Polymeric Additives Research Group, Stuttgart, Germany
July 14, 2026
Chemical Products Testing
InquiryThrough our global network of testing experts and analytical equipment including chromatography (HPLC, GC, GC/MS) and atomic absorption spectroscopy (AAS, GFA, FIAS), Our goal is to provide test services as efficiently as possible to maximize our customers' profits. For more information about our services, contact one of our experts today.
Note: this service is for Research Use Only and Not intended for clinical use.
Alfa Chemistry chemicals analysis is a leading testing service in composition analysis, content detection, formula detection of chemicals. Chemical products are inseparable from our daily lives or industrial production, but not all chemicals meet the requirements of daily use and industrial production. So it is important to ensure they are produced efficiently and in compliance to regulatory standards. Alfa Chemistry, as a provider of inspection services that enjoys the worldwide reputation, we work with all the important international standards and guidelines including ISO, GOST, USDA and FDA to offer a variety of chemical products analysis.
Alfa Chemistry has many analytical techniques and equipment for chemicals to provide you with tailor-made services that exceed expectations and straightforwardly solve your local and global challenges.
The chemical products can be analyzed by Alfa Chemistry include:
Chemical raw materials
➢ Inorganic raw materials (Inorganic salts, non-metallic minerals, inorganic bases, inorganic acids, industrial gases)
➢ Organic raw materials(Alkanes and their derivatives, olefins and their derivatives, alkynes and derivatives, heterocycles, carboxylic acids and derivatives, aromatic hydrocarbons and derivatives) etc.
Resin
➢ Epoxy resin, acrylic resin, alkyd resin, silicone resin, ion exchange resin, etc.
Industrial chemicals
➢ Pesticide (Insecticides, herbicides, fungicides, plant growth regulators, biological pesticides)
➢ Fertilizer (Biological fertilizer, compound fertilizer, phosphate fertilizer, potassium fertilizer and nitrogen fertilizer)
➢ Petrochemical products, adhesives & sealantspigments, coating & paint, inks, etc.
Daily chemicals
➢ Washing powder, toothpaste, soap, hand sanitizer, etc.
Chemical Auxiliary
➢ Additives, adhesives, plasticizers, catalysts, plasticizers, fixing agents, defoamers, waterproofing agents, etc.
Chemical Reagent
➢ Inorganic chemical reagents, organic chemical reagents, reference reagents, etc.
Detergent and Cleaner
➢ Industrial cleaning agent (cutting fluid, brightener, ultrasonic cleaning agent)
➢ Civil cleaning agent (washing powder, laundry detergent, car air conditioner cleaning agent, stainless steel cleaning agent)
➢ Water-based cleaning agent (soap, electroplating agent, rust removal cleaning agent, water-based metal cleaning agent)
Solvent cleaning agent (phosphating solution, paint remover)
The testing services for chemical products include:
| Services | Testing items |
|---|---|
| Inorganic performance testing | Compound content, moisture, chloride, heavy metal content, ignition residue, pH value, boiling point, melting point, insoluble content, density, whiteness, volatile at 105°C, residue on sieve, oil absorption, particle size distribution, determination of activation, bulk density, etc. |
| Organic performance testing | Purity and impurity content, acidity, moisture, chromaticity, evaporation residue, crystallization point, hydroxyl compounds, polymerization inhibitors, peroxides, pH value, total aldehyde content, boiling range, boiling point, melting point, alcohol content, density, etc. |
| Component analysis | Composition analysis, formula analysis, qualitative analysis, quantitative analysis, chemical composition analysis, deformulation analysis, etc. |
Why do you need a chemical products testing report?
For sale. According to the third-party test report, you can make your products show certain advantages in sales.
Improve product quality. Through the test report, find out the problems of products, improve the quality of products and reduce the production cost.
Research and development. Some problems encountered in the R&D process can be solved according to some data of the test report, so as to shorten the R&D cycle.
Import and export of products.
Product quality control.
Techniques for chemical products testing
Gas chromatography
Used to separate and analyze volatile compounds in a sample.
Mass spectrometry
Used to identify and quantify chemical compounds in a sample.
Infrared spectroscopy
Used to identify functional groups in organic compounds.
UV-Vis spectroscopy
Used to analyze the absorption or transmission of light by a sample.
Nuclear magnetic resonance (NMR) spectroscopy
Used to determine the structure and molecular composition of a sample.
High-performance liquid chromatography (HPLC)
Used to separate and quantify compounds in a sample based on their interaction with a liquid mobile phase.
Fourier transform infrared spectroscopy (FTIR)
Used to identify chemical compounds based on their infrared absorption spectra.
Differential scanning calorimetry (DSC)
Used to study the thermal properties of a sample, such as melting and boiling points.
X-ray diffraction
Used to determine the crystalline structure of a material.
Titrators
Used to determine the concentration of a specific chemical in a sample through a titration process.
Industry articlesFAQsCustomer Reviews
Determination of Chemical Purity and Analysis of Menaquinone-7 (MK7)
Jedynak, Łukasz, et al. Journal of Pharmaceutical and Biomedical Analysis 135 (2017): 116-125.
