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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: 500kg
Update Time: 2025-05-28

Product Details

Product Name: 2-(2-aminoethoxy)-1,1-dimethoxyethane CAS No.: 1228258-40-9
Min. Order: 1kg Purity: 0.99
Supply Ability: 500kg Release date: 2025/05/28

?Baloxavir Impurity (CAS 1228258-40-9)?
Google Keywords: Baloxavir Impurity, CAS 1228258-40-9, Antiviral Drug Impurity, Influenza Treatment, GMP Reference Standard


?? ?Product Overview?

?Baloxavir Impurity? (CAS 1228258-40-9) is a high-purity reference standard used in the quality control and analytical profiling of ?Baloxavir Marboxil?, a novel antiviral drug targeting influenza. This impurity is critical for ensuring compliance with regulatory requirements during API manufacturing and formulation studies.

  1. ?Primary Function?: Serves as a certified impurity marker for method validation and batch release.

  2. ?Applications?: Pharmaceutical QC/QA, stability studies, and regulatory submissions.


? ?Key Advantages?

?? ?Ultra-High Purity? | ≥98% (HPLC/GC-MS verified) | Traceable to USP/EP standards.
?? ?Regulatory Compliance? | Meets ICH Q3A/B guidelines for impurities in APIs.
?? ?Stability? | Certified stability data under ICH storage conditions (-20°C, 24 months).


?? ?Applications?

  • ?Antiviral Drug Development?: Essential for impurity profiling in Baloxavir Marboxil production.

  • ?Quality Control Labs?: Used in HPLC/LC-MS method development and validation.

  • ?Regulatory Compliance?: Supports EMA/FDA filings for influenza drug approvals.


?? ?Quality Assurance?

  • ?Testing Methods?: HPLC, GC-MS, NMR, and FTIR for structural confirmation.

  • ?Standards?: Complies with USP <1086>, EP 10.0, and GMP requirements.


?? ?Market Trends?

The global influenza treatment market is projected to reach ?$1.8 billion by 2027? (CAGR 5.2%), driven by rising demand for targeted antivirals like Baloxavir. As regulatory scrutiny on impurity control intensifies, this reference standard addresses critical needs in drug safety and efficacy.


Ensure precision in your antiviral drug development with Baloxavir Impurity – certified quality, compliance, and traceability for global regulatory success.

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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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