Pyrroloquinoline Quinone Disodium Salt
Pyrroloquinoline Quinone Disodium Salt (PQQ) is a novel functional compound used in dietary supplements for its role in mitochondrial health and cellular energy metabolism. It is not listed in Reg. (EU) 432/2012 for authorised health claims. In gummy manufacturing, PQQ is heat-stable and soluble, making it suitable for inclusion in premium formulations. Brands typically position it for mitochondrial biogenesis, cognitive vitality, and healthy ageing.
- mitochondrial health
- energy metabolism
- cognitive function
At a glance
- Definition
- Pyrroloquinoline Quinone Disodium Salt (PQQ) is a novel functional compound used in dietary supplements for its role in mitochondrial health and cellular energy metabolism. It is not listed in Reg. (EU) 432/2012 for authorised health claims. In gummy manufacturing, PQQ is heat-stable and soluble, making it suitable for inclusion in premium formulations. Brands typically position it for mitochondrial biogenesis, cognitive vitality, and healthy ageing.
- Common positionings
- mitochondrial biogenesis
- cellular energy
- cognitive vitality
- healthy ageing
- antioxidant support
- Format suitability
- Reviewed for gummies and sachets — confirmed per project.
Where this ingredient fits in the DAT Supply catalogue
Every format chip links through to its manufacturing hub and to the private-label catalogue for that format. The category chip routes to the matching vertical hub on the categories index.
- Energy & performance
- Browse all ingredients
What it is
Pyrroloquinoline Quinone Disodium Salt, commonly known as PQQ, is a redox-active quinone molecule that has attracted commercial interest for its role in supporting mitochondrial function and cellular energy metabolism. It is not a vitamin or mineral but is classified as a novel functional compound. In the EU, PQQ is under novel food assessment and does not carry authorised health claims under Reg. (EU) 432/2012. Brands use it as a premium ingredient for positioning around mitochondrial health, cognitive vitality, and healthy ageing.
For private-label gummy manufacturers, PQQ offers good applicability due to its heat stability and solubility in gummy matrices. Its premium cost tier positions it for high-value product ranges targeting consumers interested in energy, cognitive function, and longevity. Because no EU-authorised claims exist for PQQ, any claim coverage must come from co-formulated nutrients with authorised claims, such as Vitamin B6 or Magnesium for nervous-system function, or Vitamin C for antioxidant protection.
Origin and history
Pyrroloquinoline Quinone was first identified in 1979 as a novel redox cofactor in bacteria. It was later found to be present in small amounts in various foods, including fermented soybeans, green tea, and certain fruits and vegetables. Its biological significance in mammals was established through research demonstrating its role in mitochondrial biogenesis and cellular energy production. Commercial interest in PQQ as a dietary supplement ingredient grew in the early 2000s, particularly in the US and Asian markets.
Industrial production of PQQ disodium salt is achieved through chemical synthesis or microbial fermentation. The disodium salt form is the most common commercial variant due to its improved stability and solubility compared to the free acid form. In the EU, PQQ is classified as a novel food ingredient and is subject to pre-market authorisation under Regulation (EU) 2015/2283. As of the current date, it remains under assessment, meaning it cannot be marketed as a food supplement ingredient in the EU without authorisation.
Scientific overview
PQQ functions primarily as a redox cofactor, participating in electron transfer reactions within cells. Its most studied biological role is the stimulation of mitochondrial biogenesis — the process by which new mitochondria are formed within cells. This is mediated through the activation of the PGC-1α pathway, a key regulator of mitochondrial function. PQQ also exhibits antioxidant properties, protecting cells from oxidative stress by scavenging reactive oxygen species. These mechanisms underpin its positioning for energy metabolism, cognitive function, and healthy ageing.
Bioavailability of PQQ disodium salt is moderate, with oral administration leading to measurable plasma levels in human studies. The compound is absorbed in the small intestine and distributed to tissues including the brain, liver, and kidneys. The disodium salt form offers improved solubility and stability compared to the free acid, making it the preferred form for supplement manufacturing. Typical human studies use doses ranging from 10–20 mg per day.
From a manufacturing perspective, PQQ is heat-stable and soluble in gummy matrices, which simplifies formulation. Its premium cost tier means it is typically used at low doses (10–20 mg per serving) to manage cost per unit. No specific formulation conflicts or synergies have been documented in the available data, but DAT reviews these per project. Standard processing conditions apply, and no special handling is required beyond standard good manufacturing practices.
