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2,3:4,5-Di-O-isopropylidene-D-gulonic acid methyl ester 2,3:4,5-Di-O-isopropylidene-D-gulonic acid methyl ester is a pharmaceutical intermediate that can play a vital role in drug synthesis. Notably, it is often used in the research and development of certain antiviral drugs targeting diseases such as influenza and Hepatitis C. Synonyms: D-Gulonic acid, 2,3:4,5-bis-O-(1-methylethylidene)-, methyl ester; Methyl 2,3:4,5-bis-O-(1-methylethylidene)-D-gulonate. CAS No. 1714993-08-4. Molecular formula: C13H22O7. Mole weight: 290.31. BOC Sciences 3
(-)-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 is a useful research chemical. Synonyms: 2,3:4,6-Di-o-isopropylidene-2-keto-L-gulonic acid monohydrate; Dikegulac monohydrate. CAS No. 68539-16-2. Molecular formula: C12H20O8. Mole weight: 292.28. BOC Sciences 2
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: Dikegulac sodium; Dikegulac-sodium; Atrinal; Cutlass; Sodium 2,3:4,6-Di-O-isopropylidene-a-L-xylo-2-hexulofuranosonate. CAS No. 52508-35-7. Molecular formula: C12H17NaO7. Mole weight: 296.25. BOC Sciences 3
2,3:5,6-Bis-O-(1-methylethylidene)-D-gulonic acid g-lactone 2,3:5,6-Bis-O-(1-methylethylidene)-D-gulonic acid g-lactone, a paramount compound extensively applied in the biomedical sector, showcases prodigious proficiency in managing an assortment of ailments and conditions, particularly liver disorders like nonalcoholic fatty liver disease (NAFLD) and liver fibrosis. Renowned for its extraordinary chemical attributes, this remarkable product unveils auspicious therapeutic prospects and presents novel avenues for counteracting these afflictions. Synonyms: D-Gulonic acid, 2,3:5,6-bis-O-(1-methylethylidene)-, γ-lactone; 2,3:5,6-Di-O-isopropylidene-D-gulono-1,4-lactone; (3aR,6S,6aR)-6-((R)-2,2-Dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyldihydrofuro[3,4-d][1,3]dioxol-4(3aH)-one. CAS No. 67642-42-6. Molecular formula: C12H18O6. Mole weight: 258.27. BOC Sciences 3
2,3,5,6-Tetra-O-acetyl-D-gulonic acid-1,4-lactone 2,3,5,6-Tetra-O-acetyl-D-gulonic acid -1,4-lactone, an indispensable compound in the biomedical field, assumes a pivotal function in the synthesis of ascorbic acid, making it of utmost importance in the manufacturing of vitamin C. CAS No. 136345-68-1. Molecular formula: C14H18O10. Mole weight: 346.29. BOC Sciences 3
2,3-Diketo-L-gulonic acid 2,3-Diketo-L-gulonic acid is predominantly invoked in the synthesis of the ubiquitously recognized ascorbic acid - Vitamin C - serves as an indispensable tool in biotechnological methodologies. Synonyms: (4R,5S)-4,5,6-Trihydroxy-2,3-Dioxo-hexanoic acid; L-threo-2,3-Hexodiulosonic acid. CAS No. 3445-22-5. Molecular formula: C6H8O7. Mole weight: 192.12. BOC Sciences 3
2,3-O-Isopropylidene-L-gulonic acid-1,4-lactone 2,3-O-Isopropylidene-L-gulonic acid-1,4-lactone, an indispensable molecular entity extensively employed in the highly specialized field of biomedicine, serves as a pivotal intermediary constituent in the intricate synthesis pathways of diverse pharmacological agents. Remarkably versatile in nature, this unique structural configuration assumes a fundamental function in the amelioration of a wide spectrum of ailments ranging from neoplastic malignancies to aberrations affecting the cardiovascular system and autoimmune dysfunctions. Synonyms: L-Gulonic acid, 2,3-O-(1-methylethylidene)-, γ-lactone; 2,3-O-Isopropylidene-L-gulono-1,4-lactone. CAS No. 94840-08-1. Molecular formula: C9H14O6. Mole weight: 218.21. BOC Sciences 3
2-Keto-L-gulonic acid 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. Grade: ≥95%. CAS No. 526-98-7. Molecular formula: C6H10O7. Mole weight: 194.14. BOC Sciences 4
