A directory of where to buy chemicals in the USA, including: distributors, industrial manufacturers, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the suppliers website for prices or more information.
| Product | Description | |
|---|---|---|
| Ceftiofur | Ceftiofur is a semisynthetic antibiotic, with activity against various gram-positive and gram-negative, aerobic and anaerobic bacteria encountered by domestic animals [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 80370-57-6. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg. Product ID: HY-N7102. |  |
| Ceftiofur hydrochloride | Ceftiofur hydrochloride is a semisynthetic antibiotic, with activity against various gram-positive and gram-negative, aerobic and anaerobic bacteria encountered by domestic animals [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 103980-44-5. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0026. | |
| Ceftiofur hydrochloride | Ceftiofur hydrochloride. Group: Biochemicals. Alternative Names: (6R, 7R) -7-[[ (2Z) -2- (2-Amino-4-thiazolyl) -2- (methoxyimino) acetyl]amino]-3-[[ (2-furanylcarbonyl) thio]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid; Excenel; Excenel RTU. Grades: Highly Purified. CAS No. 103980-44-5. Pack Sizes: 100g, 250g, 500g, 1kg. Molecular Formula: C19H18ClN5O7S3. US Biological Life Sciences. |  Worldwide |
| Ceftiofur hydrochloride | analytical standard. Group: Application areaspharma & vet compounds & metabolitespharma & vet compounds & metabolites. Alternative Names: U 67279A, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[(2-furanylcarbonyl)thio]methyl]-8-oxo-, monohydrochloride, [6R-[6?,7?(Z)]]-, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[(2-furanylcarbonyl)thio]methyl]-8-oxo-, monohydrochloride, (6R,7R)- (9CI), Excenel, Ceftiofur hydrochloride, Spectramast LC, Aviar, Cefalus, Excenel RTU, U 64279A,5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-3-[[(2-furanylcarbonyl)thio]methyl]-8-oxo-, hydrochloride (1:1), (6R,7R)-. |  |
| Ceftiofur hydrochloride | analytical standard. Uses: For analytical and research use. Group: Application areas; pharma & vet compounds & metabolites; pharma & vet compounds & metabolites. Alternative Names: U 67279A, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[(2-furanylcarbonyl)thio]methyl]-8-oxo-, monohydrochloride, [6R-[6?,7?(Z)]]-, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-3-[[(2-furanylcarbonyl)thio]methyl]-8-oxo-, monohydrochloride, (6R,7R)- (9CI), Excenel, Ceftiofur hydrochloride, Spectramast LC, Aviar, Cefalus, Excenel RTU, U 64279A,5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-3-[[(2-furanylcarbonyl)thio]methyl]-8-oxo-, hydrochloride (1:1), (6R,7R)-. Grades: analytical standard. CAS No. 103980-44-5. Pack Sizes: 100MG. IUPAC Name: (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(furan-2-carbonylsulfanylmethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;hydrochloride. Molecular formula: C19H17N5O7S3.ClH. Mole weight: 560.02. Catalog: APS103980445. SMILES: Cl.CO\N=C(/C(=O)N[C@H]1[C@H]2SCC(=C(N2C1=O)C(=O)O)CSC(=O)c3occc3)\c4csc(N)n4. Format: Neat. Shipping: Room Temperature. | |
| Ceftiofur, Hydrochloride ( (6R, 7R) -7-[[ (2Z) -2- (2-Amino-4-thiazolyl) -2- (methoxyimino) acetyl]amino]-3-[[ (2-furanylcarbonyl) thio]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid, U-67279A) | An antibacterial. Group: Biochemicals. Alternative Names: (6R, 7R) -7-[[ (2Z) -2- (2-Amino-4-thiazolyl) -2- (methoxyimino) acetyl]amino]-3-[[ (2-furanylcarbonyl) thio]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid; U-67279A. Grades: Highly Purified. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Ceftiofur Hydrochloride Liposome | Ceftiofur hydrochloride is a potent cephalosporin antibiotic that exerts a robust bactericidal effect against both gram-positive and gram-negative bacteria. This product is a pre-formulated liposome with ceftiofur hydrochloride. It is only for research purposes and for the injection to laboratory animals. Group: Drug-loaded liposome. Categories: liposomes, niosomes, ethosomes, and transfersomes. |  |
