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(6R,7S)-Cefoperazone is the enantiomer of Cefoperazone as an impurity. Synonyms: (6R,7S)-7-[[(2R)-2-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]-2-(4-hydroxyphenyl)acetyl]amino]-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid. Grades: > 95%. CAS No. 1315481-36-7. Molecular formula: C20H20N6O7S4. Mole weight: 584.67.
Cefoperazone sodium
Cefoperazone Sodium is a third generation cephalosporin antibiotic for inhibition of rMrp2-mediated [3H]E217βG uptake with IC50 of 199 μM, used in the treatment of bacterial infections caused by susceptible microorganisms. Uses: Broad spectrum third generation cephalosporin antibiotic. an antibacterial. Synonyms: sodium;(6R,7R)-7-[[(2R)-2-[(4-ethyl-2,3-dioxopiperazine-1-carbonyl)amino]-2-(4-hydroxyphenyl)acetyl]amino]-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate. Grades: ≥95%. CAS No. 62893-20-3. Molecular formula: C25H26N9NaO8S2. Mole weight: 667.64.
Cefoperazone sodium salt
Cefoperazone sodium salt (CP 52640-2), a semisynthetic cephalosporin, has a broad spectrum of antibacterial activity [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: CP 52640-2. CAS No. 62893-20-3. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-B0210A.
Cefoperazone sodium salt
5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C25H26N9NaO8S2. CAS No. 62893-20-3. Prepack ID 45309164-5g. Molecular Weight 667.65. See USA prepack pricing.
Cefoperazone sodium salt
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C25H26N9NaO8S2. CAS No. 62893-20-3. Prepack ID 45309164-1g. Molecular Weight 667.65. See USA prepack pricing.
Cefoperazone sodium salt, ~90%
Cefoperazone sodium salt, ~90%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g, 25g, 100g. US Biological Life Sciences.
Worldwide
Cefoperazone, Sodium Salt (CP-52640-2, T-1551, Bioperazone, Cefazone, Cefobid)
Cefoperazone is a third generation cephalosporin antibiotic. Cefoperazone exerts its bactericidal effect by inhibiting the bacterial cell wall synthesis, and sulbactam acts as a beta-lactamase inhibitor, to increase the antibacterial activity of cefoperazone against beta-lactamase producing organisms. It is one of few cephalosporin antibiotics effective in treating Pseudomonas bacterial infections which are otherwise resistant to these antibiotics. Group: Biochemicals. Alternative Names: CP-52640-2, T-1551, Bioperazone, Cefazone, Cefobid; (6R, 7R) -7-[[ (2R) -2-[[ (4-Ethyl-2, 3-dioxo-1-piperazinyl) carbonyl]amino]-2- (4-hydroxyphenyl) acetyl]amino]-3-[[ (1-methyl-1H-tetrazol-5-yl) thio]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid Sodium Salt. Grades: Highly Purified. CAS No. 62893-20-3. Pack Sizes: 5g, 10g, 25g. US Biological Life Sciences.
Worldwide
Cefoperazone (sodium salt) (Standard)
Cefoperazone (sodium salt) (Standard) is the analytical standard of Cefoperazone (sodium salt). This product is intended for research and analytical applications. Cefoperazone sodium salt (CP 52640-2), a semisynthetic cephalosporin, has a broad spectrum of antibacterial activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 62893-20-3. Pack Sizes: 25 mg; 50 mg; 100 mg; 250 mg. Product ID: HY-B0210AR.
It is produced by the strain of Semisynthetic second generation cephalosporin for injection. Ceforanide is a beta-lactam, broad-spectrum antibiotic. It has bactericidal activity and is used in the sterilization in various medical procedures. It causes inhibition of bacterial cell wall synthesis by inactivating penicillin binding proteins (PBPs) thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units which are a component of the cell wall. It has a longer elimination half-life than any currently available cephalosporin. Uses: Ceforanide has bactericidal activity and is used in the sterilization in various medical procedures. Synonyms: Precef; Ceforanido; Ceforanidum; 7-(o-(Aminomethyl)phenylacetamido)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid; (6R,7R)-7-(2-(alpha-Amino-o-tolyl)acetamido)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid; (6R-trans)-7-(((2-(Aminomethyl)phenyl)acetyl)amino)-3-(((1-(carboxymethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid; Antibiotic BL-S 786. Grades: 95%. CAS No. 60925-61-3. Molecular formula: C20H21N7O6S2. Mole weight: 519.55.
Ceforanide
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Ceforanide
Ceforanide is a second generation cephalosporin administered intravenously or intramuscularly. Ceforanide has a spectrum of in vitro antibacterial activity [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 60925-61-3. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-B1297.