Why brands use Pyrroloquinoline Quinone Disodium Salt
Brands use PQQ in gummies to target the growing consumer interest in mitochondrial health, cellular energy, and healthy ageing. It is one of the most familiar and commercially understood novel functional compounds across EU and US markets. Its premium positioning allows brands to differentiate their product ranges and command higher price points. Common positioning angles include mitochondrial biogenesis, cognitive vitality, energy metabolism, and antioxidant support. Because no EU-authorised health claims exist for PQQ, brands must rely on co-formulated nutrients with authorised claims or use non-health claims such as "with PQQ" or "supports mitochondrial function" (where permitted under local regulations).
From a formulation and manufacturing standpoint, PQQ is well-suited to gummy production. It is heat-stable, soluble, and does not require special processing conditions. Its premium cost tier means it is typically used at low doses, which helps manage cost per unit. The absence of documented taste issues simplifies flavour masking. DAT confirms the final dosage, form, and stability per project after reviewing the target claim, market, and regulatory status.
For pack copy, brands must exercise strict claim discipline. No disease claims are permitted. No "anti-inflammatory" language is allowed in EU pack copy. No certification promises (vegan, kosher, halal, organic, non-GMO) can be made on pack until confirmed per project and batch documentation. No guaranteed shelf-life can be stated until confirmed with stability data. DAT reviews all claims per project and confirms regulatory compliance before final label approval.
Formats this ingredient is reviewed for
DAT Supply covers gummy, capsule, softgel, tablet, powder, oral strip, liquid drop, shot, jelly and pet formats. The list below reflects every format this ingredient is reviewed for — chips link through to the manufacturing hub for each format. Final compatibility, dose and matrix are confirmed per project.
Formulation notes
Verified formulation reference across the formats this ingredient is reviewed for — the Supported formats section lists every product format this active is approved for, and the per-format Considerations section below covers matrix-specific guidance. Final formulation, dose and on-pack copy are confirmed per project.
- Gummy fit
- Good
- Heat stable
- Yes
- Soluble in matrix
- Yes
- Cost tier
- Premium
Forms available
- Disodium salt (standard commercial form)
Dosage reference
No established EU NRV. Typical brand positioning ranges from 10–20 mg per serving. DAT confirms the final dosage per project after reviewing the target claim, market, and regulatory status.
Taste & sensory
Not characterized. Standard masking and flavour systems apply.
Manufacturing notes
No specific formulation notes. Standard processing applies.
Per-format formulation notes
Safe-baseline considerations for each format this ingredient is reviewed for. Final formulation, dose and on-pack copy are confirmed per project.
Gummies
- Taste masking and aroma load against the cooked-base flavour — confirmed per project.
- Heat exposure during cooking; coated or encapsulated forms may be required — confirmed per project.
- Matrix choice (pectin vs gelatin) and its effect on ingredient stability — confirmed per project.
- Per-gummy dose and serving count needed to hit the label claim — confirmed per project.
Sachets
- Powder flow and dose accuracy at single-serve sachet weights — confirmed per project.
- Barrier requirements (oxygen, moisture) for the active — confirmed per project.
- Reconstitution behaviour when the sachet is dosed into water — confirmed per project.
EU-authorised health claims
EU-authorised wording for this ingredient is reviewed per project against Reg. 1924/2006 and the authorised list under Reg. 432/2012. No final claim wording is implied by this page.
Authorised at ≥15% NRV per daily serving. Claim wording must appear verbatim on consumer packaging. DAT reviews final pack copy per project against EU 1924/2006 and the authorised list under EU 432/2012.
Pyrroloquinoline Quinone Disodium Salt is a novel food ingredient under EU assessment. It does not have authorised health claims under Reg. (EU) 432/2012. Any consumer-facing claims must be based on co-formulated nutrients with authorised claims or be non-health claims (e.g., ingredient presence). DAT reviews regulatory status per project and market.
Studies & evidence
External peer-reviewed sources and regulatory opinions. Citations only — DAT does not endorse the publishers.
Harris CB, Chowanadisai W, Mishchuk DO, et al.·Journal of Nutritional Biochemistry·2013
Rucker R, Chowanadisai W, Nakano M·Nutrients·2021
Itoh Y, Hine K, Miura H, et al.·Journal of Clinical Biochemistry and Nutrition·2016
Stites TE, Mitchell AE, Rucker RB·Annual Review of Nutrition·2000
European Commission·EUR-Lex·2023
Synergies & conflicts
Pairs well with
Synergy data needs review. DAT reviews per project.
Care when combining with
Conflict data needs review. DAT reviews per project.
Similar ingredients
Ingredients that frequently sit alongside this one in private-label supplement briefs.

