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Phosphatidylserine for smarter formulations: field notes from the supply chain I’ve spent enough time in formulation rooms to know when an ingredient just “behaves.” Phosphatidylserine Soybean Extract Powder 50% Nootropics Herbal Extract Raw Material is one of those steady performers—clean sourcing, predictable HPLC data, easy to blend. Origin-wise, it’s shipped from Building 23B1, No.2 Yuanboyuan St., Zhengding Area of China (Hebei) Pilot Free Trade Zone. The lot files I’ve seen read like you want them to: Non-GMO, BSE/TSE-free, non-irradiated, allergen-free. Why PS 50% is trending (and where it actually fits) Cognitive support is still hot—particularly nootropics for knowledge workers, esports, and “focus” blends for students. Brands ask for consistent 50% PS because it plays nicely with choline sources, L-theanine, and bacopa in capsules, sachets, and functional beverages. To be honest, it’s also about trust: many customers say PS is a “feelable” ingredient, even though claims are tightly regulated in the US and EU. How it’s made (real-world process flow) Materials: food-grade soy lecithin (non-GMO), L-serine, food ethanol (Class 3 solvent) Method: enzymatic transphosphatidylation (phospholipase D) to enrich phosphatidylserine; ethanol extraction; concentration; deodorization Finishing: spray-drying onto a suitable carrier to achieve ≈50% PS; sieving; metal detection Testing: assay by HPLC per USP -style chromatography; residual solvents to ICH Q3C(R8); heavy metals per modern ICP-MS limits; microbial per dietary supplement specs Service life: around 24 months sealed, cool and dry; PS is oxidation-sensitive—nitrogen-flushed bags help Industries: dietary supplements, functional foods, ready-to-mix nootropics, and even premium skincare (phospholipid systems) Key specifications (typical COA targets) Item Spec (≈, real-world use may vary) Assay (Phosphatidylserine, HPLC) ≥ 50% Source / Used Part Soy lecithin / Fruit listed per vendor data Extract Solvent Ethanol (Class 3), ICH Q3C limit ≤ 5000 ppm Heavy Metals (Pb/Cd/As/Hg) Meets modern limits (e.g., USP/ICH-aligned) Microbial Limits TPC, yeast/mold within dietary supplement specs Certifications Non-GMO, BSE/TSE-free, Non-irradiation, Allergen-free; ISO/FSSC available on request Vendor comparison at a glance Factor Phosphatidylserine Soybean Extract Powder 50% Nootropics Herbal Extract Raw Material Typical Trader Local Mill Assay consistency Tight, HPLC-verified batches Varies lot-to-lot Good, limited scale Regulatory files Complete CoA, MSDS, MoA, allergen Basic CoA only Partial Lead time Stocked SKUs; predictable Uncertain Short, small runs Customization and formulation notes Options: carrier system, particle size, flow aids for tableting, flavored premixes Compatibility: pairs well with bacopa, ginkgo, L-tyrosine; avoid high heat and moisture Labeling: “Phosphatidylserine (from soy lecithin)”—check regional regs; claims must follow local rules Mini case studies Case A (capsule): A US brand swapped a 20% PS for Phosphatidylserine Soybean Extract Powder 50% Nootropics Herbal Extract Raw Material and cut fill weights by ≈30%, improving capsule closure and yield. Customer feedback: “cleaner focus stack” and fewer soft capsules required per serving. Case B (stick packs): An APAC beverage startup used 50% PS with natural flavors. Stability at 40°C/75% RH hit 24 weeks with nitrogen flushing—assay held within ±5% (accelerated), which surprised the team given PS’s sensitivity. Standards and test methods we align to Safety: PS (soy) recognized via FDA GRAS notice framework [1] Residual solvents: ICH Q3C(R8) (ethanol Class 3) [2] HPLC: USP General Chapter <621> for chromatography conditions [3] Phospholipids profiling: AOCS methods (e.g., Ja 7-95) [4] References: 1. FDA GRAS Notice Inventory (Phosphatidylserine from soybean, industry references): https://www.fda.gov/food/generally-recognized-safe-gras-gras/gras-notice-inventory 2. ICH Q3C(R8) Residual Solvents: https://database.ich.org/sites/default/files/Q3C-R8_Guideline_Step4_2021_0412.pdf 3. USP General Chapter <621> Chromatography: https://www.uspnf.com/notices/general-chapter-621-chromatography 4. AOCS Official Methods for Phospholipids (e.g., Ja 7-95): https://www.aocs.org/attain-lab-services/methods/methods/search
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Advanced molecular distillation and microencapsulation technology. Extremely bioavailable trace carotenoids Intuitively soluble.
Advanced molecular distillation and microencapsulation
technology. Extremely bioavailable 
trace carotenoids Intuitively soluble.
Liposomes are biocompatible, biodegradable,
and do not cause an immune response.
They also enhance drug solubility and distribution,
and can be modified for targeted release.
Liposomes are biocompatible, biodegradable, and do not cause an immune response. They also enhance drug solubility and distribution, and can be modified for targeted release.
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Building 23B1, No.2 Yuanboyuan St., Zhengding Area of China (Hebei) Pilot Free Trade Zone
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