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| Product | Description | |
|---|---|---|
| Sugarcane P.E. 10:1 | Sugarcane P.E. 10:1. |  CA, FL & NJ |
| Sugar , Compressible | Sugar , Compressible. Product ID: PE-0487. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Sugar , Compressible; Sweeteners Excipients; Sweetening agent. UNII: NA. Grade: Pharmceutical Excipients. Administration route: Oral. Dosage Form: Capsules; Tablets. Stability and Storage Conditions: Compressible sucrose is stable at room temperature and low humidity. Store in an airtight container in a cool, dry place. Source and Preparation: This product is prepared by co-crystallization of sucrose and other excipients such as maltodextrin. Compressible sucrose can also be prepared by dry granulation process. Applications: Compressible sucrose is mainly used for direct compression of chewable tablets. Small changes in water content affect the properties of tablet forming. |  |
| Sugar, Confectioner's | Sugar, Confectioner's. Product ID: PE-0492. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Sugar, Confectioner's; Sweeteners Excipients; Sweetening agent; /; /. UNII: NA. Administration route: Oral. Dosage Form: Capsules, Tablets. Stability and Storage Conditions: This product is stable in air under normal storage conditions at room temperature and low relative humidity. Over 160°C becomes caramelized and decomposes. It is easier than granular sucrose to absorb moisture, dilute solution or dry storage can cause microbial growth. Store in an airtight container in a cool, dry place. Source and Preparation: Refined sucrose granules are ground with corn starch to form a fine powder. Anti-caking agents can be added, such as tricalcium phosphate, and various silicates. Applications: Powdered sucrose is used in formulations for flavoring or sweetening when sugar is required to dissolve rapidly. It can be used as a diluent in the prescription of solid preparations when it is necessary to mix tiny active ingredients with small sucrose particles to achieve content uniformity. In solution, a high concentration of powdered sugar (70% w/v) increases viscosity and has some anti-corrosion properties. Can be used as sugar coating solution, wet granular binder/thinner. | |
| sugar-phosphatase | Has a wide specificity, acting on aldohexose 1-phosphates, ketohexose 1-phosphates, aldohexose 6-phosphates, ketohexose 6-phosphates, both phosphate ester bonds of fructose 1,6-bisphosphate, phosphoric esters of disaccharides, and on pentose and triose phosphates, but at a slower rate. Group: Enzymes. Enzyme Commission Number: EC 3.1.3.23. CAS No. 9023-7-8. Sugar-phosphatase. 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-3626; sugar-phosphatase; EC 3.1.3.23; 9023-07-8. Cat No: EXWM-3626. |  |
| Sugar-phosphatase from Escherichia coli, Recombinant | In enzymology, a sugar-phosphatase (EC 3.1.3.23) is an enzyme that catalyzes the chemical reaction: sugar phosphate + H2O <-> sugar + phosphate. Thus, the two substrates of this enzyme are sugar phosphate and H2O, whereas its two products are sugar and phosphate. This enzyme belongs to the family of hydrolases, specifically those acting on phosphoric monoester bonds. The systematic name of this enzyme class is sugar-phosphate phosphohydrolase. Group: Enzymes. Synonyms: Sugar-phosphate phosphohydrolase. Enzyme Commission Number: EC 3.1.3.23. CAS No. 9023-7-8. Purity: >95 % as judged by SDS-PAGE. Sugar-phosphatase. Mole weight: 34233.0 Da. Activity: 7.786 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Escherichia coli str. K-12 substr. MG1655. Sugar-phosphate phosphohydrolase; EC 3.1.3.23; Sugar-phosphatase. Cat No: NATE-1228. | |
| Sugars - IR Identification PT | Proficiency Testing Material. Group: Atomic absorption spectroscopy (aas). |  |
