Liposomal Coenzyme Q10 Powder 50%

Liposomal Coenzyme Q10; assay 50.0% by HPLC; phospholipid-encapsulated powder form; supported by representative batch LXLP260415.

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Description

LIPOSOMAL DELIVERY INGREDIENT

Liposomal Coenzyme Q10 Powder

Liposomal Coenzyme Q10 is supplied as a phospholipid-encapsulated powder for formulators who need the active dispersed in a lipid bilayer rather than as a free crystalline solid. This grade is offered as a B2B raw material: 50% coenzyme Q10 of the active on a phospholipid carrier, produced by thin-film hydration followed by high-pressure homogenisation and spray drying. It is intended for further processing by the buyer (capsules, stick packs, sachets, liquid or powder blends). The material is characterised by phospholipid identity, particle-size distribution and encapsulation-related parameters rather than by crystallinity, so the specification below is written accordingly.

Saturated yellow-orange liposomal coenzyme Q10 powder texture close-up

COA-Backed Specification

Ingredient system Liposomal Coenzyme Q10 (phospholipid bilayer encapsulation)
Form and colour Fine yellow to orange powder
Assay 50.0%
Method HPLC
Particle size 98% through 80 mesh
Loss on drying <=5.0%
Ash <=5.0%
Heavy metals Within the limits of the approved specification
Microbiological limits Within the limits of the approved specification
Representative batch LXLP260415
Manufacture date 15 Apr 2026
Shelf life Two years when stored properly

Representative values do not replace the current shipment COA.

Liposomal coenzyme Q10 powder on a stainless steel drum top

Buyer Decision Guide

Liposomal grades are specified differently from plain powders. Buyers should agree on three things before approval: the carrier system (phosphatidylcholine from sunflower or soy lecithin, or a synthetic phospholipid), the declared active content of the encapsulated system, and the dispersion behaviour in the buyer’s own matrix. Confirm the intended final dosage form at enquiry stage.

  • Active content: 50% coenzyme Q10 on a phospholipid carrier, expressed on the encapsulated system rather than on total powder mass.
  • Carrier declaration: phosphatidylcholine source and phospholipid content are stated on the COA for identity control.
  • Particle size: micro-dispersible powder, specification agreed against the dispersion test the buyer will run.
  • Dispersion: designed to disperse in water and in oil-free aqueous matrices; evaluate in your own base before scale-up.
  • Handling: hygroscopic, sensitive to heat and oxygen; keep sealed, cool and dry, and open only under controlled conditions.
  • This material is a raw material for further processing, not a finished consumer product.
Liposomal coenzyme Q10 powder in a glass vial standing in a white dish

How This Grade Differs

Liposomal Coenzyme Q10 is not interchangeable with plain Coenzyme Q10 powder on a weight-for-weight basis. The active is held in a phospholipid bilayer, so the declared content refers to the encapsulated system, and the material behaves differently in dispersion, taste masking and flow. Buyers comparing quotations should normalise on the active content stated on the COA, not on the price per kilogram of powder.

Compare these related grades before approval:

For a substitution review, compare botanical identity, plant part, assay target, analytical method, physical form and the current offered-batch COA.

Application Areas

  • Hard capsules and two-piece capsule filling
  • Stick packs and single-serve sachets
  • Powder blends and dry mixes
  • Beverage and liquid concentrate systems, subject to the buyer’s process validation

Packaging and Delivery

  • Evaluation sample typically 10-20 g, subject to stock
  • Regular MOQ typically 1 kg
  • 1 kg foil bag or 25 kg fibre drum with inner food-grade liner
  • Custom packing and private-label options subject to confirmation
  • Typical lead time 7-15 working days after deposit

Quality and Documentation

Representative batch LXLP260415 supports the specification table above. Use the cited record for preliminary comparison and request the offered-lot COA for final technical approval. Batch COA, specification sheet, agreed third-party testing and export documents are available for buyer verification.

Frequently Asked Questions

Which particle size or presentation applies?

98% through 80 mesh

How long can we hold stock before use?

Two years when stored properly from the manufacture date when the pack stays sealed and dry.

Which safety parameters are tested every lot?

Moisture <=5.0%; result 3.40%, ash <=5.0%; result 3.40%, heavy metals and microbiology against the approved specification.

What assay does Liposomal Coenzyme Q10 Powder 50% carry on the certificate of analysis?

Assay 50.0%, determined by HPLC.

How recent is the representative batch shown?

The batch referenced is LXLP260415; your shipment is released on its own certificate rather than the representative one.

How is the material shipped?

Air and sea freight are both arranged, with the mode chosen against volume, destination and required date. Documents and the HS code are issued with the shipping instructions.

Which documents come with the shipment?

Batch COA, specification sheet, agreed third-party testing where required, commercial invoice, packing list, certificate of origin and transport documents. The exact set is confirmed against the product and destination market.

What packing options are available?

Standard packing is a sealed food-grade inner liner inside an export carton or fibre drum. Pack size, labelling and private-label artwork are agreed in the written specification.

Request COA, Sample or Quotation

Send your target specification, application, order quantity, destination country and required test limits.

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