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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-#-Bz0072-50mg Atorvastatin impurity 7 Product Name:Atorvastatin impurity 7 CAS No.:125971-94-0 Molecular Formula:
Product Number:PCL-#-Qu001-50mg Quetiapine EP impurity A Product Name:Quetiapine EP impurity A CAS No.:844639-07-2 Molecular Formula:
Product Number:PCL-#-Li115-100mg Linezolid impurity V Product Name:Linezolid impurity V CAS No.:496031-56-2 Molecular Formula:
Product Number:PCL-#-Bz0188-50mg Domperidone impurity B Product Name:Domperidone impurity B CAS No.:1346598-11-5 Molecular Formula:
Product Number:PCL-#-Az538-30mg Azithromycin EP impurity Q((3'-N-{[4- (acetyl) phenyl] sulfonyl }- 3'-(N,N- demethyl) azithromycin) Product Name:Azithromycin EP impurity Q((3'-N-{[4- (acetyl) phenyl] sulfonyl }- 3'-(N,N- demethyl) azithromycin) CAS No.:2095879-65-3 Molecular Formula:
Product Number:PCL-#-Bz0087-50mg Urapidil double oxidized impurity Product Name:Urapidil double oxidized impurity CAS No.:N/A Molecular Formula:
Product Number:PCL-#-Nd104-50mg N-Formyl-3,5-dimethyladamantane; N-Formyl-3,5-dimethyladamantane Hydrochloride Imp Product Name:N-Formyl-3,5-dimethyladamantane; N-Formyl-3,5-dimethyladamantane Hydrochloride Imp CAS No.:351329-88-9 Molecular Formula:
Product Number:PCL-#-Chp0335-50mg Fluoxetine hydrochloride impurity III (N-methyl-3-phenylpropylamine) Product Name:Fluoxetine hydrochloride impurity III (N-methyl-3-phenylpropylamine) CAS No.:30684-07-2 Molecular Formula:
Product Number:PCL-#-Bz0109-50mg Chlorpheniramine impurity R Product Name:Chlorpheniramine impurity R CAS No.:N/A Molecular Formula:
Product Number:PCL-#-Bz0425-50mg Nifedipine impurity 12 Product Name:Nifedipine impurity 12 CAS No.:34785-00-7 Molecular Formula:
Product Number:PCL-#-Ta102-50mg trans-4-Aminocyclohexanol Product Name:trans-4-Aminocyclohexanol CAS No.:27489-62-9 Molecular Formula:
Product Number:PCL-#-Ri121-20mg Rivaroxaban impurity A Product Name:Rivaroxaban impurity A CAS No.:898543-06-1 Molecular Formula:
Product Number:PCL-#-Pi115-25mg Pimovanserin Product Name:Pimovanserin CAS No.:706779-91-1 Molecular Formula:
Product Number:PCL-#-Ni021-100mg Nicorandil impurity C Product Name:Nicorandil impurity C CAS No.:88598-33-8 Molecular Formula:
Product Number:PCL-#-Me045-30mg 1-[1-(2,3-dimethylphenyl)-ethyl]-1H imidazole (impurity G) Product Name:1-[1-(2,3-dimethylphenyl)-ethyl]-1H imidazole (impurity G) CAS No.:2240179-63-7 Molecular Formula:
Product Number:PCL-#-To042-100mg Tofacitinib impurity A Product Name:Tofacitinib impurity A CAS No.:1092578-47-6 Molecular Formula:
Product Number:PCL-#-Bz0041-50mg Pantoprazole impurity 13 Product Name:Pantoprazole impurity 13 CAS No.:72830-07-0 Molecular Formula:
Product Number:PCL-#-Os104-100mg Methyl (3R,4R,5S)-4-acetamido-5-amino-3-(1-ethyl-propoxy)cyclohex-1-ene-1-carboxylate; Oseltamivir EP Impurity E Product Name:Methyl (3R,4R,5S)-4-acetamido-5-amino-3-(1-ethyl-propoxy)cyclohex-1-ene-1-carboxylate; Oseltamivir EP Impurity E CAS No.:208720-78-9 Molecular Formula:
Product Number:PCL-#-Ad103-50mg Adefovir impurity 1 Product Name:Adefovir impurity 1 CAS No.:1215101-40-8 Molecular Formula:
Product Number:PCL-#-Bz0154-50mg 4-hydroxy-2-methylquinoline Product Name:4-hydroxy-2-methylquinoline CAS No.:607-67-0 Molecular Formula:
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