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| Product | Description | |
|---|---|---|
| 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. |  |
| Saccharin sodium | Saccharin sodium. CAS No. 128-44-9. Product ID: PE-0004. Molecular formula: C7H5NNaO3S. Mole weight: 206.17. Category: Corrective Excipients. Product Keywords: Pharmaceutical Excipients; Liquid Dosage Form; Corrective Excipients; Saccharin sodium; PE-0004; C7H5NNaO3S; 128-44-9; 128-44-9. Appearance: White crystals or a white, crystalline efflorescent powder. Purity: 0.99. EC Number: 204-886-1. Synonym(s): 1,2-Benzothiazol-3(2H)-one 1,1-dioxide sodium salt;Sodium 1,1-dioxo-1,2-benzothiazol-2-id-3-one;2-Sodio-1,2-benzisothiazol-3(2H)-one 1,1-dioxide. Solubility: H2O: 1 M at 20 °C, clear, colorless; sparingly soluble in ethanol. Storage: 0-6°C. Melting Point: >300°C. Density: 1.69[at 20°C]. |  |
| Saccharin sodium | Saccharin sodium is an orally active, non-caloric artificial sweeteners (NAS). Saccharin sodium has bacteriostatic and microbiome-modulating properties [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 128-44-9. Pack Sizes: 500 mg. Product ID: HY-B1390A. |  |
| Saccharin Sodium BP | Saccharin Sodium BP. CAS No. 82385-42-0. Molecular formula: C7H4NNaO3S.xH2O. |  |
| Saccharin sodium hydrate | Saccharin sodium hydrate is an orally active, non-caloric artificial sweeteners (NAS). Saccharin sodium hydrate has bacteriostatic and microbiome-modulating properties [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 82385-42-0. Pack Sizes: 500 mg; 1 g. Product ID: HY-B1390B. | |
| Saccharin sodium salt | Saccharin sodium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 128-44-9. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. Molecular Formula: C7H4NNaO3S. US Biological Life Sciences. |  Worldwide |
| Saccharin sodium salt dihydrate | Sweeteners. Alternative Names: 1,2-Benzisothiazol-3(2h)-one 1,1-dioxide hydrate. CAS No. 82385-42-0. Mole weight: 223.18. Purity: 95%+. IUPACName: Sodium;1,1-dioxo-1,2-benzothiazol-2-id-3-one;hydrate. Canonical SMILES: C1=CC=C2C(=C1)C(=O)[N-]S2(=O)=O. O. [Na+]. | |
| Saccharin Sodium Salt Dihydrate | Saccharin Sodium Salt Dihydrate 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. 6155-57-3. Pack Sizes: 5g, 25g. Molecular Formula: C7H4NNaO3S; 2(H2O). US Biological Life Sciences. | Worldwide |
| Sodium cyclamate Sodium Saccharin Sorbitol Stevia. | Sodium cyclamate Sodium Saccharin Sorbitol Stevia. Group: Sweeteners. |  |
| Sodium Saccharin | Sodium Saccharin. Market: Food Additives / Preservatives, Cosmetics & Personal Care. PK Chem Industries: We supply chemicals related to Cosmetic, Personal Care, Food, Pharmaceutical, Feed, Agriculture and Mining Industries. |  |
| Sodium saccharinate (dihydrate) | Sodium saccharinate (dihydrate). Uses: For analytical and research use. Group: Impurity standards. CAS No. 6155-57-3. Molecular Formula: C7H8NNaO4S. Mole Weight: 225.19. Catalog: APB6155573. |  |
| 3-Bromopiperidin-2,6-dione | 3-Bromopiperidin-2,6-dione was in reaction with sodium saccharin to synthesize glutarimides derivatives to observe their activities against Ehrlich ascites carcinoma in Swiss albino mice. Group: Biochemicals. Grades: Highly Purified. CAS No. 62595-74-8. Pack Sizes: 5mg, 25mg. Molecular Formula: C5H6BrNO2, Molecular Weight: 192.01. US Biological Life Sciences. | Worldwide |
| DL-Alanine | DL-alanine, an orally active amino acid , is the racemic compound of L- and D-alanine. DL-alanine is employed both as a reducing and a capping agent, used with silver nitrate aqueous solutions for the production of nanoparticles. DL-alanine can be used for the research of transition metals chelation, such as Cu(II), Zn(II), Cd(11). DL-alanine, a sweetener, is classed together with glycine and sodium saccharin. DL-alanine plays a key role in the glucose-alanine cycle between tissues and liver [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Natural products. Alternative Names: DL-2-Aminopropionic acid. CAS No. 302-72-7. Pack Sizes: 25 g; 50 g; 100 g. Product ID: HY-N2362. | |