| Ceftiofur sodium | Ceftiofur sodium. Group: Biochemicals. Grades: Highly Purified. CAS No. 104010-37-9. Pack Sizes: 100mg, 250mg, 500mg, 1g. US Biological Life Sciences. | Worldwide |
| Ceftiofur sodium | Ceftiofur sodium (sodium ceftiofur) is a semisynthetic antibiotic with antimicrobial activity against a wide range of Gram-positive and Gram-negative bacteria, aerobic and anaerobic, targeting livestock [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: sodium ceftiofur. CAS No. 104010-37-9. Pack Sizes: 10 mM * 1 mL; 25 mg; 50 mg; 100 mg; 500 mg; 1 g. Product ID: HY-B0898. | |
| Ceftiofur sodium | Ceftiofur sodium, one of the third generation antibiotics, is a cephalosporin based antibacterial compound that has been approved to be used in veterinary medicine. Uses: Anti-bacterial agents. Synonyms: CCRIS 7601; CCRIS7601; CCRIS-7601; CM 31 916; CM31916; CM 31 916 Naxcel; [6R-[6α , 7β (Z)]]-7-[[ (2-amino-4-thiazolyl) (methoxyimino)acetyl]amino]-3-[[ (2-furanylcarbonyl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid Monosodium Salt. Grades: 96%. CAS No. 104010-37-9. Molecular formula: C19H16N5NaO7S3. Mole weight: 545.54. |  |
| Ceftiofur Sodium | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmacopeia & metrological institutes standards. | |
| Ceftiofur Sodium Liposome | Cefoperazone sodium (CS) is a third-generation cephalosporin with animal-specific activity, widely used for its effectiveness against most Gram-negative and some Gram-positive bacteria. This product is a pre-formulated liposome encapsulating Ceftiofur Sodium. It is only for research purposes. Group: Drug-loaded liposome. Categories: Niosomes, ethosomes, and transfersomes. | |
| Ceftiofur sodium salt | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C19H16N5NaO7S3. CAS No. 104010-37-9. Prepack ID 89966470-1g. Molecular Weight 545.55. See USA prepack pricing. |  |
| Ceftiofur (sodium) (Standard) | Ceftiofur (sodium) (Standard) is the analytical standard of Ceftiofur (sodium). This product is intended for research and analytical applications. Ceftiofurna sodium is a third-generation cephalosporin antibiotic approved for veterinary use. Uses: Scientific research. Group: Signaling pathways. CAS No. 104010-37-9. Pack Sizes: 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B0898R. | |
| Ceftizoxime | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Ceftizoxime | Ceftizoxime is a bacterial inhibitor which acts by interfering with bacterial cell wall synthesis and inhibiting cross-linking of the peptidoglycan. Uses: Scientific research. Group: Signaling pathways. CAS No. 68401-81-0. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B1596. | |
| Ceftizoxime | It is produced by the strain of Semisynthetic third generation cephalosporin for injection. Its sodium salt is used in preparations. Cefazide can be used for parenteral administration. Unlike other third-generation cephalosporins, the entire C-3 side chain of cefotaxime has been removed to prevent hydrolase inactivation. It is quite similar in nature to cefotaxime, but is not affected by metabolism. Uses: Anti-bacterial agents. Synonyms: Ceftizoxima; Ceftizoximum; Cefizox; Epocelin; Eposerin; FK-749; FR 13749; 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7- ( ( (2-amino-4-thiazolyl) (methoxyimino)acetyl)amino)-8-oxo-, (6R-(6alpha,7beta(Z)))-. Grades: > 95%. CAS No. 68401-81-0. Molecular formula: C13H13N5O5S2. Mole weight: 383.41. | |
| Ceftizoxime sodium | Ceftizoxime sodium. Group: Biochemicals. Grades: Highly Purified. CAS No. 68401-82-1. Pack Sizes: 100mg, 250mg, 500mg, 1g, 2g. Molecular Formula: C13H12N5NaO5S2. US Biological Life Sciences. | Worldwide |
| Ceftizoxime sodium | A semisynthetic cephalosporin antibiotic for the treatment of infections due to susceptible strains of microorganisms. It is third generation cephalosporin effective against Gram-negative and Gram-positive bacteria. Uses: Anti-bacterial agents. Synonyms: Ceftizoxim-Natrium. Grades: ≥98%. CAS No. 68401-82-1. Molecular formula: C13H12N5NaO5S2. Mole weight: 405.38. | |
