Colorless transport powder
70-18-8
C10H17N3O6S
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Product Description
Reduced L-glutathione, commonly abbreviated as GSH, is a naturally occurring tripeptide composed of L-glutamic acid, L-cysteine and glycine. Its chemical name is γ-L-glutamyl-L-cysteinylglycine.
Commercial reduced glutathione is normally supplied as a white or almost white crystalline powder. Its CAS number is 70-18-8, molecular formula is C₁₀H₁₇N₃O₆S, and molecular weight is 307.32 g/mol.
The cysteine residue contains a reactive sulfhydryl group responsible for the reducing properties of GSH. Exposure to oxygen, elevated temperature, unsuitable pH or trace metals can convert reduced glutathione into oxidized glutathione, also known as GSSG.
The term “glutathione” should not be used without identifying whether the supplied material is reduced GSH or oxidized GSSG.
Property | Information |
|---|---|
Product name | Reduced L-Glutathione |
Abbreviation | GSH |
Chemical name | γ-L-Glutamyl-L-cysteinylglycine |
CAS number | 70-18-8 |
EC number | 200-725-4 |
Molecular formula | C₁₀H₁₇N₃O₆S |
Molecular weight | 307.32 g/mol |
Composition | Tripeptide of glutamate, cysteine and glycine |
Appearance | White or almost white crystalline powder |
Water solubility | Soluble in water |
Typical assay | 98.0–101.0% on a dried basis |
Important impurity | Oxidized glutathione, GSSG |
Common production route | Controlled microbial fermentation |
Applications | Nutritional, food, cosmetic, biochemical and qualified pharmaceutical formulations |
Storage | Sealed, dry, protected from heat, light, oxygen and moisture |
The exact grade, production route, specification and regulatory suitability should be confirmed in the AOZUN quotation and batch documentation.
Reduced and oxidized glutathione are related but different substances.
Property | Reduced glutathione | Oxidized glutathione |
Abbreviation | GSH | GSSG |
Representative CAS number | 70-18-8 | 27025-41-8 |
Molecular form | Single tripeptide with a free sulfhydryl group | Two glutathione units connected by a disulfide bond |
Molecular weight | 307.32 g/mol | Approximately 612.63 g/mol |
Function in redox systems | Reducing form | Oxidized form |
Purchasing significance | Main active material | Process- and storage-related impurity or separately sold reagent |
A high total-glutathione result does not necessarily prove a high reduced-GSH content. Buyers should request a method capable of distinguishing GSH from GSSG.
Reduced glutathione can oxidize during manufacturing, drying, storage, solution preparation and formulation.
If the analytical method does not separate GSH and GSSG, the result may not accurately describe the amount of reduced glutathione in the product.
For quality-sensitive applications, the specification should separately address:
Reduced glutathione assay
GSSG
Individual related compounds
Total organic impurities
Water or loss on drying
Solution clarity and color
Reduced glutathione quality should be evaluated using identity testing, a validated quantitative assay and impurity-specific analysis. HPLC or another suitable separation method can distinguish the desired reduced form from oxidized glutathione and related compounds more effectively than a nonspecific total assay.
Testing only appearance and total assay may miss oxidation or closely related impurities.
An appropriate chromatographic method can support evaluation of:
Reduced glutathione content
Oxidized glutathione
Individual related substances
Total organic impurities
Batch-to-batch consistency
Stability changes
The analytical method and reference standard should be stated in the specification or test procedure.
Test item | Specification |
Appearance | White or almost white crystalline powder |
Appearance of solution | Clear and colorless |
Assay, dried basis | 98.0–101.0% |
Specific optical rotation | −17.5° to −15.5° |
Chloride | ≤200 ppm |
Sulfate | ≤300 ppm |
Ammonium | ≤200 ppm |
Iron | ≤10 ppm |
Heavy metals, as Pb | ≤10 ppm |
Loss on drying | ≤0.5% |
Sulfated ash | ≤0.1% |
For food, nutritional, cosmetic or pharmaceutical qualification, buyers may also require GSSG, related compounds, elemental impurities and microbiological limits.
Final acceptance criteria must be confirmed using the current AOZUN specification and batch COA.
