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| Product | Description | |
|---|---|---|
| 1,1-Dioxide-5-(4-bromophenyl)-1,2,5-thiadiazolidin-3-one | 1,1-Dioxide-5-(4-bromophenyl)-1,2,5-thiadiazolidin-3-one isused in the preparation of phenyl thiadiazolidinones as inhibitors of protein tyrosine phosphatase 1B (PTP1B) for treatment of diabetes mellitus. Group: Biochemicals. Grades: Highly Purified. CAS No. 692765-79-0. Pack Sizes: 10mg, 100mg. Molecular Formula: C8H7BrN2O3S, Molecular Weight: 291.12. US Biological Life Sciences. |  Worldwide |
| 1,2-Benzisothiazol-3(2H)-one 1,1-dioxide, ammonium salt | Sweeteners. Alternative Names: 2-Ammonio-1,2-benzisothiazol-3(2H)-one 1,1-dioxide. CAS No. 6381-61-9. Mole weight: 200.22. Purity: 95%+. IUPACName: Azane;1,1-dioxo-1,2-benzothiazol-3-one. Canonical SMILES: C1=CC=C2C(=C1)C(=O)NS2(=O)=O.N. Density: 1.4342 g/cm³. |  |
| 2-Methylthieno[2,3-d]isothiazol-3(2H)-one 1,1-Dioxide | 2-Methylthieno[2,3-d]isothiazol-3(2H)-one 1,1-Dioxide is an impurity of Tenoxicam (T019500), a nonsteroidal anti-inflamatory agent. Group: Biochemicals. Grades: Highly Purified. CAS No. 94040-09-2. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C6H5NO3S2, Molecular Weight: 203.24. US Biological Life Sciences. | Worldwide |
| 3-Chloro-6-methyl-dibenzo[c, f][1, 2]thiazepin-11(6H)-one 5,5-dioxide | 3-Chloro-6-methyl-dibenzo[c, f][1, 2]thiazepin-11(6H)-one 5,5-dioxide. Group: Biochemicals. Alternative Names: 3-Chloro-6, 11-dihydro-6-methyl-5, 5, 11-trioxodibenzo[c, f][1, 2]thiazepine. Grades: Highly Purified. CAS No. 26638-53-9. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. Molecular Formula: C14H10ClNO3S. US Biological Life Sciences. | Worldwide |
| 3H-1,2-Benzodithiol-3-one-1,1-dioxide, ≥95% | 3H-1,2-Benzodithiol-3-one-1,1-dioxide, ≥95%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g. US Biological Life Sciences. | Worldwide |
| 3-iodo-6-methyldibenzo[c,f][1,2]thiazepin-11(6H)-one 5,5-dioxide | An impurity of Tianeptine, which is a selective serotonin reuptake enhancer (SSRE) used for treating major depressive episodes. Synonyms: SCHEMBL18659752; 3-iodo-6-methyldibenzo[c,f][1,2]thiazepin-11(6H)-one 5,5-dioxide; 1809279-00-2. CAS No. 1809279-00-2. Molecular formula: C14H10INO3S. Mole weight: 399.2. |  |
| 4-(3-Methylphenyl)-2H-pyrido[4,3-e]-1,2,4-thiadiazin-3(4H)-one 1,1-Dioxide Sodium Salt | 4-(3-Methylphenyl)-2H-pyrido[4,3-e]-1,2,4-thiadiazin-3(4H)-one 1,1-Dioxide Sodium Salt. Uses: For analytical and research use. Group: Impurity standards. Pack Sizes: 10MG. Catalog: APS004614. Format: Neat. Shipping: Room Temperature. |  |
| 4-(3-Methylphenyl)-2H-pyrido[4,3-e]-1,2,4-thiadiazin-3(4H)-one 1,1-Dioxide Sodium Salt (Torsemide im | 4-(3-Methylphenyl)-2H-pyrido[4,3-e]-1,2,4-thiadiazin-3(4H)-one 1,1-Dioxide Sodium Salt (Torsemide im. Uses: For analytical and research use. Group: Impurity standards. CAS No. 72810-61-8. IUPAC Name: 4-(3-methylphenyl)-1,1-dioxopyrido[4,3-e][1,2,4]thiadiazin-3-one. Molecular Formula: C13H11N3O3S. Mole Weight: 289.31. Catalog: APS72810618. SMILES: Cc1cccc (c1)N2C (=O)NS (=O) (=O)c3cnccc23. Format: Neat. | |
| 4-(3-Methylphenyl)-2H-pyrido[4,3-e]-1,2,4-thiadiazin-3(4H)-one 1,1-Dioxide (Torsemide impurity) | An impurity of Torsemide. Group: Biochemicals. Grades: Highly Purified. CAS No. 72810-61-8. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 4,6-Diphenylthieno[2,4-d]-1,3-dioxol-2-one-5,5-dioxide | 4,6-Diphenylthieno[2,4-d]-1,3-dioxol-2-one-5,5-dioxide. Group: Biochemicals. Alternative Names: TDO-carbonate; Steglich's reagent. Grades: Highly Purified. CAS No. 54714-11-3. Pack Sizes: 2g, 5g. US Biological Life Sciences. | Worldwide |
| 4,6-Diphenylthieno[2,4-d]-1,3-dioxol-2-one-5,5-dioxide 98+% | 4,6-Diphenylthieno[2,4-d]-1,3-dioxol-2-one-5,5-dioxide 98+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 54714-11-3. Pack Sizes: 1g, 5g. US Biological Life Sciences. | Worldwide |
| 5-Phenyl-1,2,5-thiadiazolidin-3-one 1,1-Dioxide | 5-Phenyl-1,2,5-thiadiazolidin-3-one 1,1-Dioxide. Group: Biochemicals. Grades: Highly Purified. CAS No. 612532-44-6. Pack Sizes: 50mg. Molecular Formula: C8H8N2O3S, Molecular Weight: 212.23. US Biological Life Sciences. | Worldwide |
| 6-methyl-3-(trimethylsilyl)dibenzo[c, f][1, 2]thiazepin-11(6H)-one 5,5-dioxide | An impurity of Tianeptine, which is a selective serotonin reuptake enhancer (SSRE) used for treating major depressive episodes. CAS No. 1809278-99-6. Molecular formula: C17H19NO3SSi. Mole weight: 345.49. | |
| 6-methyldibenzo[c,f][1,2]thiazepin-11(6H)-one 5,5-dioxide | An impurity of Tianeptine, which is a selective serotonin reuptake enhancer (SSRE) used for treating major depressive episodes. Synonyms: Dibenzo[c,f][1,2]thiazepin-11(6H)-one, 6-methyl-, 5,5-dioxide; 10-methyl-9; SCHEMBL19194634; DTXSID901180125; 6-methyl-5,5-dioxobenzo[c][1,2]benzothiazepin-11-one; 10-methyl-9|E?-thia-10-azatricyclo[9.4.0.0?,?]pentadeca-1(11),3(8),4,6,12,14-hexaene-2,9,9-trione. CAS No. 26638-46-0. Molecular formula: C14H11NO3S. Mole weight: 273.31. | |
| Benzo[B]Thiophene-3(2H)-One 1,1-Dioxide | Thiophenes. Alternative Names: Benzo[B]Thiophen-3(2H)-One 1,1-Dioxide; 1-Benzothiophen-3(2h)-One 1,1-Dioxide. CAS No. 1127-35-1. Molecular formula: C8H6O3S. Mole weight: 182.19. Catalog: ACM1127351. | |
