Pure Melatonin Powder

10% Water-Soluble Microencapsulated Melatonin Powder for Beverage Formulations

Assay: ≥ 10.0% on Dried Basis (HPLC Monograph)

Source: Microbial Fermentation (Non-Synthetic)

Appearance: White to off-white fine powder

Solubility: 100% Instant cold-water soluble; Transmittance ≥ 98.0% (at 420nm via UV-Vis)

Stability: pH 3.0 – 7.5 Stable; Thermal processing resistant without recrystallization

Certificate: BRCGS, IFS, Organic (USDA/EU), COSMOS, Halal, Kosher

Compliance: Compliant with USP / EP / FCC Standard Monographs & EU Regulation 2023/915

Sample: 10-50g Free Sample Available for R&D

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  • Whatis Water-Soluble Microencapsulated Melatonin Powder?


    Standardized 10% Water-Soluble Melatonin Powder is a tech-driven functional raw material engineered specifically for liquid nutraceutical and beverage manufacturing lines. Utilizing an industrial supramolecular microencapsulation technology, this ingredient alters the naturally hydrophobic crystalline structure of pure melatonin into a highly hydro-dispersible matrix, bypassing the solubility limitations of standard lipophilic materials to ensure uniform active delivery in aqueous systems.

    Technologie printemps vert standardizes this specialized ingredient into an ultra-fine, 100% cold-water soluble powder that achieves complete visual dissolution within 60 seconds at 20°C without mechanical heat acceleration. Formulated under verified BRC and ISO food safety frameworks, the dissolved matrix delivers a measured spectrophotometric transmittance rate exceeding 98%, directly preventing industrial risks of turbidity, bottom sediment, or surface ring formation in automated ready-to-drink (RTD) filling lines.

    The processed matrix features complete organoleptic neutrality, isolating the native bitter off-flavors of the active molecule to allow direct incorporation into functional waters, relaxation shots, and adaptogenic liquid blends without altering the end-product's baseline flavor profile. This calibrated chemical and physical stabilization provides beverage formulators and R&D managers with a highly predictable, repeatable, and non-reactive input for continuous scaling.


    spécification   

    Nom du produit

    Water-Soluble Microencapsulated Melatonin Powder

    Source:

    Microbial Fermentation

    CAS non.

    Numéro de téléphone: 73-31-4

    analyse

    ≥ 10.0% on Dried Basis

    Méthode d’essai

    HPLC Monograph

    Carrier MatrixFood-Grade Supramolecular Carbohydrate Complex
    Solubility

    100% Instant cold-water soluble (≤ 60 seconds at 20°C for 1% w/v)

    Solution ClarityTransparent solution; Light Transmittance ≥ 98.0% (at 420nm via UV-Vis)
    apparence

    White to off-white fine powder (Homogeneous, free-flowing)

    pH Stability Range3.0 – 7.5 (Stable aqueous dispersion without recrystallization)

    Particle Size

    100% Through 80 mesh (≤ 180 μm) determined via USP <786>

    Loss on Drying (LOD)≤ 5.0% determined via USP <731> at 105°C to Constant Weight
    Heavy MetalsPb ≤ 1.0 ppm, As ≤ 0.5 ppm, Hg ≤ 0.1 ppm, Cd ≤ 0.2 ppm [ICP-MS via USP <233>]

    Microbiological Control

    TAMC ≤ 1,000 cfu/g, TYMC ≤ 100 cfu/g, Salmonella/E. coli: Absent [USP <61>/<62>]

    Résidus de pesticides

    Compliant with EU Regulation (EC) No 396/2005 (GC-MS / LC-MS-MS)

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    Quality & Compliance


    Standardized Manufacturing & Laboratory Integrity

    Production processes operate under standardized GMP, ISO 9001, and ISO 22000 food safety frameworks. An internal chemical laboratory utilizing validated HPLC, GC, and ICP-MS instrumentation monitors every production lot to ensure strict batch-to-batch physical and chemical uniformity.

    Monograph & International Regulatory Alignment

    This 10% Water-Soluble Melatonin is engineered with comprehensive documentation to streamline multi-country product registration and import qualification. The raw material fully satisfies the analytical identity and purity requirement thresholds of USP, EP, and FCC standard monographs.

    Calibrated Volatiles & Impurities Control

    Validated GC-HS-FID analysis restricts residual food-grade ethanol to ≤1,000 ppm in accordance with USP <467> and EP 5.4. Every batch undergoes elemental quantification under USP <233> to guarantee strict compliance with EU Regulation 2023/915 contaminants limits.

    Global Food Safety & Customs Authority

    Green Spring Technology maintains top-tier global food safety validations to accelerate cross-border shipping and port routing. The manufacturing facility is certified under BRCGS (Grade A), IFS Food (Higher Level), and maintains an active FDA Facility Registration.

    Dietary Identity & Nutricosmetic Inclusivity

    Supply lots are maintained under annual Halal and Kosher certified criteria, alongside recognized COSMOS Compliant, EU Organic, and USDA Organic credentials. This extensive portfolio ensures complete clean-label compliance for global dietary supplement, functional beverage, and nutricosmetic production lines.


    Green Spring Technology Certificates


    Key Advantages


    Dissolution Kinetics & Optical Clarity

    Achieves complete visual dissolution within 60 seconds in 20°C water, delivering a spectrophotometric transmittance rate ≥98% (at 420nm via UV-Vis). This kinetic parameter eliminates industrial risks of turbidity, phase separation, or bottom sediment.

    pH & Thermal Processing Stability

    Maintains physical and chemical stability across a beverage pH range of 3.0–7.5. The microencapsulated matrix undergoes no active potency degradation or recrystallization during continuous pasteurization or UHT sterilization workflows.

