from contamination. Buyers typically prioritise durability, proper shelving capacity, and chemical resistance when purchasing used units. Industry sentiment favours equipment with adjustable configurations to accommodate evolving laboratory needs. Common strengths include robust construction and long operational lifespan when maintained correctly. When buying used, inspectors should examine structural integrity, verify compatibility with existing lab layouts, and confirm any specialised coating or material specifications remain intact for intended applications.

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