| Dihydro-5,5-dimethyl-2H-thiopyran-3(4H)-one-1,1-dioxide | Heterocyclic Organic Compound. Alternative Names: 1049093-43-7, SureCN4971863, AKOS015950429, RP08898, FT-0685952, 5,5-dimethyl-1$l^{6}-thiane-1,1,3-trione, Dihydro-5,5-dimethyl-2H-thiopyran-3(4H)-one-1,1-dioxide. CAS No. 1049093-43-7. Molecular formula: C7H12O3S. Mole weight: 176.24. Purity: 0.96. IUPACName: 5,5-dimethyl-1,1-dioxothian-3-one. Canonical SMILES: CC1(CC(=O)CS(=O)(=O)C1)C. Catalog: ACM1049093437. | |
| 1-Nonadecanol | 1-Nonadecanol is one of the compositions of supercritical carbon dioxide (SC-CO 2 ) essential oil of Heracleum thomsonii. 1-Nonadecanol is also an important aroma compound in Neotinea ustulata [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 1454-84-8. Pack Sizes: 1 g; 5 g; 25 g. Product ID: HY-W004297. |  |
| (±)-1-Octen-3-ol | (±)-1-Octen-3-ol, is one of the volatiles responsible for mold`s odor. It can be used in combination with carbon dioxide to attract insects in order to kill them. In animal study, 1-Octen-3-ol has been shown to interfere with dopamine transport in the brain of fruit flies, so it might be an environmental agent involved in parkinsonism. Group: Biochemicals. Grades: Highly Purified. CAS No. 3391-86-4. Pack Sizes: 10g, 25 g. Molecular Formula: C8H16O. US Biological Life Sciences. | Worldwide |
| (1R,2R)-(-)-[1,2-Cyclohexanediamino-N,N'-bis(3,5-di-t-butylsalicylidene)]aluminum(III) chloride, 98% | Aluminum salen complexes as catalysts for the kinetic resolution of terminal epoxides via carbon dioxide coupling. Efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis. Catalyst used for the asymmetric hydrocyanation of nitroolefins. Catalyst used in the reaction of epoxides with heterocumulenes. Group: Heterocyclic organic compound. CAS No. 250611-13-3. Molecular formula: C36H52AlClN2O2. Mole weight: 607.26. Purity: 0.96. IUPACName: aluminum; 2, 4-ditert-butyl-6- [ [ [ (1R, 2R) -2- [ (3, 5-ditert-butyl-6-oxocyclohexa-2, 4-dien-1-ylidene) methylamino] cyclohexyl] amino] methylidene] cyclohexa-2, 4-dien-1-one; trichloride. Canonical SMILES: CC (C) (C)C1=CC (=CNC2CCCCC2NC=C3C=C (C=C (C3=O)C (C) (C)C)C (C) (C)C)C (=O)C (=C1)C (C) (C)C. [Al+3]. [Cl-]. [Cl-]. [Cl-]. ECNumber: 607-518-1. Catalog: ACM250611133. | |
| (1S)-(+)-Camphorlactone-sulfonyloxaziridine | Heterocyclic Organic Compound. Alternative Names: (1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE;5H-4a,7-Methano-4H,9H-oxazirino2,3-boxepino3,4-cisothiazol-9-one, dihydro-10,10-dimethyl-, 2,2-dioxide, 4aS-(4a.alpha., 7.alpha., 9aS*)-;(1S)-(+)-CAMPHORLACTONE-SULFONYLOXAZIRIDINE 98+%. CAS No. 127411-75-0. Molecular formula: C10H13NO5S. Mole weight: 259.28. Catalog: ACM127411750. | |
| 2-Hydroxyisobutyric Acid | 2-Hydroxyisobutyric Acid is used as a reagent in the preparation of fully functionalized tetronic acids. Also used in the synthesis of bioisosteres of trimethadione, N-derivative-1,2,3-oxathiazolidine-4-one-2,2-dioxides from α-hydroxyamides which display anticonvulsant activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 594-61-6. Pack Sizes: 5g, 10g. Molecular Formula: C4H8O3, Molecular Weight: 104.1. US Biological Life Sciences. | Worldwide |
| 2-oxoglutarate dioxygenase (ethylene-forming) | This is one of two simultaneous reactions catalysed by the enzyme, which is responsible for ethylene production in bacteria of the Pseudomonas syringae group. In the other reaction [EC 1.14.11.34, 2-oxoglutarate/L-arginine monooxygenase/decarboxylase (succinate-forming)] the enzyme catalyses the mono-oxygenation of both 2-oxoglutarate and L-arginine, forming succinate, carbon dioxide and L-hydroxyarginine, which is subsequently cleaved into guanidine and (S)-1-pyrroline-5-carboxylate.The enzymes catalyse two cycles of the ethylene-forming reaction for each cycle of the succinate-forming reaction, so that the stoichiometry of the products ethylene and succinate is 2:1. Group: Enzymes. Synonyms: ethylene-forming enzyme; EFE. Enzyme Commission Number: EC 1.13.12.19. 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-0611; 2-oxoglutarate dioxygenase (ethylene-forming); EC 1.13.12.19; ethylene-forming enzyme; EFE. Cat No: EXWM-0611. |  |
| 2-oxoglutarate/L-arginine monooxygenase/decarboxylase (succinate-forming) | This is one of two simultaneous reactions catalysed by the enzyme, which is responsible for ethylene production in bacteria of the Pseudomonas syringae group.In the other reaction [EC 1.13.12.19, 2-oxoglutarate dioxygenase (ethylene-forming)] the enzyme catalyses the dioxygenation of 2-oxoglutarate forming ethylene and three molecules of carbon dioxide.The enzyme catalyses two cycles of the ethylene-forming reaction for each cycle of the succinate-forming reaction, so that the stoichiometry of the products ethylene and succinate is 2:1. Group: Enzymes. Synonyms: ethylene-forming enzyme; EFE. Enzyme Commission Number: EC 1.14.11.34. 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-0652; 2-oxoglutarate/L-arginine monooxygenase/decarboxylase (succinate-forming); EC 1.14.11.34; ethylene-forming enzyme; EFE. Cat No: EXWM-0652. | |
| 4-Ethyl-2H-1,2,4-benzothiadiazin-3(4H)-on-1,1-dioxide | Heterocyclic Organic Compound. Alternative Names: 4-Ethyl-2H-1,2,4-benzothiadiazin-3(4H)-on-1,1-dioxide;4-Ethyl-2H-1,2,4-benzothiadiazin-3(4H)-on-1,1-. CAS No. 102308-74-7. Molecular formula: C9H10N2O3S. Mole weight: 226.2523. Purity: 0.96. IUPACName: 4-ethyl-1,1-dioxo-1$l^{6},2,4-benzothiadiazin-3-one. Canonical SMILES: CCN1C2=CC=CC=C2S(=O)(=O)NC1=O. Density: 1.379g/cm³. Catalog: ACM102308747. | |
