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Postion:Product Catalog >Organic Chemistry>Amides>Amino compound>2-(2-aminoethoxy)-1,1-dimethoxyethane
2-(2-aminoethoxy)-1,1-dimethoxyethane
  • 2-(2-aminoethoxy)-1,1-dimethoxyethane
  • 2-(2-aminoethoxy)-1,1-dimethoxyethane
  • 2-(2-aminoethoxy)-1,1-dimethoxyethane

2-(2-aminoethoxy)-1,1-dimethoxyethane NEW

Price Get Latest Price
Package 1kg 25kg
Min. Order: 1kg
Supply Ability: 600kg
Update Time: 2025-07-23

Product Details

Product Name: 2-(2-aminoethoxy)-1,1-dimethoxyethane CAS No.: 1228258-40-9
Min. Order: 1kg Purity: 0.99
Supply Ability: 600kg Release date: 2025/07/23

Baloxavir Marboxil Intermediate (CAS 1228258-40-9)?
Google Keywords: Baloxavir Intermediate, CAS 1228258-40-9, Antiviral API Synthesis, Influenza Drug Intermediates, GMP Pharmaceutical Manufacturing


?? ?Product Overview?

?Baloxavir Marboxil Intermediate? (CAS 1228258-40-9) is a high-purity chemical intermediate crucial for synthesizing ?Baloxavir Marboxil?, a cap-dependent endonuclease inhibitor approved for treating influenza A and B infections. This intermediate ensures precision and scalability in antiviral API production, meeting stringent pharmaceutical quality standards.

  • ?Primary Function?: Acts as a key building block in the synthesis of Baloxavir Marboxil API, enabling targeted antiviral activity.

  • ?Applications?: Influenza drug development, antiviral manufacturing, and large-scale API production.


? ?Key Advantages?

?? ?Ultra-High Purity? | ≥99.0% (HPLC/GC verified) | Complies with ICH Q11 guidelines for intermediates.
?? ?Scalable Synthesis? | Optimized for high-yield production with minimal impurities, reducing time-to-market.
?? ?Regulatory Compliance? | Fully characterized by NMR, HRMS, and FTIR to support FDA/EMA submissions and GMP audits.


?? ?Applications?

  1. ?API Production?: Enables efficient synthesis of Baloxavir Marboxil with consistent batch-to-batch quality.

  2. ?Process Optimization?: Facilitates R&D in refining synthetic pathways for cost-effective manufacturing.

  3. ?Quality Control?: Used in analytical method validation and stability testing during batch release.


?? ?Quality Assurance?

  • ?Testing Methods?: HPLC, GC, NMR, HRMS, and FTIR for structural confirmation and purity analysis.

  • ?Standards?: Meets USP <1086>, EP 10.0, and ISO 9001:2015 certified manufacturing protocols.


?? ?Market Trends?

The ?global antiviral drugs market? is projected to grow at a ?CAGR of 3.8%?, reaching ?$78.5 billion by 2030?, driven by rising influenza outbreaks and demand for single-dose therapies like Baloxavir. This intermediate is vital for accelerating generic and novel antiviral drug development post-patent expiry.


Elevate your influenza drug production with Baloxavir Intermediate – engineered for purity, scalability, and regulatory excellence.


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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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