A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
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
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.
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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 (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
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.
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.
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
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
analytical standard. Group: Application areas.
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
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-[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
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
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-[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
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
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
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
analytical standard. Group: Application areaspharma & vet compounds & metabolitesstandards for environmental regulatory methodspharma & vet compounds & metabolites. Alternative Names: Sonilyn, Sulfachlorpyridazine, Ciba 10370, Sulpirazina,Benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)-, Consulid, N1-(6-Chloro-3-pyridazinyl)sulfanilamide, Sulfarene, BA 10370, Nefrosul, Sulfochlorpyridazine, Renalsulfa, Sulfaclorazina, 6-Sulfanilamido-3-chloropyridazine, Cosulid, Sulfanilamide, N1-(6-chloro-3-pyridazinyl)- (6CI,7CI,8CI), 3-Chloro-6-sulfanilamidopyridazine, Durasulf, Bactolin.
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.
Sulfachloropyridazine-[13C6]
Sulfachloropyridazine-[13C6] is an isotope labelled Sulfachloropyridazine, which is an antibiotic used for bacterial infections. Synonyms: Sulfachloropyridazine-13C6; 4-amino-N-(6-chloropyridazin-3-yl)(1,2,3,4,5,6-13C6)benzene-1-sulfonamide; N1-(6-Chloro-3-pyridazinyl)sulfanilamide-13C6; 3-Chloro-6-sulfanilamidopyridazine-13C6; 6-Sulfanilamido-3-chloropyridazine-13C6; Cosulid-13C6; Durasulf-13C6; Nefrosul-13C6; Renalsulfa-13C6. Grade: 95% by HPLC; 98% atom 13C. Molecular formula: C4[13C]6H9ClN4O2S. Mole weight: 290.68.
Sulfachloropyridazine sodium
Sulfachloropyridazine sodium. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N-(6-CHLORO-3-PYRIDAZINE)-4-AMINOBENZENESULFONAININO SODIUM MONOHYDRATE;SULFACHLOROPYRIDAZINE SODIUM;SULFACHLOROPYRIDAZINE SODIUM H2O;SPDZ;Sodium N-(6-chloropyridazin-3-yl)sulphanilamidate;sulphachlorpyridazine sodium ;Sulfachlorpyridazine Sodium SPDZ;SULFACHLOROPYRIDAZINE SODIUM(SPDZ):N-(6-CHLORO-3-PYRIDAZINE)-4-AMINOBENZENESULFONAININO SODIUM MONOHYDRATE. CAS No. 23282-55-5. Molecular formula: C10H8ClN4NaO2S. Mole weight: 306.7. Purity: 0.98. IUPACName: sodium;(4-aminophenyl)sulfonyl-(6-chloropyridazin-3-yl)azanide. Canonical SMILES: C1=CC(=CC=C1N)S(=O)(=O)[N-]C2=NN=C(C=C2)Cl.[Na+]. Density: 1.588g/cm³. ECNumber: 245-553-0. Product ID: ACM23282555. Alfa Chemistry ISO 9001:2015 Certified.
Sulfachloropyridazine (Standard)
Sulfachloropyridazine (Standard) is the analytical standard of Sulfachloropyridazine. This product is intended for research and analytical applications. Sulfachloropyridazine is a broad spectrum sulfonamide used against both Gram-positive and Gram-negative aerobic bacteria. Uses: Scientific research. Group: Signaling pathways. CAS No. 80-32-0. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B1781R.
Sulfachlorpyrazine
Sulfachlorpyrazine. Uses: Designed for use in research and industrial production. Additional or Alternative Names: sulfachlorpyrazine. Product Category: Heterocyclic Organic Compound. CAS No. 1672-91-9. Mole weight: 0. Product ID: ACM1672919. Alfa Chemistry ISO 9001:2015 Certified.
Sulfachlorpyridazine
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsapi standards. Alternative Names: Cosulid, 3-Chloro-6-sulfanilamidopyridazine, Durasulf, Bactolin, Consulid, Sonilyn, 6-Sulfanilamido-3-chloropyridazine, Nefrosul, Sulpirazina, BA 10370, Ciba 10370, Sulfochlorpyridazine, N1-(6-Chloro-3-pyridazinyl)sulfanilamide, Renalsulfa, Sulfanilamide, N1-(6-chloro-3-pyridazinyl)- (6CI,7CI,8CI),Benzenesulfonamide, 4-amino-N-(6-chloro-3-pyridazinyl)-, Sulfachlorpyridazine, Sulfaclorazina, Sulfarene.
Sulfachlorpyridazine
Sulfachlorpyridazine. Group: Biochemicals. Alternative Names: 4-Amino-N-(6-chloro-3-pyridazinyl)-benzenesulfonamide; 3-Chloro -6-sulfanilamidopyridazin e; Sulfaclorazina. Grades: Highly Purified. CAS No. 80-32-0. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C10H9ClN4O2S. US Biological Life Sciences.
