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| Product | Description | |
|---|---|---|
| OXA (17-33) | OXA (17-33) is a peptide orexin OX1 receptor agonist with EC50 value of 8.29 nM. It is a drug candidate for the treatment of heart failure and hypertension. Alternative Names: Orexin A (17-33) trifluoroacetate salt H-Tyr-Glu-Leu-Leu-His-Gly-Ala-Gly-Asn-His-Ala-Ala-Gly-Ile-Leu-Thr-Leu-NH2 trifluoroacetate salt; BDBM50445183. Grades: >97%. CAS No. 343268-91-7. Molecular formula: C79H125N23O22. Mole weight: 1749. |  |
| OXABETRINIL | OXABETRINIL. Alternative Names: alpha-((1,3-dioxolan-2-ylmethoxy)imino)-benzeneacetonitril; alpha-((1,3-dioxolan-2-ylmethoxy)imino)benzeneacetonitrile; alpha-[(1,3-dioxolan-2-ylmethoxy)imino]-benzeneacetonitril; cga92194; n-(1,3-dioxolan-2-ylmethoxy)iminobenzacetonitrile; CONCEP II; OXABETRI. CAS No. 74782-23-3. Molecular formula: C12H12N2O3. Mole weight: 232.24. | |
| Oxaceprol | Oxaceprol (N-Acetyl-L-hydroxyproline), an orally active derivative of L-proline, possesses distinct anti-inflammatory activity. Oxaceprol is usually used for the research of osteoarthritis and rheumatoid arthritis[1][2]. Uses: Scientific research. Category: Signaling pathways. Alternative Names: N-Acetyl-L-hydroxyproline. CAS No. 33996-33-7. Pack Sizes: 10 mM * 1 mL in DMSO; 5 g; 10 g; 25 g; 50 g; 100 g. Product ID: HY-17490. |  |
| Oxaceprol | Oxaceprol derived from L-proline, inhibiting inflammatory cell infiltration and bone damage in the adjuvant-injected paw. Uses: An anti-inflammatory drug used in the treatment of osteoarthritis. Alternative Names: trans-1-Acetyl-4-hydroxy-L-proline;N-Acetyl-L-hydroxyproline; Oxaceprol; Jonctum; AHP 200; AHP-200; AHP200; Oxaceprolum; Tejuntivo; EINECS 251-780-6. Grades: ≥98%. CAS No. 33996-33-7. Molecular formula: C7H11NO4. Mole weight: 173.17. | |
| Oxacillin EP Impurity D (Mixture of Diastereomers) | Oxacillin EP Impurity D (Mixture of Diastereomers). Uses: For analytical and research use. CAS No. 1642559-63-4. Molecular formula: C18H21N3O4S. Mole weight: 375.44. Catalog: APB1642559634. |  |
| Oxacillin EP Impurity J | Oxacillin EP Impurity J. Uses: For analytical and research use. Alternative Names: 6-APA Dimer Ozolamide; (2S,5R,6R)-6-((R)-2-((2R,4S)-4-carboxy-5,5-dimethylthiazolidin-2-yl)-2-(5-methyl-3-phenylisoxazole-4-carboxamido)acetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid. Molecular formula: C27H31N5O8S2. Mole weight: 617.69. Catalog: APB01962. | |
| Oxacillin Impurity 10 | Oxacillin Impurity 10. Uses: For analytical and research use. Molecular formula: C18H21N3O4S. Mole weight: 375.44. Catalog: APB08983. | |
| Oxacillin Impurity 11 | Oxacillin Impurity 11. Uses: For analytical and research use. Molecular formula: C19H21N3O6S. Mole weight: 419.45. Catalog: APB08984. | |
| Oxacillin Impurity 2 | Oxacillin Impurity 2. Uses: For analytical and research use. CAS No. 36231-30-8. Molecular formula: C19H19N3O6S. Mole weight: 417.44. Catalog: APB36231308. | |
| Oxacillin Impurity 3 | Oxacillin Impurity 3. Uses: For analytical and research use. Molecular formula: C20H23N3O6S. Mole weight: 433.48. Catalog: APB08979. | |
| Oxacillin Impurity 4 | Oxacillin Impurity 4. Uses: For analytical and research use. Molecular formula: C21H23N3O7S. Mole weight: 461.49. Catalog: APB08980. | |
| Oxacillin Impurity 5 | Oxacillin Impurity 5. Uses: For analytical and research use. Molecular formula: C19H19N3O5S. Mole weight: 401.44. Catalog: APB08978. | |
