Contract preparative HPLC purification services

Precision purification of natural compounds, APIs and impurities through preparative HPLC. From sample receipt to purified material and CoA, managed by a PhD-level analytical team in Lugo, Spain.

ENAC-accredited producer

Nº 2/PMR003
Catalogue

About the service

CIFGA offers a contract purification service based on extensive experience in the purification of complex mixtures and natural extracts. The service specialises in precision purification through preparative HPLC, targeting purity above 95% where technically feasible with the analytical documentation laboratories need for research, development and regulatory purposes.

All projects are managed with direct communication between client and analyst from initial enquiry through to final delivery. Confidentiality agreements are available before any technical discussion begins.

Who uses this service

The service is used by laboratories and organisations across several sectors:

  • Pharmaceutical manufacturers and CROs requiring impurity isolation for regulatory submissions, unknown impurity characterisation, or API purification ahead of formulation development.
  • Analytical laboratories developing in-house reference standards for compounds not available in any commercial catalogue. Purified material can be further characterised by qNMR and issued with a CoA documenting purity and structural identity.
  • Universities and research centres isolating biologically active natural products or fractionating complex extracts for activity or bioassay studies.
  • Standard developers across food, textile, cosmetic, environmental and pharmaceutical sectors requiring purified compounds as the starting point for certified reference material production.

Applications

The service covers a broad range of purification objectives:

  • Cost-efficient purification of natural compounds
  • Isolation of biologically active natural products
  • Drug development: API and impurities purification
  • Unknown impurity identification, isolation and characterisation
  • Purification of synthesis products
  • Purification of target organic compounds from chemical reactions
  • Low-pressure, cost-effective fractionation for activity or bioassay studies
  • Plant-based extract fractionation
  • Development of analytical standards for food, textile, cosmetic, pharmaceutical, environmental and research applications


Sample quantities accepted: 5 mg to 50 g. Laboratories with requirements outside that range are welcome to contact the team to discuss feasibility.

Analytical equipment

The service is supported by a full suite of chromatographic and spectroscopic instrumentation for both preparative separation and structural characterisation.

NMR Varian 500 MHz and NMR Bruker 750 MHz For NMR analyses: 1H, 13C, DEPT, COSY, HMBC, HSQC. The Bruker 750 MHz provides high-resolution NMR data, supporting structural elucidation, and qNMR purity assignments.

Preparative HPLC System of Waters Autosampler and fraction collector coupled to a Waters 3100 single quadrupole mass detector. Core instrument for preparative separations with mass-directed fraction collection. The system can also be configured with UV or FLD detection.

UPLC Waters Acquity Equipped with XEVO TQMS. Used for UPLC/MS/MS analyses supporting impurity identification and purity confirmation.

HPLC Waters Alliance Equipped with a Waters dual absorbance detector.

Service flow

1
On-demand enquiry

Contact the team with details of your compound and purification objective. A confidentiality agreement can be arranged before technical discussions begin.

2
Technical evaluation

The team evaluates available options and presents a method strategy with expected purity outcomes. Concept testing is available to assess feasibility before committing to a full run, particularly useful when working with novel or complex starting materials.. A timeline and quote are sent for client approval.

3
Sample dispatch

Samples are sent to CIFGA’s facility in Lugo, Spain. Required quantity: 5 mg to 50 g. Please provide information on sample condition, solubility, handling requirements and any known toxicity before dispatch.

4
Purification and follow-up

The team runs the purification and maintains direct contact with the client throughout. The service typically targets purity above 95%, depending on sample complexity and project feasibility. Specific purity requirements can be agreed at the evaluation stage.

5
Open communication

The client is welcome to contact the team at any stage of the process.

6
Delivery

Purified material is returned with an analysis report or Certificate of Analysis (CoA) documenting purity, structural identity and the analytical methods used.

A typical impurity isolation project illustrates the process: a synthesis product containing a target compound at 60–70% purity in a complex matrix is received, a preparative HPLC method is developed, and after the purification run the isolated compound is confirmed by NMR and delivered with a CoA documenting purity above 95%.

Complementary analytical services

Beyond preparative purification, the team offers a range of analytical services that can be requested independently or as part of a combined project:

  • NMR structure elucidation: from small molecules to complex compounds
  • Quantitative NMR (qNMR): absolute purity determination, applicable to isolated compounds and reference standard development
  • Safety data sheets (SDS): documentation service
  • Chemical and physical stability studies: long-term stability and forced degradation studies
FAQ

Frequently asked questions

What purity level does the service achieve?

The standard target is above 95% purity. Higher purity requirements can be discussed at the project evaluation stage, depending on matrix complexity and the intended use of the purified material.

Timelines depend on the complexity of the separation and the characterisation scope agreed. Where concept testing is recommended, timing is confirmed during the technical evaluation stage. Full purification projects are scoped individually at the evaluation stage, and a timeline is provided with the initial quote.

Yes. A confidentiality agreement is signed before any technical discussion. Clients working with proprietary compounds or unpublished structures can request NDA terms at the initial enquiry stage.

Yes. Purification for standard development is one of the established applications of the service. Purified material can be further characterised by qNMR to assign purity values, with a CoA documenting the analytical basis for those values.

Useful information includes: compound name or structure, matrix, known solubility and stability data, quantity of starting material available, purity target, and intended downstream use.

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