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| Product | Description | |
|---|---|---|
| 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. Grades: >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-13C6 | Sulfadiazine-13C6 is a labeled Sulfadiazine.Sulfadiazine can be used to treat systemic infections. It has a broad antibacterial spectrum and has inhibitory effects on most Gram-positive and negative bacteria. It has strong inhibitory effects on Neisseria meningitidis, Streptococcus pneumoniae, Neisseria gonorrhoeae, and hemolytic Streptococcus. Can penetrate into the cerebrospinal fluid through the blood-brain barrier. Group: Isotope-labeled environmental contaminants. CAS No. 1189426-16-1. Molecular formula: 13C6C4H10N4O2S. Mole weight: 256.23. Canonical SMILES: O=S ([13C]1=[13C][13C]=[13C] (N)[13C]=[13C]1) (NC2=NC=CC=N2)=O. Catalog: ACM1189426161. |  |
| 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-d4 | Heterocyclic Organic Compound. Alternative Names: SULFADIAZINE-D4;sulfadiazine vetranal;2-(4-Aminobenzenesulfonamido-d4)pyrimidine;2-Sulfanilylaminopyrimidine-d4;4-Amino-N-2-pyrimidinylbenzenesulfonamide-d4;Adiazin-d4;Adiazine-d4;Debenal-d4. CAS No. 1020719-78-1. Molecular formula: C10H6D4N4O2S. Mole weight: 254.3. Appearance: Off-White to Pale Yellow Solid. Catalog: ACM1020719781. | |
| Sulfadiazine-d4 | The isotopically labeled drug Sulfadiazine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Sulfadiazine Impurity F | An impurity of Sulfadiazine. Sulfadiazine is an antibiotic. It is commonly used to treat urinary tract infections and burns. Grades: > 95%. Molecular formula: C4H5N3 HCl. Mole weight: 95.10 36.46. | |
| 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. Grades: >95%. CAS No. 547-32-0. Molecular formula: C10H9N4NaO2S. Mole weight: 272.26. | |
| Sulfadiazine sodium salt | 25g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C10H9N4NaO2S. CAS No. 547-32-0. Prepack ID 24036127-25g. Molecular Weight 272.26. See USA prepack pricing. |  |
| Sulfadiazine sodium salt | Sulfadiazine sodium salt. Group: Biochemicals. Grades: Highly Purified. CAS No. 547-32-0. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C10H9N4NaO2S. US Biological Life Sciences. | Worldwide |
| Sulfadiazine sodium salt, 99.0-100.5% USP | Sulfadiazine sodium salt, 99.0-100.5% USP. Group: Biochemicals. Grades: USP. Pack Sizes: 25g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| N-Acetyl sulfadiazine | Heterocyclic Organic Compound. Alternative Names: N-[4-[ (2-Pyrimidinylamino) sulfonyl]phenyl]acetamide; 2-[ (p-Acetamidophenyl) sulfonamido]pyrimidine; N4-Acetylsulfadiazine; 4'-(2-Pyrimidinylsulfamoyl)acetanilide; 4N-Acetylsulfadiazine. CAS No. 127-74-2. Molecular formula: C12H12N4O3S. Mole weight: 292.31. Appearance: White Solid. Catalog: ACM127742. | |
| N-Acetyl sulfadiazine | N-Acetyl sulfadiazine is a metabolite of sulfadiazine, an antibiotic used for the treatment of bacterial infections. Uses: A major metabolite of sulfadiazine. Synonyms: 2-[ (p-Acetamidophenyl) sulfonamido]pyrimidine; N4-Acetylsulfadiazine; 4'-(2-Pyrimidinylsulfamoyl)acetanilide; 4N-Acetylsulfadiazine; N(4)-Acetylsulfadiazine; N4-Acetylsulfadiazine. CAS No. 127-74-2. Molecular formula: C12H12N4O3S. Mole weight: 292.31. | |