| Oxacillin Impurity 7 | Oxacillin Impurity 7. Uses: For analytical and research use. CAS No. 94419-27-9. Molecular formula: C18H21N3O4S. Mole weight: 375.44. Catalog: APB94419279. | |
| Oxacillin Impurity 8 | Oxacillin Impurity 8. Uses: For analytical and research use. Molecular formula: C19H18N3NaO5S. Mole weight: 423.42. Catalog: APB08982. | |
| Oxacillin Impurity 9 | Oxacillin Impurity 9. Uses: For analytical and research use. Molecular formula: C27H29N5O7S2. Mole weight: 599.68. Catalog: APB08981. | |
| Oxacillin Impurity F | Oxacillin Impurity F. Uses: For analytical and research use. Alternative Names: Thioxacillin; (2R,5R,6R)-3,3-dimethyl-6-(5-methyl-3-phenylisoxazole-4-carboxamido)-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carbothioic S-acid. CAS No. 5053-35-0. Molecular formula: C19H19N3O4S2. Mole weight: 417.50. Catalog: APB5053350. | |
| Oxacillin Impurity G | Oxacillin Impurity G. Uses: For analytical and research use. CAS No. 724695-30-1. Molecular formula: C19H18ClN3O5S. Mole weight: 435.88. Catalog: APB724695301. | |
| Oxacillin Related Compound C | Oxacillin Related Compound C. Uses: For analytical and research use. CAS No. 1136-45-4. Mole weight: 203.19. Catalog: AP1136454. | |
| Oxacillin sodium EP Impurity B | Oxacillin sodium EP Impurity B. Uses: For analytical and research use. CAS No. 1642629-95-5. Molecular formula: C19H21N3O6S. Mole weight: 419.45. Catalog: APB1642629955. | |
| Oxacillin sodium EP Impurity C | Oxacillin sodium EP Impurity C. Uses: For analytical and research use. CAS No. 1136-45-4. Molecular formula: C11H9NO3. Mole weight: 203.2. Catalog: APB1136454. | |
| Oxacillin sodium EP Impurity D | Oxacillin sodium EP Impurity D. Uses: For analytical and research use. Molecular formula: C18H21N3O4S. Mole weight: 375.44. Catalog: APB08971. | |
| Oxacillin sodium EP Impurity F | Oxacillin sodium EP Impurity F. Uses: For analytical and research use. Molecular formula: C19H19N3O4S2. Mole weight: 417.5. Catalog: APB08972. | |
| Oxacillin sodium EP Impurity G | Oxacillin sodium EP Impurity G. Uses: For analytical and research use. Molecular formula: C20H22ClN3O5S. Mole weight: 451.92. Catalog: APB08973. | |
| Oxacillin sodium EP Impurity I | Oxacillin sodium EP Impurity I. Uses: For analytical and research use. Molecular formula: C27H29N5O7S2. Mole weight: 599.68. Catalog: APB08974. | |
| Oxacillin sodium EP Impurity J | Oxacillin sodium EP Impurity J. Uses: For analytical and research use. Molecular formula: C27H31N5O8S2. Mole weight: 617.69. Catalog: APB08975. | |
| Oxacillin sodium EP Impurity J (Mixture of Diastereomers) | Oxacillin sodium EP Impurity J (Mixture of Diastereomers). Uses: For analytical and research use. Molecular formula: C37H31N5O8S2. Mole weight: 617.69. Catalog: APB08977. | |
| Oxacillin sodium salt | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C19H18N3NaO5S. CAS No. 1173-88-2. Prepack ID 89967565-1g. Molecular Weight 423.42. See USA prepack pricing. |  |
| Oxacillin sodium salt | Oxacillin sodium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 1173-88-2. Pack Sizes: 5g. US Biological Life Sciences. |  Worldwide |
| Oxacillin sodium salt | Oxacillin sodium salt is an orally active synthetic penicillin with good bactericidal activity against staphylococci and other gram-positive pathogens[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 1173-88-2. Pack Sizes: 10 mM * 1 mL in DMSO; 100 mg. Product ID: HY-B0925. | |