The synthesis of menaquinone-7 (MK7) is a complex process that may produce many different MK7 isomers. The chromatographic behavior of these isomers is very similar, requiring the use of a chromatographic column with high selectivity for these similar compounds.
An HPLC method using a C30 reversed-phase analytical column with UV detection was developed to determine the chemical purity and analyze menaquinone-7 (MK7) in a single chromatographic run. This method allows for the separation and quantification of MK7 in the presence of its isomers.
Enantioselective Separation and Determination of Ibuprofen
Vashistha, Vinod Kumar, et al. Chirality 36.2 (2024): e23647.
Ibuprofen (IBP) is the 29th most prescribed drug in the United States in 2019 and is a widely used non-steroidal anti-inflammatory drug (NSAID) composed of two enantiomers, (R)-IBP and (S)-IBP, collectively referred to as (RS)-IBP. The enantioselective separation and determination of IBP enantiomers are crucial for pharmaceutical and clinical applications.
Chromatographic techniques used for the separation and determination of ibuprofen enantiomers include high-performance liquid chromatography (HPLC), gas chromatography (GC), liquid chromatography-tandem mass spectrometry (LC-MS/MS), and other techniques.
Analysis of Major Impurities in Ultra-Pure Bisphenol A
Krämer, Anke, Peter Bauer, and Felix H. Schacher. Journal of Chromatography A 1677 (2022): 463293.
Although the use of bisphenol A (BPA) and the production of polycarbonate (PC) through a condensation process are well-known, and the research on these processes has been ongoing for over 60 years, the understanding and quantification of side reactions during the polymerization process are still unresolved issues. Particularly, the purity of the raw material BPA greatly affects the properties of the resulting polymer.
A simple and reliable reversed-phase separation method has been developed for the separation of seven known bisphenol A (BPA) impurities, including 4-isopropenylphenol and its dimer isomers, o-, p-BPA, and triphenol. The method was validated using triple quadrupole mass spectrometry (qqqMS) and diode array detection (DAD).
What are the standard turnaround times (TAT) for routine chemical product testing, and how does expedited processing work?
Standard turnaround times typically range from 5 to 10 business days upon receipt and logging of the sample, depending on the analytical techniques required (e.g., HPLC, GC-MS, ICP-OES). For urgent projects, we offer expedited priority testing that reduces lead times significantly. Our project managers coordinate directly with the lab to fast-track sample preparation and analysis without compromising precision or data integrity.
What sample quantity and condition requirements must be met before submitting a batch for analysis?
Required sample quantities vary based on the number of assays requested and the detection limits needed, but generally, 10 to 50 grams (or milliliters) are sufficient for a comprehensive suite of tests. Samples must be chemically stable, properly labeled with a unique identifier, and accompanied by a completed chain-of-custody form and Safety Data Sheet (SDS) where applicable. Specific storage conditions—such as refrigeration or light-sensitive packaging—must be maintained during transit.
How do you ensure data accuracy, instrument calibration, and compliance with recognized analytical standards?
All analytical workflows operate under strict quality management systems aligned with ISO/IEC 17025 principles. Instruments undergo routine calibration using certified reference materials, and every analytical batch includes method blanks, matrix spikes, and duplicate samples for quality control. Our chemists follow validated methodologies published by ASTM, ISO, EPA, or pharmacopoeial bodies, and final data packages undergo a multi-tier review before release.
Can custom test methods be developed or validated for proprietary chemical formulations and non-standard matrices?
Yes. When standard methods do not fit novel or complex formulations, our method development and validation team collaborates closely with clients to design customized analytical protocols. We establish method specificity, linearity, limit of detection (LOD), limit of quantification (LOQ), accuracy, and robustness, providing a full validation report suited for regulatory submissions or internal quality assurance.
What format is used for final analytical reports, and how are raw data and out-of-specification results handled?
Final reports are delivered securely in digital PDF format containing clear method summaries, instrument parameters, quantified results, chromatograms or spectra where applicable, and a statement of compliance or uncertainty. In the event of out-of-specification (OOS) or unexpected results, our technical team halts the reporting process, investigates potential laboratory-induced anomalies, and notifies the client immediately to discuss root-cause analysis and retesting options.
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"We contracted the team to perform structural verification and impurity profiling on a series of newly synthesized organophosphorus flame retardants using high-resolution NMR and LC-MS. The turnaround was exceptionally fast, and the data package included detailed spectral overlays and integration tables that saved our internal team weeks of troubleshooting. Excellent scientific communication throughout the project."
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"Dealing with complex surfactant mixtures often leads to poor chromatographic separation, but their analytical team successfully resolved our co-eluting peaks using optimized HPLC-ELSD parameters. The resulting purity assay data and moisture content quantification met all our internal specifications for European market export. Highly professional technical support and reliable reporting."
Specialty Surfactants Corp., New Jersey, USA
June 28, 2026
⭐⭐⭐⭐⭐
"We needed independent heavy metal screening and volatile organic compound (VOC) residual testing for a new bio-based epoxy resin formulation. The lab provided clear guidance on sample packaging and delivered the ICP-MS and headspace GC-MS reports within our tight project window. The clarity of the calibration data and method references gave our quality assurance department total confidence."
CleanTech Coatings Ltd., Manchester, UK
May 19, 2026
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