CAS No 2244161-73-5 DOLUTEGRAVIR IMPURITY Pharmaceutical Intermediates

Product name	DOLUTEGRAVIR IMPURITY
CAS No.	2244161-73-5
EINECS	/
Formula	C28H24F4N4O6
Molecular Weight	588.51
Purity	≥98%
Type	Pharmaceutical Intermediates

- High Purity Standard: DOLUTEGRAVIR IMPURITY is produced under strict quality control, ensuring minimal contamination and high reliability for pharmaceutical applications.
- Quality Control is Critical: Mainly used in the development and testing of DOLUTEGRAVIR formulas, it plays a vital role in ensuring product safety and effectiveness.
- Integrated Production and Trading: As a production and trading integrated factory, we provide a seamless supply chain from manufacturing to delivery.
- Regulatory Compliance: Our products comply with all necessary industry regulations and standards, ensuring customer safety and reliability.
- Expertise and Experience: With many years of experience in the pharmaceutical industry, we are committed to quality and customer satisfaction.

product details

Product details

introduce

DOLUTEGRAVIR Impurity is a critical ingredient in the pharmaceutical industry, particularly in the development and quality control of DOLUTEGRAVIR, an antiretroviral drug used to treat HIV. As a by-product of DOLUTEGRAVIR synthesis, this impurity is critical to ensure that the final product meets the required safety and efficacy standards. Our DOLUTEGRAVIR Impurity is manufactured in a state-of-the-art facility, ensuring that every batch meets the highest quality standards.

Physical and chemical properties

- Molecular formula: C28H24F4N4O6
- Molecular weight: 588.51 g/mol
- Solubility: Soluble in organic solvents, limited solubility in water, flexible formulation.
- Stability: Demonstrates good stability under standard storage conditions, which is critical to maintaining the integrity of the drug product.

advantage

- Quality Assurance: DOLUTEGRAVIR Impurities is critical to the quality control process of DOLUTEGRAVIR formulations. It helps identify and quantify impurities to ensure that the final product is safe for patients.
- Regulatory Compliance: Regulatory agencies often require detection of dolutegravir impurities as part of testing protocols. This ensures that pharmaceutical companies can meet the stringent requirements for drug approval and market access.
- Enhanced formulation development: Understanding the behavior of dolutegravir impurities can help formulators optimize their processes to produce more effective and safer drugs.
- Cost-effective solution: By providing high-quality Dolutegravir impurities, we help pharmaceutical companies reduce the risk of costly recalls and rework due to quality issues.
- Expert Support: Our team of experts can assist customers in understanding the impact of DOLUTEGRAVIR impurities in their formulations and provide valuable insights and support throughout the development process.

Uses in the pharmaceutical industry

In conclusion,DOLUTEGRAVIR Impurities are an essential ingredient for pharmaceutical manufacturers focused on developing high-quality DOLUTEGRAVIR formulations. It is a key ingredient in the pharmaceutical industry due to its excellent physical and chemical properties, and the recognized role it plays in quality assurance and regulatory compliance. Partner with us to enhance your pharmaceutical products and meet the growing demand for high-quality antiretroviral drugs. Contact us today to learn more about our DOLUTEGRAVIR Impurities and how we can support your business needs.