Worldwide
Sulfachlorpyridazine Sodium
Sulfachlorpyridazine is an antibacterial compound. Group: Biochemicals. Alternative Names: 4-Amino-N-(6-chloro-3-pyridazinyl)-benzenesulfonamide Sodium; 3-Chloro -6-sulfanilamidopyridazin e Sodium; N1- (6-Chloro-3-pyridazinyl) sulfanilamide Monosodium Salt; Prinzone; Sodium Sulfachloropyridazine; Sodium Sulfachlorpyridazine; Sulfachloropyridazine Sodium; Sulfachlorpyridazine Sodium Salt; Vetisulid. Grades: Highly Purified. CAS No. 23282-55-5. Pack Sizes: 100mg. US Biological Life Sciences.
Worldwide
Sulfaclozine
Sulfaclozine, a sulfonamide derivative, is a potent antibacterial and anticoccidial agent which is commonly used as a veterinary drug. Uses: Sulfaclozine is a potent antibacterial and anticoccidial agent which is commonly used as a veterinary drug. Synonyms: N-(5-CHLORO-3-PYRAZINE)-4-AMINOBENZENESULFONAININO SODIUM MONOHYDRATE; SULFACHLOROPYRAZINE SODIUM; SULFACHLOROPYRAZINE SODIUM H2O; SULFACHLORPYRAZINE SODIUM; sulfaclozine; SULFACLOZINE SODIUM; SPZ; SULFACHLOROPYRAZINE SODIUM(SPZ):N-(5-CHLORO-3-PYRAZINE)-4-AMINO. Grade: ≥98%. CAS No. 102-65-8. Molecular formula: C10H9ClN4O2S. Mole weight: 284.72.
Sulfaclozine sodium
analytical standard. Group: Application areas.
Sulfaclozine Sodium Monohydrate
Sulfaclozine is a competitive antagonist of para-aminobenzoic acid (PABA), a precursor of folic acid, in protozoa and bacteria. It is indicated for treatment of coccidiosis in poultry due to infection with Eimeria species, fowl typhoid due to infection with Salmonella gallinarum and fowl cholera due to infection with Pasteurella multocida. Group: Biochemicals. Alternative Names: Sodium sulfachloropyrazine monohydrate; sodium ( (4-aminophenyl)sulfonyl) (6-chloropyrazin-2-yl)amide hydrate. Grades: Highly Purified. CAS No. 1392129-96-2. Pack Sizes: 50mg. Molecular Formula: C10H8ClN4O2SNa·H2O, Molecular Weight: 324.72. US Biological Life Sciences.
Worldwide
Sulfacytine
Sulfacytine is a short-acting sulfonamide antibiotic. Sulfacytine is active against bacteria and is an effective agent for the research of acute uncomplicated urinary tract infections [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 17784-12-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-16472.
Sulfadiazine
One of the short-acting Sulfonamides used in combination with Pyrimethamine to treat toxoplasmosis in patients with acquired immunodeficiency syndrome and in newborns with congenital infections. Sulfadiazine is a Sulfonamide Antibacterial. The chemical classification of sulfadiazine is Sulfonamides. Sulfadiazine is a synthetic pyrimidinyl sulfonamide derivative, short-acting bacteriostatic Sulfadiazine inhibits bacterial folic acid synthesis by competing with para amino benzoic acid. It is used in combination with pyrimethamine to treat toxoplasmosis in patients with acquired immunodeficiency syndrome and in newborns with congenital infections. Group: Biochemicals. Alternative Names: -Amino-N-2-pyrimidinyl Benzene sulfonamide; 2- (4-Amino Benzene sulfonamido) pyrimidine; 2-Sulfanilyl aminopyrimidine; Adiazin; Adiazine; Debenal; Liquadiazine; Microsulfon; Sulfazine; Sulfolex; Sulphadiazine; Theradiazine. Grades: Highly Purified. CAS No. 68-35-9. Pack Sizes: 50g, 100g, 250g, 500g, 1Kg. Molecular Formula: C10H10N4O2S, Molecular Weight: 250.28. US Biological Life Sciences.
Worldwide
Sulfadiazine
Sulfadiazine is a sulfonamide antibiotic. It has activity against both Gram-positive and Gram-negative bacteria. Synonyms: RP-2616; RP2616; RP 2616; Liquadiazine; Microsulfon; 2-(4-Aminobenzenesulfonamido)pyrimidine; 2-Sulfanilylaminopyrimidine; Adiazin; Adiazine; Debenal; Sulfolex; Sulphadiazine; Theradiazine. Grade: >98%. CAS No. 68-35-9. Molecular formula: C10H10N4O2S. Mole weight: 250.28.
Sulfadiazine
Sulfadiazine is a sulfonamide antibiotic with antimalarial activity. Sulfadiazine can be used for toxoplasmosis research [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 68-35-9. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0273.
