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Postion:Product Catalog >Pharmaceutical intermediates>Heterocyclic compound>7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione
7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione
  • 7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione
  • 7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione
  • 7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione

7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione NEW

Price Get Latest Price
Package 1kg 25kg
Min. Order: 1kg
Supply Ability: 850kg
Update Time: 2025-05-08

Product Details

Product Name: 7-(Benzyloxy)-3,4,12,12a-tetrahydro-1H-[1,4]oxazino[3,4-c]pyrido[2,1-f][1,2,4]triazine-6,8-dione CAS No.: 1370250-39-7
Min. Order: 1kg Purity: 0.99
Supply Ability: 850kg Release date: 2025/05/08

?Baloxavir Intermediate (CAS 1370250-39-7)?
Google Keywords: Baloxavir Intermediate, CAS 1370250-39-7, Antiviral API Synthesis, Influenza Drug Production, GMP Pharmaceutical Intermediates


?? ?Product Overview?

?Baloxavir Intermediate? (CAS 1370250-39-7) is a high-purity chemical intermediate essential for synthesizing ?Baloxavir Marboxil?, a groundbreaking antiviral API used to treat influenza A and B infections. This intermediate enables precise and scalable manufacturing of the drug, ensuring compliance with stringent pharmaceutical quality standards.

  1. ?Primary Function?: Facilitates efficient synthesis of Baloxavir Marboxil with controlled impurity profiles.

  2. ?Applications?: Antiviral drug production, clinical trial material preparation, and generic API development.


? ?Key Advantages?

?? ?Ultra-High Purity? | ≥99.0% (HPLC/GC verified) | Residual solvents <50 ppm.
?? ?Regulatory Compliance? | Aligns with ICH Q11 guidelines and GMP requirements for intermediates.
?? ?Scalability? | Validated for consistent performance in commercial-scale API manufacturing.


?? ?Applications?

  • ?Influenza Therapeutics?: Critical for synthesizing Baloxavir Marboxil, a single-dose oral antiviral.

  • ?Clinical Development?: Supports formulation studies and stability testing for regulatory submissions.

  • ?Generic Drug Manufacturing?: Enables cost-effective production post-patent expiration.


?? ?Quality Assurance?

  • ?Testing Methods?: HPLC, GC, NMR, and LC-MS for identity, purity, and impurity analysis.

  • ?Standards?: Complies with USP <1086>, EP 10.0, and ISO 9001:2015 certified processes.


?? ?Market Trends?

The global ?antiviral drug market? is projected to reach ?$78.5 billion by 2030? (CAGR 4.3%), driven by rising influenza outbreaks and demand for novel therapies like Baloxavir. This intermediate addresses the growing need for efficient, scalable API production in pandemic preparedness.


Drive innovation in antiviral drug development with Baloxavir Intermediate – precision, compliance, and scalability for global health solutions.


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Company Profile Introduction

Wuhan Biocar Pharmaceutical Co., Ltd. is a high-tech and innovative enterprise specializing in the research, development, production, and sales of APIs and pharmaceutical intermediates (excluding finished drugs). Located in the heart of Optics Valley Biological City, our company leverages the cutting-edge facilities of the Wuhan University Scientific Research Laboratory and benefits from the region's favorable policies to advance the field of biomedicine. Guided by our business philosophy—"Driven by market demand, powered by technological innovation, and enabled by e-commerce"—we are committed to delivering biomedical products that are precise, high-quality, fast, and reliable. Our offerings serve pharmaceutical companies, university research institutions, hospital outpatient services, reagent providers, and distributors worldwide.

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