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2-Keto-L-gulonic acid, an indispensable constituent in the biomedical sector, embodies exceptional pharmacological attributes. It assumes a pivotal role as a fundamental constituent in the synthesis of vitamin C, paramount in bolstering immune competency and holistic well-being. Uses: Provitamins. Synonyms: L-xylo-2-Hexulosonic acid; L-xylo-Hexulosonic acid; Gulonic acid, 2-keto-, L-; Idonic acid, 2-keto-, L-; 2-keto-L-Gulonic acid; 2-Keto-L-idonic acid; L-Xylohexulosonic acid. Grades: ≥95%. CAS No. 526-98-7. Molecular formula: C6H10O7. Mole weight: 194.14.
2-Keto-L-gulonic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 2-KETO-L-GULONIC ACID;2-KETO-L-GULONIC ACID HYDRATE;2-Keto-L-gulonic acid hydrate,90%;L-xylo-2-Hexulosonicacid, hydrate (9CI);2-Keto-L-gulonic acid hydrateE chem. Product Category: Heterocyclic Organic Compound. CAS No. 342385-52-8. Molecular formula: C6H10O7. Mole weight: 194.14. Product ID: ACM342385528. Alfa Chemistry ISO 9001:2015 Certified.
2-Keto-L-gulonic Acid
2-Keto-L-gulonic Acid is used in biological studies for the formation of sorbitol metabolism by Acetobacter melanogenus. Group: Biochemicals. Alternative Names: L-Xylo-2-Hexulosonic Acid; L-Xylo-Hexulosonic Acid; 2-Keto-L-idonic Acid; 2-Keto-L-gulonic Acid; 2-Keto-L-Gulonic Acid; L-Xylohexulosonic Acid. Grades: Highly Purified. CAS No. 526-98-7. Pack Sizes: 250mg, 1g. Molecular Formula: C?H??O?, Molecular Weight: 194.14. US Biological Life Sciences.
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2-Keto-L-gulonic acid H2O (1:x)
2-Keto-L-gulonic acid H2O (1:x) is an indispensable compound in the biomedical field, serving as a pivotal constituent for the compoundion of L-ascorbic acid, more commonly referred to as Vitamin C. Given its reliability and efficacy, this compound presenting an unparalleled remedy in the research of Vitamin C insufficiency and its associated ailments. Uses: Provitamins. Synonyms: 2-Keto-L-gulonic acid; 526-98-7; L-xylo-Hex-2-ulosonic acid; L-sorbosonic acid; L-xylo-2-Hexulosonic acid; L-Xylohexulosonic acid; 2-Oxo-l-gulonic acid; (3S,4R,5S)-3,4,5,6-tetrahydroxy-2-oxohexanoic acid; 3-keto-L-Gulonic acid; L-Ketoidonate; 2-dehydro-L-idonic acid; L-Ketoidonic acid; L-sorbosonate; 2-keto-L-gulonate; 342385-52-8; I49386U15C; Gulonic acid, 2-oxo-; UNII-I49386U15C; EINECS 208-403-5; l-xylo-hexulosonic acid; EC 208-403-5; Idonic acid, 2-keto-, L-; SCHEMBL149382; CHEBI:19543; VBUYCZFBVCCYFD-NUNKFHFFSA-N; DTXSID901031512; 2-KETO-L-GULONIC ACID [MI]; AKOS006282126; ASCORBIC ACID IMPURITY C [EP IMPURITY]; E72647; EN300-25692370; Q27109187; 6DBA7178-9A91-4E10-8B9E-22EBA19458C8. CAS No. 342385-52-8. Molecular formula: C6H10O7.xH2O. Mole weight: 194.139 (anhydrous).
2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid sodium salt
2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid sodium salt, a pivotal bioactive compound extensively utilized in the biomedical sector, serves as a fundamental catalyst for the synthesis of L-ascorbic acid, widely recognized as vitamin C. This indispensable entity not only ensures the efficacious treatment of scurvy but also facilitates the augmentation of collagen synthesis while fortifying the immune system. Synonyms: Sodium 2,3. CAS No. 52508-35-7. Molecular formula: C12H17NaO7. Mole weight: 296.25.
2-C-hydroxy-2,3:4,6-bis-O-(1-methylethylidene)-L-Gulonic acidis mainly used in the manufacture of antiviral drug compounds. Its vital role permeates into the therapeutic attempts against maladies such as HIV and Hepatitis C. Synonyms: 2,3:4,6-Di-o-isopropylidene-2-keto-L-gulonic acid monohydrate; (-)-2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid monohydrate; 2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonicacidmonohydrate; (1R, 2S, 6R, 8S)-4, 4, 11, 11-tetramethyl-3, 5, 7, 10, 12-pentaoxatricyclo[6.4.0.02, 6]dodecane-6-carboxylic acid; hydrate; Dikegulac monohydrate; 60481-94-9; (3aS,3bR,7aS,8aR)-2,2,5,5-tetramethyltetrahydro-3aH-[1,3]dioxolo[4',5':4,5]furo[3,2-d][1,3]dioxine-8a-carboxylic acid hydrate;2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid;(-)-2,3:4,6-Di-O-isoproyplidene-2-keto-L-gulonic acid monohydrate; (-)-2,3:4,6-Di-O-isopropylidene-2-keto-L-gulonic acid monohydrate, 98%; 2,3:4,6-bis-O-(1-methylethylidene)-|A-L-xylo-2-Hexulofuranosonic acid hydrate (1:1). CAS No. 60481-94-9. Molecular formula: C12H20O8. Mole weight: 292.286.
L-sorbose 1-dehydrogenase
The product, L-sorbosone, is an intermediate in bacterial 2-keto-L-gulonic-acid formation. The activity of this membrane-bound enzyme is stimulated by Fe(III) or Co2+ but is inhibited by Cu2+. The enzyme is highly specific for L-sorboseas other sugars, such as glucose, mannitol and sorbitol, are not substrates. Phenazine methosulfate and DCIP can act as artificial acceptors. Group: Enzymes. Synonyms: SDH. Enzyme Commission Number: EC 1.1.99.32. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0461; L-sorbose 1-dehydrogenase; EC 1.1.99.32; SDH. Cat No: EXWM-0461.
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