Depending on the application, the following tests may be requested:
Additional test | Example purchasing consideration |
GSSG | A defined maximum, such as ≤1.5%, when applicable |
Total organic impurities | A defined maximum, such as ≤2.0% |
Individual impurity | Method- and grade-specific |
Lead | Destination- and application-specific |
Arsenic | Destination- and application-specific |
Cadmium | Destination- and application-specific |
Mercury | Destination- and application-specific |
Total aerobic microbial count | Application-specific |
Yeast and mold | Application-specific |
Specified pathogens | Based on intended use |
Residual solvents | According to production route and application |
Pesticide residues | When required |
GMO status | Based on fermentation organism and customer policy |
Allergen statement | Based on raw materials and facility controls |
Solubility | Clear, colorless solution at the declared concentration |
Reference limits are not automatically part of the standard AOZUN specification. They must be agreed before order confirmation.
The assay indicates the measured glutathione content. The result should state whether it is calculated on an as-is or dried basis.
A reported value above 100% can occur because of analytical uncertainty and dried-basis calculation. It does not mean that the sample physically contains more than 100% material.
Glutathione contains chiral amino-acid residues. Specific optical rotation helps confirm stereochemical identity and can reveal major differences in composition.
The concentration, solvent, temperature and optical path used in the test must be stated.
GSSG is the oxidized form of glutathione. Elevated GSSG may indicate oxidation during processing or storage.
A dedicated GSSG limit is more informative than relying only on total assay.
Loss on drying estimates moisture and other volatile matter. Excess moisture can affect assay, stability, flowability and oxidation rate.
These inorganic ions may originate from raw materials, fermentation, purification or pH adjustment. Limits help establish purification consistency.
Residual ammonium can be associated with fermentation nutrients or downstream processing. Sensitive food, cosmetic and pharmaceutical applications may require a controlled limit.
Trace iron and other transition metals can catalyze oxidation. A low iron level can therefore support both purity and stability.
Sulfated ash estimates nonvolatile inorganic residue. A high result may indicate salts or other inorganic contamination.
A generic “heavy metals as Pb” test may not be sufficient for every regulated application. Modern qualification may require individual results for lead, arsenic, cadmium and mercury.
Material intended for food, nutritional or cosmetic formulations may require defined microbial limits.
A high chemical assay does not demonstrate acceptable microbiological quality.
Commercial reduced glutathione is commonly produced through controlled microbial fermentation followed by separation, purification, concentration, crystallization and drying.
A typical manufacturing sequence may include:
Preparation of the fermentation medium
Controlled microbial fermentation
Cell separation or extraction
Purification
Concentration
Crystallization
Drying
Milling or sieving
Quality testing
Moisture- and oxygen-protective packaging
The actual production organism, fermentation substrate and processing aids should be confirmed with the supplier.
Fermentation is widely used for commercial reduced glutathione because it can provide the required stereochemical form and support industrial-scale production.
Buyers should still verify:
Microorganism identity
GMO or non-GMO status
Fermentation substrate
Animal-origin status
Allergen risks
Processing aids
Residual solvents
Purification controls
Batch traceability
“Fermentation-derived” does not automatically establish food, pharmaceutical, vegetarian, vegan, non-GMO, halal or kosher compliance.
Material intended for supplements or food products may require:
Appropriate food-manufacturing controls
Microbiological limits
Elemental-impurity limits
Allergen statement
GMO statement
Residual-solvent controls
Compliance with destination-country rules
Permission to use glutathione in foods or supplements varies by country.
Cosmetic-grade GSH should have controlled color, odor, purity, GSSG, metals and microbiological quality.
The finished cosmetic manufacturer remains responsible for formulation safety, stability, claims and regulatory notification.
Pharmaceutical applications may require:
Compliance with an applicable pharmacopeial monograph
GMP manufacturing
Validated analytical methods
Impurity profiling
Elemental-impurity evaluation
Stability data
Change control
Regulatory support
A 98% or 99% assay alone does not establish pharmaceutical grade.
Laboratory applications may prioritize:
Identity
Assay
GSSG
Enzyme-assay suitability
Solution clarity
Trace metals
Consistent analytical performance
Reagent grade is not automatically suitable for food, cosmetic or clinical use.
Glutathione may be used in certain wine-production applications where permitted. Oenological material may require defined GSH content, moisture, elemental impurities, labeling and production-source information.
Use must comply with the applicable OIV standard and local wine regulations.
Qualified reduced glutathione may be used as an ingredient in capsules, tablets, powders, beverages or other supplement formats where legally permitted.
Formulators should evaluate:
Permitted ingredient status
Maximum or recommended use level
Product stability
Interactions with minerals and oxidizing ingredients
Taste and odor
Finished-product testing
Permitted label claims
This raw-material page does not provide dosing or medical advice.
Glutathione may be used in certain food, beverage and oenological applications, subject to local regulations.
