Liposomal NAD Powder 70%

Liposomal NAD (beta-Nicotinamide adenine dinucleotide); assay 70.0% by HPLC; phospholipid-encapsulated powder form; supported by representative batch LXLP260617.

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Description

LIPOSOMAL DELIVERY INGREDIENT

Liposomal NAD (beta-Nicotinamide adenine dinucleotide) Powder

Liposomal NAD (beta-Nicotinamide adenine dinucleotide) 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: 70% NAD 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.

Off-white to pale cream liposomal NAD powder texture close-up

COA-Backed Specification

Ingredient system Liposomal NAD (beta-Nicotinamide adenine dinucleotide) (phospholipid bilayer encapsulation)
Form and colour Fine off-white to pale cream powder
Assay 70.0%
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 LXLP260617
Manufacture date 17 Jun 2026
Shelf life Two years when stored properly

Representative values do not replace the current shipment COA.

Liposomal NAD powder in an unmarked stainless steel bowl on a steel bench

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: 70% NAD 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 NAD powder in a glass petri dish with its lid half-open

How This Grade Differs

Liposomal NAD (beta-Nicotinamide adenine dinucleotide) is not interchangeable with plain NAD (beta-Nicotinamide adenine dinucleotide) 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 LXLP260617 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

What assay does Liposomal NAD Powder 70% carry on the certificate of analysis?

Assay 70.0%, determined by HPLC.

How long can we hold stock before use?

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

How recent is the representative batch shown?

The batch referenced is LXLP260617; your shipment is released on its own certificate rather than the representative one.

What do you declare for moisture and ash?

Both are released against the limits on the approved specification; the measured result for your lot appears on its COA.

What is the usual lead time?

Regular production normally takes 7-15 working days after deposit, depending on stock, volume, testing and customisation requirements.

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.

Can I review the COA before I pay?

Yes. Request the current or representative COA and check identity, method, limits and results before approving the purchase order.

Request COA, Sample or Quotation

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

Get the current batch COA, a sample or a quotation