D8132

Dehydro-L-(+)-ascorbic acid dimer

≥80% (enzymatic)

• Sinónimos: Bis(dehydro-L-ascorbic acid), Bis-DHA, DHA
• Fórmula empírica (notación de Hill): C₁₂H₁₂O₁₂
• Número CAS: 72691-25-9
• Peso molecular: 348.22
• UNSPSC Code: 12352205
• PubChem Substance ID: 24894191
• NACRES: NA.79
• Beilstein/REAXYS Number: 84277
• MDL number: MFCD00066467

Propiedades

• biological source: synthetic
• Quality Segment: 200
• assay: ≥80% (enzymatic)
• form: powder
• color: faint beige to beige, faint brown to light brown, white to yellow
• shipped in: dry ice
• storage temp.: −20°C
• SMILES string: O1[C@@H](C(=O)C(=O)C1=O)[C@@H](O)CO
• InChI: 1S/C6H6O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-8H,1H2/t2-,5+/m0/s1
• InChI key: SBJKKFFYIZUCET-JLAZNSOCSA-N

Descripción

General description

Dehydro-L-(+)-ascorbic acid dimer is a water soluble molecule, which is produced by vitamin C in the lumen of gastrointestinal tract.

Application

Dehydro-L-(+)-ascorbic acid dimer has been used to study its transformation and stability under the influence of pH, concentration and temperature.

Biochem/physiol Actions

Dehydro-L-(+)-ascorbic acid dimer is used to regenerate ascorbic acid(AA). AA oxidation to dehydroascorbic acid (DHA) takes place in extracellular fluid and cells. AA acts as an antioxidant and enzyme cofactor. It is used in a wide variety of applications, including cell culture. It also acts as a reducing agent, that helps reduce oxidative stress. L-Ascorbate can be regenerated from dehydroascorbic acid (DHA) by biological systems.

Other Notes

Dimer in crystalline form; hydrated monomer in aqueous solution

Información de seguridad

• Clase de almacenamiento: 11 - Combustible Solids
• ¿Qué está pasando?: WGK 3
• Punto de inflamación (°F): Not applicable
• Punto de inflamación (°C): Not applicable
• EPI (equipos de protección individual): Eyeshields, Gloves, type N95 (US)