First Choice Peptides

For laboratory research use only. This compound is not FDA approved and is not for human or veterinary use. All data presented is drawn from published laboratory and preclinical literature for reference purposes.

L-Glutathione

Cell Biology

L-Glutathione

Reduced L-glutathione tripeptide

GSHL-Glutathione reducedCAS: 70-18-8

Reduced L-glutathione is an endogenous gamma-glutamyl tripeptide used in biochemical and cell-biology research involving redox chemistry, thiol-dependent reactions, enzymatic assays, oxidative-stress models, and analytical method development. This material is intended exclusively for laboratory research and is not supplied for human or veterinary use.

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$149.99

Quantity

1

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Frequently researched together

Other laboratory research compounds available in our catalog.

Compound information

Technical specifications

What is L-Glutathione?

L-Glutathione is a three-residue peptide whose sequence corresponds to the endogenous gamma-glutamyl tripeptide found in the cells of essentially every aerobic organism. The catalogue supplies the reduced form, listed under the synonyms GSH and L-glutathione reduced, in 600 mg and 1500 mg presentations. It is supplied strictly for laboratory research use and is not for human or veterinary use.

The sequence is gamma-Glu-Cys-Gly. The prefix gamma is the defining structural feature: the bond joining glutamate to cysteine is formed from the side-chain carboxyl rather than the alpha-carboxyl, producing an isopeptide linkage that resists ordinary aminopeptidases and gives the molecule a dedicated enzymatic degradation route. The central cysteine carries a free sulfhydryl group, the chemically active centre of the molecule, which on oxidation joins two molecules through a disulfide bond to give the dimer GSSG.

L-Glutathione is catalogued under CAS 70-18-8 with the molecular formula C10H17N3O6S and a molecular weight of 307.33 g/mol, values that describe the reduced monomer rather than the oxidised dimer. The single sulphur atom in the formula is the cysteine thiol. It is used as a bulk reagent in redox chemistry, thiol-dependent reactions, enzymatic assays, oxidative-stress model systems and analytical method development.

Read the compound guide
GSHL-Glutathione reducedCAS: 70-18-8
CAS number
70-18-8
Molecular formula
C10H17N3O6S
Molecular weight
307.33 g/mol

Stability information

Recommended handling and storage conditions for retaining compound identity and integrity in the laboratory.

Lyophilized

-20°C · Protect from light

Reconstituted

2-8°C

Regulatory information

Development origin and regulatory status, compiled for reference.

Research compound · Not FDA-approved

Frequently asked

Questions about L-Glutathione

What purity is L-Glutathione supplied at, and is a Certificate of Analysis available?

Yes. Each lot of L-Glutathione is tested by a third-party laboratory using HPLC for purity, and the certificate of analysis for the current lot is linked on this page and in the certificate library.

How is the identity of L-Glutathione verified?

Identity is confirmed by mass spectrometry against the expected molecular weight of 307.33 g/mol, alongside HPLC retention behaviour. Both results are recorded on the lot certificate.

How should L-Glutathione be stored on receipt?

Lyophilized: -20°C (Protect from light); Reconstituted: 2-8°C.

Where is L-Glutathione shipped from?

Orders ship from the United States in discreet, tracked packaging. Shipping is available to US addresses only.

Is L-Glutathione supplied for research use only?

Yes. L-Glutathione is sold strictly as a laboratory research material. It is not for human or veterinary use, not for diagnostic procedures, and has not been evaluated by the U.S. Food and Drug Administration. See the research use disclaimer for the full terms.

Answers describe how this material is tested, stored and shipped. They are not guidance on any use, and this compound is not for human or veterinary use.

Sources & references

Published literature in which this compound has been the subject of laboratory or preclinical study. Listed for bibliographic reference only.

Research and educational purposes only. These references are provided for bibliographic context. They are not evidence of safety or efficacy, and nothing here is medical advice or a claim about any use in humans or animals.

Cellular and molecular life sciences : CMLS

Mechanisms of ferroptosis

2016DOI: 10.1007/s00018-016-2194-1PMID: 27048822
View source

Molecules (Basel, Switzerland)

Glutathione-Related Enzymes and Proteins: A Review

2023DOI: 10.3390/molecules28031447PMID: 36771108
View source

Antioxidants & redox signaling

Glutathione Degradation

2017DOI: 10.1089/ars.2017.7136PMID: 28537416
View source

Biochimica et biophysica acta

Nuclear glutathione

2013DOI: 10.1016/j.bbagen.2012.10.005PMID: 23069719
View source