2-Keto-L-gulonic acid 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. Alfa Chemistry. 4
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. USBiological 10
Worldwide
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 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 H2O; 2-Keto-L-gulonic acid hydrate. CAS No. 342385-52-8. Molecular formula: C6H10O7.xH2O. Mole weight: 194.139 (anhydrous). BOC Sciences 4
3,4:5,6-Di-O-isopropylidene-L-gulonic acid methyl ester 3,4:5,6-Di-O-isopropylidene-L-gulonic acid methyl ester, a compound of utmost importance within the realm of biomedical research and pharmaceutical progression, serves as a beacon of potential in the treatment and understanding of a myriad of afflictions. With its multifaceted capabilities, it proudly contributes to combating the likes of cardiovascular disorders, diabetes mellitus, and immune-related conditions. Molecular formula: C13H22O7. Mole weight: 290.31. BOC Sciences 4
3-Azido-3-deoxy-5,6-O-isopropylidene-D-gulonic acid g-lactone 3-Azido-3-deoxy-5,6-O-isopropylidene-D-gulonic acid g-lactone demonstrates remarkable versatility, making it an indubitably significant compound within the field of biomedicine. Serving as a pivotal intermediate in the synthesis of diverse pharmaceuticals, encompassing antivirals, antibiotics, and anticancer agents, this compound embraces a paramount position. Furthermore, its applications extend to combating formidable ailments such as HIV/AIDS, bacterial infections, and select cancer variants. Synonyms: D-Gulonic acid, 3-azido-3-deoxy-5,6-O-(1-methylethylidene)-, γ-lactone. CAS No. 244057-17-8. Molecular formula: C9H13N3O5. Mole weight: 243.22. BOC Sciences 4
5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone 5,6-O-Isopropylidene-L-gulonic acid-1,4-lactone is a valuable compound in the biomedical industry, utilized in the research and development of pharmaceutical drugs targeting various diseases such as cancer, viral infections is and inflammatory conditions. Synonyms: 5,6-O-Isopropylidene-L-gulono-1,4-lactone; 5,6-Isopropylidene-L-gulonic acid γ-lactone; L-Gulonic acid, 5,6-O-(1-methylethylidene)-, γ-lactone. CAS No. 94697-68-4. Molecular formula: C9H14O6. Mole weight: 218.20. BOC Sciences 5
5-Azido-5,6-dideoxy-2,3-O-isopropylidene-D-gulonic acid-1,4-lactone 5-Azido-5,6-dideoxy-2,3-O-isopropylidene-D-gulonic acid-1,4-lactone, a remarkable compound in the biomedical realm, assumes an indispensable role as an intermediate. Its pervasive utilization in research endeavors propels scientific advancements. Demonstrating its significance, this compound serves as a pivotal building block for synthesizing a myriad of drugs and compounds that distinctly target a spectrum of diseases. Synonyms: D-Gulonic acid, 5-azido-5,6-dideoxy-2,3-O-(1-methylethylidene)-, γ-lactone. CAS No. 185741-56-4. Molecular formula: C9H13N3O4. Mole weight: 227.22. BOC Sciences 5
6-Deoxy-2,3:4,5-di-O-isopropylidene-D-gulonic acid methyl ester 6-Deoxy-2,3:4,5-di-O-isopropylidene-D-gulonic acid methyl ester is a prominent biomedical agent employed solely for scientific exploration, finding utility in the chemical amalgamation of potent antiviral therapeutics. With its acclaimed attributes, this compound stands as a quintessential precursor employed in studying the virulent impact of prevailing viral afflictions. Synonyms: Methyl 6-deoxy-2,3:4,5-bis-O-(1-methylethylidene)-D-gulonate; D-Gulonic acid, 6-deoxy-2,3:4,5-bis-O-(1-methylethylidene)-, methyl ester. CAS No. 1979119-24-8. Molecular formula: C13H22O6. Mole weight: 274.31. BOC Sciences 5
