Dihydroberberine 98% (DHB)

Canonical DHB route for berberine-family differentiation, stability review, and post-GLP-1 metabolic companion concepts.

Dihydroberberine (DHB) supplier specification

Nutrition BioTech is a bulk dihydroberberine ingredient supplier and manufacturer, supplying DHB powder at 98% minimum by HPLC (CAS 483-15-8), produced by controlled reduction of berberine, for B2B nutraceutical and dietary-supplement formulation.

Every lot ships with a Certificate of Analysis stating identity, HPLC assay and the assay basis, from an ISO 22000 and FSSC 22000 certified quality system. Samples, specifications and COAs are available on request for formulation trials.

Ingredient name Dihydroberberine (DHB)
Synonyms DHB; 7,8-dihydroberberine; reduced berberine; protoberberine-class isoquinoline alkaloid
CAS number 483-15-8
Machine-readable identifiers InChIKey FZAGOOYMTPGPGF-UHFFFAOYSA-N · PubChem CID 10217
Molecular formula C20H19NO4
Molecular weight 337.37 g/mol
Assay / purity 98% minimum by HPLC; other grades available on request.
Production route Controlled reduction of berberine (itself obtained from Phellodendron and Coptis botanical sources). Route and starting material are stated in the lot documentation.
Appearance Yellow to yellow-brown crystalline powder
Solubility Practically insoluble in water; soluble in methanol, ethanol and DMSO. DHB is oxidation-sensitive; protective packaging and handling guidance are supplied with the specification.
Typical applications Capsules, tablets and low-dose powder blends for B2B dietary-supplement programs; stability-focused formats reviewed per project.
Documentation Download public specification sheet
Public sheet prepared from the current product-page specification block; not a batch-specific Certificate of Analysis. Lot-specific COA and supporting records are available for qualified buyer review when appropriate.
Quality system ISO 22000:2018, FSSC 22000 and HACCP based quality system, GMP-aligned manufacturing; certificates available on request.
Supplier Nutrition BioTech, 1601 W. Mission Blvd, Suite 103 (DL#29), Pomona, CA 91766, United States

DHB Pro-Stable / stability-first product route

DHB Pro-Stable: the berberine upgrade has to survive the launch path.

Dihydroberberine can give metabolic-wellness brands a premium upgrade story, but the buyer review should not stop at a single headline. The real launch questions are stability, bitterness, color, packaging, sensory direction and technical file readiness.

Request DHB file packageView Post-GLP-1 route

Buyer reframe

Getting attention is easy. Passing formulation review is harder.

Many DHB products compete on headline bioavailability. A serious B2B launch has to go further: how the material behaves in sachets, powders, capsules or chewables; whether bitterness and color can be managed; what packaging route is realistic; and which files R&D, QA and regulatory teams need before launch planning.

Stability

Review the intended format, storage condition, water activity direction and packaging assumptions before choosing the finished-product route.

retention reviewpackaging

Taste and color

Bitterness, yellowing, appearance and sensory direction matter early, especially for powders, sachets, gummies and chewables.

bitternesscolor drift

File readiness

DHB should move with a clear technical review path: COA/spec, assay, safety files, allergen/GMO/vegan statements as applicable, and launch-language support.

COA/specclaim boundary

Best-fit applications

Where DHB Pro-Stable fits

  • Post-GLP-1 companion sachets paired with protein, fiber, creatine or gut-metabolic support ingredients.
  • Premium berberine-family upgrade concepts where the brand needs a sharper technical reason to exist.
  • Powder and stick-pack formats where stability, bitterness, color and packaging need early review.
  • Capsule or tablet lines where DHB is used as the technical upgrade while Berberine Pro-Micelle supports the broader platform story.

DHB launch review checklist

What a serious buyer should review before choosing a DHB route

Material identity

  • DHB assay and specification.
  • Source identity and production route discussion where available.
  • COA and method notes for buyer review.

Format risk

  • Stability discussion for the target dosage form.
  • Bitterness, appearance and color notes.
  • Packaging recommendation for the intended route.

Commercial readiness

  • Sample and application review route.
  • QA / regulatory file package as applicable.
  • Supplement-category launch wording and claim-boundary support.

Connected route

Use DHB Pro-Stable as the technical upgrade, then build the platform around the formula job.

DHB Pro-Stable is strongest when the buyer needs a premium berberine-family route with stability, taste, color, packaging and file review. Berberine Pro-Micelle can carry the broader routine-fit and dispersion discussion.

Together, they give Post-GLP-1 companion concepts a product-first architecture: material selection first, platform logic second, application and file package third.

Review Berberine Pro-Micelle

FAQ for brand teams

DHB Pro-Stable FAQ

Is DHB only an absorption story?

No. For a serious product launch, the better question is whether the ingredient route can support the target format, taste, color, packaging, file package and supplement-category language.

Which formats should be reviewed first?

Capsules and tablets are the simpler starting point. Sachets, powders, gummies and chewables need earlier review of bitterness, color, water exposure, processing route and packaging direction.

What should a buyer request first?

Ask for sample availability, COA/spec, assay method, stability discussion for the intended format, sensory direction, packaging recommendation and file-package support.

