Glutathione 1500mg/vial Promotes Detoxification And Brightens Skin Tone

Glutathione 1500mg/bottle core introduction

Medical-grade high-purity glutathione | Made in China glutathione 1500mg/bottle

Generic name : Reduced glutathione

English name : Reduced L-Glutathione

Chemical name : γ-glutamyl-cysteine-glycine

CAS No .: 70-18-8

Molecular formula : C₁₀H₁₇N₃O₆S

Molecular weight : 307.32 g/mol

Appearance : White crystalline powder

Purity : ≥98.5% (HPLC)

Content : ≥99.0%

Specific curl : -19.0° to -17.0°

Storage : Refrigerate at 2-8℃, away from light, sealed, and stored in a dry place.

Usage and Storage Guide

1. Reconstitution and preparation :

Recommended solvent :

Sterile water for injection : used in the preparation of injectable dosage forms

0.9% Sodium Chloride Injection : For preparation for intravenous infusion.

Specialized Solvents : Some products come with a specialized reconstitution solvent.

Solvents for cell experiments : PBS buffer or special culture medium

Standard preparation procedure :

Preparation for aseptic procedures :

Clean the work surface with 75% ethanol before operation.

Operators must wear sterile gloves, masks, and caps.

Use disposable sterile syringes and needles.

Solvent extraction :

Draw an appropriate amount of solvent (2-4 mL of sterile water is recommended) using a syringe.

The recommended final concentration is generally 300-600 mg/mL.

Reconstitution procedure :

Slowly pour the solvent along the bottle wall.

Gently rotate the vial to dissolve the powder.

Vigorous shaking is strictly prohibited to prevent oxidation and degradation.

Concentration calculation example :

Dissolve 1500 mg of glutathione in 3 mL of sterile water.

Final concentration: 500 mg/mL

Calculation formula: 1500mg ÷ 3mL = 500mg/mL

Key points to note :

Dissolution rate : This product dissolves relatively slowly; patient rotation is required for dissolution.

To avoid oxidation : Reconstitution should be carried out in an inert gas (nitrogen) environment.

Light protection : The reconstitution process must be carried out in the absence of light.

Stability : The reconstituted solution is easily oxidized at room temperature; refrigeration at 2-8℃ is recommended.

Usage time limit : It should be used within 2 hours after reconstitution.

2. Storage conditions :

Unopened raw materials :

Long-term storage : Store frozen at -20℃, shelf life 36 months

Short-term storage : Refrigerate at 2-8℃, shelf life 12 months.

Light protection requirement : Must be stored in the original packaging aluminum foil bag or light-proof container.

Humidity control : Relative humidity ≤ 60%

Reconstituted solution :

Use immediately : Use immediately after reconstitution.

Short-term storage : If storage is necessary, refrigerate at 2-8℃ for no more than 4 hours.

Freezing is strictly prohibited : Reconstituted solutions must not be frozen.

Transportation conditions :

Cold chain transportation : refrigerated transport at 2-8℃

Dry ice transportation : Long-term transportation is recommended below -20℃.

Light-proof packaging : Requires wrapping with light-proof material.

Moisture-proof packaging : built-in desiccant

3. Concentration reference standard :

Injection concentration : 300-600 mg/mL

Intravenous infusion concentration : The final diluted concentration shall not exceed 20 mg/mL

Cellular experimental concentration : 0.1-10 mM

In vitro study concentration : adjusted according to the experimental design.

4. Incompatibilities :

Do not mix :

Vitamin K

Vitamin B12

Antihistamines

sulfonamides

Note the compatibility :

Compatible with most electrolyte solutions

Compatible with amino acid solutions

It is recommended to infuse separately.

Quality Advantages of Chinese Manufacturers

This product is manufactured by a well-known Chinese pharmaceutical company, strictly adhering to cGMP standards, and its quality meets the standards of the Chinese Pharmacopoeia, the United States Pharmacopoeia, and the European Pharmacopoeia.

✅Advanced production technology :

Fermentation production : using patented yeast strains for fermentation production.

Multi-step purification process :

Ion exchange chromatography

Activated carbon decolorization

Molecular sieve separation

Crystallization Refining

Fully enclosed production line : prevents oxidation and contamination

Online quality monitoring : Full-process quality monitoring

✅Strict quality control :

Content determination : determined by HPLC method, content ≥99.0%

Purity analysis : Total impurities of related substances <1.5%

Chiral purity : L-glutathione purity ≥ 99.9%

Residue control :

Heavy metals <10ppm

Arsenic salt <2ppm

Bacterial endotoxin <0.5 EU/mg

Aseptic test meets the requirements

Stability study :

Accelerated test: 40℃±2℃, RH75%±5%, 6 months

Long-term test: 25℃±2℃, RH60%±5%, 36 months

✅ Professional packaging system :

Neutral borosilicate glass bottles : good chemical stability

Butyl rubber stoppers : low adsorption

Aluminum-plastic composite cap : Good sealing performance

Nitrogen purging protection : to prevent oxidation

Single-dose packaging : to avoid cross-contamination

✅Complete document system :

Batch production records

Batch inspection record

Stability Study Report

Quality Inspection Report (COA)

Drug registration documents

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