| 5-Chloro Acesulfame | 5-Chloro Acesulfame. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 5-Chloro-6-methyl-1,2,3-oxathiazin-4(3H)-one 2,2-dioxide, Acesulfam Potassium Imp. B (EP). CAS No. 72827-08-8. Pack Sizes: 10MG. IUPAC Name: 5-chloro-6-methyl-2,2-dioxooxathiazin-4-one. Molecular Formula: C4H4ClNO4S. Mole Weight: 197.60. Catalog: APS72827088. SMILES: CC1=C(Cl)C(=O)NS(=O)(=O)O1. Format: Neat. Shipping: Room Temperature. | |
| 5-Hydroxy lornoxicam | Heterocyclic Organic Compound. Alternative Names: 5-HYDROXY LORNOXICAM;3-e)-1,2-thiazine-3-carboxamide,6-chloro-4-hydroxy-n-(5-hydroxy-2-2h-thieno(;pyridinyl)-2-methyl-,1,1-dioxide. CAS No. 123252-96-0. Molecular formula: C13H10ClN3O5S2. Mole weight: 387.82. Appearance: Greenish Yellow Solid. Purity: 0.96. IUPACName: (3E)-6-chloro-3-[hydroxy-[(5-hydroxypyridin-2-yl)amino]methylidene]-2-methyl-1,1-dioxothieno[2,3-e]thiazin-4-one. Density: 1.814g/cm³. Catalog: ACM123252960. | |
| 5-Hydroxy Lornoxicam | 5-Hydroxy Lornoxicam is one of lornoxicam metabolites. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: 6-Chloro-4-hydroxy-N-(5-hydroxy-2-pyridinyl)-2-methyl-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-Dioxide; 2H-Thieno(2,3-e)-1,2-thiazine-3-carboxamide, 6-chloro-4-hydroxy-N-(5-hydroxy-2-pyridinyl)-2-methyl-, 1,1-dioxide. Grades: 98%. CAS No. 123252-96-0. Molecular formula: C13H10ClN3O5S2. Mole weight: 387.82. | |
| 6-Hydroxy Bentazon | A metabolite of Bentazon, a selective post-emergence herbicide. Group: Biochemicals. Alternative Names: 6-Hydroxy-3-(1-methylethyl)-1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-Dioxide; 6-Hydroxybentazone. Grades: Highly Purified. CAS No. 60374-42-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 6-Nitrosaccharin | 6-Nitrosaccharin. Group: Biochemicals. Alternative Names: 6-Nitrobenzo [d]isothiazol-3 (2H) -one 1,1-dioxide; 6-Nitro-1,2-benzothiazol-3(2h)-one 1,1-dioxide. Grades: Highly Purified. CAS No. 22952-24-5. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C7H14N2O5S. US Biological Life Sciences. | Worldwide |
| 8-Hydroxybentazone | 8-Hydroxybentazone. Group: Biochemicals. Alternative Names: 8-Hydroxybentazon; 8-Hydroxy-3-(1-methylethyl)-1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-Dioxide. Grades: Highly Purified. CAS No. 60374-43-8. Pack Sizes: 1mg. Molecular Formula: C10H12N2O4S, Molecular Weight: 256.279999999999. US Biological Life Sciences. | Worldwide |
| Acesulfame | Acesulfame. Synonyms: RARECHEM AM UC 0205;SWEET ONE;SUNETTE;POTASSIUM 6-METHYL-1,2,3-OXATHIAZIN-4(3H)-ONE 2,2-DIOXIDE;1,2,3-oxathiazin-4(3h)-one,6-methyl-,2,2-dioxide;6-methyl-1,2,3-oxathiazin-4(3h)-one2,2-dioxide;6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide. CAS No. 33665-90-6. Product ID: CDF4-0163. Molecular formula: C4H5NO4S. Category: Sweeteners. Product Keywords: Food Ingredients; Sweeteners; Acesulfame; CDF4-0163; 33665-90-6; C4H5NO4S; 251-622-6; 33665-90-6. Purity: 0.99. EC Number: 251-622-6. Melting Point: 123-123.5°. Density: 1.83 g/mL. |  |
| Acesulfame-[d4] Potassium Salt | Acesulfame-[d4] Potassium Salt is a labelled version of Acesulfame Potassium. Acesulfame potassium is a non-nutritive sweetener. Synonyms: 6-Methyl-1,2,3-oxathiazin-4(3H)-one-d4 2,2-Dioxide Potassium Salt; Acesulfam H-d4 Potassium Salt; 3,4-Dihydro-6-methyl-1,2,3-oxathiazin-4-one-d4 2,2-Dioxide Potassium Salt. CAS No. 1623054-53-4. Molecular formula: C4D4KNO4S. Mole weight: 205.27. | |
| Acesulfame-d4 Potassium Salt | New generation', heat-stable sweetener that has not been suspected to cause cancer nor be genotoxic. Allelic variation of the Tas1r3 gene affects behavioral taste responses to this molecule, suggesting that it is a T1R3 receptor ligand. Group: Biochemicals. Alternative Names: 6-Methyl-1,2,3-oxathiazin-4(3H)-one-d4 2,2-Dioxide Potassium Salt; Acesulfam H-d4 Potassium Salt; 3,4-Dihydro-6-methyl-1,2,3-oxathiazin-4-one-d4 2,2-Dioxide Potassium Salt. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Acesulfame Potassium | Acesulfame Potassium. CAS No. 55589-62-3. Product ID: PE-0484. Molecular formula: C4H4KNO4S. Mole weight: 201.24. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Acesulfame Potassium; Sweeteners Excipients; Sweetening agent; C4H4KNO4S; 55589-62-3; 55589-62-3. UNII: NA. Chemical Name: 6-Methyl-1, 2, 3-oxathiazin-4(3H)-one-2, 2-dioxide potassium salt. Grade: Pharmceutical Excipients. Administration route: Oral. Dosage Form: Oral preparations. Stability and Storage Conditions: Acetylsul panpotassium has good stability. Stored in bulk at room temperature for many years without signs of decomposition. The sweetness of aqueous solution (pH 3.0 - 3.5, 20°C) did not decrease for about two years. Although some decomposition after storage at 40°C for several months, it has good stability at temperature rise. Neither sterilization nor pasteurization affected the sweetness of acetylsulpanpotassium. Bulk products should be stored in airtight containers in a dry place. Source and Preparation: Acetylsul panpotassium is synthesized from tert-butyl acetoacetate and fluorosulfonyl isocyanate. The resulting product is converted to fluorosulfonyl acetoacetamide and cyclized into dioxythiazone cyclization in the presence of potassium hydroxide. Because this compound is strongly acidic, it can directly form potassium salt. Another route for the synthesis of acetylsulfamide be | |