| Ceftizoxime sodium | Ceftizoxime sodium (SKF-88373) is third generation cephalosporin effective against Gram-negative and Gram-positive bacteria. It binds penicillin-binding proteins (PBPs) and inhibits the bacterial cell wall synthesis. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SKF-88373. CAS No. 68401-82-1. Pack Sizes: 50 mg; 100 mg. Product ID: HY-B1596A. | |
| Ceftizoxime sodium, 850-995ug/mg (HPLC) USP | Ceftizoxime sodium, 850-995ug/mg (HPLC) USP. Group: Biochemicals. Grades: USP. CAS No. 68401-82-1. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences. | Worldwide |
| Ceftizoxime sodium salt | 100mg Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C13H12N5NaO5S2. CAS No. 68401-82-1. Prepack ID 41432628-100mg. Molecular Weight 405.39. See USA prepack pricing. | |
| Ceftizoxime S-Oxide Impurity | an impurity of ceftizoxime. Synonyms: 5-Thia-1-azabicyclo[4.2.0]?oct-2-ene-2-carboxylic acid, 7-[[(2Z)?-2-(2-amino-4-thiazolyl)?-2-(methoxyimino)?acetyl]?amino]?-8-oxo-, 5-oxide, (6R,?7R)?-. Grades: > 95%. CAS No. 79226-66-7. Molecular formula: C13H13N5O6S2. Mole weight: 399.41. | |
| Ceftobiprole | Ceftobiprole (Ro 63-9141) is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci with a MIC 90 value of 2 μg/mL for MRSA. Ceftobiprole also inhibits gram-positive and gram-negative pathogens. Ceftobiprole can be used for the study of hospital-acquired pneumonia (excluding ventilator-associated pneumonia) and community-acquired pneumonia [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 63-9141; BAL 9141. CAS No. 209467-52-7. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112579. | |
| Ceftobiprole | Ceftobiprole is a cephalosporin prodrug with potent bactericidal activity against methicillin-resistant MRSA and penicillin-resistant Streptococcus pneumoniae (PRSP). Synonyms: (6R,7R)-7-[[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-ylidene)-2-nitrosoacetyl]amino]-8-oxo-3-[(E)-[2-oxo-1-[(3R)-pyrrolidin-3-yl]pyrrolidin-3-ylidene]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; BAL 9141; BAL9141. Grades: >95%. CAS No. 209467-52-7. Molecular formula: C20H22N8O6S2. Mole weight: 534.57. | |
| Ceftobiprole | Ceftobiprole (Ro 63-9141) is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci with a MIC90 value of 2 μg/mL for MRSA. Ceftobiprole also inhibits gram-positive and gram-negative pathogens. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Ceftobiprole;5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylicacid,7-[[(2Z)-2-(5-aMino-1,2,4-thiadiazol-3-yl)-2-(hydroxyiMino)acetyl]aMino]-8-oxo-3-[(E)-[(3R)-2-oxo[1,3-bipyrrolidin]-3-ylidene]Methyl]-,(6R,7R)-. Product Category: Inhibitors. CAS No. 209467-52-7. Molecular formula: C20H22N8O6S2. Mole weight: 534.576. Purity: ≥95.0%. Product ID: ACM209467527. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Ceftobiprole medocaril sodium | Ceftobiprole medocaril (BAL5788) sodium is the parenteral proagent of Ceftobiprole (HY-112579). Ceftobiprole is a parenteral pyrrolidinone cephalosporin. Ceftobiprole is a broad-spectrum cephalosporin with high levels of in vitro activity against methicillin- (MRSA) and vancomycin-resistant staphylococci (VRSA) and penicillin-resistant streptococci. Ceftobiprole also inhibits gram-positive and gram-negative pathogens [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: BAL5788 sodium. CAS No. 252188-71-9. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106574A. | |
| Ceftobiprole medocaril sodium | Ceftobiprole medocaril sodium is a water-soluble prodrug ceftobiprole, a 5th-generation cephalosporin for the treatment of hospital-acquired pneumonia (excluding ventilator-associated pneumonia) and community-acquired pneumonia. Ceftobiprole binds to penicillin-binding proteins (PBPs) and inhibits their transpeptidase activity. Synonyms: Ceftobiprole medocaril; BAL5788; BAL-5788. CAS No. 252188-71-9. Molecular formula: C26H25N8NaO11S2. Mole weight: 712.6. | |
