Quality + R&D +
Laboratory
LUBESOLUT's technical capability is not a sales argument. It is the real infrastructure underpinning every formulation, every batch and every commitment to the client.
Technical capabilities
What underpins our ability to manufacture with rigour and guarantee batch-to-batch consistency.
Formulation and development
Our R&D team formulates from scratch or adapts existing formulations. Selection of bases and additive systems oriented towards the real application, not minimum raw material cost.
- Formulation design for specific application
- Base selection: mineral, synthetic (PAO, esters), semi-synthetic
- Anti-wear, EP, anti-corrosion, antioxidant additive systems
Laboratory and testing
Formulations are validated before reaching production. We work with standardised methods and proprietary tests adapted to client conditions.
- Viscometric analysis (kinematic and dynamic)
- Tribological tests (Four-Ball, Timken, FZG)
- Oxidative stability, flash point, RPVOT
- In-service oil analysis (client)
Batch quality control
Every batch produced is analysed before leaving the facility. The certificate of analysis accompanies the product. Traceability is complete: from raw material to delivery.
- COA (Certificate of Analysis) per batch
- Retained reference sample per batch
- Full traceability in internal system
Continuous improvement
The quality system is not a file of certificates. It is how we work: formula review, incident monitoring and constant updating of references.
- Periodic review of active formulations
- Non-conformity management and corrective actions
- Updating of technical and safety data sheets
Technical documentation
All the documentation an industrial client requires: technical data sheet, safety data sheet and certificate of analysis. Adaptable to specific client or approval requirements.
- Technical Data Sheet (TDS) per product and reference
- Safety Data Sheet (SDS)
- Updated REACH / SVHC documentation
Regulatory compliance
We work with current regulations regarding composition, labelling and safety. We do not invent compliance: we work with rigour and prudence in every statement.
- REACH — Registration and restriction of substances
- CLP — Classification and labelling
- H1 range with FDA 21 CFR §178.3570 compliance
Note: The capabilities described reflect our real infrastructure and working methodology. We do not claim specific certifications beyond those we have documented. If you need compliance information for a specific application, please contact us directly.
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