| sugar-terminal-phosphatase | Acts on sugars and polyols phosphorylated on the terminal carbon, with a preference for sugars with a D-erythro-configuration, e.g. good substrates are glucose 6-phosphate, mannose 6-phosphate, 6-phosphogluconate, erythrose 4-phosphate and xylitol 5-phosphate. Group: Enzymes. Synonyms: xylitol-5-phosphatase. Enzyme Commission Number: EC 3.1.3.58. CAS No. 99283-70-2. 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-3663; sugar-terminal-phosphatase; EC 3.1.3.58; 99283-70-2; xylitol-5-phosphatase. Cat No: EXWM-3663. | |
| Sugemalimab | Sugemalimab is a fully human, full length, anti-programmed death ligand 1 ( PD-L1 ) immunoglobulin G4 (IgG4) monoclonal antibody (mAb). Sugemalimab shows anticancer activities and can be used for non-small cell lung cancer research [1]. Uses: Scientific research. Group: Inhibitory antibodies. CAS No. 2256084-03-2. Pack Sizes: 1 mg; 5 mg. Product ID: HY-P99114. |  |
| Sugiol | Sugiol is an abietane diterpenoid, can be isolated from Calocedrus formosana bark. Sugiol has anti-inflammatory activity, could effectively reduce intracellular reactive oxygen species (ROS) production in lipopolysaccharide (LPS)-stimulated macrophages. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. Appearance: Powder. CAS No. 511-05-7. Molecular formula: C20H28O2. Mole weight: 300.4. Purity: 0.98. IUPACName: 6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one. Canonical SMILES: CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O. Product ID: ACM511057. Alfa Chemistry ISO 9001:2015 Certified. |  |
| s(-)-Uh-301 hydrochloride(s(-)-5-fluoro-8-hydroxy-dpat hydroc | s(-)-Uh-301 hydrochloride(s(-)-5-fluoro-8-hydroxy-dpat hydroc. Uses: Designed for use in research and industrial production. Additional or Alternative Names: UNII-1T7773JH5N. Product Category: Heterocyclic Organic Compound. CAS No. 127126-22-1. Molecular formula: C16H24FNO??·HCl. Mole weight: 301.83. Purity: ≥98%. IUPACName: (7S)-7-(dipropylamino)-4-fluoro-5,6,7,8-tetrahydronaphthalen-1-ol;hydrochloride. Canonical SMILES: CCCN(CCC)C1CCC2=C(C=CC(=C2C1)O)F.Cl. Product ID: ACM127126221. Alfa Chemistry ISO 9001:2015 Certified. Categories: 5-Fhdpat. | |
| Sulanemadlin | Sulanemadlin (ALRN-6924) is a potent and cell-permeating p53-based peptidomimetic macrocycles. Sulanemadlin is a inhibitor of the p53-MDM2, p53-MDMX, or both p53 and MDM2 and MDMX protein-protein interactions. Sulanemadlin can be used for cancers research[1]. Uses: Scientific research. Group: Peptides. Alternative Names: ALRN-6924; MP-4897. CAS No. 1451199-98-6. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-P4210. | |
| Sulbactam | Sulbactam is a β-lactamase inhibitor. This drug is given in combination with β-lactam antibiotics to inhibit β-lactamase, an enzyme produced by bacteria that destroys the antibiotics. Synonyms: RO-1-9213; RO 1-9213; RO1-9213. Grade: >98%. CAS No. 68373-14-8. Molecular formula: C8H11NO5S. Mole weight: 233.24. |  |
| Sulbactam | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metaboliteseuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: CP 45899, Penicillanic acid sulfone, (2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-Dioxide, Penicillanic acid dioxide,Sulbactam, (2S-cis)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-Dioxide, Betamaze, Penicillanic acid S,S-dioxide, Sulbactam, Penicillanic acid 1,1-dioxide. | |
| Sulbactam | Sulbactam (CP45899) is a competitive, irreversible beta-lactamase inhibitor. Sulbactam shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 68373-14-8. Molecular formula: C8H11NO5S. Purity: 0.9971. Product ID: ACM68373148. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sulbactam | Sulbactam (CP45899) is a competitive, irreversible beta-lactamase inhibitor. Sulbactam shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus -- Acinetobacter baumannii (Acb) complex [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP45899. CAS No. 68373-14-8. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0334. | |
