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High Bioavailability Liposomal L-Theanine Powder Green Tea Extract Liposome Bulk Raw Material Supply

Other Name

Liposomal Theanine

Appearance

White Powder

Specifications

70%

Price

120-150 USD

MOQ

1KG

Application

Health care

Certificates

HACCP, ISO22000, Kosher, Halal, TÜVRheinland, EU Organic Certificate, USDA, NOP, FDA

    Free Samples
    High-Absorption Amino Acid Delivery

    LIPOSOMAL
    L-THEANINE POWDER (70%)

    Liposomal L-Theanine Powder delivers 70% active L-Theanine (CAS 3081-61-6) encapsulated within a phospholipid bilayer via industrial emulsification and spray-drying. This free-flowing powder integrates directly into capsule, tablet, powder blend, and functional beverage premix production lines. A reliable B2B ingredient for manufacturers serving the global relaxation, focus, and sleep-support supplement markets.

    CAS 3081-61-6 Bulk Production 70% Loading GMP Compatible
    L-Theanine 1

    TECHNICAL SPECIFICATIONS

    Product Name
    Liposomal L-Theanine Powder
    Active Ingredient
    L-Theanine (CAS 3081-61-6)
    Active Loading Capacity
    70%
    Encapsulation Efficiency (EE%)
    ≥ 85% (Typical)
    Particle Size
    80nm – 250nm (Rehydrated)
    PDI
    ≤ 0.35
    Appearance
    White to Off-White Powder
    Solubility
    Dispersible in water (stable liposomal suspension)
    Loss on Drying
    ≤ 5.0%
    Heavy Metals (as Pb)
    ≤ 10 ppm
    Storage
    Cool, dry, sealed container; protect from light
    Shelf Life
    Refer to batch-specific COA

    LIPOSOMAL DELIVERY PRINCIPLE

    L-Theanine is highly water-soluble, so liposomal encapsulation here targets controlled release and process compatibility rather than solubility enhancement. Unencapsulated L-Theanine dissolves rapidly in aqueous systems, causing uneven powder blend distribution and hygroscopicity-driven clumping during storage.

    Our process embeds L-Theanine within phospholipid bilayer vesicles via controlled high-shear emulsification, then converts the preparation into a free-flowing powder by spray-drying. Key production benefits: (1) improved blend homogeneity in V-blender operations; (2) moisture resistance under standard warehouse conditions; (3) extended compatibility with multi-phase beverage systems for consistent per-batch dosing.

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    CERTIFICATE OF ANALYSIS (COA)

    Product Name Liposomal L-Theanine Powder Batch No. CRS20260601
    CAS No. 3081-61-6 Test Date 2026-06-02
    Mfg. Date 2026-06-01 Expiry Date 2028-05-31
    Items Specification Methods Results
    Assay (L-Theanine) 70% HPLC 70.2%
    Encapsulation Efficiency ≥ 85% Dialysis/HPLC 87.3%
    Particle Size 80–250nm DLS 145nm
    PDI ≤ 0.35 DLS 0.22
    Appearance White to Off-White Powder Visual Conformity
    Loss on Drying ≤ 5.0% Gravimetric 3.2%
    Heavy Metals (as Pb) ≤ 10 ppm ICP-MS Conformity
    Arsenic (As) ≤ 1 ppm ICP-MS Conformity
    Cadmium (Cd) ≤ 1 ppm ICP-MS Conformity
    Mercury (Hg) ≤ 0.1 ppm ICP-MS Conformity
    TPC ≤ 1,000 CFU/g Plate Count Conformity
    Yeast & Mold ≤ 100 CFU/g Plate Count Conformity
    E. coli Negative/25g USP <62> Conformity
    Salmonella Negative/25g USP <62> Conformity
    Shelf Life Please refer to batch-specific COA for exact expiry date.
    Package 1kg/foil bag or 25kg/drum; nitrogen flushed, light-protected.
    Storage Store cool, dry, dark, sealed below 25°C.

    QUALITY VERIFICATION

    1. HPLC Active Assay

    Every batch tested to confirm 70% L-Theanine loading. Batch-specific CoA provided with each shipment.

    2. DLS Particle Size Analysis

    Verifies stable liposome formation (80–250nm) upon rehydration — consistent nano-scale vesicle dimensions across every production run.

    3. Encapsulation Efficiency (EE%)

    EE% ≥ 85% confirms genuine encapsulation within the liposome structure, not simple physical blending with phospholipids.

    4. Heavy Metal & Microbial Screening

    Full compliance: Pb ≤10ppm, As/Cd ≤1ppm, Hg ≤0.1ppm; TPC & Yeast/Mold per USP standards.


    L-theanine01

    FUNCTIONAL ROLES

    1. Relaxation Without Sedation

    Promotes calm, relaxed alertness via alpha-brainwave activity — without drowsiness. A high-demand daytime relaxation active with strong repeat-purchase market dynamics.

    2. Focus & Cognitive Performance

    Widely paired with caffeine in nootropic formulations. Smooths stimulant edge while supporting sustained focus — a consistent B2B demand driver for functional beverage and supplement brands.

    3. Sleep Quality Support

    Supports sleep quality by promoting a relaxed pre-sleep state without direct sedation. Popular co-active alongside melatonin and magnesium in evening formulations.

    4. Stress Management

    Supports a balanced physiological response to everyday mental stressors. Staple ingredient across the growing stress-management and adaptogenic supplement categories.


    INDUSTRIAL APPLICATIONS

    l-theanine
    health supplements

    1. Bulk Capsule Manufacturing

    200–400mg single-active or multi-ingredient cognitive/relaxation complexes; excellent flowability for high-speed capsule filling lines.

    2. Functional Beverage Premixes

    Dry premix formats for stick packs, sachets, and bulk drink mixes. Liposomal carrier supports uniform dispersion upon reconstitution.

    3. Tablet & Caplet Production

    Compatible with direct-compression and wet-granulation. Standalone L-Theanine or multi-active stress-relief and focus tablet formulas.

    4. OEM / Private Label Formulas

    Ready-to-encapsulate or blend for cognitive wellness, stress-management, and sleep-support private-label supplement lines.


    OEM & PACKING

    OEM

    OEM

    Certificates

    CERTIFICATES

    Transportation

    TRANSPORTATION

    Packaging

    PACKAGING


    TECHNICAL FAQ

    Q1: What is the monthly production capacity for bulk liposomal L-Theanine orders?

    Our line supports multi-ton monthly output. For capacity allocation, lead times, and volume pricing, please contact our sales team with your projected annual requirements.

    Q2: Can you customize the L-Theanine loading percentage?

    Yes. Custom specs (e.g., 50%, 85%) are available for qualified large-volume OEM projects. MOQ and development lead times apply.

    Q3: How is batch-to-batch consistency verified?

    Every batch undergoes HPLC assay (target: 70%) with batch-specific CoA upon shipment. EE% and DLS particle size are monitored as routine QC across every production run.

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