Pharmaceutical grade Vinpocetine 42971-09-5

Vinpocetine More Info

Vinpocetine, with CAS registry number 42971-09-5, is a semisynthetic derivative of the alkaloid vincamine, which is obtained from the leaves of the periwinkle plant (Vinca minor). Initially developed and approved as a pharmaceutical compound in Hungary in the 1970s, it has been widely studied for its potential effects on cerebral metabolism and blood flow. Its molecular structure is designed to enhance bioavailability and target specific pathways related to neurological function. While it is regulated as a prescription drug in some countries, it is also available as a dietary supplement in others, reflecting its dual status as both a pharmaceutical and a nutraceutical ingredient.

Primary Uses and Applications

Vinpocetine is primarily utilized to support cognitive health, particularly in contexts related to memory, focus, and cerebral circulation. In pharmaceutical applications, it has been investigated for use in cognitive decline, cerebrovascular disorders, and age-related cognitive impairment. As a dietary supplement ingredient, it is commonly formulated in products targeting mental clarity, brain energy, and neurological wellness. Its mechanism of action is believed to involve phosphodiesterase inhibition, modulation of cerebral blood flow, and neuroprotective effects, though research outcomes vary across regions and applications.

Application Market

The market for Vinpocetine is segmented into pharmaceutical and nutraceutical sectors, with varying regulatory statuses across regions. In countries like Russia, Hungary, and China, it is often approved as a prescription drug, while in the United States and parts of Europe, it is primarily available as a dietary supplement ingredient. Supply chains include pharmaceutical manufacturers, nutraceutical companies, and ingredient distributors catering to brain health products. Demand is driven by consumer interest in cognitive enhancement, aging populations, and growing awareness of neurological health, with distribution channels ranging from healthcare providers to retail and online supplement stores.

Handling and Regulatory Considerations

Regulatory status for Vinpocetine varies significantly by jurisdiction; it is essential to comply with regional laws regarding its classification as either a drug or supplement ingredient. In markets where it is considered a pharmaceutical, it must be manufactured under Good Manufacturing Practice (GMP) guidelines and adhere to drug approval processes. As a dietary ingredient, labeling and marketing claims must conform to local supplement regulations (e.g., FDA DSHEA in the U.S.). Proper handling should follow general chemical safety protocols, including the use of personal protective equipment (PPE) and adherence to storage conditions specified in safety data sheets (SDS). Businesses should conduct due diligence to ensure full compliance with import, sale, and usage requirements in target markets.

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Suitable for more than 50kg 
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2. Packaging photo
3. COA, MSDS, etc
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For commercial orders
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Company Profile

Established in 2013, Hyper Chem has exclusive tie-ups with leading manufacturers, supplying raw materials produced in GMP and ISO 9002 certified facilities, and provides high-quality ingredients and raw materials to cater to the requirements of our diverse range of clients.

Among them, our key client industrial sectors around the global are:

Pharmaceuticals
Nutrition Ingredients/ Dietary supplements
Cosmetic Ingredients
Food Ingredients
Veterinary API
Agriculture fertilizer
Custom Synthesis lab supply

HyperChem provides to its wonderful and honorable clients comprehensive purchasing and distribution services which ensure that we are delivering the right generic, raw, or customized product, make sure that we are delivering it at the right time, ensure that it is delivered in the specified amount, and in the right kind of packaging to clients and customers of all types of industries irrespective of their size of operation.