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Glatiramer (CAS 147245-92-9) is a synthetic polypeptide polymer, accidentally discovered during research at the Weizmann Institute of Science in the 1960s. Initially used in animal models for multiple sclerosis (MS), it has since become a key therapeutic agent for MS. Produced from four amino acids – L-alanine, L-glutamic acid, L-lysine and L-tyrosine – it is synthesized via precisely controlled copolymerization. Advanced protection chemistry and dialysis purification ensure compliance with international pharmaceutical standards, with environmentally friendly, non-hazardous production.
Technical Specifications
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Product Name |
Glatiramer |
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Synonyms |
Glatiramer API, Glatiramer Powder |
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Characteristics |
A white to off-white lyophilized powder |
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CAS Number |
147245-92-9 |
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Assay |
≥98.0% (HPLC, Subject to the COA) |
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Formula |
C25H45N5O13 |
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Package |
Technical Package |
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Storage |
Long-term: Keep tightly sealed, protected from light & dry; stable for 3 years at ≤-20°C, 2 years at 2–8°C (refrigerated). Short-term: Sealed & light-protected; may be stored at 15–25°C (room temperature) for up to 1 month. Avoid freezing/thawing cycles, intense light & high temperature. |
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Structure |
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As an immunomodulator, Glatiramer API is mainly indicated for relapsing forms of multiple sclerosis, including clinically isolated syndrome, relapsing-remitting and active secondary progressive MS. It acts by competing for MHC II binding and inducing anti-inflammatory immune cells. It serves pharmaceutical companies, research institutes and medical institutions worldwide for MS drug manufacturing and neuroscience research. Stored at 2–8°C and administered subcutaneously, it is a cornerstone in MS treatment and drives progress in neuroimmunology.
Product Features
This product is a synthetic polypeptide pharmaceutical raw material, precisely copolymerized from four natural amino acids. It appears as a white to off-white Glatiramer Powder, with purity meeting pharmacopoeial standards, stable production and low impurities to support global regulatory filing for MS drug development.
Viatris glatiramer acetate is manufactured under a unified global quality system with full cold-chain control, sealed and light-proof storage at 2–8°C, delivering excellent batch consistency for large-scale and long-term supply to formulation enterprises.
As a core immunomodulatory API, it mimics myelin basic protein with well-defined clinical applications, mainly for R&D and production of relapsing MS formulations. Its safety and efficacy are validated by long-term clinical data and widely recognized in the industry.
The product shows excellent physicochemical stability and compatibility. It may be stored sealed and light-protected at 15–25°C for short-term use, while long-term storage at 2–8°C is recommended. Freeze-thaw cycles are prohibited, supporting global logistics and reliable supply to drug manufacturers.
Full-Cycle Quality Control & Consistent Quality
From raw material selection to finished goods delivery, a full-process quality control system is implemented with real-time monitoring of key procedures. Purity, impurities and physicochemical indicators are strictly controlled to ensure every batch of Glatiramer meets international pharmaceutical quality standards with stable and reliable performance.
Viatris glatiramer acetate relies on standardized production and mature quality control to achieve batch consistency in large-scale manufacturing, minimizing quality variation and providing traceable, high-reliability raw materials for downstream formulation clients.
Based on industry demand and market supply, the product maintains high quality while supporting competitive Glatiramer price, offering stable costs and continuous supply for long-term quality and economic benefits to partners.
Strict sample retention and stability studies are performed to monitor appearance and purity under various storage conditions. Quality control points are continuously optimized to maintain stable quality throughout storage, transportation and usage, complying with global regulatory filing standards.
Application Scenarios
As a widely used immunomodulatory API, Glatiramer (CAS 147245-92-9) features stable quality and clear pharmacological effects, serving pharmaceutical R&D, formulation production and scientific research to support industry development.
It is mainly used in the production of formulations for relapsing multiple sclerosis, serving as a key raw material for subcutaneous injections to support large-scale manufacturing. Viatris glatiramer acetate is a preferred choice for many formulation companies due to its strict quality control.
It is applied in pharmaceutical R&D for formula optimization, dosage form improvement and mechanism studies of novel MS drugs, supplying high-purity raw materials for research institutions to boost efficiency in neuroimmunological studies.
It supports global formulation registration and GMP-compliant production, meeting standards of ChP, FDA and other major authorities to enable pharmaceutical enterprises to expand global markets with compliant and steady raw material supply.
It fits pharmaceutical supply chain support with customizable packaging and supply plans based on client needs. With reliable quality and timely delivery plus favorable Glatiramer price, it helps partners reduce supply chain costs.
Packaging and Transportation
As a highly active pharmaceutical API, Glatiramer (CAS 147245-92-9) requires professional packaging and transport to preserve quality. Scientific packaging and strict logistics control are adopted in line with physicochemical properties and industry standards to ensure safe delivery.
Products are sealed in food-grade pharmaceutical aluminum foil bags, with outer waterproof, light-proof and shock-resistant cartons, desiccants and cushioning materials to isolate moisture, light and physical impact. Viatris glatiramer acetate uses the same standard packaging for safe storage and transport.
Packing specifications can be customized, with regular options of 1g, 5g, 10g per bag and 25kg sealed drums for bulk orders. Each batch is clearly labeled for full traceability, suitable for various order sizes.
Transport follows cold-chain standards with refrigerated vehicles maintaining 2–8°C and real-time temperature monitoring. High temperature, freezing and severe vibration are avoided to preserve physicochemical stability and product integrity.
Transportation complies with global pharmaceutical logistics regulations, supported by complete COA and transport documentation. It balances efficiency and cost control, with reasonable Glatiramer price to reduce customers' overall supply chain expenses.
Our Advantages
We own standardized production bases and advanced manufacturing processes enabling large-scale production of Glatiramer API. Each procedure is strictly controlled to ensure purity and impurities meet international pharmaceutical standards with excellent batch consistency.
We provide full-cycle quality control from raw material incoming to finished goods delivery with full monitoring and traceability. We also support competitive Glatiramer price to offer cost-effective products and lower cooperation costs.
Our professional R&D and service team provides Customized Glatiramer solutions including packaging and supply plans, responding promptly to inquiries and ensuring smooth cooperation.
With years of industry experience, we understand global pharmaceutical regulations and market demands. We supply products complying with major pharmacopoeias and maintain a stable supply chain to ensure on-time delivery and avoid supply shortages.
FAQ
We supply high-quality Glatiramer (CAS 147245-92-9) to global customers with mature technology, full-cycle QC and reliable supply chains. All procedures comply with international pharmaceutical standards to ensure batch consistency, complete documentation and on-time delivery. Customer-focused, we provide flexible solutions and professional support with cost efficiency. We seek long-term strategic partnerships with pharmaceutical companies and research institutes worldwide to advance drug development in neuroimmunology.
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