| N-Acetyl Sulfadiazine | A major metabolite of Sulfadiazine. Group: Biochemicals. Alternative Names: N- [4- [ (2-Pyrimidinylamino) sulfonyl] phenyl] acetamide; 2- [ (p-Acetamidophenyl) sulfonamido] pyrimidine; N4-Acetylsulfadiazine; 4- (2-Pyrimidinylsulfamoyl) acetanilide; 4N-Acetylsulfadiazine. Grades: Highly Purified. CAS No. 127-74-2. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| N-Acetyl Sulfadiazine-13C6 | A major metabolite of Sulfadiazine. Group: Biochemicals. Alternative Names: N-[4-[ (2-Pyrimidinylamino) sulfonyl]phenyl-13C6]acetamide; 2- [ (p-Acetamidophenyl-13C6) sulfonamido] pyrimidine; N4-Acetylsulfadiazine-13C6; 4- (2-Pyrimidinylsulfamoyl) acetanilide-13C6; 4N-Acetylsulfadiazine-13C6. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| N-Acetyl Sulfadiazine-d4 | A major labeled metabolite of Sulfadiazine. Group: Biochemicals. Alternative Names: N-[4-[ (2-Pyrimidinylamino) sulfonyl]phenyl-d4]acetamide; 2- [ (p-Acetamidophenyl-d4) sulfonamido] pyrimidine; N4-Acetylsulfadiazine-d4; 4- (2-Pyrimidinylsulfamoyl) acetanilide-d4; 4N-Acetylsulfadiazine-d4. Grades: Highly Purified. CAS No. 1219149-66-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Silver sulfadiazine | Silver sulfadiazine (AgSD), a sulfonamide antibiotic, effects a dual inhibitory action on bacterial growth by its sulfa moiety (SD-SDZ) that prevents bacterial folate absorption and subsequent DNA synthesis. The silver that is released from Silver sulfadiazine binds and disrupts the DNA structure, precluding bacterial DNA replication [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: AgSD. CAS No. 22199-08-2. Pack Sizes: 1 g. Product ID: HY-B1497. | |
| Silver sulfadiazine | Silver sulfadiazine (AgSD), a sulfonamide antibiotic, effects a dual inhibitory action on bacterial growth by its sulfa moiety (SD-SDZ) that prevents bacterial folate absorption and subsequent DNA synthesis. The silver that is released from Silver sulfadiazine binds and disrupts the DNA structure, precluding bacterial DNA replication. Group: Electrolytes. Alternative Names: 4-Amino-n-2-pyrimidinylbenzenesulfonamide monosilver salt. CAS No. 22199-08-2. Product ID: Silver; (4-aminophenyl)sulfonyl-pyrimidin-2-ylazanide. Molecular formula: 357.14. Mole weight: C10H9AgN4O2S. C1=CN=C (N=C1)[N-]S (=O) (=O)C2=CC=C (C=C2)N. [Ag+]. InChI=1S/C10H9N4O2S. Ag/c11-8-2-4-9(5-3-8)17(15, 16)14-10-12-6-1-7-13-10; /h1-7H, 11H2; /q-1; +1. UEJSSZHHYBHCEL-UHFFFAOYSA-N. 99%+. |  |
| Silver sulfadiazine | Silver sulfadiazine (AgSD), a sulfonamide antibiotic, effects a dual inhibitory action on bacterial growth by its sulfa moiety (SD-SDZ) that prevents bacterial folate absorption and subsequent DNA synthesis. The silver that is released from Silver sulfadiazine binds and disrupts the DNA structure, precluding bacterial DNA replication. Group: Inhibitors. Alternative Names: 4-Amino-n-2-pyrimidinylbenzenesulfonamide monosilver salt. CAS No. 22199-08-2. Molecular formula: C10H9AgN4O2S. Mole weight: 357.14. Appearance: White to off-white powder. Purity: 99%+. IUPACName: Silver;(4-aminophenyl)sulfonyl-pyrimidin-2-ylazanide. Canonical SMILES: C1=CN=C (N=C1)[N-]S (=O) (=O)C2=CC=C (C=C2)N. [Ag+]. ECNumber: 244-834-5. Catalog: ACM22199082. | |
| Silver sulfadiazine | Silver sulfadiazine. Group: Biochemicals. Grades: Highly Purified. CAS No. 22199-08-2. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C10H9AgN4O2S. US Biological Life Sciences. | Worldwide |
| Silver Sulfadiazine USP | Silver Sulfadiazine USP. Categories: silver sulfadiazine; 22199-08-2. |  CA, FL & NJ |
| Sulfamerazine-d4 | Sulfadiazine-d4 is a deuterium-labeled sulfadiazine. This product is a medium-effective sulfonamide for the treatment of systemic infections. It has a broad antibacterial spectrum and has inhibitory effects on most Gram-positive and negative bacteria. It inhibits Neisseria meningitidis, Streptococcus pneumoniae, Neisseria gonorrhoeae, and hemolytic Streptococcus. It has a strong effect and can penetrate into the cerebrospinal fluid through the blood-brain barrier. Group: Isotope-labeled synthetic intermediates. CAS No. 1020719-84-9. Molecular formula: C11H8D4N4O2S. Mole weight: 268.33. Canonical SMILES: O=S (C1=C ([2H])C ([2H])=C (N)C ([2H])=C1[2H]) (NC2=NC=CC (C)=N2)=O. Catalog: ACM1020719849. | |
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