Description
HIGH-PURITY SPECIALTY INGREDIENT
L-Glutathione (reduced)
L-Glutathione (reduced) is supplied as a high-purity B2B raw material at 98.0%. This grade is produced to a declared purity with controlled identity, residual solvents and heavy metals, and is released against a batch-specific COA. It is intended for further processing by the buyer or for use as a reference material in development work; it is not a finished consumer product.
COA-Backed Specification
| Identity | L-Glutathione (reduced) |
|---|---|
| Form and colour | Fine white crystalline powder |
| Assay | 98.0% |
| Method | HPLC |
| Particle size | 98% through 80 mesh |
| Loss on drying | <=5.0% |
| Ash | <=5.0% |
| Heavy metals | Within the limits of the approved specification |
| Microbiological limits | Within the limits of the approved specification |
| Representative batch | LXGZ260516 |
| Manufacture date | 16 May 2026 |
| Shelf life | Two years when stored properly |
Representative values do not replace the current shipment COA.
Buyer Decision Guide
Buyers approving L-Glutathione (reduced) normally agree four points before the first order: the assay method and acceptance range, the identity and isomeric form, the residual solvent limits applicable to the destination market, and the physical form required by the buyer’s process. Confirm these at enquiry stage so the shipment is released to the right specification.
- Assay: 98.0% by HPLC, released batch by batch against the current COA.
- Identity: confirmed by the analytical methods stated in the specification table above.
- Residual solvents and heavy metals: reported per batch and reviewed against the destination market’s limits.
- Physical form: powder as standard; packaging and particle size agreed against the buyer’s process.
- Documentation: COA, specification sheet and safety data sheet accompany each shipment.
- Regulatory status, permitted uses and labelling requirements are the buyer’s responsibility for the destination market.
How This Grade Differs
L-Glutathione (reduced) is often quoted alongside materials of the same or a closely related name at a different purity or in a different form. The two are not interchangeable: purity, residual solvent profile and physical form all change the buyer’s processing yield. Compare quotations on the released assay and the reported impurity profile, not on the headline percentage alone.
Compare these related grades before approval:
For a substitution review, compare botanical identity, plant part, assay target, analytical method, physical form and the current offered-batch COA.
Application Areas
- Hard capsules and two-piece capsule filling
- Stick packs and single-serve sachets
- Powder blends and dry mixes
- Beverage and liquid concentrate systems, subject to the buyer’s process validation
Packaging and Delivery
- Evaluation sample typically 10-20 g, subject to stock
- Regular MOQ typically 1 kg
- 1 kg foil bag or 25 kg fibre drum with inner food-grade liner
- Custom packing and private-label options subject to confirmation
- Typical lead time 7-15 working days after deposit
Quality and Documentation
Representative batch LXGZ260516 supports the specification table above. Use the cited record for preliminary comparison and request the offered-lot COA for final technical approval. Batch COA, specification sheet, agreed third-party testing and export documents are available for buyer verification.
Frequently Asked Questions
Which specification figure should the purchase order reference for Reduced L-Glutathione Powder 98%?
The figure 98.0%, measured by HPLC.
What do you declare for moisture and ash?
Both are released against the limits on the approved specification; the measured result for your lot appears on its COA.
How is lot traceability handled?
Each lot keeps batch records and a retained sample, and the certificate for LXGZ260516 carries the same batch reference used in the quotation.
How does the material behave in your process?
It is supplied as Fine white crystalline powder at 98% through 80 mesh, so bulk density and flow are confirmed against your process before the first order.
How should the material be stored after arrival?
Two years when stored properly. Keep the pack sealed; moisture uptake is the main risk for this grade.
Which documents come with the shipment?
Batch COA, specification sheet, agreed third-party testing where required, commercial invoice, packing list, certificate of origin and transport documents. The exact set is confirmed against the product and destination market.
Can I get a sample before placing the order?
Yes. An evaluation sample is normally available before a formal order. Sample quantity, courier account and destination are confirmed at the time of request.
What is the usual lead time?
Regular production normally takes 7-15 working days after deposit, depending on stock, volume, testing and customisation requirements.
Request COA, Sample or Quotation
Send your target specification, application, order quantity, destination country and required test limits.
Get the current batch COA, a sample or a quotation
Specification comparison: Before comparing this grade with a conventional or liposomal-labelled form, review our liposomal versus conventional active buyer guide. It explains which identity, active-content basis and composition questions to put in your purchasing brief.