| Sulbactam | Sulbactam. Group: Biochemicals. Grades: Highly Purified. CAS No. 68373-14-8. Pack Sizes: 1g, 2g, 5g, 10g, 25g. US Biological Life Sciences. |  Worldwide |
| Sulbactam acid | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C8H11NO5S. CAS No. 68373-14-8. Prepack ID 69388315-1g. Molecular Weight 233.24. See USA prepack pricing. |  |
| Sulbactam-[d3] | An isotope labelled Sulbactam. Sulbactam is an irreversible inhibitor of β-lactamase. It binds to the enzyme and does not allow it to degrade the antibiotic. Synonyms: (2S,5R)-3-(D3)methyl-3-methyl-4,4,7-trioxo-4λ6-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid. Grade: >95%. Molecular formula: C8H8D3NO5S. Mole weight: 236.26. | |
| Sulbactam Impurity 11 | Sulbactam Impurity 11. Uses: For analytical and research use. Group: Impurity standards. CAS No. 15058-64-7. Molecular formula: C8H11NO4S. Mole weight: 217.24. Catalog: APB15058647. | |
| Sulbactam Impurity 19 | Sulbactam Impurity 19. Uses: For analytical and research use. Group: Impurity standards. CAS No. 139595-42-9. Molecular formula: C8H9Br2NO3S. Mole weight: 359.03. Catalog: APB139595429. | |
| Sulbactam pivoxil | Sulbactam pivoxil is a proagent of sulbactam. Sulbactam is a β-lactamase inhibitor which poorly adsorbed from gastrointestinal tract. Sulbactam pivoxil has a better absorption than the parent agent and provides high serum levels after oral administration [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP 47904. CAS No. 69388-79-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-108288. | |
| Sulbactam Pivoxil | Sulbactam Pivoxil is a prodrug of the semi-synthetic β-lactamase inhibitor Sulbactam. Group: Biochemicals. Alternative Names: (2S, 5R)-3, 3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid (2,2-Dimethyl-1-oxopropoxy)methyl Ester 4,4-Dioxide; (Pivaloyloxy)methyl Penicillanate S,S-Dioxide; CP 47904; (2S-cis)-3, 3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid (2,2-dimethyl-1-oxopropoxy)methyl Ester 4,4-Dioxide. Grades: Highly Purified. CAS No. 69388-79-0. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Sulbactam Related Compound A | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sulbactam Related Compound D | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sulbactam Related Compound E | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sulbactam Related Compound F | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sulbactam sodium | Sulbactam (CP45899) sodium is a competitive, irreversible beta-lactamase inhibitor. Sulbactam sodium shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus -- Acinetobacter baumannii (Acb) complex [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP45899 sodium. CAS No. 69388-84-7. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0334A. | |
| Sulbactam Sodium | A beta-lactamase inhibitor with very weak antibacterial action. The compound prevents antibiotic destruction of beta-lactam antibiotics by inhibiting beta-lactamases, thus extending their spectrum activity. Combinations of sulbactam with beta-lactam antibiotics have been used successfully for the therapy of infections caused by organisms resistant to the antibiotic alone. Alternative Names: Sulbactam sodium salt. Sodium sulbactam. Sulbactam (sodium). CAS No. 69388-84-7. Product ID: API69388847. Molecular formula: C8H10NNaO5S. EINECS: 273-984-4. SMILES: CC1([C@@H](N2[C@H](S1(=O)=O)CC2=O)C(=O)[O-])C.[Na+]. Appearance: White Crystalline Powder. Standard: EP/USP/BP. Category: Antibiotic APIs. |  |
| Sulbactam Sodium | Sulbactam is an irreversible inhibitor of β-lactamase. It binds to the enzyme and does not allow it to degrade the antibiotic. Synonyms: (2S,5R)-3,3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic Acid 4,4-Dioxide Sodium Salt; CP 45899-2; Penicillanic Acid 1,1-Dioxide Sodium Salt; Sodium 1,1-Dioxypenicillanate; Sodium Penicillanate 1,1-Dioxide; Sodium Sulbactam; Sulbactam Sodium Salt; Unasyn IM. Grade: Assay: 88.6%. CAS No. 69388-84-7. Molecular formula: C8H10NNaO5S. Mole weight: 255.22. | |
