CAS No 1973402-05-9 DOLUTEGRAVIR IMPURITY E Pharmaceutical Intermediates

- High Purity: Dolutegravir Impurity E is produced under strict quality control measures to ensure high purity suitable for pharmaceutical applications.

- Critical for Quality Control: This impurity is critical for the quality assessment of dolutegravir formulations to ensure compliance with regulatory standards.

- Multiple Applications: It is used in various drug formulations and research applications, particularly in the development of antiretroviral therapies.

- Integrating production and trading: As a factory integrating production and trading, we provide customers with competitive prices and reliable supply chain.

- Commitment to Quality: Our advanced manufacturing processes and quality assurance protocols ensure that every batch of Dolutegravir Impurity E meets the highest industry standards.

product details

Product details

Product detail

Dolutegravir Impurity E is a byproduct produced during the synthesis of dolutegravir, an integrase inhibitor used to treat HIV. Understanding and controlling impurities such as Dolutegravir Impurity E is critical for pharmaceutical manufacturers to ensure the safety, efficacy, and quality of their products. This impurity is particularly important in terms of regulatory compliance as it helps manufacturers meet the strict requirements set by health authorities.

138982-67-9 ZIPRASIDONE HYDROCHLORIDE 外包装3

product detail

CAS No.	40856-44-8
EINECS	609-874-3
Formula	C9H11NO2
Molecular Weight	165.19
Appearance	White to Off-White solid
Purity	≥98%
Type	Pharmaceutical Intermediates

Physical and Chemical Properties

Dolutegravir impurity E has several key physical and chemical properties that contribute to its effectiveness in pharmaceutical applications:

- Molecular formula: C20H19F2N3O5

- Molecular weight: 419.38 g/mol

- Appearance: Yellow solid

- Solubility: Soluble in organic solvents such as methanol and dimethyl sulfoxide (DMSO), with limited solubility in water, providing a wide range of formulation possibilities.

- Melting Point: Approximately 150-155 °C, indicating stability under standard laboratory conditions.

These properties not only enhance the performance of the drug formulation but also ensure that Dolutegravir Impurity E can be effectively utilized in various applications without compromising stability or efficacy.

Advantages

1. Quality Assurance: The presence of impurity E in dolutegravir is critical for quality control in the production of dolutegravir to ensure that the final product meets safety and efficacy standards.

2. Regulatory Compliance: Understanding and controlling impurities such as Impurity E in Dolutegravir is critical to complying with international regulatory standards, making it an essential component of drug development.

3. Multiple Research Applications: Dolutegravir Impurity E is used in multiple research applications including stability studies and formulation development, providing valuable insights into the behavior of dolutegravir in different environments.

4. Cost-effective: As a factory integrating production and trading, we have streamlined the operation process and provide competitive prices without compromising quality, making Dolutegravir Impurity E an economical choice for pharmaceutical companies.

5. Committed to R&D: Our dedicated research team is constantly exploring new applications and formulations for Dolutegravir Impurity E, ensuring we are always at the forefront of pharmaceutical innovation.

Committed to quality and innovation

Across our integrated facilities, we are committed to maintaining the highest standards of quality and innovation. Our state-of-the-art manufacturing facilities are equipped with advanced technologies that allow us to precisely and consistently produce Dolutegravir Impurity E. Our team of researchers and quality control experts work diligently to ensure that every batch of our product meets the highest standards of purity and potency.

We understand the importance of a reliable supply chain in the pharmaceutical industry. Therefore, we have built a strong logistics and distribution network to ensure timely delivery of products to customers around the world. Our customer-centric approach means we are always ready to work with our partners to meet their specific needs and requirements.

In summary

Dolutegravir Impurity E is the first choice for pharmaceutical manufacturers seeking a high-quality, potent and versatile impurity for quality control and research applications. With its superior physical and chemical properties, coupled with our commitment to quality and innovation, we are confident that Dolutegravir Impurity E will enhance your product offerings and meet the needs of the evolving pharmaceutical landscape. Choose Dolutegravir Impurity E for your next formulation and experience the difference in quality and performance.