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| Product | Description | |
|---|---|---|
| Calcium Saccharate Tetrahydrate | Calcium Saccharate is used in the synthesis of hydroxyapatite particles. Synthesized from the nitric acid oxidation of D-glucose. Group: Biochemicals. Grades: Highly Purified. CAS No. 5793-89-5. Pack Sizes: 5g, 10g. Molecular Formula: C6H8O8Ca 4[H2O]. US Biological Life Sciences. |  Worldwide |
| Calcium Saccharate USP | Calcium Saccharate USP. CAS No. 5793-89-5. Molecular formula: C6H8CaO8.4H2O. |  |
| Calcium D-saccharate tetrahydrate | 100g Pack Size. Group: Biochemicals, Carbohydrates. Formula: C6H8CaO8 · 4H2O. CAS No. 5793-88-4. Prepack ID 31685470-100g. Molecular Weight 320.26. See USA prepack pricing. |  |
| Calcium D-saccharate tetrahydrate | Calcium D-saccharate tetrahydrate is a biomedical compound used in the research of conditions related to calcium deficiencies, such as osteoporosand hypocalcemia. Synonyms: D-Glucaric acid calcium salt; D-Saccharic acid calcium salt; Glucaric acid calcium salt tetrahydrate; Calcium D-glucarate; Glucosaccharic acid calcium salt tetrahydrate. Grades: 98%. CAS No. 5793-89-5. Molecular formula: C6H8CaO8 4H2O. Mole weight: 320.26. |  |
| Calcium D-saccharate tetrahydrate, 98.5-102.0% USP | Calcium D-saccharate tetrahydrate, 98.5-102.0% USP. Group: Biochemicals. Grades: USP. CAS No. 5793-89-5,5793-88-4. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Calcium Gluconate | Calcium Gluconate. Synonyms: D-Glucaric acid, calcium salt (1:1) tetrahydrate; Calcium Saccharate. CAS No. 299-28-5. Product ID: PE-0617. Molecular formula: C6H8CaO8·4H2O. Category: Metal Stabilizer; Buffer. Product Keywords: Other Materials; Stabilizers; PE-0617; Calcium Gluconate; Metal Stabilizer; Buffer; C6H8CaO8·4H2O; 299-28-5. UNII: NA. Chemical Name: D-Glucaric acid, calcium salt (1:1) tetrahydrate. Grade: Pharmceutical Excipients. Administration route: Oral administration; Intravenous injection; Intramuscular injection; Subcutaneous injection. Stability and Storage Conditions: In an airtight container. Commonly used amount and the maximum amount: Maximum dosage of calcium gluconate monohydrate for each administration route: oral: 420mg; Intravenous injection: 20mg; Intramuscular injection: 20mg; Subcutaneous injection: 20mg. |  |
| Saccharated lime | Use as emulsion stabilizer, dispersing agent. Group: Anionic surfactants. Alternative Names: Calcium saccharate. CAS No. 5793-88-4. Molecular formula: C6H8CaO8. Mole weight: 248.2. Catalog: ACM5793884. |  |
| Calcium Saccharin | Calcium Saccharin. Synonyms: Calcium benzosulphimide; Saccharin Calcium; Calcium o-benzosulfimide; Calciumo-benzosulphimide; Calcium 2-benzosulphimide. CAS No. 6485-34-3. Product ID: PE-0500. Molecular formula: C14H8CaN2O6S·3(1/2)H2O. Mole weight: 467.48. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Calcium Saccharin; Sweeteners Excipients; Sweetening agent; C14H8CaN2O6S·3(1/2)H2O; 6485-34-3; 6485-34-3. UNII: 5101OP7P2I. Administration route: Oral. Dosage Form: Syrups and solutions. Source and Preparation: Saccharin reacts with half equivalent calcium hydroxide in water medium to form calcium salt, concentrates the reaction liquid to crystallization, and then dries. Safety: Limit: FDA and USDA rules, same as "saccharin". Toxicity: ADI 0-5 (Total ADI of saccharin and its salts; FAO/WHO, 2001). | |
| 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. | |
| Calcium Saccharin USP | Calcium Saccharin USP. CAS No. 6381-91-5. Molecular formula: C14H8CaN2O6S2 ·3½ H2O. | |
| Inorganic Pyrophosphatase from Saccharomyces cerevisiae, Recombinant | Pyrophosphatase (or inorganic pyrophosphatase) is an enzyme (EC 3.6.1.1) that catalyzes the conversion of one molecule of pyrophosphate to two phosphate ions. This is a highly exergonic reaction, and therefore can be coupled to unfavorable biochemical transformations in order to drive these transformations to completion. The functionality of this enzyme plays a critical role in lipid metabolism (including lipid synthesis and degradation), calcium absorption and bone formation, and DNA synthesis,as well as other biochemical transformations. Inorganic pyrophosphatase (ppase) catalyzes the hydrolysis of inorganic pyrophosphate to form orthophosphate. a variety ...actions that can be pulled far in the synthesis direction by the action of inorganic pyrophosphatase. Applications: Enhancing yields of rna in transcription reactions. Group: Enzymes. Synonyms: Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. CAS No. 9024-82-2. Inorganic pyrophosphatase. Mole weight: 71 kDa. Storage: at -20°C. Form: 20 mM Tris-HCl (pH 8.0), 100 mM KCl, 0.1 mM EDTA, 1 mM dithiothreitol and 50% glycerol. Source: E. coli. Species: Saccharomyces cerevisiae. Pyrophosphate phosphohydrolase; inorganic pyrophosphatase; EC 3.6.1.1; 9024-82-2; iphosphate phosphohydrolase. Cat No: NATE-1281. |  |
| Saccharin Calcium Hydrate | Saccharin Calcium Hydrate is a non-nutritive sweetener; pharmaceutic aid (flavor). Saccharin was formerly listed as reasonably anticipated to be a human carcinogen; delisted because the cancer data are not sufficient to meet the current criteria for this listing. Group: Biochemicals. Grades: Highly Purified. CAS No. 6381-91-5. Pack Sizes: 10g, 100g. Molecular Formula: C14H8CaN2O6S2 3.5[H2O], Molecular Weight: 404.43. US Biological Life Sciences. | Worldwide |
| Sodium Cyclamate | Sodium Cyclamate. CAS No. 139-05-9. Product ID: PE-0486. Molecular formula: C6H12NNaO3S. Mole weight: 201.22. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Sodium Cyclamate; Sweeteners Excipients; Sweetening agent; C6H12NNaO3S; 139-05-9; 139-05-9. UNII: NA. Chemical Name: Sodium N-cyclohexylsulfamate. Grade: Pharmceutical Excipients. Stability and Storage Conditions: Sodium cyclolatate is hydrolyzed slowly by sulfuric acid and cyclohexylamine at a rate proportional to hydrogen ion concentration. Therefore, it is relatively stable in practice. The solution is stable to light, heat and air over a fairly wide pH range. Tablets containing sodium cylatate and saccharin showed no decrease in sweetness after up to 20 years of storage. Raw materials should be stored in an airtight container and kept in a cool and dry place. Source and Preparation: This product is prepared by sulfonic acid reaction of cyclohexylamine under alkaline conditions. Commercially, sulfonating agents include sulfamic acid, sulfate, or sulfur trioxide. Quaternary amine compounds such as trihexamine or trimethylamine can be used as binding agents. The resulting cyclohexylate amine salt is treated with appropriate metal oxides, and the corresponding sodium salt, calcium salt, potassium salt or magnesium salt can be prepared. Applications: As a strong sweetener, sodium cyclolatate can be use | |
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