| Ceftolozane | Ceftolozane (CXA-101 free base; FR264205 free base) is a cephalosporin antibiotic with potent activity against Pseudomonas aeruginosa and strains Enterobacteriaceae, with MIC s of 0.5 and 0.25-0.5 mg/L [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CXA-101 free base; FR264205 free base. CAS No. 689293-68-3. Pack Sizes: 1 mg. Product ID: HY-19806. | |
| Ceftolozane | Ceftolozane is a 5th generation cephalosporin antibiotic. It is a semi-synthetic beta-lactam antibiotic and is used for the treatment of infections with gram-negative bacteria, or gram-positive bacteria that have become resistant to conventional antibiotics. It is also used for the treatment of complicated urinary tract infections and complicated intra abdominal infections combined with the β-lactamase inhibitor tazobactam. Uses: Ceftolozane is used for the treatment of infections with gram-negative bacteria, or gram-positive bacteria that have become resistant to conventional antibiotics. it is also used for the treatment of complicated urinary tract infections and complicated in. Synonyms: 7-{[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-{[(2-carboxypropan-2-yl)oxy]imino}acetyl]amino}-3-[ (5-amino-4-{[(2-aminoethyl)carbamoyl]amino}-1-methyl-1H-pyrazol-2-ium-2-yl)methyl]-3,4-didehydrocepham-4-carboxylate; CXA-101; CXA101. Grades: 98%. CAS No. 689293-68-3. Molecular formula: C23H30N12O8S2. Mole weight: 666.69. | |
| Ceftolozane sulfate | Ceftolozane (CXA-101) sulfate is an antipseudomonal cephalosporin. Ceftolozane binds to P. aeruginosa essential PBPs (1b, 1c, 2 and 3) with high affinity. Ceftolozane inhibits cell wall synthesis by binding the PBPs. Ceftolozane sulfate inhibits P. aeruginosa and Enterobacteriaceae [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CXA-101; FR264205. CAS No. 936111-69-2. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-19806A. | |
| Ceftolozane TFA | Ceftolozane TFA is a cephalosporin antibiotic that can be used to inhibit Gram-negative bacterial infections. Ceftolozane TFA can be used to synthesize new antibiotic that are more potent and safer [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1628046-32-1. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-106257A. | |
| Ceftolozane TFA salt | Ceftolozane TFA salt is the salt of Ceftolozane, which is the fifth-generation cephalosporin antibiotic. It is a semi-synthetic β-lactam antibiotic used to treat Gram-negative or Gram-positive bacterial infections that have developed resistance to conventional antibiotics. Synonyms: 5-Amino-2-(((6R,7R)-7-((Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(((2-carboxypropan-2-yl)oxy)imino)acetamido)-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl)methyl)-4-(3-(2-aminoethyl)ureido)-1-methyl-1H-pyrazol-2-ium 2,2,2-trifluoroacetate; 1H-Pyrazolium, 5-amino-4-[[[(2-aminoethyl)amino]carbonyl]amino]-2-[[(6R,7R)-7-[[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-[(1-carboxy-1-methylethoxy)imino]acetyl]amino]-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl]-1-methyl-, 2,2,2-trifluoroacetate (1:1); 5-Amino-4-{[(2-aminoethyl)carbamoyl]amino}-2-{[(6R,7R)-7-{[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-{[(2-carboxy-2-propanyl)oxy]imino}acetyl]amino}-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-1-methyl-1H-pyrazol-2-ium trifluoroacetate; CXA-101 TFA salt; Ceftolozane trifluoroacetate. Grades: ≥95%. CAS No. 1628046-32-1. Molecular formula: C23H30N12O8S2.C2HF3O2. Mole weight: 780.71. | |
| Ceftriaxone | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C18H18N8O7S3. CAS No. 73384-59-5. Prepack ID 76468654-1g. Molecular Weight 554.58. See USA prepack pricing. | |
| Ceftriaxone | Ceftriaxone (Ro 13-9904 free acid) is a broad spectrum β-lactam third-generation cephalosporin antibiotic, which has good antibacterial activity against a variety of gram-negative and positive bacteria. Ceftriaxone is a covalent inhibitor of GSK3β with IC 50 value of 0.78 μM. Ceftriaxone is an inhibitor of Aurora B. Ceftriaxone has anti-inflammatory, antitumor and antioxidant activities. Ceftriaxone can be used in the study of bacterial infections and meningitis [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 13-9904 free acid. CAS No. 73384-59-5. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-B0712. | |