Its reducing character may influence oxidation, color and flavor stability, but the effect depends on the complete formulation and processing conditions.
Generic industrial or reagent-grade material should not be used in food.
Reduced glutathione may be incorporated into qualified cosmetic formulations as an antioxidant or skin-conditioning ingredient where legally permitted.
Formulators should verify:
Ingredient regulatory status
Concentration
pH
Oxidation stability
Color development
Odor
Preservative compatibility
Packaging
Finished-product safety
Permitted cosmetic claims
A raw-material supplier should not guarantee skin whitening, removal of pigmentation, wrinkle reduction or a specific time to visible results.
Qualified pharmaceutical-grade glutathione may be used as an API, excipient or processing material in approved pharmaceutical applications.
Bulk ingredient material must not be represented as an injectable or finished medicine. Sterile products require separate manufacturing, sterilization, container-closure and regulatory controls.
Reduced glutathione is used in:
Biochemical assays
Enzyme research
Redox-system studies
Protein chemistry
Buffer formulations
Cell-culture research
Analytical standards
Laboratory reducing systems
Researchers should select a grade appropriate for the test method and required purity.
GSH contains a reactive sulfhydryl group and can oxidize in solution.
Important formulation variables include:
pH
Temperature
Dissolved oxygen
Light exposure
Trace iron and copper
Water activity
Other oxidizing ingredients
Packaging headspace
Processing time
Preservative system
A high-quality raw material cannot compensate for an unstable finished formulation.
Two reduced glutathione molecules can form a disulfide bond, producing oxidized glutathione.
Oxidation may accelerate when GSH is exposed to:
Air
Elevated temperature
Alkaline conditions
Light
Trace metals
Oxidizing agents
Long solution-holding times
Repeated container opening
The change may not always be visible, so chemical testing is required.
Depending on the intended product, formulators may evaluate:
Suitable pH control
Low-oxygen processing
Nitrogen headspace
Chelating agents
Low-metal raw materials
Light-protective packaging
Reduced processing temperature
Shorter solution-holding time
Compatible antioxidants
Appropriate water activity
Finished-product stability studies
Any stabilization system must comply with the applicable food, cosmetic or pharmaceutical regulations.
For analytical or manufacturing use:
Use suitable-quality water.
Use clean, low-metal equipment.
Prepare only the amount required.
Minimize air exposure.
Avoid unnecessary heating.
Control pH.
Protect the solution from light where appropriate.
Use the solution promptly unless validated stability data support storage.
Monitor GSH and GSSG during stability studies.
Aqueous GSH solutions generally oxidize more readily than the sealed dry powder.
Before commercial formulation, test compatibility with:
Copper and iron salts
Peroxides
Strong oxidizers
Alkaline ingredients
Mineral premixes
Botanical extracts
Flavor systems
Preservatives
Surfactants
Packaging materials
Metal-containing ingredients may significantly affect oxidation.
A qualified supplier should be able to confirm:
Reduced form, GSH
CAS number
Production method
Assay method and calculation basis
GSSG limit
Related-substance limits
Optical rotation
Moisture or loss on drying
Elemental impurities
Microbiological limits
Fermentation organism
GMO and allergen status
Animal-origin status
Packaging
Storage and shelf life
COA, TDS and SDS availability
Change-control procedure
Regulatory suitability for the intended market
A supplier should not rely solely on a purity result when offering material for regulated applications.
Depending on the grade, buyers may verify:
Packaging integrity
Label and batch number
Appearance
Solution clarity
Identification
Assay
Specific optical rotation
GSSG
Related compounds
Loss on drying
Residue on ignition
Chloride
Sulfate
Ammonium
Iron
Elemental impurities
Microbiological quality
COA compliance
Retained samples should be protected from moisture, heat, light and oxygen.
A typical industrial package may use:
Double food-compatible PE inner bags
Light- and moisture-resistant outer bag
Sealed fiber or cardboard drum
25 kg net weight
Smaller foil bags for samples or specialty orders
Actual package size and liner material should be confirmed in the quotation.
For regulated uses, packaging materials may require food-contact, pharmaceutical or other application-specific documentation.
Store reduced glutathione in a tightly sealed container in a cool, dry place protected from:
Direct sunlight
Heat
Moisture
Oxygen
Strong oxidizers
Trace-metal contamination
Repeated container opening
Some reagent grades are stored at 2–8°C, while other validated bulk grades may have different labeled conditions. Follow the storage instructions and shelf life stated for the purchased product.
After opening, reseal the inner bag promptly and minimize headspace exposure.