| Acesulfame Potassium | Acesulfame Potassium is used as a potent sweetener in cosmetics, foods and beverage products, table-top sweeteners, vitamins and pharmaceutical preparations, including powder mixtures, tablets and liquid products. Synonyms: Acesulfame K; ace K; acesulfamum kalicum; E950; 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4(3H)-one-2,2-dioxide potassium salt; potassium 6-methyl-2,2-dioxo-oxathiazin-4-olate; Sunett; Sweet One; 6-Methyl-1,2,3-oxathiazin-4(3H)-one 2,2-Dioxide Potassium Salt; 6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-Dioxide Potassium Salt; Otizon; Potassium Acesulfame. Grades: ≥97%. CAS No. 55589-62-3. Molecular formula: C4H4KNO4S. Mole weight: 201.24. | |
| Acesulfame Potassium | New generation', heat-stable sweetener that has not been suspected to cause cancer nor be genotoxic. Allelic variation of the Tas1r3 gene affects behavioral taste responses to this molecule, suggesting that it is a T1R3 receptor ligand. Group: Biochemicals. Alternative Names: 6-Methyl-1,2,3-oxathiazin-4(3H)-one 2,2-Dioxide Potassium Salt; 6-Methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-Dioxide Potassium Salt; E 950; Otizon; Potassium Acesulfame; Sunett; Sunnett; Sweet One. Grades: Highly Purified. CAS No. 55589-62-3. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Azane; 1,1-dioxo-1,2-benzothiazol-3-one | Heterocyclic Organic Compound. Alternative Names: 1,2-Benzisothiazolin-3-one,1,1-dioxide,ammonium salt; AMMONIUM SACCHARIN; Ammonium O-benzosulfimide; EINECS 228-971-8; Ammonium 1,2-benzisothiazolin-3-one 1,1-dioxide; Saccharin ammonium; Daramin. CAS No. 128-43-8. Molecular formula: C7H8N2O3S. Mole weight: 200.215 g/mol. Purity: 0.96. IUPACName: azane;1,1-dioxo-1,2-benzothiazol-3-one. Canonical SMILES: C1=CC=C2C(=C1)C(=O)NS2(=O)=O.N. ECNumber: 228-971-8. Catalog: ACM128438. | |
| Beaucage reagent | Beaucage reagent. Group: Biochemicals. Alternative Names: 3H-1,2-Benzodithiol-3-one-1,1-dioxide. Grades: Highly Purified. CAS No. 66304-01-6. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| Bentazon | Bentazon. Group: Biochemicals. Alternative Names: 3-(1-Methylethyl)-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide; 3,4-Dihydro-3-isopropyl-1H-2,1,3-benzothiadiazin-4-one 2,2-dioxide; 3-Isopropyl-1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide. Grades: Highly Purified. CAS No. 25057-89-0. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C10H12N2O3S. US Biological Life Sciences. | Worldwide |
| Biotin (D-Biotin, Vitamin H, Coenzyme R, Bioepiderm) | Biotin is used as a growth factor in mammalian cell culture as well as having numerous immunological purification roles in avidin/streptavidin-biotin binding mechanisms. Biotin, also known as vitamin H or B7, is a water-soluble B-complex vitamin which is composed of an ureido (tetra hydroimidizalone) ring fused with a tetrahydrothiophene ring. A valeric acid substituent is attached to one of the carbon atoms of the tetrahydrothiophene ring. Biotin is a cofactor in the metabolism of fatty acids and leucine, and it plays a role in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids. It plays a role in the citric acid cycle, which is the process by which biochemical energy is generated during aerobic respiration. Biotin not only assists in various metabolic reactions, but also helps to transfer carbon dioxide. Biotin is also helpful in maintaining a steady blood sugar level. Biotin is often recommended for strengt Group: Biochemicals. Alternative Names: (3aS,4S,6aR)-Hexahydro-2-oxo-1H-thieno[3,4-d]imidazole-4-pentanoic Acid; (+)-Biotin; Vitamin B7; Coenzyme R; D(+)-Biotin; Factor S; Lutavit H2; Meribin; NSC 63865; Rovimix H2. Grades: Molecular Biology Grade. CAS No. 58-85-5. Pack Sizes: 1g, 5g, 10g, 25g. Molecular Formula: C??H??N?O?S, Molecular Weight: 244.31. US Biological Life Sciences. | Worldwide |
| Biotin (Glucose Oxidase) | Biotin is used as a growth factor in mammalian cell culture as well as having numerous immunological purification roles in avidin/streptavidin-biotin binding mechanisms. Biotin, also known as vitamin H or B7, is a water-soluble B-complex vitamin which is composed of an ureido (tetra hydroimidizalone) ring fused with a tetrahydrothiophene ring. A valeric acid substituent is attached to one of the carbon atoms of the tetrahydrothiophene ring. Biotin is a cofactor in the metabolism of fatty acids and leucine, and it plays a role in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids. It plays a role in the citric acid cycle, which is the process by which biochemical energy is generated during aerobic respiration. Biotin not only assists in various metabolic reactions, but also helps to transfer carbon dioxide. Biotin is also helpful in maintaining a steady blood sugar level. Biotin is often recommended for strengt Group: Biochemicals. Alternative Names: Vitamin H, Coenzyme R, Bioepiderm. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| CALCIUM SACCHARIN | CALCIUM SACCHARIN. Synonyms: SACCHARIN CALCIUM;SACCHARIN CALCIUM SALT;SYNCAL (R) CAS;CALCIUM SACCHARIN;Bis[(2,3-dihydro-1,2-benzisothiazole 1,1-dioxide)-2-yl]calcium salt;1,1-Dioxide-1,2-benzisothiazol-3(2H)-one, calcium salt;1,2-Benzisothiazol-3(2H)-one, 1,1-dioxide, calcium salt (2:1);1,2-Benzisothiazolin-3-one, 1,1-dioxide, calcium salt. CAS No. 6485-34-3. Product ID: CDF4-0170. Molecular formula: C7H7CaNO3S. Category: Sweeteners. Product Keywords: Food Ingredients; Sweeteners; CALCIUM SACCHARIN; CDF4-0170; 6485-34-3; C7H7CaNO3S; 229-349-9; 6485-34-3. Purity: 0.99. EC Number: 229-349-9. | |
