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D-Chiro-Inositol 99% HPLC

D-Chiro-Inositol 99% HPLC is a defined inositol stereoisomer used in women’s-health and metabolic-wellness formulations.

GoodNutrition supplies this ingredient for supplement, functional food and personal care manufacturers. We support bulk purchasing with specification review, sample evaluation and export documentation for ongoing B2B supply projects.

Please confirm assay, appearance, solubility, packaging format and intended application with our team before order placement so the material profile matches your formula and market requirements.

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COA / MSDS documents

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GoodNutrition supplies botanical extracts and nutraceutical ingredients for supplement, functional food and personal care manufacturers. Contact us to confirm specification, assay, solubility, sample availability, MOQ, packaging and current lead time for this item.

We support B2B purchasing with COA documentation, production coordination and repeat-order planning for wholesale ingredient projects.

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ISO Certificate Documents

Published ISO certificates identify Good Nutrition Biotechnology Co., Ltd. Review each document's scope before supplier qualification.

ISO 9001:2015 standard markISO 9001:2015 ISO 22000:2018 standard markISO 22000:2018

ISO 9001 covers plant extracts and pharmaceutical intermediates. ISO 22000 covers the named extracts and food additives listed in its certificate, including NAD and MSM. These management-system documents do not certify every catalogue product.

Current status must be confirmed with CQC and the applicable surveillance audit acceptance notice. For Halal, Kosher or organic requirements, request product-specific evidence and confirm availability before ordering.

D-Chiro-Inositol 99% HPLC is a defined inositol stereoisomer used in women's-health and metabolic-wellness formulations.

D-chiro-inositol should be distinguished from myo-inositol because the two isomers are used at different ratios and inclusion levels. Isomer identity, chromatographic assay and blend uniformity are central purchasing and formulation considerations.

Product Specification

Product NameD-Chiro-Inositol 99% HPLC
Material IdentityD-chiro-inositol
AppearanceWhite to off-white powder
Key SpecificationD-chiro-inositol 99% by HPLC

Key Characteristics

  • Specific inositol stereoisomer with high chromatographic purity
  • Water-soluble crystalline powder
  • Often used at lower levels than myo-inositol in combination products

Formulation & Handling

  • Suitable for capsules, tablets, sachets and powder blends
  • Use validated premixing when combining with larger amounts of myo-inositol
  • Confirm isomer ratio and finished-product serving size during development

Quality Parameters to Review

  • Isomer identity and HPLC assay
  • Related inositol isomers and water content
  • Heavy metals and microbiological limits

Final suitability should be confirmed against the agreed product specification, batch COA, destination-market requirements and the buyer’s finished-product validation.

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Buyer FAQ

What should buyers verify for D-Chiro-Inositol 99% HPLC?

Review Isomer identity and HPLC assay; Related inositol isomers and water content; Heavy metals and microbiological limits. Final acceptance should follow the agreed specification and batch COA.

How is D-Chiro-Inositol 99% HPLC commonly formulated?

Suitable for capsules, tablets, sachets and powder blends; Use validated premixing when combining with larger amounts of myo-inositol; Confirm isomer ratio and finished-product serving size during development

What is D-Chiro-Inositol 99% HPLC commonly used for?

Common application directions include Women's metabolic-wellness supplements; Hormone-balance-positioned nutrition products; Myo-inositol and D-chiro-inositol combination formulas. Finished-product claims and suitability must be reviewed for the destination market.

B2B purchasing details

Review key sourcing details before bulk ordering

For bulk D-Chiro-Inositol 99% HPLC purchasing, buyers commonly review assay, purity, identity, particle size, heavy metals and microbiological limits before confirming sample evaluation, MOQ, packaging and lead time.

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