| Sulbactam sodium salt | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C8H10NNaO5S. CAS No. 69388-84-7. Prepack ID 90004872-1g. Molecular Weight 255.22. See USA prepack pricing. | |
| Sulbactam sodium salt | 5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C8H10NNaO5S. CAS No. 69388-84-7. Prepack ID 90004872-5g. Molecular Weight 255.22. See USA prepack pricing. | |
| Sulbactam Sodium Salt | A semi-synthetic β-lactamase inhibitor. It is used in combination with β-lactam antibiotics as antibacterial. Group: Biochemicals. Alternative Names: (2S, 5R)-3, 3-Dimethyl-7-oxo-4-thia-1-azabicyclo[3. 2. 0]heptane-2-carboxylic Acid 4,4-Dioxide Sodium Salt; CP 45899-2; Penicillanic Acid 1,1-Dioxide Sodium Salt; Sodium 1,1-Dioxypenicillanate; Sodium Penicillanate 1,1-Dioxide; Sodium Sulbactam; Sulbactam Sodium; Sulbactam Sodium Salt; Unasyn IM. Grades: Highly Purified. CAS No. 69388-84-7. Pack Sizes: 100mg, 1g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Sulbactam (sodium) (Standard) | Sulbactam (sodium) (Standard) is the analytical standard of Sulbactam (sodium). This product is intended for research and analytical applications. Sulbactam (CP45899) sodium is a competitive, irreversible beta-lactamase inhibitor. Sulbactam sodium shows antimicrobial activity against multidrug-resistant (MDR) acinetobacter calcoaceticus--Acinetobacter baumannii (Acb) complex [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 69388-84-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0334AR. | |
| Sulbenicillin | Sulbenicillin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 6α-[Phenyl(sulfo)acetylamino]penicillanic acid. Product Category: Heterocyclic Organic Compound. CAS No. 34779-28-7. Product ID: ACM34779287. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sulbenicillin sodium | Sulbenicillin is a penicillin antibiotic. Synonyms: Sulbenicillin disodium; Sulfobenzylpenicillin; (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[(2-phenyl-2-sulfonatoacetyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate disodium salt. CAS No. 28002-18-8. Molecular formula: C16H16N2O7S2Na2. Mole weight: 458.42. | |
| Sulbutiamine | Sulbutiamine. Categories: sulbutiamine; bisibutiamine. | CA, FL & NJ |
| Sulbutiamine | Sulbutiamine is a synthetic analogue of vitamin B1 used for the treatment of asthenia. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Bisibuthiamine. CAS No. 3286-46-2. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B2229. | |
| Sulbutiamine | Sulbutiamine (isobutyryl thiamine disulfide) is a lipophilic derivative of thiamine used for the treatment of asthenia and other related pathological conditions. Sulbutiamine is available over-the-counter in several countries as a component of nutritional supplements. Group: Biochemicals. Alternative Names: 2-Methylpropanoic Acid 1, 1'- [Dithiobis [3- [1- [ [ (4-amino-2-methyl-5-pyrimidinyl) methyl] formylamino] ethylidene] -3, 1-propanediyl] ] Ester; Bisibutiamine; O-Isobutyroylthiamine Disulfide; O-Isobutyrylthiamine Disulfide; Vitaberin. Grades: Highly Purified. CAS No. 3286-46-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Sulbutiamine | It is highly lipophilic, allowing it to cross the blood-brain barrier more easily than other thiamine derivatives. Although its clinical efficacy is not yet defined, sulbutiamine is used to treat asthenia. While its other uses include improvement of erectile dysfunction and reduction of psycho-behavioural inhibition, sulbutiamine showed evidence of modulatory effect on dopaminergic and glutamatergic cortical transmissions. The chronic administration of the drug has demonstrated to improve long term memory formation in mice. Alternative Names: Sulbutiamine. bisibutiamine. Bisibuthiamine. Vitaberin. CAS No. 3286-46-2. Product ID: API3286462. Molecular formula: C32H46N8O6S2. Mole weight: 702.89. EINECS: 221-937-3. SMILES: CC1=NC=C(C(=N1)N)CN(/C(=C(/SS/C(=C(/N(C=O)CC2=CN=C(N=C2N)C)\C)/CCOC(=O)C(C)C)\CCOC(=O)C(C)C)/C)C=O. Appearance: White to Off-White Solid. Category: Nutrition & Healthcare APIs. | |