| carbamoyl-phosphate synthase (ammonia) | The enzyme catalyses the first committed step in the urea cycle. The reaction proceeds via three separate chemical reactions: phosphorylation of hydrogencarbonate to carboxyphosphate; a nucleophilic attack of ammonia on carboxyphosphate yielding carbamate; and the phosphorylation of carbamate forming carbamoyl phosphate. Two moles of ATP are utilized for the synthesis of one molecule of carbamyl phosphate, making the reaction essentially irreversible. The enzyme requires the allosteric activator N-acetyl-L-glutamate. cf. EC 6.3.5.5, carbamoyl-phosphate synthase (glutamine-hydrolysing). Group: Enzymes. Synonyms: carbon-dioxide-ammonia ligase; carbamoylphosphate synthase; carbamylphosphate synthetase; carbamoylphosphate synthase (ammonia); carbamoylphosphate synthetase; carbamylphosphate s. Enzyme Commission Number: EC 6.3.4.16. CAS No. 9026-23-7. 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-5785; carbamoyl-phosphate synthase (ammonia); EC 6.3.4.16; 9026-23-7; carbon-dioxide-ammonia ligase; carbamoylphosphate synthase; carbamylphosphate synthetase; carbamoylphosphate synthase (ammonia); carbamoylphosphate synthetase; carbamylphosphate synthetase I; CPSI (gene name); carbon-dioxide:ammonia ligase (ADP-forming, carbamate-phosphorylating). Cat No: EXWM-5785. | |
| Carbonic Anhydrase II from Bovine, Recombinant | The carbonic anhydrases (or carbonate dehydratases) form a family of enzymes that catalyze the rapid interconversion of carbon dioxide and water to bicarbonate and protons (or vice versa), a reversible reaction that occurs relatively slowly in the absence of a catalyst. The active site of most carbonic anhydrases contains a zinc ion; they are therefore classified as metalloenzymes. Carbonic anhydrase is a zinc-containing enzyme that catalyzes the reversible conversion of carbon dioxide to bicarbonate. one of its main physiological roles is to maintain the acid-base balance in blood and other tissues. lack of carbonic anhydrase results in carbonic anhydrase type ii defi...ns: Carbonic anhydrase is used to create carbon dioxide capture systems and to research various purification techniques. carbonic anhydrase is also used to study acid-base regulation in fish and carbonic anhydrase type ii deficiency syndrome. bovine carbonic anhydrase ii (ca II), has been widely used as a model protein in the investigation of the protein folding process. Group: Enzymes. Synonyms: carbonic anhydrases; carbonate dehydratases; EC 4.2.1.1; anhydrase; carbonate anhydrase; carbonic acid anhydrase; carboxyanhydrase; carbonic anhydrase A; carbonate hydro-lyase. Enzyme Commission Number: EC 4.2.1.1. CAS No. 9001-03-0. Purity: >90% by SDS-PAGE. Carbonic Anhydras | |
| Cetrimonium saccharinate | Leveling agent in cationic dyes, antistatic agent, softening agent in textile, fiber, leather. Group: Oil fieldtextile industry. Alternative Names: 1-Hexadecanaminium, N,N,N-trimethyl-, salt with 1,2-benzisothiazol-3(2H)-one 1,1-dioxide (1:1). CAS No. 2478-29-7. Molecular formula: C26H46N2O3S. Mole weight: 466.72. IUPACName: 1,1-Dioxo-1,2-benzothiazol-3-olate;hexadecyl(trimethyl)azanium. Canonical SMILES: CCCCCCCCCCCCCCCC[N+](C)(C)C. C1=CC=C2C(=C1)C(=NS2(=O)=O)[O-]. Catalog: ACM2478297. | |
| Dibenzothiophene sulfone | Dibenzo[b,d]thiophene sulfone has been recognized as one of the most attractive building blocks for the synthesis of H2-production polymer photocatalysts. Group: Heterocyclic organic compound. CAS No. 1016-05-3. Molecular formula: C12H8O2S. Mole weight: 216.26. Purity: MP 223-224deg. IUPACName: dibenzothiophene 5,5-dioxide. Canonical SMILES: O=S1(=O)c2ccccc2-c3ccccc13. ECNumber: 213-805-9. Catalog: ACM1016053-2. | |
| Dibenzothiophene sulfone | Dibenzothiophene sulfone. Uses: Dibenzo[b,d]thiophene sulfone has been recognized as one of the most attractive building blocks for the synthesis of h2-production polymer photocatalysts. Group: other electronic materials. CAS No. 1016-05-3. Product ID: dibenzothiophene 5,5-dioxide. Molecular formula: 216.26. Mole weight: C12H8O2S. O=S1(=O)c2ccccc2-c3ccccc13. 1S/C12H8O2S/c13-15 (14)11-7-3-1-5-9 (11)10-6-2-4-8-12 (10)15/h1-8H. IKJFYINYNJYDTA-UHFFFAOYSA-N. MP 223-224deg. |  |
| DIDOPO | DI-DOPO is one phosphate ester organic compound, no halogen environmental protection flame retardant, can fully meet the environmental requirements of the European Union.This product has high efficiency flame retardant to polyester and nylon products, with excellent compatibility with polyester and nylon, excellent spinnability in the spinning process, continuous silk, good coloring performance;It has good flame retardant effect in CCL board, with low Dk, Df characteristics. Group: Dopo flame retardant. Alternative Names: 6H-dibenz[c, e][1, 2]oxaphosphorin, 6, 6'-(1, 2-ethanediyl)bis-6, 6'-dioxide DIDOPO. CAS No. 1239439-38-3. Molecular formula: C26H20O4P2. Mole weight: 458.38. Purity: 99% min. Catalog: ACM1239439383. | |
