Olanzapine Reference Standard (CAS 132539-06-1) & Impurity Standards

To ensure accurate results in testing procedures, the use of high-purity Olanzapine reference standard (CAS 132539-06-1) and Olanzapine impurity standards is essential. Olanzapine is an atypical antipsychotic drug, belonging to the thienobenzodiazepine class and acting as a dopamine antagonist. It’s used in the treatment of schizophrenia and bipolar disorder.

We provide pharmaceutical reference standards solutions, including:

  • Olanzapine reference standard.
  • Pharmacopoeial and non-pharmacopoeial Olanzapine impurity standards.
  • Stable isotopes of Olanzapine.

Benefits of our products:

  • Ensure the highest purity and accuracy for your testing and manufacturing processes.
  • Support compliance with international pharmacopoeial standards.
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    Product Details

    Olanzapine Reference Standard (CAS 132539-06-1) and Impurity Standards

    Olanzapine, a crucial active pharmaceutical ingredient (API) in the treatment of mental disorders, is increasingly asserting its indispensable role in the healthcare sector. As a dopamine antagonist belonging to the thienobenzodiazepine class, Olanzapine is widely used in the treatment of schizophrenia and bipolar disorder. It is an atypical antipsychotic drug. To ensure the absolute therapeutic effectiveness and safety of the drug, strict quality control through the use of high-purity Olanzapine reference standards (CAS 132539-06-1) and Olanzapine impurity standards is extremely essential. This article will introduce a reliable solution for supplying reputable reference and impurity standards, meeting all the stringent requirements of the pharmaceutical industry.

    Detailed information about Olanzapine

    • Chemical Name: Olanzapine
    • CAS Number: 132539-06-1
    • Molecular Formula: C17H20N4S
    • Molecular Weight: 312.43
    • Synonyms: 2-Methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b][1,5]benzodiazepine; Integrol; LY 170053; Lanzac; Oleanz; Oliza; Oltal; Zyprexa
    • Classification: Intermediates, impurities, metabolites, pharmaceutical standards, pure chemicals
    • Appearance: Yellow solid
    • Storage Conditions: 2-8°C (refrigerator)

    Overriding Importance of Olanzapine Reference Standard and Olanzapine Impurity Standards

    In the field of pharmaceutical manufacturing and quality control, quality assurance is a crucial factor in ensuring product safety, efficacy, and regulatory compliance. For Olanzapine, the use of pharmaceutical reference standards and Olanzapine impurity standards plays an extremely important role in many aspects:

    • Qualitative and Quantitative Analysis: Olanzapine reference standard (CAS 132539-06-1) helps accurately determine the Olanzapine content in the final product, ensuring correct dosage and therapeutic efficacy.
    • Purity Control: Olanzapine impurity standards help assess the presence and content of impurities that may arise during synthesis or storage. Impurity control is mandatory to prevent undesirable substances from affecting the drug’s quality and safety.
    • Research and Development (R&D): Reference and impurity standards support the API synthesis process, formulation optimization, and stability testing of Olanzapine under various conditions.
    • Ensuring Compliance with International Pharmacopoeias: The use of pharmacopoeial reference and impurity standards is a mandatory requirement for pharmaceutical manufacturers to comply with stringent industry regulations, thereby ensuring that products are approved for global market circulation.

    Reliable Source for Olanzapine Reference and Impurity Standards

    We are proud to be a reputable supplier of high-quality Olanzapine reference standards (CAS 132539-06-1) and Olanzapine impurity standards, meeting all the stringent requirements of the pharmaceutical industry. Our product portfolio includes Olanzapine reference standards, and pharmacopoeial and non-pharmacopoeial impurities, as well as stable isotopes. Specifically:

    • Olanzapine Reference Standard: The purest form of the active ingredient for use as a primary reference standard.
    • Pharmacopoeial Impurities of Olanzapine: Includes impurities listed and controlled according to international pharmacopoeias.
    • Non-Pharmacopoeial Impurities of Olanzapine: Other impurities that may arise but are not officially listed in the pharmacopoeia, still requiring control to ensure product safety.
    • Stable Isotopes of Olanzapine: Isotopic versions of Olanzapine used in advanced research, mass spectrometry analysis, and bioavailability testing.

    Benefits of choosing our products:

    • Guaranteed Quality: All reference standards and impurity standards undergo rigorous testing, ensuring the highest purity and accuracy, accompanied by a complete Certificate of Analysis (CoA).
    • Diverse Product Range: Meeting all needs from research and development to manufacturing and quality control in pharmaceutical laboratories.
    • International Standard Compliance: Our products meet and exceed international standards, helping customers easily comply with regulations.
    • Fast Delivery: With readily available stock, we commit to prompt delivery, ensuring your production and testing processes are uninterrupted.
    • In-depth Technical Support: Our team of experienced specialists is always ready to provide dedicated technical consultation and support, ensuring customers use the products most effectively.
    • Optimal Storage and Transportation: Products are stored under ideal conditions (2-8°C) and transported under standard conditions to maintain the best quality from our warehouse to the customer.

    Contact Us Now to Elevate Your Pharmaceutical Quality

    Investing in high-quality Olanzapine reference standards (CAS 132539-06-1) and Olanzapine impurity standards is not just a mandatory requirement but also a key factor in ensuring the safety and efficacy of your pharmaceutical products. Let us be your trusted partner in the journey of quality control.

    Contact us now for a quote and detailed consultation on our Olanzapine reference standards and impurity standards – reliable solutions for every pharmaceutical laboratory and business.