    Volatiles & Purity Specification

    Derived from microbial fermentation and verified free from Peak E contaminants. Validated GC-HS-FID analysis restricts residual food-grade ethanol to ≤1,000 ppm in accordance with USP <467> and EP 5.4.

    Powder Rheology & Blending Metrics

    Calibrated to a stable bulk density of 0.40–0.55 g/mL and a particle profile of 100% through 80 Mesh. This engineering metric controls powder flowability to mitigate material segregation in compounding hoppers and manage plant-floor dust.

    Organoleptic Neutrality & Matrix Integration

    Features complete organoleptic neutrality to isolate the native bitter flavors of the melatonin molecule. The ingredient integrates into functional liquids and ready-to-drink (RTD) bases without changing the end-product's baseline sensory profile.


    Applications


    Liquid Formulations & Ready-to-Drink (RTD) Beverages

    Engineered for aqueous matrix systems including 50ml–100ml liquid shots and functional beverages. A monitored spectrophotometric transmittance rate ≥98% (at 420nm via UV-Vis) ensures optimal visual clarity, preventing industrial risks of turbidity, phase separation, or ring formation in automated filling lines.

    Concentrated Oral Liquids, Drops & Sprays

    Applicable for high-potency oral liquid drop matrices and throat spray delivery systems. Complete hydro-dispersibility allows for uniform active ingredient distribution and precise dosing accuracy, serving as a tech-driven alternative for formulations targeting consumers with solid dosage swallowing limitations.

    Thermal-Processed Dairy & Plant-Based Matrices

    Thermally calibrated to withstand industrial heat preservation protocols without chemical degradation. The microencapsulated powder integrates into milk, soy, and almond bases, remaining stable during pasteurization and Ultra-High Temperature (UHT) sterilization without affecting baseline matrix viscosity.

    Gummies & Hydrocolloid-Based Confectionery

    Optimized to ensure uniform homogeneity within pectin, gelatin, or starch hydrocolloid carrier bases during molten phase blending. This physical dispersion calibration limits active marker stratification, ensuring precise dose containment and compliance with regulatory batch uniformity standards.

    Dry-Blended Instant Powder Mixes & Sachets

    Suitable for instant herbal tea blends, cocoa powder matrices, and single-serve sachet delivery lines. The powder disperses within 60 seconds in both hot and cold aqueous solvents without mechanical heat acceleration, leaving no insoluble residue or bottom sediment in the reconstituted beverage.


    water-soluble-melatonin-applications-beverages-drops-gummies

    Applications of Green Spring Technology's water-soluble melatonin powder in sleep shots, oral drops, and gummies.


    Technical FAQ


    Q1: How does pH fluctuation affect the chemical stability and spectrophotometric clarity of this 10% Water-Soluble Melatonin Powder within acidic beverage matrices?

    A: This engineered 10% Melatonin Powder remains chemically stable and clear across a wide pH range of 3.0 to 7.5. In low-pH beverage matrices (pH 3.2–4.5), the food-grade supramolecular carbohydrate microencapsulation shield prevents active macromolecule aggregation or acid hydrolysis. Spectrophotometric validation confirms zero sediment, precipitation, or active assay degradation over a continuous simulated shelf-life, managing the industrial risk of crystalline crystallization.


    Q2: Does thermal processing or continuous pasteurization induce active degradation or color shifting in Water-Soluble Stinging Nettle-Aligned Fermented Melatonin Powder?

    A: No. The thermally resilient microencapsulated matrix withstands conventional heating thresholds without degradation. This Fermented Melatonin Powder endures standard High-Temperature Short-Time (HTST) pasteurization at 85°C–90°C, hot-filling, and Ultra-High Temperature (UHT) sterilization with a measured active HPLC assay loss of <0.5%. The dissolved matrix maintains structural visual neutrality post-heating, causing zero Maillard browning, color shifting, or off-flavor generation.


    Q3: Are there complexation or interfacial tension disruption risks when formulating industrial-grade Standardized Melatonin Microcapsules alongside GABA, L-Theanine, or botanical extracts?

    A: The hydro-matrix optimized by Green Spring Technology features a non-ionic, neutral surface charge that prevents cross-ingredient complexation. When co-formulated with GABA, L-Theanine, or magnesium salts, the Standardized Melatonin Microcapsules avoid electrostatic binding or interfacial tension disruptions. The barrier coating isolates the active core from natural organic acids and polyphenols in plant-derived extracts, preventing oil-out separation or secondary sediment formation in continuous large-scale run.


    Why Partner With Green Spring Technology?


    • 25+ Years of Fermentation Infrastructure

    • Established in 2000, Green Spring Technology operates a quarter-century of bio-fermentation infrastructure. This industrial heritage ensures multi-stage process controls and verifiable batch-to-batch chemical uniformity.

    • Global Certification & Regulatory Alignment

    • Manufacturing lines are backed by active BRCGS (Grade A) and IFS Food (Higher Level) certifications. The facility maintains an active FDA Facility Registration, ISO 9001, and ISO 22000 for import compliance.

    • Internal Laboratory & Formulation Support

    • The analytical laboratory utilizes validated HPLC, GC, and ICP-MS instrumentation for batch consistency controls. The technical department collaborates with client engineers to resolve bulk density and aqueous solubility limits.

    • Secured Supply Chain & Logistics Continuity

    • Maintains a permanent stock threshold of 2,000 kg+ within temperature-and-humidity-controlled warehouses. This logistical hub enables rapid international dispatch, ensuring friction-free port entry across European and North American customs.

    • Customized Specification Engineering

    • The facility calibrates material physical metrics to fit industrial plant-floor requirements. Production options include specialized Direct Compression (DC) granules and 10% Water-Soluble microencapsulated powder for automated beverage lines.


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