| Ethanolamine hydrochloride | Ethanolamine hydrochloride, is an organic compound used in various industrial applications. It is a white or colorless solid that is soluble in water and has a faint odor. One of the major uses of Ethanolamine hydrochloride is in the production of detergents and surfactants. Used as a raw material in the manufacture of compounds such as ethylenediaminetetraacetic acid (EDTA) and diethanolamine, which are commonly used in household and industrial cleaning products. Ethanolamine hydrochloride is also used in the synthesis of pharmaceuticals, agrochemicals and rubber processing agents. It acts as a buffer in certain chemical reactions, helping to adjust pH and maintain stability. Ethanolamine hydrochloride can be used for gas purification and metal corrosion inhibitor. Its ability to react with acid gases such as carbon dioxide and sulfur dioxide makes it useful for removing impurities from natural gas and other industrial gases. Overall, Ethanolamine hydrochloride is a multifunctional compound with many potential industrial applications. Its ability to act as a buffer, chelating agent, and corrosion inhibitor makes it an important tool in a variety of industries. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 2-Aminoethanol hydrochloride. CAS No. 2002-24-6. Pack Sizes: 25 g; 50 g. Product ID: HY-W035903. | |
| Fluphenazine Di N'-Oxide | Fluphenazine Di N'-Oxide is one of Fluphenazine metabolites. Fluphenazine is a phenothiazine antipsychotic, a dopaminergic antagonist and an antiviral agent. Synonyms: 1-Piperazineethanol, 4-[3-[2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-, 1,4-dioxide. Grades: 98%. CAS No. 76005-60-2. Molecular formula: C22H26F3N3O3S. Mole weight: 469.52. | |
| Fluphenazine N4-Oxide Sulphoxide | Fluphenazine N4-Oxide Sulphoxide is one of Fluphenazine intermediates. Fluphenazine is a phenothiazine antipsychotic, a dopaminergic antagonist and an antiviral agent. Synonyms: 4-[3-[2-(Trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazineethanol S,1-Dioxide; 4-[3-[5-Oxido-2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazineethanol 1-Oxide; 1-Piperazineethanol, 4-[3-[5-oxido-2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-, 1-oxide; Fluphenazine Decanoate Impurity 14. Grades: 96%. CAS No. 76005-61-3. Molecular formula: C22H26F3N3O3S. Mole weight: 469.52. | |
| Fluphenazine Sulphone | Fluphenazine Sulphone is one of Fluphenazine impurities. Fluphenazine is a phenothiazine antipsychotic, a dopaminergic antagonist and an antiviral agent. Synonyms: 4-[3-[5,5-Dioxido-2-(trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazineethanol; 4-[3-[2-(Trifluoromethyl)-10H-phenothiazin-10-yl]propyl]-1-piperazineethanol S,S-Dioxide; UNII-V6267DR81T; Fluphenazine S,S-dioxide; Fluphenazine Dihydrochloride EP Impurity B. Grades: 98%. CAS No. 1476-79-5. Molecular formula: C22H26F3N3O3S. Mole weight: 469.52. | |
| Iodinin | Iodinin is an antibiotic produced by the strain of Chromobacterium iodinum etc. It has antibacterial and fungal properties. Synonyms: 5,6-dihydroxy-10-oxidophenazin-10-ium-1-one; 1,6-Phenazinediol 5,10-dioxide. CAS No. 68-81-5. Molecular formula: C12H8N2O4. Mole weight: 244.20. | |
| Ipsapirone | Ipsapirone is a selective partial agonist of the serotonin (5-HT) receptor 5-HT1A. Its Ki value is 10 nM in hippocampal membranes. It reduces 5-HT release in rat ventral hippocampus in vivo. It also inhibits passive avoidance behavior and foot shock-induced aggression in rats. It has anxiolytic effects in vivo. It has been used to treat borderline personality disorder and depression. Uses: Anti-anxiety agents. Synonyms: TVX Q 7821; 1,1-Dioxo-2-[4-(4-pyrimidin-2-ylpiperazin-1-yl)butyl]-1,2-benzothiazol-3-one; 2-[4-[4-(2-Pyrimidinyl)-1-piperazinyl]butyl]-1,2-benzisothiazol-3(2H)-one-1,1-dioxide. Grades: ≥99% by HPLC. CAS No. 95847-70-4. Molecular formula: C19H23N5O3S. Mole weight: 401.48. | |
| Lornoxicam Impurity 1 | Lornoxicam Impurity 1 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: N-Des(2-pyridinyl)-N-(5-carboxy-2-thiazolyl) Lornoxicam; 6-Chloro-4-hydroxy-2-methyl-N-(5-carboxy-2-thiazolyl)-2H-thieno[2,3-e]-1,2-thiazine-3-carboxamide 1,1-Dioxide; MTB-2. Grades: > 98%. CAS No. 1246819-40-8. Molecular formula: C12H8ClN3O6S3. Mole weight: 421.86. | |
| Lornoxicam Impurity 16 | Lornoxicam Impurity 16 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: 2-methyl-2,3-dihydro-4H-thieno[2,3-e][1,2]thiazin-4-one 1,1-dioxide; 2-Methyl-2H-thieno[2,3-e][1,2]thiazin-4(3H)-one 1,1-dioxide; 2-methyl-3H-thiopheno[2,3-e]1,2-thiazine-1,1,4-trione; 4H-Thieno[2,3-e]-1,2-thiazin-4-one, 2,3-dihydro-2-methyl-, 1,1-dioxide. Grades: 98%. CAS No. 72975-44-1. Molecular formula: C7H7NO3S2. Mole weight: 217.27. | |
| Lornoxicam Impurity 2 | Lornoxicam Impurity 2 is one of lornoxicam impurities. Lornoxicam is a non-steroidal COX-1/COX-2 inhibitor and a non-steroidal anti-inflammatory drug (NSAID), with analgesic, anti-pyretic, anti-thrombotic and anti-inflammatory activities. Synonyms: N-Des(2-pyridinyl)-N-(5-hydroxymethyl-2-thiazolyl) Lornoxicam; 6-chloro-4-hydroxy-N-(5-(hydroxymethyl)thiazol-2-yl)-2-methyl-2H-thieno[2,3-e][1,2]thiazine-3-carboxamide 1,1-dioxide; MTB-1. Grades: > 98%. CAS No. 1246818-50-7. Molecular formula: C12H10ClN3O5S3. Mole weight: 407.87. | |
