D5392

Dithiodiglykolsäure

≥98%

• Synonym(e): 2,2′-Dithiodiacetic acid
• Empirische Formel (Hill-System): C₄H₆O₄S₂
• CAS-Nummer: 505-73-7
• Molekulargewicht: 182.22
• EG-Nummer: 208-019-8
• MDL-Nummer: MFCD00039607
• UNSPSC-Code: 12352100
• PubChem Substanz-ID: 57654100
• NACRES: NA.22

Eigenschaften

• Assay: ≥98%
• Form: powder
• Lagertemp.: −20°C
• SMILES String: OC(=O)CSSCC(O)=O
• InChI: 1S/C4H6O4S2/c5-3(6)1-9-10-2-4(7)8/h1-2H2,(H,5,6)(H,7,8)
• InChIKey: DLLMHEDYJQACRM-UHFFFAOYSA-N

Beschreibung

Anwendung

• Enhancement of octacalcium phosphate via Dithiodiglycolic acid: Research on the interlayer expansion of octacalcium phosphate illustrates the forced oxidation of Dithiodiglycolic acid intercalated molecules within its interlayers, showcasing a novel application in material science and chemical engineering (Sugiura et al., 2023).
• Drug delivery systems: A study on redox-responsive self-assembly PEG nanoparticles enhanced by triptolide, where Dithiodiglycolic acid plays a critical role, demonstrates its potential in improving the efficacy of antitumor treatments, providing insights into pharmaceutical applications (Wang et al., 2018).
• Synthesis and medicinal applications: A comprehensive study on the synthesis and biological evaluation of Dithiodiglycolic acid derivatives via oxidative coupling of thiols highlights its utility in medicinal chemistry, offering new avenues for drug design and development (Bakulina et al., 2019).
• Redox-sensitive coordination polymers: The development of redox-sensitive nanoscale coordination polymers for drug delivery and cancer theranostics utilizes Dithiodiglycolic acid, providing significant advancements in cancer treatment strategies (Zhao et al., 2017).

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Persönliche Schutzausrüstung: dust mask type N95 (US), Eyeshields, Gloves