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Everolimus, Reference Standards

 :   USP
Everolimus, Reference Standards
 :  USP
 
Everolimus, Reference Standards

 

 

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

Everolimus System Suitability Mixture: This is a mixture of everolimus, everolimus oxepane isomer and 9-O-hydroxyethyl sirolimus

 : US Pharmacopea Reference Standard

 

 

 

  • Catalog No:
  • 1268976.
  • 1268987.
  • Popis:
  • Everolimus
  • Everolimus System Suitability Mixture
  • Čí. CAS:
  • 159351-69-6
  • Č. UN:
  • 3077
  • 3077

 

Product Family Options

 

  • Popis
    Standard
    Typ balení
    Bal.
     
     
  • Everolimus
    USP reference standard
    Vial
    300 mg
       
       
    1 * 300 mg
    1 * 300 mg - 58 830,00 Kč
    58 830,00 Kč
    1 * 300 mg
       58 830,00 Kč

     
     
    Specifications
    Cat. No.
    1268976.
    Popis
    Everolimus
    Čí. CAS
    159351-69-6
    Č. UN
    3077
  • Everolimus System Suitability Mixture
    USP reference standard
    Vial
    25 mg
       
       
    1 * 25 mg
    1 * 25 mg - 63 020,00 Kč
    63 020,00 Kč
    1 * 25 mg
       63 020,00 Kč

     
     
    Specifications
    Cat. No.
    1268987.
    Popis
    Everolimus System Suitability Mixture
    Čí. CAS
    Č. UN
    3077