6-Deoxy-6-iodo-2,3:4,5-di-O-isopropylidene-D-gulonic acid methyl ester 6-Deoxy-6-iodo-2,3:4,5-di-O-isopropylidene-D-gulonic acid methyl ester is a valuable compound used in the field of biomedicine, serving as a crucial component in the research and development of various drugs targeting specific diseases that ranges from cardiovascular medicines to cancer therapeutics. Synonyms: Methyl 6-deoxy-6-iodo-2,3:4,5-bis-O-(1-methylethylidene)-D-gulonate; D-Gulonic acid, 6-deoxy-6-iodo-2,3:4,5-bis-O-(1-methylethylidene)-, methyl ester. CAS No. 1979119-22-6. Molecular formula: C13H21IO6. Mole weight: 400.21. BOC Sciences 5
6-O-tert-butyldimethylsilyl-2,3-O-isopropylidene-5-O tolenesulfonyl-L-gulonic acid γ-lactone 6-O-tert-butyldimethylsilyl-2,3-O-isopropylidene-5-O tolenesulfonyl-L-gulonic acid γ-lactone. Molecular formula: C22H34O8SSi. Mole weight: 486.65. BOC Sciences 5
6-O-tert-butyldimethylsilyl-2,3-O-isopropylidene-L-gulonic acid γ-lactone 6-O-tert-butyldimethylsilyl-2,3-O-isopropylidene-L-gulonic acid γ-lactone is a valuable compound in biomedicine used for the treatment of various diseases. Its unique chemical structure allows it to effectively target and inhibit specific enzymes involved in pathogenic processes. This compound shows promising activity against viral infections and has also demonstrated potential in cancer therapy, showing selective toxicity towards tumor cells. Its versatile applications in the biomedical industry make it a valuable tool for drug discovery and development. Synonyms: L-Gulonic acid, 6-O-[(1,1-dimethylethyl)dimethylsilyl]-2,3-O-(1-methylethylidene)-, γ-lactone. CAS No. 118464-47-4. Molecular formula: C15H28O6Si. Mole weight: 332.47. BOC Sciences 5
D-Gulonic acid-1,4-lactone D-Gulonic acid-1,4-lactone is a vital compound found in the biomedical industry. It plays a crucial role in the synthesis of L-ascorbic acid (vitamin C). With its antioxidant properties, D-Gulonic acid-1,4-lactone is utilized in various drugs and treatments for diseases associated with vitamin C deficiency such as scurvy. It serves as a precursor in the production of essential antioxidants, supporting overall health and immune function. Synonyms: D-Gulonolactone. CAS No. 6322-7-2. Molecular formula: C6H10O6. Mole weight: 178.14. BOC Sciences 7
2,3,4,5,6-Pentahydroxyhexanoic acid 2,3,4,5,6-Pentahydroxyhexanoic acid. Uses: Designed for use in research and industrial production. Additional or Alternative Names: L-Gulonic Acid. Product Category: Heterocyclic Organic Compound. CAS No. 526-97-6. Molecular formula: C6H12O7. Mole weight: 0. Density: 1.763g/cm³. Product ID: ACM526976. Alfa Chemistry — ISO 9001:2015 Certified. Categories: gluconic acid. Alfa Chemistry. 5
Ascorbic acid EP Impurity D An impurity of Ascorbic acid. Ascorbic acid is a water-soluble vitamin essential for human health. It is found in citrus fruits, berries, and vegetables and is widely used to prevent and treat scurvy, a disease caused by Vitamin C deficiency. Vitamin C plays a crucial role in tissue repair, collagen formation, and the production of certain neurotransmitters. It also functions as an antioxidant and supports immune system function. Synonyms: Methyl L-xylo-hex-2-ulosonate; Methyl L-sorbosonate; L-xylo-2-Hexulosonic acid, methyl ester; L-xylo-Hexulosonic acid, methyl ester; Gulonic acid, 2-keto-, methyl ester, L-; Methyl L-xylo-2-hexulosonate; 2-keto-L-Gulonic acid methyl ester; Methyl 2-keto-L-gulonate; Methyl L-xylo-hexulosonate; NSC 163924; Ascorbic acid Impurity D. Grade: ≥95%. CAS No. 3031-98-9. Molecular formula: C7H12O7. Mole weight: 208.17. BOC Sciences 6
Ascorbic acid impurity C Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmaceutical impuritieseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Ascorbic Acid Imp. C (EP): D-Sorbosonic Acid, 2-Keto-D-gulonic acid, D-xylo-Hexulosonic acid. Alfa Chemistry Analytical Products 2