| Oxacillin sodium salt 99+% | Oxacillin sodium salt 99+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 1173-88-2. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| Oxacillin sodium salt monohydrate | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C19H18N3NaO5S ·H2O. CAS No. 7240-38-2. Prepack ID 52575358-5g. Molecular Weight 441.43. See USA prepack pricing. | |
| Oxacillin Sodium Salt Monohydrate | Semi-synthetic antibiotic related to Penicillin. Antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R, 6R) -3, 3-Dimethyl-6-[[ (5-methyl-3-phenyl-4-isoxazolyl) carbonyl]amino]-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid Sodium Salt Hydrate; Penicillin P-12 Hydrate; Sodium Oxacillin Hydrate; BRL-1400 Hydrate; Bactocill Hydrate; Bristopen Hydrate; Stapenor Hydrate. Grades: Highly Purified. CAS No. 7240-38-21. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Oxacillin Sodium Salt Monohydrate | Oxacillin sodium monohydrate is a semi-synthetic antibacterial agent and is a narrow spectrum beta-lactam antibiotic of the penicillin class. Alternative Names: (2S,5R,6R)-3,3-Dimethyl-6-[[(5-methyl-3-phenyl-4-isoxazolyl)carbonyl]amino]-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid Sodium Salt Hydrate; Penicillin P-12 Hydrate; Sodium Oxacillin Hydrate; BRL-1400 Hydrate; Bactocill Hydrate; Bristopen Hydrate; Stapenor Hydrate; Oxacillin sodium hydrate; Cryptocillin; Prostaphlin; Stapenor; BAY-M-1099; BAY M 1099. Grades: 96%. CAS No. 7240-38-2. Molecular formula: C19H18N3NaO5S.H2O. Mole weight: 441.43. | |
| Oxacillin sodium USP Impurity K | Oxacillin sodium USP Impurity K. Uses: For analytical and research use. Molecular formula: C19H19N3O5S. Mole weight: 401.44. Catalog: APB08976. | |
| Oxacycloheptadec-10-en-2-one | Oxacycloheptadec-10-en-2-one. Alternative Names: AMBRETTOLIDE; 16-HYDROXY-7-HEXADECENOIC ACID O-LACTONE; HEXADECEN-8-OLIDE; FEMA 2555; OMEGA-6-HEXADECENLACTONE; Oxacycloheptadec-10-en-2-on; 16-Hydroxy-9-hexadecenoic acid lactone; 1-Oxacycloheptadeca-10-en-2-one. CAS No. 28645-51-4. Molecular formula: C16H28O2. Mole weight: 252.39. | |
| Oxacyclohexane open ring tacrolimus | Oxacyclohexane open ring tacrolimus is an impurity of Tacrolimus, which is a macrolide drug that is widely used as a potent immunosuppressant. Alternative Names: Tacrolimus Open Ring Impurity; Tacrolimus related compound, tacrolimus open ring; 3H-Pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,19,21(4H,8H,12H,23H)-tetrone, 5,6,11,13,14,15,16,17,18,20,24,25,26,26a-tetradecahydro-5,15,20,20-tetrahydroxy-3-[(1E)-2-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(2-propen-1-yl)-, (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,26aS)-; (3S,4R,5S,8R,9E,12S,14S,15R,16S,18R,26aS)-5,6,11,13,14,15,16,17,18,20,24,25,26,26a-Tetradecahydro-5,15,20,20-tetrahydroxy-3-[(1E)-2-[(1R,3R,4R)-4-hydroxy-3-methoxycyclohexyl]-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(2-propen-1-yl)-3H-pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,19,21(4H,8H,12H,23H)-tetrone; 3H-Pyrido[2,1-c][1,4]oxaazacyclotricosine-1,7,19,21(4H,8H,20H,23H)-tetrone, 5,6,11,12,13,14,15,16,17,18,24,25,26,26a-tetradecahydro-5,15,20,20-tetrahydroxy-3-[2-(4-hydroxy-3-methoxycyclohexyl)-1-methylethenyl]-14,16-dimethoxy-4,10,12,18-tetramethyl-8-(2-propenyl)-, [3S-[3R*[E(1S*,3S*,4S*)],4S*,5R*,8S*,9E,12R*,14R*,15S*,16R*,18S*,26aR*]]-. Grades: ≥90% by HPLC. CAS No. 144432-23-5. Molecular formula: C44H71NO13. Mole weight: 822.03. | |