Sulfadiazine
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitesstandards for environmental regulatory methodspharma & vet compounds & metabolitesapi standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)impurity standardspharmaceutical toxicologypharmacopoeial standards. Alternative Names: Diazovit, Lipo-Diazine, Coco-Diazine, N1-2(1H)-Pyrimidinylidenesulfanilamide, N1-2-Pyrimidinylsulfanilamide, 2-(4-Aminobenzenesulfonamido)pyrimidine, Sterazine, Adiazine, SDA, 2-Sulfanilylaminopyrimidine, Sulphadiazine E, Cremodiazine, Sulfadimidine Imp. B (Pharmeuropa), 4-Amino-N-(2-pyrimidinyl)benzenesulfonamide, Sulfolex, Liquadiazine, N1-2-Pyrimidinylsulfanilamide, Deltazina, Lipo-Levazine, Pyrimal, SN 112, Eskadiazine, 4-Amino-N-(2-pyrimidyl)benzenesulfonamide, Diazolone, Sulfazine, Sulfadiazina Reig Jofre, Sulfapyrimidine, Debenal, Adiazin, Microsulfon, 2-Sulfanilamidopyrimidine, NSC 35600, Spofadrizine, Neazine,4-Amino-N-pyrimidin-2-ylbenzenesulfonamide, Theradiazine, Sulfazin (Russian pharmaceutical), N1-2-Pyrimidylsulfanilamide, Diazyl, Sulfapirimidin, RP 2616, Pirimal, Di-Azo-Mul, 4-[[(Pyrimidin-2-yl)amino]sulfonyl]aniline, Sulphadiazine, Honey diazine, 2-(4-Aminobenzenesulfonylamino)pyrimidine, Sulfazin, Diazin, 2-(p-Aminobenzenesulfonamido)pyrimidin, Piridisir, Sulfadiazin, Sulfadiazine, Sanodiazine, A 306.
Sulfadiazine-13C6
The isotopically labeled drug Sulfadiazine. Antibacterial. Group: Biochemicals. Alternative Names: 4-Amino-N-2-pyrimidinyl Benzene sulfonamide-13C6. Grades: Highly Purified. CAS No. 1189426-16-1. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Sulfadiazine-[13C6]
Sulfadiazine-[13C6] is the labelled analogue of Sulfadiazine, which is an antibiotic. It is commonly used to treat urinary tract infections and burns. Synonyms: Sulfadiazine-13C6; 4-Amino-N-pyrimidin-2-yl-benzene-13C6-sulfonamide; 4-Amino-N-2-pyrimidinylbenzenesulfonamide-13C6; 2-(4-Aminobenzenesulfonamido-13C6)pyrimidine; 2-Sulfanilylaminopyrimidine-13C6; Adiazin-13C6; Adiazine-13C6; Debenal-13C6; Liquadiazine-13C6; Microsulfon-13C6; Sulfazine-13C6; Sulfolex-13C6; Sulfadiazine-(phenyl-13C6). Grade: 95% by HPLC; 98% atom 13C. CAS No. 1189426-16-1. Molecular formula: C4[13C]6H10N4O2S. Mole weight: 256.21.
Sulfadiazine-d4
The isotopically labeled drug Sulfadiazine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Sulfadiazine-[d4]
Sulfadiazine-[d4] is the labelled analogue of Sulfadiazine. Sulfadiazine is an antibiotic. It is commonly used to treat urinary tract infections and burns. Synonyms: Sulfadiazine D4; 4-Amino-N-2-pyrimidinylbenzenesulfonamide-d4; 2-(4-Aminobenzenesulfonamido-d4)pyrimidine; 2-Sulfanilylaminopyrimidine-d4. Grade: 95% by HPLC; 95% atom D. CAS No. 1020719-78-1. Molecular formula: C10H6D4N4O2S. Mole weight: 254.30.
Sulfadiazine-(phenyl-13C6)
analytical standard. Group: Application areas.
Sulfadiazine Silver Salt
Coordination compound. Antibacterial. Group: Biochemicals. Alternative Names: [4-Amino-N- (2-pyrimidinyl-kN1) benzenesulfonamidato-kO]silver. Grades: Highly Purified. CAS No. 22199-08-2. Pack Sizes: 10mg, 100mg, 10g, 25g. Molecular Formula: C10H9AgN4O2S, Form: Supplied as an off-white. US Biological Life Sciences.
Worldwide
Sulfadiazine sodium
Sulfadiazine sodium is a sulfonamide antibiotic with antimalarial activity. Sulfadiazine can be used for toxoplasmosis research [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 547-32-0. Pack Sizes: 10 mM * 1 mL; 500 mg. Product ID: HY-B0273A.
Sulfadiazine Sodium
Sulfadiazine sodium is a bacteriostatic sulfonamide antibiotic. It is used to treat systemic infections caused by sensitive bacteria in domestic animals, such as respiratory and urinary tract infections and mastitis, uterine sarcoiditis, peritonitis, etc. It is also effective for swine toxoplasmosis. Synonyms: (n(sup1)-2-pyrimidinylsulfanilamido)-sodium; 2-sulfanilamidopyrimidine sodium salt; 4-amino-n-2-pyrimidinyl-benzenesulfonamidmono sodium salt; monosodium 2-sulfanilamidopyrimidine; n(sup1)-2-pyrimidinylsulfanilamide monosodium salt. Grade: >95%. CAS No. 547-32-0. Molecular formula: C10H9N4NaO2S. Mole weight: 272.26.