Ascorbic acid impurity D Ascorbic acid impurity D. Uses: For analytical and research use. Group: European pharmacopoeia (ph. eur.); pharmacopoeial standards. Alternative Names: Ascorbic Acid Imp. D (EP),Methyl D-xylo-hex-2-ulosonate, D-xylo-2-Hexulosonic acid methyl ester, 2-Keto-gulonic acid methyl ester, Methyl D-sorbosonate. CAS No. 67776-07-2. IUPAC Name: methyl (3R,4S,5R)-3,4,5,6-tetrahydroxy-2-oxohexanoate. Molecular formula: C7H12O7. Mole weight: 208.17. Catalog: APS67776072. SMILES: COC(=O)C(=O)[C@H](O)[C@@H](O)[C@H](O)CO. Format: Neat. Shipping: Room Temperature. Alfa Chemistry Analytical Products 4
D-Gulono-1,4-lactone D-Gulono-1,4-lactone. Group: Biochemicals. Alternative Names: D-gulonic acid gamma-lactone. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. USBiological 3
Worldwide
D-Talono-1,4-lactone D-Talono-1,4-lactone is an indispensable compound for the research of Alzheimer's, Parkinson's and diverse neurodegenerative maladies, intricately operating as a neuroactivity modifier. Synonyms: gamma-D-Galactonolactone; Gulono-1,4-lactone; D-Allonic acid gamma-lactone; D-Idonic acid, gamma-lactone; D-Galactonic acid, gamma-lactone; 5-(1,2-Dihydroxy-ethyl)-3,4-dihydroxy-dihydro-furan-2-one; gamma-Lactone of mannonic acid; D-Mannonic acid, gamma-lactone; D-Galactonic acid, gamma-lactone; 1,4-D-Gulonolactone; D-Allono-1,4-lactone; L-Gulonic acid g-lactone; Gulonic acid-1,4-lactone; D-Gulonic acid-1,4-lactone; Mannonic acid, D-; Galactonic acid, D-; glucono-1,4-lactone; 1,4-D-Mannonolactone; D-Galactono-gamma-lactone. CAS No. 23666-11-7. Molecular formula: C6H10O6. Mole weight: 178.14. BOC Sciences 7
Gulonolactone Gulonolactone. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Gulonolactone, D-galactonolactone, D-Gulono gamma-lactone, D-Gulono-1,4-lactone, Gulonic acid-1,4-lactone, Gulonic acid, gamma-lactone, D-Gulonic acid gamma-lactone, D-(-)-Gulono-1,4-lactone, 219355_ALDRICH, STOCK1N-51779, MolPort-002-525-586, CID165105, ZINC00901647, BAF290D4-5A2B-424C-9F26-37DBB214E76B, 3327-64-8. Appearance: Off white powder. CAS No. 3327-64-8. Molecular formula: C6H10O6. Mole weight: 178.14. Purity: RG. IUPACName: (3R,4S,5S)-5-[(1R)-1,2-dihydroxyethyl]-3,4-dihydroxyoxolan-2-one. Product ID: ACM3327648. Alfa Chemistry — ISO 9001:2015 Certified. Alfa Chemistry. 2
L-gulonate 3-dehydrogenase Also oxidizes other L-3-hydroxyacids. Group: Enzymes. Synonyms: L-3-aldonate dehydrogenase; L-3-aldonic dehydrogenase; L-gulonic acid dehydrogenase; L-β-hydroxyacid dehydrogenase; L-β-hydroxy-acid-NAD-oxidoreductase; L-3-hydroxyacid dehydrogenase. Enzyme Commission Number: EC 1.1.1.45. CAS No. 9028-51-7. 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-0330; L-gulonate 3-dehydrogenase; EC 1.1.1.45; 9028-51-7; L-3-aldonate dehydrogenase; L-3-aldonic dehydrogenase; L-gulonic acid dehydrogenase; L-β-hydroxyacid dehydrogenase; L-β-hydroxy-acid-NAD-oxidoreductase; L-3-hydroxyacid dehydrogenase. Cat No: EXWM-0330. Creative Enzymes
L-Gulono-1,4-lactone L-Gulono-1,4-lactone. Group: Biochemicals. Alternative Names: L-gulonic acid gamma-lactone. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. USBiological 3
Worldwide
L-gulono-1,4-lactone-[UL-13C6] A labelled analogue of L-Gulono-1,4-lactone. L-Gulono-1,4-lactone is one of the many forms of Vitamin C and a precursor in the biosynthesis of ascorbic acid. Synonyms: L-[UL-13C6]gulono-1,4-lactone; L-[UL-13C6]gulonic acid gamma-lactone. Molecular formula: [13C]6H10O6. Mole weight: 184.09. BOC Sciences 2
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. Creative Enzymes