| Oxadiazon | Oxadiazon. Group: Biochemicals. Alternative Names: 3-[2,4-Dichloro-5-(1-methylethoxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2(3H)-one; 2-tert-Butyl-4-(2,4-dichloro-5-isopropoxyphenyl)-1,3,4-oxadiazolin-5-one; 2-tert-Butyl-4-(2,4-dichloro-5-isopropoxyphenyl)-5-oxo-1,3,4-oxadiazoline. Grades: Highly Purified. CAS No. 19666-30-9. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C15H18Cl2N2O3. US Biological Life Sciences. | Worldwide |
| Oxalacetic acid | Oxalacetic acid is a four-carbon dicarboxylic acid that acts as an intermediate of the citric acid cycle. Oxaloacetate is synthesized by malate dehydrogenase from the oxidation of L-malate. Nutritional supplement in health care products. Uses: Ingredient of health care products. Alternative Names: Oxaloacetic acid; 2-Oxosuccinic acid; 2-Oxobutanedioic acid; Oxaloacetate; 2-oxobutanedioic acid. Grades: 98%. CAS No. 328-42-7. Molecular formula: C4H4O5. Mole weight: 132.071. | |
| Oxalacetic acid | Oxalacetic acid. Alternative Names: Oxalacetic acid 2-Oxosuccinic. CAS No. 328-42-7. Purity: >97.0%. Product ID: FFC-AR-328427. Molecular formula: C4H4O5. Mole weight: 132.07. IUPAC Name: 2-oxobutanedioic acid. Alfa Chemistry - ISO 9001:32057 Certified. |  |
| Oxalacetic acid | 25g Pack Size. Group: Analytical Reagents, Biochemicals, Diagnostic Raw Materials. Formula: C4H4O5. CAS No. 328-42-7. Prepack ID 21309006-25g. Molecular Weight 132.07. See USA prepack pricing. | |
| Oxalacetic Acid | Oxalacetic Acid. Categories: oxalacetic acid; oxaloacetic acid. |  CA, FL & NJ |
| Oxalacetic acid 98+% | Oxalacetic acid 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 5g, 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| Oxalacetic Acid(CAS 328-42-7) | Oxalacetic Acid(CAS 328-42-7). CAS No. 328-42-7. Cenik is your partner of choice for specialised chemicals. We don't just provide products - we supply solutions to your technical and regulatory specifications. |  |
| Oxalacetic acid diethyl ester sodium salt | Oxalacetic acid diethyl ester sodium salt. Group: Biochemicals. Alternative Names: Diethyl oxalacetate sodium salt. Grades: Highly Purified. CAS No. 40876-98-0,52980-17-3. Pack Sizes: 250g, 500g, 1kg. US Biological Life Sciences. | Worldwide |
| Oxalacetic acid diethylester sodium salt | 100g Pack Size. Group: Building Blocks, Organics. Formula: C8H11O5Na. CAS No. 40876-98-0. Prepack ID 10451984-100g. Molecular Weight 210.16. See USA prepack pricing. | |
| Oxalacetic acid diethylester sodium salt | 25g Pack Size. Group: Building Blocks, Organics. Formula: C8H11O5Na. CAS No. 40876-98-0. Prepack ID 10451984-25g. Molecular Weight 210.16. See USA prepack pricing. | |
| Oxalacetic acid diethyl ester sodium salt ≥96% (GC) | Oxalacetic acid diethyl ester sodium salt ≥96% (GC). Group: Biochemicals. Grades: GC. Pack Sizes: 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Oxalacetic Acid (Oxaloacetic acid) | A four carbon dicarboxylic acid that is an intermediate in the citric acid cycle and glucogenesis. It has been shown to inhibit succinate dehydrogenase. Oxaloacetic acid, in the form of its conjugate base oxaloacetate, is a metabolic intermediate in many processes that occur in animals. It takes part in the: gluconeogenesis, urea cycle, glyoxylate cycle, amino acid synthesis, fatty acid synthesis and citric acid cycle. Gluconeogenesis[1] is a metabolic pathway consisting of a series of eleven enzyme-catalyzed reactions, resulting in the generation of glucose from non-carbohydrates substrates. The beginning of this process takes place in the mitochondrial matrix, where pyruvate molecules are found. A pyruvate molecule is carboxylated by a pyruvate carboxylase enzyme, activated by a molecule each