| Ceftriaxone | It is produced by the strain of Semisynthetic third generation cephalosporin for injection. It has the third-generation cephalosporin commonness. It is characterized by a plasma elimination half-life of up to 7.1h, and one dose per day. Synonyms: Biotrakson; Rocefin; Rocephalin; Rophex. Grades: >98%. CAS No. 73384-59-5. Molecular formula: C18H18N8O7S3. Mole weight: 554.58. | |
| Ceftriaxone disodium salt hemi(heptahydrate) | analytical standard. Group: Application areas. | |
| Ceftriaxone, Disodium Salt, Hemiheptahydrate, 84+% (Ro-13-9904/001, Rocefin Rocephine) | An antibacterial. Group: Biochemicals. Alternative Names: Ro-13-9904/001, Rocefin Rocephine. Grades: Highly Purified. CAS No. 104376-79-6. Pack Sizes: 5g, 10g, 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| Ceftriaxone Impurity 1 | Ceftriaxone Impurity 1. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (E)-S-benzo[d]thiazol-2-yl 2-(2-aminothiazol-4-yl)-2-(methoxyimino)ethanethioate. CAS No. 1684396-27-7. Molecular formula: C13H10N4O2S3. Mole weight: 350.44. Catalog: APB1684396277. | |
| Ceftriaxone Impurity C | Reagent used in the preparation of Cefalosporins. Synonyms: Tetrahydro-2-methyl-3-thioxo-1,2,4-triazine-5,6-dione; Ro 11-8390; 2-Methyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazine-3-thiol; USP Ceftriaxone Triazine Analog. Grades: > 95%. CAS No. 58909-39-0. Molecular formula: C4H5N3O2S. Mole weight: 159.17. | |
| Ceftriaxone Impurity E | An impurity of Ceftriaxone, a cephalosporin antibiotic for the treatment of various bacterial infections. Synonyms: (6R,7R)-7-Amino-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grades: > 95%. CAS No. 58909-56-1. Molecular formula: C12H13N5O5S2. Mole weight: 371.4. | |
| Ceftriaxone sodium | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C18H18N8Na2O7S3. CAS No. 74578-69-1. Prepack ID 89992119-1g. Molecular Weight 598.55. See USA prepack pricing. | |
| Ceftriaxone Sodium | Pharmaceutical Secondary Standard; Certified Reference Material. Group: Pharmacopeia & metrological institutes standards. | |
| Ceftriaxone Sodium | (6R,7R,Z)-7-(2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-((6-hydroxy-2-methyl-5-oxo-2,5-dihydro-1,2,4-triazin-3-ylthio)methyl)-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid. CAS No. 73384-59-5. Product ID: 8-04260. Molecular formula: C18H18N8O7S3Na. Mole weight: 554.58. Properties: Micronized Powder, Climara, Dihydroxyoestrin| 17-beta-Estradiol| Estra-1,3,5(10)-triene-3,17beta-diol. |  |
| Ceftriaxone Sodium | Ceftriaxone Sodium is an antibiotic, a third-generation cephalosporin. It has broad-spectrum activity against Gram-positive bacteria and expanded Gram-negative coverage. lt is useful for the treatment of a number of bacterial infections, includeing ear infections, skin infections, urinary tract infections, pneumonia, gonorrhea, pelvic inflammatory disease, bone and joint infections, intra-abdominal infections, and meningitis and so on. It is used preoperatively to reduce the risk of postoperative infections. It inhibits bacterial cell wall synthesis by means of binding to the penicillin-binding proteins. It is a stimulator of EAAT2 expression with neuroprotective effects in both in ... stimulator of eaat2 expression with neuroprotective effects in both in vitro and in vivo models, which is based in part on its ability to inhibit neuronal cell death by glutamate excitotoxicity. Synonyms: 2,5,6-tetrahydro-2-methyl-5,6-dioxo-)(methoxyimino)acetyl)amino)-8-oxo-3-(((4-triazin-3-yl)thio)methyl)-,sodiumsalt,hydrate(2:4:7)(6r-(6-alpha,7-2;beta(z)))-; [6R-[6alpha, 7beta (Z)]]-7-[[ (2-Amino-4-thiazolyl) (methoxyimino)acetyl]amino]-8-oxo-3-[[ (1, 2, 5, 6-tetrahydro-2-methyl-5, 6-dioxo-1, 2, 4-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid sodium salt. Grades: 98%. CAS No. 74578-69-1. Molecular formula: C18H16N8Na2O7S3. Mole weight: 598.54. | |
