EQUOPRO® / S-EQUOL INGREDIENT SUPPLIER
≥99% HPLC purity, clear specifications and technical documentation for supplement brands and formulation teams.
THE INGREDIENT AT A GLANCE
EquoPro is the S-stereoisomer of equol, supplied as a white powder for B2B ingredient evaluation. Start with identity and analytical limits, then review the batch-specific results.
Full specification, storage & stability →Specification basis: TDS dated 22 July 2026. Request the current controlled document and batch-specific results before purchase.
Request the current TDS & COA →EVIDENCE FOR YOUR EVALUATION
01 / HUMAN RESEARCH
An eight-week randomized trial enrolled 30 women, with 27 completing the study. Reported outcomes and limitations are available alongside the paper.
Preliminary findings; small sample, baseline imbalance and completer analysis limit interpretation.
Study design, results & original paper →All research & publication status →02 / SUPPLIER QUALIFICATION
Review the TDS, batch-report references, stability information, NSF GMP facility listing and self-affirmed GRAS statement with their applicable scope.
Facility registration and an industry award do not establish product efficacy or FDA approval.
Testing, safety & manufacturing documents →FORMULATION DEVELOPMENT
Capsules, tablets and nutritional blends are development concepts. A water-insoluble ingredient needs application-specific testing.
Evaluate loading, excipient compatibility and finished-product stability.
Assess mixing uniformity, ingredient interactions and packaging.
Investigate dispersion, flavor and stability; water solubility is not established.
SHANGHAI EGT SYNBIO GROUP CO., LTD.
Tell us your target market, application and estimated requirement. The team can discuss samples, documents and commercial terms.
S-EQUOL / FAQ
Identity, evidence and the practical steps to an ingredient evaluation.
Shanghai EGT Synbio Group Co., Ltd. supplies EquoPro®, a branded S-equol ingredient produced through microbial fermentation and conversion. Meet the supplier →
The TDS dated 22 July 2026 specifies ≥99% purity by HPLC. Review the current TDS and batch COA before purchase. Review analytical specifications →
The TDS describes the ingredient as insoluble in water. Beverage development requires specific dispersion, flavor and finished-product stability testing. Review formulation considerations →
An eight-week exploratory randomized, double-blind, placebo-controlled EquoPro study enrolled 30 perimenopausal women; 27 completed it. Small sample size and other limitations mean the results remain preliminary. Read the results and limitations →
Request the current TDS, a batch COA, relevant test reports, SDS and supporting safety and stability information. Review the version, batch and testing scope of each document. Explore the document guide →
Share your application, target market and estimated requirement. Sample availability, minimum order quantity, packaging, fees and lead time are confirmed for your project. Review the procurement process →