of ATP and water. This reaction results in the formation of oxaloacetate. NADH reduces oxaloacetate to malate. This transformation is needed to transport the molecule out of the mitochondria. On Group: Biochemicals. Alternative Names: Oxobutanedioic Acid; Oxalacetic Acid; 2-Ketosuccinic acid; 2-Oxobutanedioic acid; 2-Oxosuccinic Acid; Ketosuccinic Acid; NSC 284205; NSC 77688; OAA; Oxaloacetic Acid; Oxaloethanoic Acid; Oxosuccinic Acid; α-Ketosuccinic Acid. Grades: Reagent Grade. CAS No. 328-42-7. Pack Sizes: 25g, 50g, 100g, 250g. Molecular Formula: C?H?O?, Molecular Weight: 132.07. US Biological Life Scienc | Worldwide |
| oxalate-CoA ligase | This enzyme belongs to the family of ligases, specifically those forming carbon-sulfur bonds as acid-thiol ligases. This enzyme participates in glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: oxalyl-CoA synthetase; oxalyl coenzyme A synthetase. Enzyme Commission Number: EC 6.2.1.8. CAS No. 37318-57-3. 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-5710; oxalate-CoA ligase; EC 6.2.1.8; 37318-57-3; oxalyl-CoA synthetase; oxalyl coenzyme A synthetase. Cat No: EXWM-5710. |  |
| oxalate CoA-transferase | This enzyme belongs to the family of transferases, specifically the CoA-transferases. The systematic name of this enzyme class is succinyl-CoA:oxalate CoA-transferase. Other names in common use include succinyl-beta-ketoacyl-CoA transferase, and oxalate coenzyme A-transferase. This enzyme participates in glyoxylate and dicarboxylate metabolism. Group: Enzymes. Synonyms: succinyl-β-ketoacyl-CoA transferase; oxalate coenzyme A-transferase. Enzyme Commission Number: EC 2.8.3.2. CAS No. 9026-17-9. 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-3415; oxalate CoA-transferase; EC 2.8.3.2; 9026-17-9; succinyl-β-ketoacyl-CoA transferase; oxalate coenzyme A-transferase. Cat No: EXWM-3415. | |
| oxalate decarboxylase | The enzyme from Bacillus subtilis contains manganese and requires O2 for activity, even though there is no net redox change. Group: Enzymes. Synonyms: oxalate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.2. CAS No. 9024-97-9. 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-4764; oxalate decarboxylase; EC 4.1.1.2; 9024-97-9; oxalate carboxy-lyase. Cat No: EXWM-4764. | |
| Oxalate Decarboxylase from Bacillus subtilis, recombinant | Oxalate decarboxylase (OxdC, EC4.1.1.2) is a manganese-containing enzyme, which decomposes oxalic acid and oxalate. With OxdC catalysis, oxalate is split into formate and CO2. This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. The systematic name of this enzyme class is oxalate carboxy-lyase (formate-forming). This enzyme is also called oxalate carboxy-lyase. The enzyme is composed of two cupin domains, each of which contains a Mn (II) ion. This enzyme participates in glyoxylate and dicarboxylate metabolism. This enzyme has been recognized for diagnostics in diverse biotechnological applications such as.ndustry, and agriculture to lower oxalate levels in foods and the environment. The recombinant protein made from the Bacillus Subtilis sequence includes OxdC with N-terminal His-tag. Group: Enzymes. Synonyms: Oxalate carboxy-lyase; EC 4.1.1.2; Oxalate decarboxylase; OxdC. Enzyme Commission Number: EC 4.1.1.2. CAS No. 9024-97-9. Purity: > 98% by SDS-PAGE. Mole weight: 45.9 kDa. Activity: 150U/mg. Storage: Stable for 1 year at -20°C. For long term storage, aliquot and store at -70°C. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: Bacillus subtilis. Oxalate carboxy-lyase; EC 4.1.1.2; Oxalate decarboxylase; OxdC. Cat No: NATE-1688. | |