| sulcatone reductase | Studies on the effects of growth-stage and nutrient supply on the stereochemistry of sulcatone reduction in Clostridia pasteurianum, C. tyrobutyricum and Lactobacillus brevis suggest that there may be at least two sulcatone reductases with different stereospecificities. Group: Enzymes. Enzyme Commission Number: EC 1.1.1.260. CAS No. 196522-54-0. 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-0166; sulcatone reductase; EC 1.1.1.260; 196522-54-0. Cat No: EXWM-0166. | |
| Sulcofuron-sodium monohydrate | analytical standard. Group: Pesticides & metabolites standards. | |
| Sulconazole nitrate | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standardspharmaceutical toxicologypharmacopoeial standards. Alternative Names: Myk, Sulconazole nitrate, RS 44872, RS 44872-00-10-3, 1H-Imidazole, 1-[2-[[(4-chlorophenyl)methyl]thio]-2-(2,4-dichlorophenyl)ethyl]-, (+/-)-, mononitrate, 1H-Imidazole, 1-[2-[[(4-chlorophenyl)methyl]thio]-2-(2,4-dichlorophenyl)ethyl]-, mononitrate (9CI), Sulcosyn, Exelderm,1-[2-[[(4-Chlorophenyl)methyl]thio]-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole Nitrate (1:1). | |
| Sulconazole Nitrate | Sulconazole nitrate is an organic nitrate salt, a conazole antifungal drug and an imidazole antifungal drug. Alternative Names: 82382-23-8. Exelderm. Sulconazole nitrate salt. CAS No. 61318-91-0. Product ID: API61318910. Molecular formula: C18H16Cl3N3O3S. Mole weight: 460.8. EINECS: 624-696-6. SMILES: C1=CC(=CC=C1CSC(CN2C=CN=C2)C3=C(C=C(C=C3)Cl)Cl)Cl.[N+](=O)(O)[O-]. Appearance: White to Off-white Solid. Category: Antifungal APIs. | |
| Sulcotrione | analytical standard. Group: Pesticides & metabolites standardspesticides & metabolitespesticides & metabolites. | |
| Sulcotrione | Sulcotrione is a β-triketone herbicide which can inhibit hydroxyphenylpyruvate dioxygenase ( HPPD ). Uses: Scientific research. Group: Signaling pathways. CAS No. 99105-77-8. Pack Sizes: 10 mM * 1 mL; 50 mg; 100 mg. Product ID: HY-107368. | |
| Sulcotrione-d4 (benzoyl-3-d,mesyl-d3) | analytical standard. Group: Pesticides & metabolites standards. | |
| Suldrazin | Suldrazin. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Suldrazin, CID3085327, 65566-74-7, Benzenesulfonamide, 4-amino-N-2-quinoxalinyl-, mixt. with 5-((3,4-dimethoxyphenyl)methyl)-2,4-pyrimidinediamine. Product Category: Heterocyclic Organic Compound. CAS No. 65566-74-7. Molecular formula: C27H28N8O4S. Mole weight: 560.627420 [g/mol]. Purity: 0.96. IUPACName: 4-amino-N-quinoxalin-2-ylbenzenesulfonamide; 5-[(3,4-dimethoxyphenyl)methyl]pyrimidine-2,4-diamine. Product ID: ACM65566747. Alfa Chemistry ISO 9001:2015 Certified. | |
| Sulfabenz | Sulfabenz. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 4-amino-n-phenyl-benzenesulfonamid;Benzenesulfonamide,4-amino-N-phenyl-;sulfabenz;4-aminobenzenesulfoanilide;4-Aminobenzenesulfonanilide;N-Phenyl-4-aminobenzenesulfonamide;NSC-2619;4-Amino-N-phenylbenzenesulfonamide. Product Category: Heterocyclic Organic Compound. CAS No. 127-77-5. Molecular formula: C12H12N2O2S. Mole weight: 248.3. Purity: 0.96. IUPACName: 4-amino-N-phenylbenzenesulfonamide. Canonical SMILES: C1=CC=C(C=C1)NS(=O)(=O)C2=CC=C(C=C2)N. Density: 1.373g/cm³. ECNumber: 204-865-7. Product ID: ACM127775. Alfa Chemistry ISO 9001:2015 Certified. Categories: Sulfabenzamide. | |
