Analysis and expertise laboratory

Raw material purity analysis in a laboratory

More than 140 people
More than 140 people at your service
5200 m² laboratory
5200 m² laboratory + 99% of services are provided in-house
Accredited laboratory
Accredited laboratory COFRAC ISO 17025

Your needs: carry out a purity analysis to ensure the conformity of your substance

What is product purity?

The purity of a product in chemistry refers to the degree to which a substance consists exclusively of the desired molecule or chemical element, without contamination by other substances. Purity is an essential measure for determining the quality and effectiveness of a chemical compound.

Why carry out a purity analysis of your products?

The “purity” of a material or raw material will make a major contribution to optimising its final performance. Regular checks on materials are therefore an essential stage in the production process.

In the event of a fault (visual defect, questionable solidity, appearance of an unknown substance, etc.), manufacturers from all sectors regularly call on analysis laboratories to check the purity of their raw materials or materials used.

Determining the purity of a substance

Determining the purity of a substance involves analysing its components to check its chemical composition and identify any impurities or contaminants. This process is essential in many industrial sectors, such as pharmaceuticals, cosmetics and metallurgy, to ensure that the substance complies with quality and safety standards.

Carry out chemical purity and trace element analysis

Chemical purity analysis is essential to ensure that your materials are free from contaminants. The presence of trace elements, even at extremely low concentrations, can have a significant impact on the quality, performance or safety of your products.

Trace element analysis can detect and quantify these impurities present in your materials. Advanced techniques such as inductively coupled plasma mass spectrometry (ICP-MS) are commonly used to identify heavy metals, toxic substances or non-compliant elements.

Our solutions: characterise the chemical composition of your materials to assess their purity and performance

Why call on FILAB?

The FILAB laboratory puts the expertise of its doctors and engineers and its state-of-the-art analytical equipment at your disposal, and offers you tailor-made support to assess the purity of your materials.

The FILAB laboratory has a wide range of analytical techniques at its disposal to address these purity and impurity issues.

Our technical resources for purity analysis

SEM FEG EDX purity analysis

Search for pollution (inclusion of particles)

Surface analysis

Ageing study

Purity analysis by ICP (AES ou MS)

– Contaminant detection

– Quantification and detection of heavy metals

Identification of impurities (particles, unknown deposits, etc.)

– Nickel release test

– Synthetic sweat test

Purity analysis by GC-MS, GC FID ou UPLC MS/MS

Contaminant determination (residual solvents, pesticides, allergens, etc.)

Residual solvent analysis

– VOC, BTEX, PAH, or HCT analysis

– Allergen screening

Purity analysis by NMR

Analysis of active ingredients

– Determination of optical purity

– Measurement of enantiomeric excess

Promising strong responsiveness and a personalized response to your requests, FILAB supports you in the implementation of your quality control needs before or after the marketing of your products.

Purity analysis for the pharmaceutical industry

In the pharmaceutical industry, purity testing is essential to ensure that drugs and active pharmaceutical ingredients (APIs) meet quality and safety standards. Our ISO 17025-accredited laboratory performs in-depth analyses to detect potential contaminants, impurities, or residues in raw materials, manufacturing intermediates, and finished products. By ensuring compliance with strict standards, such as the European Pharmacopoeia and USP, we help you prevent contamination risks and ensure the efficacy of your products.

Our purity testing services apply to a wide range of pharmaceutical products, including:

  • Active Pharmaceutical Ingredients (APIs): purity testing of raw materials to ensure the absence of contaminants.
  • Finished Products: evaluation of drug products for possible residual impurities from production or packaging.
  • Sterile Products: microbiological and chemical purity testing to prevent cross-contamination or toxic residue in injections and other sterile products.

FAQ

How to check the purity of your materials with FILAB?

FILAB is an accredited analytical laboratory that offers comprehensive solutions to verify the chemical purity of your materials, regardless of your industry. We use cutting-edge techniques to detect impurities and ensure the compliance of your products.

Here's how FILAB can help you:

  • Trace element analysis: using technologies such as ICP-MS to detect extremely low concentrations of heavy metals and other contaminants.
  • Chromatography: to separate and identify organic compounds present in your samples.
  • Electron microscopy: identifying particles and contaminants at the microscopic level.
How does raw material purity analysis contribute to the quality of finished products?

Raw material purity testing is essential to ensure that finished products meet quality and safety standards. Impurities in raw materials can affect the performance, stability, and compliance of final products, whether in the pharmaceutical, cosmetic, or food industries.

Identifying and eliminating potential contaminants early in the production process prevents the risk of failure or contamination, while ensuring that the final product is safe and compliant with regulatory requirements.

How does raw material purity analysis optimize your production costs?

Raw material purity testing allows you to quickly identify impurities or contaminants before they even enter the production line. By detecting these issues early, you can avoid costly malfunctions, batch losses, or unplanned production downtime. This rigorous control allows you to ensure smooth production and reliable finished products.

How can purity analysis prevent contamination risks in the cosmetics industry?

In the cosmetics industry, ingredient purity is essential to ensure consumer safety. Purity testing helps detect chemical impurities, heavy metal residues, and microbiological contaminants that may be present in formulations.

What are the benefits of purity analysis in the metallurgical industry?

Purity testing in the metallurgical industry verifies the chemical composition of alloys and detects impurities that could affect the strength and durability of materials. This ensures the quality of components used in demanding sectors such as aeronautics and automotive. Purity testing helps optimize material performance while meeting international standards.

What types of contaminants can be detected during a purity analysis of medical devices?

Purity testing of medical devices detects chemical, particulate, or microbiological contaminants that could affect the product's biocompatibility. The techniques used, such as electron microscopy and ICP-MS, comply with ISO 10993-18 and ISO 19227 standards and ensure that devices are free from harmful substances that could compromise patient health.

How does purity analysis help meet environmental standards in the chemical industry?

Purity analysis is essential in the chemical industry to detect traces of pollutants or toxic elements in products or waste. Purity analyses ensure that chemical products comply with environmental regulations, such as the REACH directive in Europe, by preventing the release of hazardous substances into the environment.

How important is material purity in the electronics industry?

In the electronics industry, material purity is important to prevent component failure. Even trace levels of impurities can impair the performance of semiconductors and other sensitive components. Purity analysis, particularly using ICP-MS and ion chromatography, helps ensure the quality of materials used and the reliability of finished products.

The filab advantages
A highly qualified team
A highly qualified team
Responsiveness in responding to and processing requests
Responsiveness in responding to and processing requests
A COFRAC ISO 17025 accredited laboratory
A COFRAC ISO 17025 accredited laboratory
(Staves available on www.cofrac.com - Accreditation number: 1-1793)
A complete analytical park of 5,200m²
A complete analytical park of 5,200m²
Tailor-made support
Tailor-made support
Anaïs DECAUX Customer Support Manager
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