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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-#-Ii108-50mg Ibuprofen EP impurity Q Product Name:Ibuprofen EP impurity Q CAS No.:36039-35-7 Molecular Formula:
Product Number:PCL-#-B512-100mg 1,2-bis(2-bromoethoxy)benzene Product Name:1,2-bis(2-bromoethoxy)benzene CAS No.:136383-33-0 Molecular Formula:
Product Number:PCL-#-Bz0136-50mg ethyl (1H-pyrazol-3-yl)acetate Product Name:ethyl (1H-pyrazol-3-yl)acetate CAS No.:82668-50-6 Molecular Formula:
Product Number:PCL-#-Os109-100mg Oseltamivir impurity 3; ethyl (1R,5R,6R)-5-(1-ethylpropoxy)-7-oxazolo[4.1.0]hept-3-ene-3-carboxylate Product Name:Oseltamivir impurity 3; ethyl (1R,5R,6R)-5-(1-ethylpropoxy)-7-oxazolo[4.1.0]hept-3-ene-3-carboxylate CAS No.:1266663-89-1 Molecular Formula:
Product Number:PCL-#-Nm336-25mg Esomeprazole sodium impurity III Product Name:Esomeprazole sodium impurity III CAS No.:784143-42-6 Molecular Formula:
Product Number:PCL-#-Cb100-50mg 4-chloro-1-butanol Product Name:4-chloro-1-butanol CAS No.:928-51-8 Molecular Formula:
Product Number:PCL-#-Mo022-100mg 1-Cyclopropyl-6-hydroxy-8-methoxy-7-(octahydropyrrolo[3,4-b]pyridin-6-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid(Moxifloxacin impurity RC-3) Product Name:1-Cyclopropyl-6-hydroxy-8-methoxy-7-(octahydropyrrolo[3,4-b]pyridin-6-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid(Moxifloxacin impurity RC-3) CAS No.:# Molecular Formula:
Product Number:PCL-#-Im101-20mg IndoRomalacetate Product Name:IndoRomalacetate CAS No.:753498-25-8 Molecular Formula:
Product Number:PCL-#-Bz0208-50mg Levocloxacinamide impurity Product Name:Levocloxacinamide impurity CAS No.:909779-33-5 Molecular Formula:
Product Number:PCL-#-Di074-100mg N,N'-dicyclohexylurea Product Name:N,N'-dicyclohexylurea CAS No.:2387-23-7 Molecular Formula:
Product Number:PCL-#-Bz0089-50mg Atropine sulfate EP impurity A Product Name:Atropine sulfate EP impurity A CAS No.:5978-81-4 Molecular Formula:
Product Number:PCL-#-To012-100mg Methyl-(4-methyl-piperidin-3-yl)-[7-(toluene-4-sulfonyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine (Tofacitinib impurity IM03-3) Product Name:Methyl-(4-methyl-piperidin-3-yl)-[7-(toluene-4-sulfonyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]-amine (Tofacitinib impurity IM03-3) CAS No.:N/A Molecular Formula:
Product Number:PCL-#-Bz0355-50mg Pabcilib Standard 012 Product Name:Pabcilib Standard 012 CAS No.:2206135-30-8 Molecular Formula:
Product Number:PCL-#-Am354-50mg 4-Amino-3,5-dichloropyridine Product Name:4-Amino-3,5-dichloropyridine CAS No.:22889-78-7 Molecular Formula:
Product Number:PCL-#-Bz0427-50mg Valsartan hydrolysis products Product Name:Valsartan hydrolysis products CAS No.:676129-92-3 Molecular Formula:
Product Number:PCL-#-Sa127-20mg Albuterol sulfate impurity J, Product Name:Albuterol sulfate impurity J, CAS No.:41489-89-8 Molecular Formula:
Product Number:PCL-#-Bz0242-50mg Atorvastatin impurity L Product Name:Atorvastatin impurity L CAS No.:873950-19-7 Molecular Formula:
Product Number:PCL-#-To038-10mg Tofacitib isomer impurity (TFC3-T1) Product Name:Tofacitib isomer impurity (TFC3-T1) CAS No.:2174011-55-1 Molecular Formula:
Product Number:PCL-#-Cp106-50mg Clindamycin phosphate impurity I Product Name:Clindamycin phosphate impurity I CAS No.:1309048-48-3 Molecular Formula:
Product Number:PCL-#-Di133-50mg dimethylammonioethyl methacrylate Product Name:dimethylammonioethyl methacrylate CAS No.:2867-47-2 Molecular Formula:
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