| Native Microorganism Phosphoenolpyruvate carboxylase | Phosphoenolpyruvate carboxylase is an enzyme in the family of carboxy-lyases found in plants and some bacteria that catalyzes the addition of bicarbonate (HCO3-) to phosphoenolpyruvate (PEP) to form the four-carbon compound oxaloacetate and inorganic phosphate: PEP + HCO3-? oxaloacetate + Pi. This reaction is used for carbon fixation in CAM (crassulacean acid metabolism) and C4 organisms, as well as to regulate flux through the citric acid cycle (also known as Krebs or TCA cycle) in bacteria and plants. The enzyme structure and its two step catalytic, irreversible mechanism have been well studied. PEP carboxylase is highly regulated, both by phosphorylation and allostery. Applications: This enzyme is useful for enzymatic determination of carbon dioxide when coupled with malate dehydrogenase in clinical analysis. Group: Enzymes. Synonyms: PEP carboxylase; PEPCase; PEPC; EC 4.1.1.31; Phosphoenolpyruvate carboxylase; PDB ID: 3ZGE. Enzyme Commission Number: EC 4.1.1.31. CAS No. 9067-77-0. PEPC. Mole weight: approx. 390 kDa (by gel filtration). Activity: Grade? 5.0U/mg-solid or more. Stability: Stable at-20°C for at least one year. Appearance: White amorphous powder, lyophilized. Source: Microorganism. PEP carboxylase; PEPCase; PEPC; EC 4.1.1.31; Phosphoenolpyruvate carboxylase; PDB ID: 3ZGE. Cat No: DIA-212. | |
| Native Streptococcus faecalis L-Tyrosine Decarboxylase | In enzymology, a tyrosine decarboxylase (EC 4.1.1.25) is an enzyme that catalyzes the chemical reaction:L-tyrosine<-> tyramine + CO2. Hence, this enzyme has one substrate, L-tyrosine, and two products, tyramine and carbon dioxide. This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in tyrosine metabolism and alkaloid biosynthesis. It employs one cofactor, pyridoxal phosphate. Applications: L-tyrosine decarboxylase from strept oc occus faecalis has been used in a study to isolate and identify the carbonyl-active site of diamine oxidase by gas chromatographic mass spectrometry. l-tyrosine decarboxylase from strept oc occus faecalis has also been used in a study to investigate the adsorption of strept oc occus faecalis on diatomite carriers for use in biotransformations. Group: Enzymes. Synonyms: tyrosine decarboxylase; EC 4.1.1.25; L-tyrosine decarboxylase; L-(-)-tyrosine apodecarboxylase; L-tyrosine carboxy-lyase; 9002-09-9. Enzyme Commission Number: EC 4.1.1.25. CAS No. 9002-9-9. L-Tyrosine Decarboxylase. Activity: > 0.1 unit/mg solid. Storage: -20°C. Source: Streptococcus faecalis. tyrosine decarboxylase; EC 4.1.1.25; L-tyrosine decarboxylase; L-(-)-tyrosine apodecarboxylase; L-tyrosine carboxy-lyase; 9002-09-9. Cat No: NATE-0421. | |
| Native Streptococcus faecalis L-Tyrosine Decarboxylase Apoenzyme | In enzymology, a tyrosine decarboxylase (EC 4.1.1.25) is an enzyme that catalyzes the chemical reaction:L-tyrosine<-> tyramine + CO2. Hence, this enzyme has one substrate, L-tyrosine, and two products, tyramine and carbon dioxide. This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in tyrosine metabolism and alkaloid biosynthesis. It employs one cofactor, pyridoxal phosphate. Applications: L-tyrosine decarboxylase apoenzyme from strept oc occus faecalis has been used in a study to purify and characterize tyrosine decarboxylase and aromatic-l-amino-acid decarboxylase. l-tyrosine decarboxylase apoenzyme from strept oc occus faecalis has also been used in a study to investigate the stereospecificity of sodium borohydride reduction of tyrosine decarboxylase. Group: Enzymes. Synonyms: tyrosine decarboxylase; EC 4.1.1.25; L-tyrosine decarb. Enzyme Commission Number: EC 4.1.1.25. CAS No. 9002-9-9. L-Tyrosine Decarboxylase. Activity: <0.005 unit/mg solid (without pyridoxal 5-phosphate),> 0.05 unit/mg solid (with excess pyridoxal 5-phosphate). Storage: -20°C. Source: Streptococcus faecalis. tyrosine decarboxylase; EC 4.1.1.25; L-tyrosine decarboxylase; L-(-)-tyrosine apodecarboxylase; L-tyrosine carboxy-lyase; 9002-09-9. Cat No: NATE-0420. | |
| N-Bromosaccharin | N-Bromosaccharin. Group: Biochemicals. Alternative Names: 2-Bromo-1,2-benzisothiazol-3(2H)-one 1,1-Dioxide. Grades: Highly Purified. CAS No. 35812-01-2. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. | Worldwide |
| N-Iodosaccharin | N-Iodosaccharin. Group: Biochemicals. Alternative Names: 2-Iodo-1,2-benzisothiazol-3(2H)-one 1,1-Dioxide. Grades: Highly Purified. CAS No. 86340-94-5. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| Olaquindox | Olaquindox, as one of the antimicrobial growth accelerants, is usually used in livestock production to improve feed efficiency. Olaquindox induced apoptosis of HepG2 cells through a caspase-9 dependent mitochondrial pathway. Besides, Olaquindox also induces autophagy in HepG2 cells and that Olaquindox-induced apoptosis can be enhanced by 3-methyladenine. Olaquindox-induced autophagy in HepG2 cells is upregulated by Beclin 1 but downregulated by ROS-dependent JNK. Uses: Antimicrobial growth accelerant. Synonyms: N-(2-HYDROXYETHYL)-3-METHYL-2-QUINOXALINECARBOXAMIDE 1,4-DIOXIDE;OLAGUINDOX; OLAQUINDOX;2-(n-(2-hydroxyethyl)karbamoyl)-3-methylchinoxalin-1,4-dioxid; 2-quinoxalinecarboxamide,n-(2-hydroxyethyl)-3-methyl-,1,4-dioxide;bayernox;bayonox; bisergon. Grades: >98%. CAS No. 23696-28-8. Molecular formula: C12H13N3O4. Mole weight: 263.25. | |
| Potassium saccharate | Potassium saccharate. Synonyms: 1,2-Benzisothiazol-3(2H)-one,1,1-dioxide, potassium salt (1:1). CAS No. 10332-51-1. Product ID: CDF4-0177. Molecular formula: C6H8K2O8. Category: Sweeteners. Product Keywords: Food Ingredients; Sweeteners; Potassium saccharate; CDF4-0177; 10332-51-1; C6H8K2O8; 10332-51-1. Purity: 0.99. | |
