Nuclear Magnetic Resonance (NMR) Spectroscopy in Pharmaceutical Analysis
Meet regulatory requirements and ensure product quality through our comprehensive Nuclear Magnetic Resonance (NMR) Spectroscopy in Pharmaceutical Analysis services. From compound verification to impurity testing, our cGMP-compliant NMR solutions deliver precise structural analysis and quantitative measurements that accelerate your pharmaceutical development process while maintaining compliance standards.

What is Nuclear Magnetic Resonance (NMR) Spectroscopy in Pharmaceutical Analysis at Element?
NMR Spectroscopy is an advanced analytical technique that provides detailed information about molecular covalent structure, stereochemistry, and conformation. At Element, we provide cGMP-compliant NMR services that enable verification of chemical synthesis, compound characterization, and impurity analysis, ensuring your product meets regulatory requirements while supporting critical stages of your pharmaceutical development process.
What can Element offer you for NMR in Pharmaceutical Analysis?
Materials we test
Materials we test
Our NMR analysis capabilities cover a wide range of pharmaceutical materials, from APIs to complex polymers. We specialize in analyzing biodegradable polymers, polysaccharides, synthetic peptides, and various pharmaceutical compounds, providing you with comprehensive structural and quantitative data.
Key tests offered
Key tests offered
- Complete structural elucidations
- Impurity determinations
- Co-monomer ratio analysis
- Residual monomer analysis
- Degree of substitution measurements
- Weight percent analysis
- Sequence confirmation
Methods and solutions offered
Methods and solutions offered
Our Nuclear Magnetic Resonance Spectroscopy services include:
- Heparin Sodium impurity determinations
- Identification, co-monomer ratios and residual monomer analysis of biodegradable polymers such as PLGA
- Determination of weight percent oxyethylene in poloxamers
- Olefins in crude oils and condensates
- Deacetylation degree of polysaccharides such as Chitosan
- Confirmation of synthetic peptide sequence
- Complete structural elucidations of Active Pharmaceutical Ingredients (API) and naturally occurring compound and in-process impurities
- Structural elucidations studies involve 1D, 1H, 13C, 31P and 19F NMR in combination with 2D {1H, 1H} (COSY, TOCSY, NOESY), 2D {1H, 13C} and {1H, 15N} HSQC and HMBC and 2D {19F, 13C} HSMBC experiments.
We employ multiple NMR techniques including:
- 1D, 1H, 13C, 31P and 19F NMR
- 2D {1H, 1H} (COSY, TOCSY, NOESY)
- 2D {1H, 13C} and {1H, 15N} HSQC and HMBC
- 2D {19F, 13C} HSMBC experiments
Which labs offer this service
Which labs offer this service
Our team operates from Life Sciences hubs across the world, providing global access to our expert capabilities. Find your nearest Life Sciences hub on our Locations Page.
Complex mixture analysis expertise
Complex mixture analysis expertise
Our NMR capabilities extend beyond single-compound analysis to analyze complex mixtures of compounds that are often amenable to NMR analysis, giving you comprehensive insights into multi-component pharmaceutical formulations. This capability is particularly valuable when dealing with combination products or investigating impurity profiles.
Materials we test
Pharmaceutical Materials:
- Active Pharmaceutical Ingredients (APIs)
- Drug substances
- Excipients
- Natural compounds
- In-process impurities
Polymers:
- Biodegradable polymers (PLGA)
- Poloxamers
- Polysaccharides (Chitosan)
- Synthetic peptides
Other:
- Heparin Sodium
- Crude oils and condensates
Your Challenges, Our Solutions
Regulatory Compliance Concerns
Quality Assurance Complexity
Complex Structural Analysis Needs
Precise Measurement Requirements
Why Choose Element
Complete GMP Compliance
Comprehensive Analysis Capabilities
Expert Support Throughout Development
Precision-Focused Results

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