Glycine, N-(N-D-γ-glutamyl-L-cysteinyl)-

Base Information

• Chemical Name: Glycine, N-(N-D-γ-glutamyl-L-cysteinyl)-
• CAS No.: 108457-42-7
• Molecular Formula: C₁₀H₁₇N₃O₆S
• Molecular Weight: 307.327
• Mol file: 108457-42-7.mol

Synonyms:Glycine,N-(N-D-g-glutamyl-L-cysteinyl)-

Chemical Property of Glycine, N-(N-D-γ-glutamyl-L-cysteinyl)-

Chemical Property:

• Melting Point: 191-193 °C (decomp)
• Boiling Point: 754.5±60.0 °C(Predicted)
• PKA: 2.21±0.10(Predicted)
• PSA: 197.62000
• Density: 1.441±0.06 g/cm3(Predicted)
• LogP: -0.72400

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: Glycine, N-(N-D-γ-glutamyl-L-cysteinyl)-, often referred to as Glutathione, is a vital molecule with diverse applications in different fields. In the field of healthcare and medicine, it is a crucial antioxidant that plays a key role in protecting cells from oxidative damage and maintaining overall health. It is used as a supplement and in intravenous treatments to support liver function, boost the immune system, and aid in detoxification processes. In the cosmetic and skincare industry, glutathione is utilized for its potential skin-lightening and anti-aging properties, contributing to the formulation of skincare products. Additionally, in research and diagnostics, it serves as a valuable tool for the study of cellular processes and oxidative stress, aiding in scientific investigations. Its multifaceted utility underscores its significance in promoting health, skincare, and scientific research, where it plays a pivotal role in wellness, cosmetic formulations, and biomedical research.

Technology Process of Glycine, N-(N-D-γ-glutamyl-L-cysteinyl)-

There total 1 articles about Glycine, N-(N-D-γ-glutamyl-L-cysteinyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ 2-(4-ammonio-4-carboxy-butyrylamino)-2-(carboxymethyl-carbamoyl)-ethylsulfanyl (70-18-8,76946-74-2,108457-42-7,128960-77-0,148102-19-6)

Guidance literature:

Glutathion, Ce⁴⁺;

DOI:10.1016/0022-2364(69)90047-X

Reference yield: 94.0%

[Pt(tris(2-diphenylphosphinoethyl)amine)Cl]Cl*4H2O + glutathione (70-18-8,76946-74-2,108457-42-7,128960-77-0,148102-19-6) → PtN(C2H4P(C6H5)2)3(O2CCHNH3C2H4CONHCHCH2SCONHCH2CO2)*2H2O=PtN(C2H4P(C6H5)2)3(O2CCHNH3C2H4CONHCHCH2SCONHCH2CO2)*2H2O

Guidance literature:

In methanol; water; to a soln. of aminoacid in water was added dropwise to a soln. of complex in water, the mixt. was stirred for 48 h at ambient temp.; filtered, lyophilised, washed with ether, dried in vac.; elem. anal.;

DOI:10.1016/S0020-1693(02)00813-7

Reference yield: 94.0%

Glutathione reduced (108457-42-7) → glutathione disulfide (464195-33-3,121-24-4,87140-29-2)

Guidance literature:

With [(η⁵-C₅Me₅)Ru(μ-1_k³SSS':2_k²SS-tpdt)Fe(η⁵-C₅Me₅)][PF₆]; oxygen; In water; at 20 ℃; for 3h; Green chemistry;

DOI:10.1039/c9cy01667h

Downstream raw materials:

glutathione disulfide

VK₃GS