| Oxalate decarboxylase, Microorganism | Oxalate decarboxylase, Microorganism (EC 4.1.1.2), a stress-response enzyme in certain soil bacteria, is a Mn-dependent enzyme in the cupin superfamily and is found in fungi and soil bacteria. Oxalate decarboxylase catalyzes the decarboxylation of the oxalate mono-anion in the soil bacterium Bacillus subtilis. Enzymatic activity of OxDC is strongly pH dependent, with a maximum at around pH 4.0[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9024-97-9. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-E70518. | |
| oxalate oxidase | Contains Mn2+ as a cofactor. The enzyme is not a flavoprotein as had been thought. Group: Enzymes. Synonyms: aero-oxalo dehydrogenase; oxalic acid oxidase. Enzyme Commission Number: EC 1.2.3.4. CAS No. 9031-79-2. 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-1211; oxalate oxidase; EC 1.2.3.4; 9031-79-2; aero-oxalo dehydrogenase; oxalic acid oxidase. Cat No: EXWM-1211. | |
| Oxalate oxidase | Oxalate oxidase. Alternative Names: Oxalate oxidase; Oxidase, oxalate; E.C. 1.2.3.4; Aero-oxalo dehydrogenase; Germin (enzyme); Germin. CAS No. 9031-79-2. | |
| Oxalate Oxidase | Oxalate Oxidase, or oxalate oxidase, catalyzes the oxidation of oxalic acid to hydrogen peroxide and carbon dioxide in the presence of oxygen. Oxalate Oxidase can be found in a variety of plants (such as barley) and microorganisms and can be used to treat wastewater and filtrates containing oxalic acid[1]. Uses: Scientific research. Category: Signaling pathways. CAS No. 9031-79-2. Pack Sizes: 5 U; 10 U. Product ID: HY-E70385. | |
| Oxalate Oxidase from barley seedlings | Oxalate Oxidase from barley seedlings. Uses: For analytical and research use. Category: Pharmacopoeial standards. CAS No. 9031-79-2. Catalog: AP9031792. | |
| Oxalate oxidase from B. subtilis, Recombinant | In enzymology, an oxalate oxidase (EC 1.2.3.4) is an enzyme that catalyzes the chemical reaction: oxalate + O2 + 2 H+ <-> 2 CO2 + H2O2.The 3 substrates of this enzyme are oxalate, O2, and H+, whereas its two products are CO2 and H2O2. This enzyme belongs to the family of oxidoreductases, specifically those acting on the aldehyde or oxo group of donor with oxygen as acceptor. The systematic name of this enzyme class is oxalate:oxygen oxidoreductase. This enzyme participates in glyoxylate and dicarboxylate metabolism. It has 2 cofactors: FAD, and Manganese. Group: Enzymes. Synonyms: OxO; OxOx; OxO_r; aero-oxalo dehydrogenase; oxalic acid oxidase. Enzyme Commission Number: EC 1.2.3.4. Mole weight: 43.6 kDa, His-tagged. Activity: > 230 mU/mg. Stability: Stable for at least 2 years as supplied. Storage: Store at -20°C. Form: Freeze dried. Source: E. coli. Species: B. subtilis. OxO; OxOx; OxO_r; aero-oxalo dehydrogenase; oxalic acid oxidase; oxalate oxidase; OxOx. Cat No: NATE-1642. | |
| oxalate oxidoreductase | Contains thiamine diphosphate and [4Fe-4S] clusters. Acceptors include ferredoxin and the nickel-dependent carbon monoxide dehydrogenase (EC 1.2.7.4). Group: Enzymes. Enzyme Commission Number: EC 1.2.7.10. 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-1224; oxalate oxidoreductase; EC 1.2.7.10. Cat No: EXWM-1224. | |
