50-81-7O=C1OC(C(O)CO)C(O)=C1OCIWBSHSKHKDKBQ-UHFFFAOYSA-NChemical: D-erythro-Hex-2-enonic acid, .gamma.-lactone
D-erythro-Hex-2-enonic acid, .gamma.-lactone is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of D-erythro-Hex-2-enonic acid, .gamma.-lactone are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
D-erythro-Hex-2-enonic acid, .gamma.-lactone: Does not have an individual approval but may be used under an appropriate group standard
Chemical: D-erythro-Hex-2-enonic acid, .gamma.-lactone
D-erythro-Hex-2-enonic acid, .gamma.-lactone is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of D-erythro-Hex-2-enonic acid, .gamma.-lactone are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)
D-erythro-Hex-2-enonic acid, .gamma.-lactone: Does not have an individual approval but may be used under an appropriate group standard
Not Known or Reasonably Ascertainable;All Other Chemical Product and Preparation Manufacturing;Plastics Material and Resin Manufacturing;Paint and Coating Manufacturing;Food, beverage, and tobacco product manufacturing
D-erythro-Hex-2-enonic acid, .gamma.-lactone: ACTIVE
BeschreibungAscorbic acid, a water-soluble dietary supplement, is consumed by humans more than any other supplement. The name ascorbic means antiscurvy and denotes the ability of ascorbic to combat this disease. Vitamin C is the l-enantiomer of ascorbic acid. Ascorbic acid deficiency in humans results in the body’s inability to synthesize collagen, which is the most abundant protein in vertebrates.
HistoryVitamin C is a general term for compounds having ascorbic acid activity, including ascorbic acid, dehydroascorbic acid, and its isomers.The understanding of vitamin C has gone through a long and painful process. Although the relationship between scurvy and stored food is obvious, but the treatments of this disease have been misguided. By 1601, British armed Captain James Lancaster discovered the disease on the ship of the East India Company and regarded the scurvy as “rot,” which could be made tissue alkaline. At the early stage of the nineteenth century, the understanding and treatment of scurvy had developed to a right approach. The exposition of scurvy etiology and metabolic theory took more than a century.By the early stage of the twentieth century, inspired by the animal model of beriberi, researchers in the Christchurch Oslo University discovered one animal that could suffer scurvy accidentally and then established a valuable scurvy animal model. This experiment demonstrated that the extract isolated from lemon had antiscurvy activity. Until 1932, many research groups obtained the anti-scurvy crystal from different plants and identified the crystal as ascorbic acid vitamin C. Next year, the chemical structure of ascorbic acid was elucidated, and then its artificial synthesis was accomplished.
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50-81-7、62624-30-0、89-65-6、89924-69-6CHEMBL1161421Verwendenantiscorbutic, antiviral
DefinitionChEBI: L-ascorbic acid is the L-enantiomer of ascorbic acid and conjugate acid of L-ascorbate. It has a role as a coenzyme, a flour treatment agent, a food antioxidant, a plant metabolite, a cofactor, a skin lightening agent and a geroprotector. It is an ascorbic acid and a vitamin C. It is a conjugate acid of a L-ascorbate. It is an enantiomer of a D-ascorbic acid.