| DL-Alanine | DL-Alanine is a racemic mixture of alanine, a non-essential alpha-amino acid. Alanine is one of the most common residues for protein synthesis and is involved in the metabolism of tryptophan and vitamin pyridoxine. Furthermore, alanine is an important source of energy for muscles and central nervous system. It strengthens the immune system, helps in the metabolism of sugars and organic acids, and displays a cholesterol-reducing effect in animals. CAS No. 302-72-7. Product ID: PAP-0005. Molecular formula: C3H7NO2. Category: Amino acid. Product Keywords: Amino Acid Series; DL-Alanine; PAP-0005; Amino acid; C3H7NO2; 302-72-7. Color: White. EC Number: 206-126-4. Physical State: Crystals or Crystalline Powder. Solubility: H2O: soluble. Storage: Keep in dark place,Inert atmosphere,Room temperature. Applications: DL-alanine is an amino acid, a racemic compound of L- and D-alanine. DL-alanine, together with aqueous silver nitrate, is used for nanoparticle generation as a reducing agent and an end-sealing agent. DL-alanine can be used for the chelation of Cu(II), Zn(II), Cd(11) and other transition metals. DL-alanine is a sweetener, placed in the same group as glycine and saccharin sodium. DL-alanine plays a key role in the glucose-alanine cycle between tissues and the liver. Boiling Point: 212.9±23.0 °C(Predicted). Melting Point: 289 °C (dec.) (lit.). Density: 1,424 g/cm3. Product Description: DL-alanine is an amino acid, a rac | |
| DL-Alanine-13C-1 | DL-Alanine- 13 C-1 is the 13 C-labeled DL-Alanine. DL-alanine, an amino acid, is the racemic compound of L- and D-alanine. DL-alanine is employed both as a reducing and a capping agent, used with silver nitrate aqueous solutions for the production of nanoparticles. DL-alanine can be used for the research of transition metals chelation, such as Cu(II), Zn(II), Cd(11). DL-alanine, a sweetener, is classed together with glycine, and sodium saccharin. DL-alanine plays a key role in the glucose-alanine cycle between tissues and liver[1][2][3][4][5][6]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: DL-2-Aminopropionic acid- 13 C-1. CAS No. 102029-81-2. Pack Sizes: 25 mg; 50 mg; 100 mg. Product ID: HY-N2362S. | |
| DL-Alanine-13C-3 | DL-Alanine- 13 C-3 is the 13 C-labeled DL-Alanine. DL-alanine, an amino acid, is the racemic compound of L- and D-alanine. DL-alanine is employed both as a reducing and a capping agent, used with silver nitrate aqueous solutions for the production of nanoparticles. DL-alanine can be used for the research of transition metals chelation, such as Cu(II), Zn(II), Cd(11). DL-alanine, a sweetener, is classed together with glycine, and sodium saccharin. DL-alanine plays a key role in the glucose-alanine cycle between tissues and liver[1][2][3][4][5][6]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: DL-2-Aminopropionic acid- 13 C-3. CAS No. 131157-42-1. Pack Sizes: 5 mg; 10 mg. Product ID: HY-N2362S1. | |
| O-Toluenesulfonamide | O-Toluenesulfonamide. CAS No. 88-19-7. Pack Sizes: 25, 100 g in poly bottle. Product ID: CDC10-0272. Molecular formula: C7H9NO2S. Category: Cosmetic Plasticizers. Product Keywords: Cosmetic Ingredients; Cosmetic Plasticizers; O-Toluenesulfonamide; CDC10-0272; 88-19-7; C7H9NO2S; 201-808-8; MFCD00007934; 88-19-7. Purity: 0.9999. Color: White to off-white. EC Number: 201-808-8. Physical State: neat. Solubility: DMSO (Slightly), Methanol (Very Slightly, Heated). Quality Level: 200. Storage: Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition sources and untrained individuals. Secure and label area. Protect containers/cylinders from physical damage. Boiling Point: 143°C(10 torr). Melting Point: 156-158°C. Density: 1.271 g/cm3. Product Description: o-Toluenesulfonamide is a major impurity in artificial sweetening substances containing saccharin. Determination of o-toluenesulfonamide in saccharin and saccharin sodium by reversed-phase HPLC method has been reported. | |
| Sodium cyclamate | Sodium cyclamate (sweetener code 952) is an artificial sweetener. It is 30 - 50 times sweeter than sucrose (table sugar), making it the least potent of the commercially used artificial sweeteners. It is often used with other artificial sweeteners, especially saccharin; the mixture of 10 parts cyclamate to 1 part saccharin is common and masks the off-tastes of both sweeteners. It is less expensive than most sweeteners, including sucralose, and is stable under heating. Group: Sweeteners. Alternative Names: N-Cyclohexylsulfamic acid sodium salt. CAS No. 139-05-9. Molecular formula: C6H12NNaO3S. Mole weight: 201.22. Appearance: White powder. Purity: 95%+. IUPACName: Sodium;N-cyclohexylsulfamate. Canonical SMILES: C1CCC(CC1)NS(=O)(=O)[O-].[Na+]. Density: 1.32 g/cm³. Catalog: ACM139059. | |
| 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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