| OxalicAcid | OxalicAcid,alsoknownasEthanedioicacid,existswidelyinplantderivedfood. Uses: Oxalicacid,(1)canbeusedasprecipitatingandresolvingagentforrareearthmetal,etc.inmetallurgyindustry;(2)canbeusedfor2133rein,uresformaldehydepowderetc.inorganicsynthesis;(3)canbeusedforpolishingofmarblestone,removingrustbleachingproductsofleather,woodandaluminiumetc.inlightindustry;(4)canbeusedasreducingagent,bleachingagentfortextileinprintinganddyeingindustry;(5)canbeusedastetracydine,oxytetracycline,hcl,borneletc.inpharmaceuticalindustry;(6)canbeusedaslaboratoryagent,solventsactivatorandbasicmaterialsforchemicalindustry. Alternative Names: ETHANEDIOICACID;DI-CARBOXYLICACID;Kyselinastavelova. Grades: Premiumgrade:99.6;Firstgrade:99.4;Premiumgrade:99. CAS No. 144-62-7. Molecular formula: C2H2O4. Mole weight: 90.03. | |
| Oxalic Acid | Oxalic Acid. We stock inventory in warehouses throughout the United States, allowing us to serve customers in all regions in a timely and cost effective manner. |  US and Canada |
| Oxalic Acid | An impurity of oxaliplatin which is a coordination complex that is used in cancer chemotherapy. A reducing agent and its conjugate base, known as oxalate (C2O42?), is a useful chelating agent for metal cations. Group: Biochemicals. Alternative Names: Ethanedioic Acid; Aktisal; Aquisal; DeerClean; NSC 132055; NSC 151956; NSC 62774; NSC 76990; Ultraplast Activate S 52. Grades: Highly Purified. CAS No. 144-62-7. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| Oxalic Acid | Oxalic Acid. Grade: ACS. CAS: 144-62-7. Packing: Plastic Drums. |  New Jersey NJ |
| Oxalic Acid | Oxalic Acid. Grades: ACS. CAS No. 6153-56-6. Pack Sizes: Kilogram Quanitites: 1 kg , 5 kg. Order Number: 2794. |  www.prochemonline.com |
| Oxalic Acid | Oxalic Acid. Category ACIDS. Pack Sizes Drums/ bags/ bulk |  |
| Oxalic Acid | While Oxalic Acid is widely recognized for its ability to eliminate iron oxide or rust stains from metal surfaces, it possesses a diverse range of applications. It can serve as a laundry rinse, wood-bleaching agent, calcium deposit remover, paint stripper, component in ink production, ink stain remover, stone cleaning and polishing agent, photographic film developer, and textile dyeing agent. Uses: Cleaning, Dyeing, Electroplating. Alternative Names: Dicarboxylic Acid, Ethanedionic Acid, Ethanedoic Acid, Oxalic Acid, Oxalic Acid Dihydrate. CAS No. 6153-56-6. Pack Sizes: 55 lb. |  USA |
| Oxalic Acid | OXALIC ACID, DIHYDRATE, ACS Reagent, crystal, (Synonym: Ethanedioic Acid, Dihydrate), Formula: HO2CCO2H.2H2O. CAS No. 6153-56-6. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Oxalic acid, 0.1N Standardized Solution | Oxalic acid, 0.1N Standardized Solution. Uses: For analytical and research use. CAS No. 144-62-7. Molecular formula: C2H2O4. Mole weight: 90.04. Catalog: APB144627-1. | |
| Oxalic Acid-(1,2-13C2) | Oxalic Acid-(1,2-13C2) is the labelled analog of Oxalic Acid (O845120) which is an impurity of oxaliplatin which is a coordination complex that is used in cancer chemotherapy. It is also a reducing agent and its conjugate base, known as oxalate (C2O42?), is a useful chelating agent for metal cations. Group: Biochemicals. Grades: Highly Purified. CAS No. 62654-02-8. Pack Sizes: 5mg, 10mg. Molecular Formula: 13C2H2O4. US Biological Life Sciences. | Worldwide |
| Oxalic acid-13C2 | Oxalic acid-13C2 is the deuterium labeled Oxalic acid, 99% (HY-Y0262)[1]. Oxalic Acid is a strong dicarboxylic acid occurring in many plants and vegetables and can be used as an analytical reagent and general reducing agent[2]. Uses: Scientific research. Category: Signaling pathways. CAS No. 62654-02-8. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-Y0262S1. | |
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