Do not launch DHB on a headline alone.

Nutrition BioTech can review DHB Pro-Stable against the target format, stability route, sensory direction, sample path, file package and public claim boundary before your brand commits to a formula.

Request DHB file and format review



Specification FAQ

What is the CAS number for Dihydroberberine?

The CAS number for Dihydroberberine is 483-15-8. The molecular formula is C20H19NO4 and the molecular weight is 337.37 g/mol. Machine-readable identifiers: InChIKey FZAGOOYMTPGPGF-UHFFFAOYSA-N · PubChem CID 10217.

What purity is Dihydroberberine supplied at, and by which method?

98% minimum by HPLC; other grades available on request.

Is Dihydroberberine soluble in water?

Practically insoluble in water; soluble in methanol, ethanol and DMSO. DHB is oxidation-sensitive; protective packaging and handling guidance are supplied with the specification.

How is Dihydroberberine produced and where does it come from?

Controlled reduction of berberine (itself obtained from Phellodendron and Coptis botanical sources). Route and starting material are stated in the lot documentation.

Published research context

Dihydroberberine, the reduced form of berberine, has a focused peer-reviewed literature on absorption, interconversion and bioanalysis. The studies below are provided as technical context for formulators evaluating this raw material. These entries summarise what the cited publications report. They are not claims about Nutrition BioTech material, and no health, therapeutic or cosmetic outcome is claimed or implied for any finished product. Buyers are responsible for the claims they make on their own labels and for confirming what is permitted in their market.

  1. Microbial reduction, absorption and solution instabilityReported that nitroreductases of the gut microbiota reduce berberine to dihydroberberine, that dihydroberberine showed an intestinal absorption rate about 5-fold that of berberine in animal experiments, and that dihydroberberine was unstable in solution and reverted to berberine in intestinal tissue through a non-enzymatic oxidation. The instability and reversion behaviour of the reduced form is directly relevant to its handling, packaging and formulation.Feng R, Shou JW, Zhao ZX, He CY, et al. Sci Rep. 2015;5:12155. PMID 26174047. DOI 10.1038/srep12155. source
  2. Human absorption kinetics of oral dihydroberberineIn a randomized, double-blind, crossover pilot trial in five adult males, measured plasma berberine after single 100 mg and 200 mg doses of dihydroberberine against a 500 mg dose of berberine: Cmax was 3.76 ± 1.4 ng/mL for 100 mg dihydroberberine versus 0.4 ± 0.17 ng/mL for 500 mg berberine, and AUC was 284.4 ± 115.9 versus 42.3 ± 17.6 ng/mL x 120 min. This is a pharmacokinetic study in volunteers, not raw-material release testing; identity and assay of supplied powder follow the methods stated in our specification and COA.Moon JM, Ratliff KM, Hagele AM, Stecker RA, et al. Nutrients. 2021;14(1):124. PMID 35010998. DOI 10.3390/nu14010124. source
  3. Metabolite profiling in Caco-2 cells and human volunteersUsing UHPLC-HRMS over a 24 h period in nine volunteers and in Caco-2 cells, reported that dihydroberberine administration gave higher blood concentrations of berberine and most berberine metabolites, while a micellar berberine formulation gave a higher proportion of unmetabolized berberine, and that individual metabolites followed distinct metabolic pathways.Chang C, Roh YS, Du M, Kuo YC, et al. Int J Mol Sci. 2024;25(11):5625. PMID 38891813. DOI 10.3390/ijms25115625. source
  4. Transdermal pharmacokinetics with validated LC-MS/MS bioanalysisDescribed transdermal formulations of berberine and dihydroberberine together with an LC-MS/MS method validated according to FDA bioanalytical guidelines, and reported in rats that bioavailability ranked by AUC0-8 as transdermal dihydroberberine above transdermal berberine, with both well above oral berberine. The matrix of this work is rat plasma, not raw-material assay.Buchanan B, Meng Q, Poulin MM, Zuccolo J, et al. PLoS One. 2018;13(3):e0194979. PMID 29579096. DOI 10.1371/journal.pone.0194979. source


Product review FAQ

Use these questions to start a claim-safe B2B sample, formulation, and documentation review.

What files can Nutrition BioTech provide for Dihydroberberine 98% (DHB)?

Available files may include COA, specification, identity, source, allergen, GMO, vegan, heavy metals, microbial limits, manufacturing flow, residual solvent, country of origin, and composition statements, depending on the material and target market.

How should a brand review Dihydroberberine 98% (DHB) before sampling?

The best first review includes the target dosage form, serving size, market channel, active marker, required documents, and any formulation constraints such as solubility, taste, density, particle behavior, or stability.

What regulatory and facility support may be available?

Regulatory review notes for the target market can be provided. Nutrition BioTech does not hold and does not claim any GRAS notification or NDI notification for this material. Facility and quality system support follows the same certificate set named in the specification table: ISO 22000:2018, FSSC 22000, HACCP and GMP. The holding entity for each certificate is named on the certificate and confirmed under buyer review.

Claim boundary: ingredient pages are for B2B technical and formulation review. Public wording should be matched to the intended market, dosage form, and applicable regulatory review.

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