Reduced glutathione is generally handled as a low-hazard solid, but normal industrial hygiene remains necessary.
Avoid:
Generating airborne dust
Breathing powder
Eye contact
Prolonged skin contact
Contamination of food or production areas
Mixing with unidentified oxidizing materials
Use suitable gloves, protective eyewear and dust control according to the current SDS and workplace risk assessment.
Reduced glutathione is commonly transported as a non-dangerous good.
Final transport status should be confirmed using:
Current supplier SDS
Product grade
Package size
Transport method
Destination-country requirements
Temperature or moisture protection may still be commercially important even when the product is not classified as dangerous goods.
Regulatory status varies according to country and application.
Before using glutathione in a food, supplement, cosmetic or pharmaceutical product, confirm:
Permitted ingredient status
Required grade
Use-level restrictions
Labeling requirements
Permitted claims
Manufacturing requirements
Import registration
Finished-product testing
Pharmacopoeial requirements, when applicable
A CAS number or UNII listing does not itself establish regulatory approval for a specific use.
Depending on application, buyers may request:
Certificate of Analysis
Safety Data Sheet
Technical Data Sheet
Product specification
Manufacturing-flow summary
GMP statement
Country of Origin
Allergen statement
GMO statement
Animal-origin or BSE/TSE statement
Residual-solvent statement
Elemental-impurity report
Microbiological report
Pesticide-residue statement
Halal certificate
Kosher certificate
Stability or retest information
Change-control statement
Only request or advertise certificates that apply to the actual supplied grade and manufacturing site.
AOZUN supports international buyers seeking reduced L-glutathione for qualified nutritional, food, cosmetic, biochemical and pharmaceutical-manufacturing applications.
Commercial support may include:
Grade and specification review
Batch-specific COA
GSH and GSSG requirement discussion
Packaging options
Sample evaluation
Documentation coordination
Export support
Third-party inspection
International shipment planning
Technical communication during supplier qualification
Product grade, specification, manufacturing source, regulatory status and intended-use suitability must be confirmed in the final quotation and contract.
For an accurate quotation, provide:
Product name: Reduced L-Glutathione
CAS number: 70-18-8
Intended application
Required grade
Assay requirement
Maximum GSSG
Related-substance limits
Elemental-impurity limits
Microbiological requirements
Required certificates
Order quantity
Packaging requirement
Destination
Sample requirement
Delivery schedule
If you are replacing an existing supplier, attach the current specification or representative COA.
Reduced L-glutathione is a tripeptide composed of glutamate, cysteine and glycine. It is commonly abbreviated as GSH.
Its CAS number is 70-18-8.
Reduced glutathione has a molecular weight of 307.32 g/mol.
The word “glutathione” is sometimes used generically. A purchase specification should state whether the product is reduced glutathione, GSH, or oxidized glutathione, GSSG.
GSSG is oxidized glutathione formed when two GSH molecules create a disulfide bond. It is an important quality and stability indicator.
Yes. Reduced glutathione is soluble in water and should produce a clear, colorless solution at an appropriate test concentration.
A total assay may not distinguish reduced glutathione from its oxidized form. Separate GSSG testing provides better information about oxidation and active GSH content.
Not automatically. Pharmaceutical grade also depends on the pharmacopoeial specification, GMP system, impurities, stability, documentation and intended regulatory use.
No. Food or bulk ingredient grade must not be used as an injectable product. Injectable use requires an approved sterile pharmaceutical product.
No. A raw-material supplier should not guarantee whitening or a specific time to visible results. Cosmetic performance depends on formulation, concentration, stability, use conditions and permitted claims.
It may be produced by fermentation, but vegan status must be supported by information about the microorganism, fermentation medium, processing aids and manufacturing facility.
No. GMO status must be confirmed using supplier documentation.
Keep it tightly sealed, cool, dry and protected from light, moisture, oxygen and oxidizing materials. Follow the storage conditions printed on the supplied product.
GSH solutions can oxidize to GSSG. Prepare solutions fresh unless validated stability data support a defined storage period.
A common bulk package is 25 kg per drum with moisture-resistant inner liners. Smaller packages may be discussed during quotation.
Sample and documentation availability can be discussed during quotation. Include your grade, GSSG, microbiological and regulatory requirements in the inquiry.
Contact AOZUN for reduced L-glutathione pricing, specifications, packaging and export information.
Send us your required grade, assay, GSSG limit, application, quantity, packaging, destination and documentation requirements. Our team will review the request and confirm an appropriate commercial specification.