| Ceftriaxone Sodium | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: Disodium (6R,7R)-7-[[(2Z)-(2-aminothiazol-4-yl)(methoxyimino)acetyl]amino]-3-[[(2-methyl-6-oxido-5-oxo-2,5-dihydro-1,2,4-triazin-3-yl)sulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 3.5 hydrate, Ceftriaxone disodium hemiheptahydrate, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-, sodium salt, hydrate (2:4:7), (6R,7R)-,Ceftriaxone sodium, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-, disodium salt, hydrate (2:7), (6R,7R)- (9CI), 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2-amino-4-thiazolyl)(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-, disodium salt, hydrate (2:7), [6R-[6alpha,7beta(Z)]]-. | |
| Ceftriaxone sodium 3.5 hydrate | Ceftriaxone sodium 3.5 hydrate. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: sodium (6R,7R)-7-((E)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetamido)-3-(((2-methyl-6-oxido-5-oxo-2,5-dihydro-1,2,4-triazin-3-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate,disodium salt,hemiseptahydrate. CAS No. 104376-79-6. Molecular formula: C18H16N8Na2O7S3·3·5H2O. Mole weight: 661.60. Catalog: APB104376796. | |
| Ceftriaxone sodium E-isomer | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Ceftriaxone sodium hydrate | Ceftriaxone sodium hydrate (Ro 13-9904 sodium hydrate) is a broad spectrum β-lactam third-generation cephalosporin antibiotic, which has good antibacterial activity against a variety of gram-negative and positive bacteria. Ceftriaxone sodium hydrate is a covalent inhibitor of GSK3β with IC 50 value of 0.78 μM. Ceftriaxone sodium hydrate is an inhibitor of Aurora B. Ceftriaxone sodium hydrate has anti-inflammatory, antitumor and antioxidant activities. Ceftriaxone sodium hydrate can be used in the study of bacterial infections and meningitis [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 13-9904 sodium hydrate. CAS No. 104376-79-6. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B0712A. | |
| Ceftriaxone sodium hydrate (2:4:7) | Ceftriaxone sodium hydrate is a third-generation cephalosporin antibiotic. Synonyms: Ceftriaxone Disodium Salt Hemiheptahydrate; (6R,7R)-7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6-dioxo-1,2,4-triazin-3-yl)thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, disodium salt, hemiheptahydrate; Rocefin; Rocephine. Grades: Assay: ≥ 795 μg/mg. CAS No. 104376-79-6. Molecular formula: C18H16N8O7S3.7/2H2O.2Na. Mole weight: 661.60. | |
| Ceftriaxone sodium salt | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C18H16N8Na2O7S3 · 3.5H2O. CAS No. 104376-79-6. Prepack ID 10212773-1g. Molecular Weight 661.6. See USA prepack pricing. | |
| Ceftriaxone sodium salt | Ceftriaxone sodium salt (Ro 13-9904) is a broad spectrum β-lactam third-generation cephalosporin antibiotic, which has good antibacterial activity against a variety of gram-negative and positive bacteria. Ceftriaxone sodium salt is a covalent inhibitor of GSK3β with IC 50 value of 0.78 μM. Ceftriaxone sodium salt is an inhibitor of Aurora B. Ceftriaxone sodium salt has anti-inflammatory, antitumor and antioxidant activities. Ceftriaxone sodium salt can be used in the study of bacterial infections and meningitis [1] [2] [3] [4] [5] [6] [7]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ro 13-9904. CAS No. 74578-69-1. Pack Sizes: 100 mg; 500 mg. Product ID: HY-B0712B. | |
| Ceftriaxone Sodium Sterile | Ceftriaxone disodium salt is a third generation semisynthetic cephalosporin antibiotic, which is chemically synthesized form 7-aminocephalosporanic acid (7-ACA). It has a broad spectrum of activity against Gram-positive and Gram-negative aerobic and anaerobic bacteria, and is generally more active against Gram-negative bacteria than the first and second generation cephalosporins. It has increased stability to β-lactamases compared with the first and second generation cephalosporins. Incorporation of the triazine substituted side chain into the 3-position of the cephalosporin nucleus markedly prolong serum half-life. Synonyms: Ceftriaxone sodium, Disodium (6R, 7R)-7-[[ (2Z)- (2-aminothiazol-4-yl) (methoxyimino)acetyl]amino]-3-[[ (2-methyl-6-oxido-5-oxo-2, 5-dihydro-1, 2, 4-triazin-3-yl)sulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylate 3.5 hydrate, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-3-[[(1,2,5,6-tetrahydro-2-methyl-5,6. CAS No. 104376-79-6. Product ID: PAP-0096. Molecular formula: C18H16N8Na2O7S3·31/2H2O. Mole weight: 661.58. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; PAP-0096; Ceftriaxone Sodium Sterile; 104376-79-6; Ceftriaxone sodium, Disodium (6R, 7R)-7-[[ (2Z)- (2-aminothiazol-4-yl) (methoxyimino)acetyl]amino]-3-[[ (2-methyl-6-oxido-5-oxo-2, 5-dihydro-1, 2, 4-triazin-3-yl) |  |
| Cefuracetime | SKF81367 is a cephalosporin antibiotic. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SKF81367. CAS No. 39685-31-9. Pack Sizes: 1 mg; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-U00154. | |
| Cefuracetime (E-isomer) Sodium Salt | Cefuracetime (E-isomer) Sodium Salt. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (6R,7R)-3-[(Acetyloxy)methyl]-7-[[(2E)-2-furanyl(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid sodium salt,5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[(acetyloxy)methyl]-7-[[2-furanyl(methoxyimino)acetyl]amino]-8-oxo-, monosodium salt, [6R-[6?,7?(E)]]- (9CI), Cefuracetime sodium (E-isomer), (6R,7R)-7-[[(E)-(Furan-2-yl)(methoxyimino)acetyl]amino]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid sodium salt, (E)-Cefuracetime sodium salt. CAS No. 97170-20-2. Pack Sizes: 10MG. IUPAC Name: sodium;(6R,7R)-3-(acetyloxymethyl)-7-[[(2E)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate. Molecular formula: C17H16N3O8S.Na. Mole weight: 445.38. Catalog: APS97170202. SMILES: [Na+].CO\N=C(\C(=O)N[C@H]1[C@H]2SCC(=C(N2C1=O)C(=O)[O-])COC(=O)C)/c3occc3. Format: Neat. Shipping: Room Temperature. | |
| Cefuroxime | analytical standard. Group: Application areasapi standardsimpurity standardspharmaceutical toxicology. Alternative Names: Zefu, Ketocef, Biofuroxim, Biofuroksym, Cefasyn, Maxalac, Cefuroxime, Multisef, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[2-furanyl(methoxyimino)acetyl]amino]-8-oxo-, [6R-[6alpha,7beta(Z)]]-, (6R,7R)-3-[[(Aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-(2-furanyl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, Cefuroxime Axetil Imp. D (EP), Cefuroxim, Cefuroxime acid, Cephuroxime, Cefaloxime,5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-(2-furanyl)-2-(methoxyimino)acetyl]amino]-8-oxo-, (6R,7R)-, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-furanyl(methoxyimino)acetyl]amino]-8-oxo-, (6R,7R)- (9CI). | |
| Cefuroxime | It is produced by the strain of Semisynthetic second generation cephalosporin. Cefuroxime is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime has a broad spectrum activity against Gram-positive and Gram-negative bacteria. Synonyms: Cephuroxime; Cefuroxim; Cefuroximo; Cefuroximum; Sharox; Zinacef; Biofuroksym; Cefuril; (6R,7R)-7-(2-(2-Furyl)glyoxylamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid 7(sup 2)-(Z)-(O-methyloxime) carbamate (ester). Grades: 98%. CAS No. 55268-75-2. Molecular formula: C16H16N4O8S. Mole weight: 424.39. | |
| Cefuroxime | Cefuroxime is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime has a broad spectrum activity against Gram-positive and Gram-negative bacteria [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Kefurox. CAS No. 55268-75-2. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-B1256A. | |
| Cefuroxime | 1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H16N4O8S. CAS No. 55268-75-2. Prepack ID 17592387-1g. Molecular Weight 424.39. See USA prepack pricing. | |
| Cefuroxime axetil | Cefuroxime Axetil, a proagent of the cephalosporin cefuroxime and an oarl broad spectrum antibiotic, inhibits several gram-positive and gram-negative organisms, including those most frequently associated with various common community-acquired infections [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 64544-07-6. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-B1325. | |