Chondroitin Sulfate
Chondroitin sulfate is a naturally occurring glycosaminoglycan found in cartilage and connective tissue. It is one of the most familiar and commercially understood joint health actives across EU and US markets. Chondroitin sulfate has no authorised health claims under Reg. (EU) 432/2012, so brands typically position it alongside co-formulated nutrients such as Vitamin C (for collagen formation) or Vitamin D (for normal bone function). It is not suitable for gummy formats due to poor solubility and high molecular weight, and is typically delivered in sachet formats.
Coenzyme Q10
Coenzyme Q10 is used in private-label supplement manufacturing. Sourcing, dose anchors and target-market documentation are reviewed per project.

Dihydroberberine
Dihydroberberine is a reduced form of berberine, a naturally occurring alkaloid found in plants such as Berberis aristata and Coptis chinensis. It is used in dietary supplements for metabolic wellness and blood sugar balance positioning. As a botanical-derived compound on the EU on-hold list, it has no authorised health claims under Reg. (EU) 432/2012.

Glucosamine Sulfate
Glucosamine is a naturally occurring amino sugar that is a structural component of cartilage and synovial fluid. In supplement form (sulfate or hydrochloride), it has been used for decades in joint-positioned ranges. Glucosamine itself has no authorised EU health claim under Reg. 432/2012; in gummy formats it is most commonly positioned for 'joint comfort' alongside co-formulated nutrients that carry authorised claims.

Lutein
Lutein is a carotenoid pigment found naturally in green leafy vegetables and egg yolks. It is one of the most familiar and commercially understood gummy actives across EU and US markets, primarily positioned for eye and macular health. Lutein has no authorised health claim under Reg. (EU) 432/2012; any claim coverage relies on co-formulated nutrients.

Melatonin
Melatonin is a hormone naturally produced by the pineal gland that regulates circadian rhythm and sleep onset. In food-supplement gummy formats it is the most commonly requested sleep-onset active, with two EU-authorised health claims under Reg. 432/2012 at 1 mg (sleep onset) and 0.5 mg (jet lag) per portion. Above these doses, EU classification typically shifts to medicinal product — Member State verification is required per project.
Adjacent reading
Pairings, resource guides and blog notes most often associated with Pyrroloquinoline Quinone Disodium Salt on DAT Supply briefs.
Common pairings
Ingredients that frequently co-formulate with Pyrroloquinoline Quinone Disodium Salt.
Develop a formula featuring Pyrroloquinoline Quinone Disodium Salt
Explore concepts already built around this ingredient, or talk to our team to scope a custom formulation.