Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 745Erstellt: 25. Oktober 2026

Glutathion

GSH · L-GLUTATHIONE REDUCED · REDUCED GLUTATHIONE · glutatione · Glutathion · Liposomal Glutathione · Glutathione powder · glutide

https://huagongshe.com/de/chemical/745

Molekülstruktur von Glutathion

Identifikatoren & physikalische Daten

CAS No.70-18-8
SummenformelC10H17N3O6S
Durchschnittliche Molmasse307,33 g/mol
Monoisotopische Masse307,08380626 g/mol
SMILESNC(CCC(=O)NC(CS)C(=O)NCC(=O)O)C(=O)O
InChIKeyRWSXRVCMGQZWBV-UHFFFAOYSA-N
PubChem CID745
ChEMBLCHEMBL100476
ChEBICHEBI:177535
DTXSIDDTXSID70859082
Lokaler NameGlutathion

Chemische & physikalische Eigenschaften

XLogP-4,5
Polarare Oberfläche (TPSA)160
H-Brücken-Donoren6
H-Brücken-Akzeptoren8
Frei drehbare Bindungen9
Schwere Atome20
Formalladung0
Komplexität389
Schmelzpunkt192-195 °C (dec.) (lit.)
Siedepunkt754.5±60.0 °C(Predicted)
Dichte1.4482 (rough estimate)
Brechungsindex-17 ° (C=2, H2O)
Lagerbedingungen2-8°C
LöslichkeitH2O: 50 mg/mLsoluble
Aggregatzustandpowder
pKa (Säurekonstante)pK1 2.12pK2 3.53pK3 8.66pK4 9.12(at 25℃)
FarbeWhite
pH3 (10g/l, H2O, 20°C)
GeruchOdorless
Merck14,4475
BRN1729812
StabilitätStable. Incompatible with strong oxidizing agents.
Kosmetik-Inhaltsstoffe FunktionenREDUCING
InChI1S/C10H17N3O6S/c11-5(10(18)19)1-2-7(14)13-6(4-20)9(17)12-3-8(15)16/h5-6,20H,1-4,11H2,(H,12,17)(H,13,14)(H,15,16)(H,18,19)/t5-,6-/m0/s1
InChIKeyRWSXRVCMGQZWBV-WDSKDSINSA-N
SMILESN[C@@H](CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O)C(O)=O
LogP (Verteilungskoeffizient)-1.645 (est)
CAS Datenbank70-18-8(CAS DataBase Reference)
EPA chemische InformationenGlutathione (70-18-8)

Sicherheit & Vorschriften

F9-23
Wassergefährdungsklasse (WGK)2
TSCA-Inventar-StatusTSCA listed
Zollcode29309070
RTECS-Nr.MC0556000
R-Sätze (R)68-36/37/38
GefahrensymboleXi
Sicherheitshinweise (S)24/25-36/37/39-27-26
Lagerklasse11 - Combustible Solids

Anwendungen & Verwendung

Beschreibung

Glutathione (GSH) is a tripeptide (γ-glutamylcysteinylglycine) widely distributed in both plants and animals. GSH serves as a nucleophilic co-substrate to glutathione transferases in the detoxification of xenobiotics and is an essential electron donor to glutathione peroxidases in the reduction of hydroperoxides. GSH is also involved in amino acid transport and maintenance of protein sulfhydryl reduction status. The concentration of GSH ranges from a few micromolar in plasma to several millimolar in tissues such as liver.