| Potassium saccharate | Sweeteners. Alternative Names: 1,2-Benzisothiazol-3(2H)-one,1,1-dioxide, potassium salt (1:1). CAS No. 10332-51-1. Mole weight: 221.28. Purity: 95%+. IUPACName: Potassium;1,1-dioxo-1,2-benzothiazol-2-id-3-one. Canonical SMILES: C1=CC=C2C(=C1)C(=O)[N-]S2(=O)=O.[K+]. | |
| Ruthenium dioxide | Ruthenium dioxide is one of the primary oxygen catalysts used in a majority of chemical reactions such as the production of chlorine oxides. Ruthenium (IV) oxide is applied as an electrochemical supercapacitor agent as it has a high potential to store charge. Ruthenium dioxide is applied as a catalyst in the Deacon process where chlorine is produced through oxidation of hydrogen chloride. The high charge potential makes Ruthenium dioxide appropriate for use as an active agent in supercapacitors. The dispersion aspect of Ruthenium dioxide enhances the capacitance of nanocomposite electrode substances for supercapacitors. Ruthenium dioxide is widely used as a doping agent, as a catalyst, and as a coating material for titanium anodes, for the elimination of hydrogen sulfide from oil refineries. Hydrogen sulfide can be divided by light in the presence of a photocatalyst-containing CdS crystals doped with Ruthenium (IV) oxide. The hydrogen obtained could be essential in the synthesis of methanol, ammonia and potentially fuel an economy driven by hydrogen. Group: Nanoparticles & nanopowders. Alternative Names: Dioxoruthenium. CAS No. 12036-10-1. Molecular formula: O2Ru. Mole weight: 133.1. Appearance: Dark blue crystal. Purity: 0.98. IUPACName: dioxoruthenium. Canonical SMILES: O=[Ru]=O. ECNumber: 234-840-6. Catalog: ACM12036101-4. | |
| Ruthenium dioxide | Ruthenium dioxide. Uses: Ruthenium dioxide is one of the primary oxygen catalysts used in a majority of chemical reactions such as the production of chlorine oxides. ruthenium (iv) oxide is applied as an electrochemical supercapacitor agent as it has a high potential to store charge. ruthenium dioxide is applied as a catalyst in the deacon process where chlorine is produced through oxidation of hydrogen chloride. the high charge potential makes ruthenium dioxide appropriate for use as an active agent in supercapacitors. the dispersion aspect of ruthenium dioxide enhances the capacitance of nanocomposite electrode substances for supercapacitors. ruthenium dioxide is widely used as a doping agent, as a catalyst, and as a coating material for titanium anodes, for the elimination of hydrogen sulfide from oil refineries. hydrogen sulfide can be divided by light in the presence of a photocatalyst-containing cds crystals doped with ruthenium (iv) oxide. the hydrogen obtained could be essential in the synthesis of methanol, ammonia and potentially fuel an economy driven by hydrogen. Group: Salt. Alternative Names: Dioxoruthenium. CAS No. 12036-10-1. Product ID: dioxoruthenium. Molecular formula: 133.1. Mole weight: O2Ru. O=[Ru]=O. InChI=1S/2O.Ru. WOCIAKWEIIZHES-UHFFFAOYSA-N. 98%. | |
| Saccharin | Saccharin is an orally active and non-caloric artificial sweetener used in beverages, foods, table-top sweeteners and oral hygiene products such as toothpastes and mouthwashs. Saccharin has bacteriostatic and microbiome-modulating properties. Synonyms: 1,2-Benzisothiazol-3(2H)-one 1,1-dioxide; 1,2-Dihydro-2-ketobenzisosulfonazole; Benzoic Sulfimide; o-Benzosulfimide; Benzosulfimide; Garantose; Glucid; Gluside; NSC 5349; Saccharimide; o-Sulfobenzimide. Grades: 95%. CAS No. 81-07-2. Molecular formula: C7H5NO3S. Mole weight: 183.18. | |
| Saccharin | Saccharin occurs as odorless white crystals or a white crystalline powder. It has an intensely sweet taste, with a metallic or bitter aftertaste that at normal levels of use can be detected by approximately 25% of the population. The aftertaste can be masked by blending saccharin with other sweeteners. Synonyms: 1, 2-Benzisothiazolin-3-one 1, 1-dioxide; benzoic acid sulfimide; benzoic sulfimide; benzosulfimide; 1, 2-dihydro-2-ketobenzisosulfonazole; 2, 3-dihydro-3-xobenzisosulfonazole; E954; Garantose; gluside; Hermesetas; sacarina; saccarina; saccharin insoluble; saccharinum; o-sulfobenzimide; o-sulfobenzoic acid imide. CAS No. 81-07-2. Product ID: PE-0483. Molecular formula: C7H5NO3S. Mole weight: 183.18. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Saccharin; Sweeteners Excipients; Sweetening agent; C7H5NO3S; 81-07-2; 81-07-2. UNII: C151H8M554. Chemical Name: 1, 2-Benzisothiazol-3(2H)-one 1, 1-dioxide. Grade: Pharmceutical Excipients. Administration route: Oral; Topical. Dosage Form: Oral solutions, syrups, tablets, and topical preparations. Stability and Storage Conditions: Saccharin is stable under the normal range of conditions employed in formulations. In the bulk form it shows no detectable decomposition and only when it is exposed to a high temperature (125°C) at a low pH (pH 2) for over 1 hour does significant decomposition occur. The decomposition pr | |
| Saccharin sodium | Nickel Plating Intermediates. Alternative Names: 1,2-Benzothiazol-3(2H)-one 1,1-dioxide sodium salt. CAS No. 128-44-9. Molecular formula: C7H4NNaO3S. Mole weight: 205.17. Appearance: Crystal. Purity: 95%+. IUPACName: Sodium;1,1-dioxo-1,2-benzothiazol-2-id-3-one. Canonical SMILES: C1=CC=C2C(=C1)C(=O)[N-]S2(=O)=O. [Na+]. Catalog: ACM128449-1. | |
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