2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone 2,3:5,6-Di-O-isopropylidene-L-gulono-1,4-lactone is a crucial organic compound widely used in the biomedical industry. This compound plays a significant role in the synthesis of Vitamin C (ascorbic acid), a vital nutrient for humans. It aids in the prevention and treatment of scurvy, a disease caused by Vitamin C deficiency. Synonyms: L-Gulonolactone diacetonide. CAS No. 7306-64-1. Molecular formula: C12H18O6. Mole weight: 258.27. BOC Sciences 3
5-Azido-6-O-(tert-butyldimethylsilyl)-2,3-O-isopropylidene L-gulono-1,4-lactone 5-Azido-6-O-(tert-butyldimethylsilyl)-2,3-O-isopropylidene L-gulono-1,4-lactone is a multifaceted compound acting as a precursor in pharmaceutical drug research and development. Furthermore, it serves as a pivotal asset in the pursuit of groundbreaking drug discovery endeavors, targeting meticulously defined diseases or pathways. Synonyms: 5-Azido-5-deoxy-6-O-[(1,1-dimethylethyl)dimethylsilyl]-2,3-O-(1-methylethylidene)-D-mannonic acid gamma-lactone. CAS No. 118464-49-6. Molecular formula: C15H27N3O5Si. Mole weight: 357.48. BOC Sciences 5
L-galactonolactone dehydrogenase This enzyme catalyses the final step in the biosynthesis of L-ascorbic acid in higher plants and in nearly all higher animals with the exception of primates and some birds. The enzyme is very specific for its substrate L-galactono-1,4-lactone as D-galactono-γ-lactone, D-gulono-γ-lactone, L-gulono-γ-lactone, D-erythronic-γ-lactone, D-xylonic-γ-lactone, L-mannono-γ-lactone, D-galactonate, D-glucuronate and D-gluconate are not substrates. FAD, NAD+, NADP+ and O2 (cf. EC 1.3.3.12, L-galactonolactone oxidase) cannot act as electron acceptor. Group: Enzymes. Synonyms: galactonolactone dehydrogenase; L-galactono-γ-lactone dehydrogenase; L-galactono-γ-lactone:ferricytochrome-c oxidoreductase; GLDHase; GLDase. Enzyme Commission Number: EC 1.3.2.3. CAS No. 9029-2-1. 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-1370; L-galactonolactone dehydrogenase; EC 1.3.2.3; 9029-02-1; galactonolactone dehydrogenase; L-galactono-γ-lactone dehydrogenase; L-galactono-γ-lactone:ferricytochrome-c oxidoreductase; GLDHase; GLDase. Cat No: EXWM-1370. Creative Enzymes
L-galactonolactone oxidase A flavoprotein. Acts on the 1,4-lactones of L-galactonic, D-altronic, L-fuconic, D-arabinic and D-threonic acids; not identical with EC 1.1.3.8 L-gulonolactone oxidase. (cf. EC 1.3.2.3 galactonolactone dehydrogenase). Group: Enzymes. Synonyms: L-galactono-1,4-lactone oxidase. Enzyme Commission Number: EC 1.3.3.12. CAS No. 69403-13-0. 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-1373; L-galactonolactone oxidase; EC 1.3.3.12; 69403-13-0; L-galactono-1,4-lactone oxidase. Cat No: EXWM-1373. Creative Enzymes
L-Gulono-1,4-lactone-13C6 L-Gulono-1,4-lactone-13C6. Group: Biochemicals. Alternative Names: Reduced Ascorbic Acid-13C; Dihydroascorbic Acid-13C. Grades: Highly Purified. Pack Sizes: 5mg. Molecular Formula: 13C6H10O6, Molecular Weight: 184.1. US Biological Life Sciences. USBiological 3
Worldwide
L-gulonolactone oxidase A microsomal flavoprotein (FAD). The product spontaneously isomerizes to L-ascorbate. While most higher animals can synthesize asborbic acid, primates and guinea pigs cannot. Group: Enzymes. Synonyms: L-gulono-γ-lactone: O2 oxidoreductase; L-gulono-γ-lactone oxidase; L-gulono-γ-lactone:oxidoreductase; GLO. Enzyme Commission Number: EC 1.1.3.8. CAS No. 9028-78-8. 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-0426; L-gulonolactone oxidase; EC 1.1.3.8; 9028-78-8; L-gulono-γ-lactone: O2 oxidoreductase; L-gulono-γ-lactone oxidase; L-gulono-γ-lactone:oxidoreductase; GLO. Cat No: EXWM-0426. Creative Enzymes

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