AquigenBio Expands Ibuprofen Impurity Standards Portfolio for Advanced Pharmaceutical Testing

AquigenBio, a trusted global provider of high-quality impurity standards and reference materials, has announced the expansion of its Ibuprofen Impurity Standards portfolio. These new offerings are designed to meet the growing demand for precise analytical tools in pharmaceutical research, quality control, and regulatory compliance.
The updated category now includes specialized impurity standards for Ibuprofen and its related compounds, delivering high-purity reference materials that meet stringent industry and regulatory requirements.

Newly Featured Ibuprofen Impurity Standards
(S)-Ibuprofen-D3
A deuterated internal standard ideal for LC-MS/MS quantitation and stability testing. Its isotopic labeling ensures accuracy and reproducibility in complex analytical methods.
👉 https://aquigenbio.com/product/s-ibuprofen-d3/

(S)-Ibuprofen Isopropyl Ester
Commonly used in degradation pathway studies and formulation stability analysis, this ester derivative helps identify and control esterification-related impurities in Ibuprofen formulations.
👉 https://aquigenbio.com/product/s-ibuprofen-isopropyl-ester/

(R,S)-N-(1-Phenylethyl) Ibuprofen Amide
A key impurity reference standard used in API synthesis monitoring and impurity profiling. This standard aids laboratories in meeting stringent pharmacopeial and regulatory guidelines.
👉 https://aquigenbio.com/product/rs-n-1-phenylethyl-ibuprofen-amide/

Why These Standards Matter
Ibuprofen, one of the most widely used non-steroidal anti-inflammatory drugs (NSAIDs), must adhere to strict quality and safety standards. Impurities-whether process-related, degradation products, or stereoisomeric variants-can impact efficacy and safety, making accurate detection and quantification crucial.
AquigenBio's Regulatory-Grade Impurity Standards are manufactured under controlled conditions and supplied with:
Comprehensive Certificates of Analysis (COAs)

Detailed analytical data, including HPLC purity, NMR, and mass spectrometry profiles

Batch-specific documentation to support regulatory filings such as ANDAs

Stability data to ensure long shelf life and consistent results

Applications Across the Pharmaceutical Value Chain
These Ibuprofen impurity standards can be integrated into:
Analytical Method Development & Validation (AMV)

Routine Quality Control (QC) Testing

Stability Studies for shelf-life prediction

Regulatory Submissions (USP, EP, ICH guidelines)

Forensic and Bioanalytical Studies

By offering both parent drug standards and related impurities, AquigenBio enables end-to-end analytical coverage, ensuring that drug manufacturers, CROs, and regulatory labs can meet the highest quality benchmarks.

AquigenBio's Commitment to Excellence
With a mission to bridge the gap between analytical needs and high-quality reference materials, AquigenBio continues to invest in research, quality assurance, and global supply chain efficiency. All products undergo stringent ISO-compliant quality checks before shipment, ensuring that customers receive only the highest purity standards.

Aquigen Bio Sciences
281/1, Plot No 41,
Hinjawadi - Pirangut Rd,
Kasar Amboli, Pirangut,
Pune, Maharashtra 412108
Visit: www.aquigenbio.com

Aquigen Bio is a leading provider of certified reference standards, impurity profiling compounds, and research chemicals to pharma, biotech, and academic institutions worldwide. With a dedication to excellence and a focus on regulatory readiness, Aquigen empowers scientists to innovate with confidence.

This release was published on openPR.