| Cefuroxime axetil | Cefuroxime is a cephalosporin antibiotic. It is used to treat many kinds of bacterial infections, including severe or life-threatening forms. Cefuroxime axetil is a prodrug of the cephalosporin cefuroxime, which is a second generation oral cephalosporin antibiotic with in vitro antibacterial activity against several gram-positive and gram-negative organisms. Synonyms: Cefuroxime 1-acetoxyethyl ester; Elobact. Grades: ≥97%. CAS No. 64544-07-6. Molecular formula: C20H22N4O10S. Mole weight: 510.47. | |
| Cefuroxime Axetil | It is the 1-(acetyloxy) ethyl ester of Cefuroxime , an injectable second generation cephalosporin with an excellent antibacterial activity. This ester has a broader spectrum of activity than cephalexin (first-generation) and is widely used to treat respiratory tract infections. Antibacterial. Group: Biochemicals. Alternative Names: (6R, 7R) -3-[[ (Aminocarbonyl) oxy]methyl]-7-[[ (2Z) -2- (2-furanyl) -2- (methoxyimino) acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid 1-(Acetyloxy)ethyl Ester; Altacef; Bioracef; CCI 15641; Cefaks; Cefazine; Ceftin; Cefurax; Cefuroxime 1-Acetoxyethyl Ester; Elobact; Forcef; Oraxim; Zinat; Zinnat. Grades: Highly Purified. CAS No. 64544-07-6. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| Cefuroxime Axetil | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardsbritish pharmacopoeiaeuropean pharmacopoeia (ph. eur.)pharmacopoeial standards. Alternative Names: (1RS)-1-(acetyloxy)ethyl (6R,7R)-3-[(carbamoyloxy)methyl]-7-[[(Z)-2-(furan-2-yl)-2(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate, CCI 15641,Cefuroxime axetil, Cefuroxime Ester E47. | |
| Cefuroxime Axetil Delta-3-Isomers | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Cefuroxime Axetil E-isomers | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. | |
| Cefuroxime axetil Impurity A | Cefuroxime axetil Impurity A. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: (6R,7R)-1-acetoxyethyl 3-((carbamoyloxy)methyl)-7-((Z)-2-(furan-2-yl)-2-(methoxyimino)acetamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate. CAS No. 123458-61-7. Molecular formula: C20H22N4O10S. Mole weight: 510.47. Catalog: APB123458617. | |
| Cefuroxime Axetil Impurity E | (αZ)-α-(Methoxyimino)-N-[(5aR,6R)-1,4,5a,6-tetrahydro-1,7-dioxo-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl]-2-furanacetamide is an impurity of Cefuroxime Axetil, the 1-(acetyloxy) ethyl ester of Cefuroxime , an injectable second generation cephalosporin with an excellent antibacterial activity. Synonyms: (αZ)-α-(Methoxyimino)-N-[(5aR,6R)-1,4,5a,6-tetrahydro-1,7-dioxo-3H,7H-azeto[2,1-b]furo[3,4-d][1,3]thiazin-6-yl]-2-furanacetamide. Grades: > 95%. CAS No. 947723-87-7. Molecular formula: C15H13N3O6S. Mole weight: 363.35. | |
| Cefuroxime-d3 | Labeled Cefuroxime. Antibacterial. Group: Biochemicals. Alternative Names: (6R, 7R) -3-[[ (Aminocarbonyl) oxy]methyl]-7-[[ (2Z) -2-furanyl (methoxy-d3-imino) acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Cefuroxime sodium | Cefuroxime sodium is a second-generation cephalosporin antibiotic resistant to beta-lactamase. It has a broad-spectrum antimicrobial activity against Gram-positive and Gram-negative bacteria. Uses: Anti-bacterial agents. Synonyms: Anaptivan; Biociclin; Biofurex; (6R,7R)-3-[[(Aminocarbonyl)oxy]methyl]-7-[[(2Z)-2-furanyl(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Sodium Salt; Cefurin; Duxima; Novocef; Zinacef. Grades: ≥95%. CAS No. 56238-63-2. Molecular formula: C16H15N4NaO8S. Mole weight: 446.36. | |
| Cefuroxime sodium | Cefuroxime sodium is an orally active second-generation cephalosporin antibiotic with increased stability to β-lactamase. Cefuroxime sodium has a broad spectrum activity against Gram-positive and Gram-negative bacteria. Uses: Designed for use in research and industrial production. Product Category: Inhibitors. CAS No. 56238-63-2. Molecular formula: C16H15N4NaO8S. Mole weight: 446.37. Purity: 0.9933. Product ID: ACM56238632. Alfa Chemistry ISO 9001:2015 Certified. | |
Our database is helping our users find suppliers everyday.
