Cranberry Extract (PACs)

Cranberry Extract (PACs)

Vaccinium macrocarpon Aiton · A-type proanthocyanidins by DMAC

American cranberry fruit extract standardised on A-type proanthocyanidins by the DMAC method, AOAC 2019.06, with A-type identity confirmation. Vegan, declared peanut-free, 25 kg drums.

Specifications

Botanical identityVaccinium macrocarpon Aiton, family Ericaceae, the American or large cranberry. Distinct from V. oxycoccos (small cranberry) and V. vitis-idaea (lingonberry).
Part used and originWhole fruit or juice press residue. Grown in North America (Wisconsin, Massachusetts, Quebec, British Columbia) and Chile; not an Indian crop. Origin chain documented.
StandardisationProanthocyanidins (PACs) by DMAC, offered across roughly 10% to 60%, with 15% and 25% the volume grades. Juice powders carry only a small fraction of this.
Assay method and standardReported by the DMAC colorimetric assay per AOAC Official Method 2019.06, stating whether procyanidin A2 or cranberry c-PAC was the calibration standard. The two differ.
Method cautionFolin and generic UV polyphenol figures are not PAC values and read much higher. A bare percentage without a named method and standard is not comparable between suppliers.
Serving arithmetic36 mg PAC per daily serving is the reference figure the trade formulates to: 240 mg of a 15% PAC extract, or 144 mg of a 25% PAC extract, by DMAC.
A-type identityCranberry PACs are predominantly A-type interflavan linked. A-type character confirmed by MALDI-TOF MS along the lines of AOAC First Action Method 2019.05.
Adulteration and allergen riskGrape seed (B-type) and peanut skin (A-type, peanut allergen) are documented PAC adulterants. Every lot is profiled and the material is declared peanut-free.
Market authenticity contextPublished surveys found about 24% of commercial extracts and 60% of finished supplements differing from authentic fruit, including Morus nigra and hibiscus adulteration.
Secondary markersCranberry anthocyanin pattern of cyanidin and peonidin galactosides and arabinosides reported on request; organic acid profile supports authenticity.
Regulatory referenceUS GRAS notice GRN 873, cranberry extract powder, received an FDA no-questions letter for beverages and RTD coffee at 150 mg per 8 oz serving.
Appearance and solubilityDeep red to reddish-brown free-flowing powder with a tart berry odour. Water-soluble; colour and stability both favour acidic systems.
Allergen and dietary statusVegan and vegetarian; no bovine, porcine, marine or insect material. Free of all FDA 9 and EU 14 allergens; peanut-free status verified, not merely attested.
Shelf life, storage24 months unopened, extendable to 36 on validated grades. Store below 25 C, RH under 60%, sealed and dark.
HS code1302 19 19 for the extract
Cranberry extract is made from the fruit of Vaccinium macrocarpon Aiton (family Ericaceae), the American or large cranberry. It is a different species from the European small cranberry, Vaccinium oxycoccos, and from lingonberry, Vaccinium vitis-idaea, and the three are not interchangeable even though customs groups their juices under one subheading. Commercial cranberry is grown in North America — Wisconsin, Massachusetts, New Jersey, Quebec and British Columbia — with additional volume from Chile; it is not an Indian crop, so this is an imported-raw-material line supplied against a documented origin chain. The extract is produced from whole fruit or from press residue by aqueous or aqueous-ethanol extraction, membrane refining and spray drying, and is distinct from cranberry juice powder, which is a juice preparation carrying fruit sugars and usually a maltodextrin carrier with only a small fraction of the PAC content. The standardisation marker is proanthocyanidin content, and the arithmetic buyers care about is straightforward: 36 mg of PAC per daily serving is the reference figure the trade formulates to, which at a 15% PAC extract means 240 mg of extract and at 25% means 144 mg. What is not straightforward is the number itself, because PAC values are method-dependent to a degree that catches new buyers out. The industry method is the 4-dimethylaminocinnamaldehyde colorimetric assay, adopted as AOAC Official Method 2019.06 following an inter-laboratory validation of the 96-well DMAC procedure; that validation compared the procyanidin A2 dimer standard against a cranberry-PAC (c-PAC) reference material, and the two standards do not give the same figure on the same sample. Folin and generic UV polyphenol numbers are higher again and are not PAC values at all. We report the method and the calibration standard alongside every assay, and we will not quote a bare percentage. Because DMAC measures a chromophore and cannot tell where the PAC came from, identity is established separately: cranberry PACs are predominantly A-type interflavan linked, and A-type character is confirmed by MALDI-TOF mass spectrometry along the lines of AOAC First Action Method 2019.05, supported by the cranberry anthocyanin pattern of cyanidin and peonidin galactosides and arabinosides. That identity work is not optional, and it carries an allergen dimension. Published market surveys have found roughly a quarter of commercial cranberry extracts and a majority of finished cranberry supplements differing materially from authentic fruit, with adulteration by Morus nigra and hibiscus among the findings, and PAC-rich extracts more broadly are adulterated with grape seed extract, which is B-type, and with peanut skin extract, which is A-type and therefore passes a naive A-type screen while introducing a peanut allergen into a product labelled free of it. We therefore declare cranberry extract explicitly peanut-free on the specification and support that with lot-level profiling rather than a supplier attestation. The extract is vegan and vegetarian, with no bovine, porcine, marine or insect material and no other FDA 9 or EU 14 allergen inputs; carriers are named with their botanical origin. Cranberry extract powder holds a US GRAS notice, GRN 873, which received an FDA no-questions letter for use in beverages, beverage bases and ready-to-drink coffee at 150 mg per 8 oz serving. Heavy metals, pesticide residues, microbiology and residual solvents are tested lot-wise and every consignment ships with COA, specification, MSDS, allergen and GMO statements and origin documentation. This record describes composition and function only; no therapeutic or disease claim is made or supported.

Applications

Capsule and tablet blendsWomen's health supplementsSachet and stick packsFunctional beverage premixesGummies and chewablesEffervescent tablet blendsFruit polyphenol complexesPet supplement formulations

Available grades

PAC-standardised extract by DMAC across roughly 10% to 60%, with 15% and 25% the volume grades and higher assays to order. Native whole-fruit concentrates supplied to an agreed drug-to-extract ratio, declared per lot. Spray-dried cranberry juice powder on a named carrier, which is a juice preparation and not a PAC-standardised extract. Water-dispersible spray-dried grade on maize maltodextrin or gum acacia for beverage work, and a carrier-free grade for tablet and capsule work. Organic (NPOP/NOP/EU) lots where the origin certification chain supports it; kosher and halal certification available. Grades differ in PAC content by more than an order of magnitude and are not interchangeable; reformulating between them requires re-qualification and a recalculated serving size.

Packaging: 25 kg fibre drums with double food-grade LDPE liners, palletised and shrink-wrapped for export; 1 kg and 5 kg aluminium foil laminate pouches for sampling and pilot batches, heat-sealed with desiccant. Cranberry powders are markedly hygroscopic and will cake if opened into humid air, so drums are packed with desiccant, sealed under low humidity and, on request, nitrogen-flushed. Open only in a conditioned room and reseal immediately. Store below 25 C at under 60% RH, out of direct light.

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