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Impurity reference standards

Impurity Reference Standards
Impurity reference standards are physical benchmarks for implementing pharmaceutical quality standards. They serve as critical carriers for metrological traceability, acting as specialized tools to assess drug quality, establish measurement baselines, determine drug authenticity and efficacy, and calibrate testing instruments and methodologies. Within national drug standards, they are state-issued reference materials for both quantitative and qualitative analysis of pharmaceuticals.

Primary Functions

  1.Quality Control Applications:
  • Used as standard substances for drug identification, purity testing, and content determination.
  • Function as specialized "measuring tools" that directly impact the accuracy and reproducibility of test results.
  2.Targeted Impurity Control:

  • Essential for increasingly stringent impurity profiling, including localization, quantification, and response factor determination of specific impurities mandated by modern pharmacopeial standards.


Selection Criteria

  1.Source Availability:
  • Common Process-Related Impurities (e.g., by-products) are typically obtainable from pharmacopeial authorities (USP, EP) or certified suppliers (e.g., LGC).
  • Unique or Rare Impurities often require in-house synthesis, extraction, or isolation. Such impurities lack commercially available reference standards and necessitate method development, validation, and calibration to enable accurate quantification in active pharmaceutical ingredients (APIs).
  2.Critical Parameters for Procurement:
  • Purity: The cornerstone of reference standard quality (e.g., ≥98% by HPLC).
  • Shelf Life: Indicates stability under specified storage conditions.
  • Documentation: Complete Certificate of Analysis (COA) and spectral data (e.g., NMR, LC-MS).
  • Supplier Credentials: ISO/IEC 17034 accreditation, GMP compliance, and traceability to international standards.
Hengyuan Fine Chemical’s PCL Impurity Reference Standards
  Hengyuan Fine Chemical supplies PCL-branded impurity reference standards with the following advantages:
  • Full Documentation: Batch-specific COA and spectral data provided.
  • Direct Manufacturing Supply: Eliminates intermediaries, ensuring cost-effectiveness and rapid delivery.
  • Comprehensive Portfolio: Covers a wide range of pharmacopeial and custom-synthesized impurities.
  • Regulatory Readiness: Supports compliance with ICH, USP, and ChP requirements.
Contact us for technical specifications or procurement inquiries.

Product Number Image Product Name CAS No. Molecular Formula
Product Number:PCL-#-Ri099-20mg 4,5 dichloro compound (rivaroxaban impurity 2) rivaroxaban impurity D Product Name:4,5 dichloro compound (rivaroxaban impurity 2) rivaroxaban impurity D CAS No.:1770812-37-7 Molecular Formula:
Product Number:PCL-#-Bz0138-50mg 5-amino-1,3-dihydroxytoluene Product Name:5-amino-1,3-dihydroxytoluene CAS No.:71176-54-0 Molecular Formula:
Product Number:PCL-#-Li098-25mg Lipoic acid impurity C Product Name:Lipoic acid impurity C CAS No.:462-20-4 Molecular Formula:
Product Number:PCL-#-Do056-25mg Donepezil impurity B Product Name:Donepezil impurity B CAS No.:120013-45-8 Molecular Formula:
Product Number:PCL-#-Ni005-100mg N-nitrosodiphenylamine Product Name:N-nitrosodiphenylamine CAS No.:86-30-6 Molecular Formula:
Product Number:PCL-#-Li012-50mg Lidocaine EP impurity A (2,6-dimethylaniline) Product Name:Lidocaine EP impurity A (2,6-dimethylaniline) CAS No.:87-62-7 Molecular Formula:
Product Number:PCL-#-To003-100mg Tofacitinib impurity J Product Name:Tofacitinib impurity J CAS No.:2328165-36-0 Molecular Formula:
Product Number:PCL-#-Me017-100mg N-methylaniline Product Name:N-methylaniline CAS No.:100-61-8 Molecular Formula:
Product Number:PCL-#-Ri026-50mg Rivaroxaban impurity G (5-chlorothiophene-2-carboxamide) Product Name:Rivaroxaban impurity G (5-chlorothiophene-2-carboxamide) CAS No.:97799-98-9 Molecular Formula:
Product Number:PCL-#-Su0312-50mg Methyl 2-methoxy-5-sulfamoylbenzoate; Product Name:Methyl 2-methoxy-5-sulfamoylbenzoate; CAS No.:33045-52-2 Molecular Formula:
Product Number:PCL-#-Gr101-100mg Granisetron EP impurity C; N-(3-lactam)-9-azabicyclo[3.3.1]non-3-yl-1-methyl-1H-indazole-3-carboxamide Product Name:Granisetron EP impurity C; N-(3-lactam)-9-azabicyclo[3.3.1]non-3-yl-1-methyl-1H-indazole-3-carboxamide CAS No.:160177-67-3 Molecular Formula:
Product Number:PCL-#-Ii110-25mg Ibuprofen EP impurity M Product Name:Ibuprofen EP impurity M CAS No.:60057-62-7 Molecular Formula:
Product Number:PCL-#-Ca043-50mg Carbol sulfonate sodium impurity 9 Product Name:Carbol sulfonate sodium impurity 9 CAS No.:70063-07-9 Molecular Formula:
Product Number:PCL-#-Bz0391-50mg Cefmetazole sodium catabolite II Product Name:Cefmetazole sodium catabolite II CAS No.:55817-29-3 Molecular Formula:
Product Number:PCL-#-Et374-50mg Ethyl 2-(1-imidazolyl)acetate Product Name:Ethyl 2-(1-imidazolyl)acetate CAS No.:17450-34-9 Molecular Formula:
Product Number:PCL-#-Li003-50mg Linezolid impurity H Product Name:Linezolid impurity H CAS No.:333753-69-8 Molecular Formula:
Product Number:PCL-#-Pr025-50mg Pranoprofen impurity I Product Name:Pranoprofen impurity I CAS No.:52549-44-7 Molecular Formula:
Product Number:PCL-#-Ap105-100mg Atropine sulfate impurity G Product Name:Atropine sulfate impurity G CAS No.:21956-47-8 Molecular Formula:
Product Number:PCL-#-Bz0122-50mg Terbutaline impurity 6 Product Name:Terbutaline impurity 6 CAS No.:882066-15-1 Molecular Formula:
Product Number:PCL-#-Az532-25mg Azithromycin EP impurity H; Azithromycin impurity III (impurity H) 3'-N-[[4-(acetylamino)phenyl]sulfonyl]-3'-N-desmethyl azithromycin Product Name:Azithromycin EP impurity H; Azithromycin impurity III (impurity H) 3'-N-[[4-(acetylamino)phenyl]sulfonyl]-3'-N-desmethyl azithromycin CAS No.:612069-30-4 Molecular Formula:
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