| Sulfabenzamide | Has anti-bacterial activity. Group: Biochemicals. Alternative Names: N-[(4-Aminophenyl)sulfonyl]-benzamide; N- (Benzoyl) -4-amino Benzene sulfonamide; N1-Benzoylsulfanilamide; NSC 74587; NSC 74587G; Sulfabenzamid. Grades: Highly Purified. CAS No. 127-71-9. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| Sulfabenzamide | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standards. Alternative Names: N-(p-Aminobenzenesulfonyl)benzamide, Sulfabenzamid, Sulfabenzid, NSC 74587, NSC 74587G,Benzamide, N-[(4-aminophenyl)sulfonyl]-, N-Sulfamylbenzamide, Benzamide, N-sulfanilyl- (6CI,7CI,8CI), Sulfabenzoylamide, Sulfabenzamide, N-Sulfanilylbenzamide, N1-Benzoylsulfanilamide, N-(Benzoyl)-4-aminobenzenesulfonamide, Sulfabenzide. | |
| Sulfabenzamide | Sulfabenzamide (N-Sulfanilylbenzamide) is an antimicrobial agent and usually consumed in combination with Sulfathiazole and Sulfacetamide. Sulfabenzamide is effective against Gram-positive and negative bacterial strains [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: N-Sulfanilylbenzamide. CAS No. 127-71-9. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B0960. | |
| Sulfabenzamide | analytical standard. Group: Application areas. | |
| Sulfabenzamide-[d4] | Sulfabenzamide-[d4] is the labelled analogue of Sulfabenzamide, an antimicrobial agent. Synonyms: Sulfabenzamide-d4; N-[(4-Aminophenyl)sulfonyl]-benzamide-d4; N-(Benzoyl)-4-aminobenzenesulfonamide-d4; N1-Benzoylsulfanilamide-d4. Molecular formula: C13H8D4N2O3S. Mole weight: 280.34. | |
| Sulfacetamide | Sulfacetamide (Sulphacetamide), a bacteriostatic sulphonamide, is a popular antibiotic prescribed for treating ocular infections [1] [2]. Uses: Scientific research. Group: Natural products. Alternative Names: Sulphacetamide. CAS No. 144-80-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-N7123. | |
| Sulfacetamide | Sulfacetamide. Group: Biochemicals. Alternative Names: N-[ (4-aminophenyl) sulfonyl]acetamide; 4- (Acetylaminosulfonyl) aniline; A 500; Acetocid; Acetosulfamin; Acetosulfamine; Albamine; Albucid; Alesten; Formosulfacetamide; N- (4-Aminobenzenesulfonyl) acetamide; N- (p-Aminophenylsulfonyl) acetamide; N-Acetylsulfanilamide; N-Sulfanilylacetamide; N-[ (4-Aminophenyl) sulfonyl]acetamide; N1-Acetylsulfanilamide; NSC 63871; N'-Acetylsulfanilamide; Ocusol; Region; Steramide; Sulamyd; Sulfacet; Sulfacetamide; Sulfacetimide; Sulfacyl; Sulphacetamide; Sulphasil; Urosulfon; p-Amino Benzene sulfonacetamide; N-[ (4-aminophenyl) sulfonyl]acetamide; N-Sulfanilyacetamide. Grades: Highly Purified. CAS No. 144-80-9. Pack Sizes: 1g. Molecular Formula: C8H10N2O3S, Molecular Weight: 214.24. US Biological Life Sciences. | Worldwide |
| Sulfacetamide | analytical standard. Group: Application areas. | |
| Sulfacetamide | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardsimpurity standardspharmaceutical toxicologypharmacopoeial standards. Alternative Names: Sulfacetamide,N-[(4-Aminophenyl)sulfonyl]acetamide, Sulfadimidine Imp. E (Pharmeuropa). | |
| Sulfacetamide | 100g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Organics, Research Organics & Inorganics. Formula: C8H10N2O3S. CAS No. 144-80-9. Prepack ID 34100925-100g. Molecular Weight 214.24. See USA prepack pricing. | |
| Sulfacetamide-[13C6] | Sulfacetamide-[13C6] is the labelled analogue of Sulfacetamide. Sulfacetamide is a sulfonamide antibiotic as a dihydropteroate Synthase inhibitor. It is a competitive inhibitor of bacterial para-aminobenzoic acid, which is required for bacterial synthesis of folic acid. Sulfacetamide is used for the treatment of skin infections and urinary tract infections. It is also used to treat acne and seborrheic dermatitis. Synonyms: Sulfacetamide-13C6; N-Acetyl-4-aminobenzene-13C6-sulfonamide; N-[(4-aminophenyl)sulfonyl]acetamide-13C6; 4-(Acetylaminosulfonyl)aniline-13C6; Acetocid-13C6; Acetosulfamine-13C6; Formosulfacetamide-13C6; N-(p-Aminophenylsulfonyl)acetamide-13C6; N-Sulfanilyacetamide-13C6. Grade: >98%. Molecular formula: C2[13C]6H10N2O3S. Mole weight: 220.20. | |
