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USP Testing for Castor Oil, Lanolin, Triclosan & Complex Excipients
Quantum Analytics Group has supported specialized USP testing for over 30 years, helping clients navigate difficult matrices, trace-level impurities, and highly specific compendial requirements with clear, defensible analytical data.
Rare Testing Capabilities
30+ years of specialized USP testing experience
One of the few labs capable of Triclosan impurity testing
Among a limited number of labs supporting Modified Lanolin USP testing
Trace impurity expertise for Lanolin and Modified Lanolin
WHY USP TESTING?
When Standard Testing Is Not Enough
Certain USP monographs require more than routine execution. They demand specialized instrumentation, deep method familiarity, and experience interpreting complex analytical requirements.
Complex
Matrices
Lipid-based, natural, modified, and antimicrobial materials require careful handling and method control.
Trace-Level Impurities
Specialized impurity testing demands sensitivity, selectivity, and strong analytical discipline.
Defensible Data
Clear, audit-ready reporting supports supplier qualification, release testing, investigations, and regulatory documentation.
TESTING
Castor Oil & Hydrogenated Castor Oil
USP-aligned testing for lipid-based raw materials.
Fatty Acid Composition by GC-FID
Triglyceride Composition by HPLC-ELSD
Ethylene Oxide and Dioxane
Limit of Ethylene Glycol & Diethylene Glycol
Limit of Nickel
LIMITED LABORATORY AVAILABILITY
Modified Lanolin & Lanolin
Specialized testing for complex natural and modified materials.
Quantum is among a limited number of laboratories capable of USP testing for Modified Lanolin.
Limit of Lanolin Alcohols
Limit of Foreign Substances
RARE CAPABILITY
Triclosan USP Impurity Testing
Trace-level impurity analysis for highly specialized requirements.
Quantum is one of the few laboratories capable of this level of Triclosan testing. Our scientists also contributed to the development of the organic impurities method in the USP monograph for Triclosan.
Monochlorophenols and 2,4-Dichlorophenol
1,3,7-Trichlorodibenzo-p-dioxin
2,8-Dichlorodibenzo-p-dioxin
2,8-Dichlorodibenzofuran
2,4,8-Trichlorodibenzofuran
Other organic impurities
WHY QUANTUM?
Experience You Can Rely On
Scientist-to-scientist communication
Fit-for-purpose analytical strategies
Advanced chromatographic and impurity analysis capabilities
Clear, defensible, audit-ready reporting
Long-term support for quality, regulatory, and supplier qualification teams
30+
Years supporting specialized USP testing for complex materials
Who We Support
Our specialized USP testing services support organizations that need reliable data for complex excipients and raw materials.
Pharmaceutical Manufacturers
Support for release testing, investigations, and regulatory documentation.
Excipient Suppliers
Testing support for qualification, specifications, and customer requirements.
Personal Care &
Cosmetics
Specialized testing for materials used in formulation and production.
CMOs & CDMOs
Analytical support for outsourced development and manufacturing workflows.
Raw Material Distributors
Documentation and testing support for customer and compliance requirements.
QA/QC & Regulatory Teams
Clear results to support confident decisions and audit readiness.
From Uncertainty to Clarity
A simple process designed to help you determine whether we can support your USP testing requirement quickly and confidently.
01.
Technical Consultation
We review your material, USP monograph, testing requirement, specification, timeline, and documentation needs.
02.
Specialized Method Execution
Our scientists apply the appropriate analytical methods, instrumentation, controls, and expertise.
03.
Clear, Actionable Results
You receive defensible analytical data and technical support to move your project forward.
Frequently asked questions
No. For Triclosan, testing for chlorinated dioxins, furans, chlorophenolics and related trace impurities requires specialized capability, sensitivity, and experience. Quantum Analytics Group is one of the few laboratories capable of supporting these specialized Triclosan analyses. We bring over 25 years of expertise in this area.
Modified Lanolin and Lanolin are complex materials with natural variability. Accurate testing requires method familiarity, matrix experience, and careful interpretation.
Yes. Our testing supports supplier qualification, incoming raw material release, quality investigations, and regulatory documentation.
Quantum supports USP-aligned methods including GC-FID for fatty acid composition and HPLC-ELSD for triglyceride composition, along with testing for ethylene oxide, dioxane, ethylene glycol and diethylene glycol, and Limit of Nickel (by GFAAS).