| Sulfacetamide sodium | Sulfacetamide sodium. Group: Biochemicals. Alternative Names: N- (p-Aminobenzenesulfonyl) acetamide. Grades: Highly Purified. CAS No. 6209-17-2. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C8H9N2O3SNa. US Biological Life Sciences. | Worldwide |
| Sulfacetamide sodium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Sulfacetamide Sodium | Sulfacetamide Sodium is a sulfonamide-active molecule used in the study of tinea versicolor and rosacea. Uses: Scientific research. Group: Signaling pathways. CAS No. 127-56-0. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-B0576. | |
| Sulfacetamide Sodium Monohydrate | Sulfacetamide Sodium Monohydrate. Uses: For analytical and research use. Group: Api standards; pharmaceutical toxicology. Alternative Names: N1-Acetylsulfanilamide sodium monohydrate, Sodium sulfacetamide monohydrate, Sodium N-sulfanilylacetamide monohydrate, Sulamyd sodium monohydrate,Sulfacetamide Sodium Monohydrate, N-[(4-Aminophenyl)sulfonyl]acetamide monosodium salt monohydrate, Sulfacetamide sodium monohydrate, N-[(4-Aminophenyl)sulfonyl]acetamide sodium salt hydrate (1:1:1), N-Sulfanilylacetamide monosodium salt monohydrate. CAS No. 6209-17-2. Molecular formula: C8H9N2NaO3.H2O. Mole weight: 236.22. Catalog: APS6209172. Format: Neat. Shipping: Room Temperature. | |
| Sulfacetamide sodium salt | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Biochemicals, Research Organics & Inorganics. Formula: C8H9N2NaO3S · H2O. CAS No. 6209-17-2. Prepack ID 68760340-25g. Molecular Weight 254.24. See USA prepack pricing. | |
| Sulfacetamide Sodium Salt | Sulfacetamide Sodium Salt is an antibiotic that blocks synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. It can be used in biological study to explore topical application of benzoyl peroxide, antibiotics, sulfur and sodium sulfacetamide, azelaic acid for treatment of acne vulgaris in humans. Group: Biochemicals. Grades: Highly Purified. CAS No. 127-56-0. Pack Sizes: 100g, 250g. Molecular Formula: C8H9N2NaO3S, Molecular Weight: 236.22. US Biological Life Sciences. | Worldwide |
| Sulfacetamide (Standard) | Sulfacetamide (Standard) is the analytical standard of Sulfacetamide. This product is intended for research and analytical applications. Sulfacetamide (Sulphacetamide), a bacteriostatic sulphonamide, is a popular antibiotic prescribed for treating ocular infections [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sulphacetamide (Standard). CAS No. 144-80-9. Pack Sizes: 50 mg; 100 mg; 250 mg. Product ID: HY-N7123R. | |
| Sulfachloropyrazine-[13C6] | Sulfachloropyrazine-[13C6] is the labelled analogue of Sulfachloropyrazine, which is an effective sulfonamide derivative with antibacterial and coccidioidal effects. Synonyms: Sulfachloropyrazine-13C6; 4-Amino-N-(6-chloropyrazin-2-yl)-benzene-13C6-sulfonamide; Sulfachloropyrazine-(phenyl-13C6); Sulfaclozine-13C6. Grade: 95% by HPLC; 98% atom 13C. CAS No. 1416711-61-9. Molecular formula: C4[13C]6H9ClN4O2S. Mole weight: 290.68. | |
| Sulfachloropyrazine-(phenyl-13C6) | analytical standard. Group: Application areas. | |
| Sulfachloropyrazine Sodium Monohydrate | Antiprotozoal agent used therapeutically in the treatment of coccidiosis in poultry and other livestock. An antiparisitic agent. Group: Biochemicals. Alternative Names: 4-Amino-N- (6-chloropyrazinyl) benzenesulfonamide Monosodium Salt Monohydrate; 4-Amino-N- (6-chloro-2-pyrazinyl) benzenesulfonamide Sodium Salt Monohydrate; N1- (6-Chloropyrazinyl) sulfanilamide Monosodium Salt Monohydrate. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Sulfachloropyridazine | Sulfachloropyridazine is a broad spectrum sulfonamide used against both Gram-positive and Gram-negative aerobic bacteria. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sulfachlorpyridazine. CAS No. 80-32-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg. Product ID: HY-B1781. | |
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