Cefoselis
It is produced by the strain of Semisynthetic fourth generation cephalosporin for injection. Cefoselis, a new parenteral cephalosporin, was active against clinical isolates of both gram-positive and gram-negative aerobic bacteria. The activity of Cefoselis was similar to that of cefpirome and cefepime and generally superior to that of ceftazidime. Cefoselis showed potent antibacterial activity against Hemophilus influenzae and Moraxella catarrhalis. Cefoselis was highly active against MSSA and MSCNS. Cefoselis was poor in the activity against MRSA, MRCNS, PRSP and Enterococcus faecalis, and had no activity for Enterococcus faecium. Synonyms: Wincef. Grades: >98%. CAS No. 122841-10-5. Molecular formula: C20H22N7O7S2. Mole weight: 536.56.
Cefoselis hydrochloride
Cefoselis, a new parenteral cephalosporin, is a widely used beta-lactam antibiotic and is active against clinical isolates of both gram-positive and gram-negative aerobic bacteria. It showed potent antibacterial activity against Hemophilus influenzae and Moraxella catarrhalis. It was highly active against MSSA and MSCNS, but it was poor in the activity against MRSA,MRCNS,PRSP and Enterococcus faecalis, and had no activity for Enterococcus faecium. Synonyms: Wincef hydrochloride. Grades: >98%. CAS No. 911212-25-4. Molecular formula: C19H23ClN8O6S2. Mole weight: 559.02.
Cefoselis sulfate
Cefoselis sulfate is a stable cephalosporin for BETA-lactamase. The drug shows antimicrobial activity for a wide range of bacteria including Pseudomonas. Synonyms: Winsef; (6R- (6alpha, 7beta (Z)))-7- ( ( (2-Amino-4-thiazolyl) (methoxyimino)acetyl)amino)-3- ( (2, 3-dihydro-2- (2-hydroxyethyl)-3-imino-1H-pyrazol-1-yl)methyl)-8-oxo-5-Thia-1-azabicyclo (4. 2. 0)oct-2-ene-2-carboxylic acid sulfate. Grades: 0.98. CAS No. 122841-12-7. Molecular formula: C19H22N8O6S2.H2SO4. Mole weight: 620.64.
Cefoselis sulfate. Group: Biochemicals. Grades: Highly Purified. CAS No. 122841-12-7. Pack Sizes: 5mg, 10mg, 25mg, 50mg, 100mg. US Biological Life Sciences.
Worldwide
Cefoselis sulfate
Cefoselis sulfate (FK-037), the fourth gen-eration of cephalosporin, is a β-lactam antibiotic. Cefoselis sulfate exhibits good activity against a wide range of Gram-positive and Gram-negative organisms. Cefoselis sulfate penetrates the blood-brain barrier [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: FK-037. CAS No. 122841-12-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-B0186B.
Cefotaxime
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N5O7S2. CAS No. 63527-52-6. Prepack ID 85979953-1g. Molecular Weight 455.47. See USA prepack pricing.
Cefotaxime
It is produced by the strain of Semisynthetic third generation cephalosporin for injection. Cefotaxime is an antibiotic with broad spectrum activity against Gram positive and Gram negative bacteria. Cefotaxime inhibits mucopeptide synthesis by binding to and inactivating penicillin binding proteins thereby interfering with the final transpeptidation step required for cross-linking of peptidoglycan units. It is used to treat joint infections, pelvic inflammatory disease, meningitis, pneumonia, urinary tract infections, sepsis, gonorrhea, and cellulitis. Synonyms: Betaksim; C-Tax; Cefabol; Cefotaxime; Cefotaxime acid; Ceftax; Cephotaxime; Claforan; Omnatax; Taxim; Zeefotax; E-cefotaxime; Cefotaximum; Cefotaxima; 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 3- ( (acetyloxy)methyl)-7- ( ( (2Z)- (2-amino-4-thiazolyl) (methoxyimino)acetyl)amino)-8-oxo-, (6R,7R)-. Grades: ≥98%. CAS No. 63527-52-6. Molecular formula: C16H17N5O7S2. Mole weight: 455.46.
Cefotaxime
Cefotaxime, a β-lactamase stable cephalosporin and a third-generation cephalosporin antibiotic, possesses broad-spectrum antibiotic activity against numerous Gram-positive and Gram-negative bacteria [1] [2] [3] [4] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefotaxim; HR-756. CAS No. 63527-52-6. Pack Sizes: 10 mM * 1 mL; 100 mg; 250 mg; 500 mg. Product ID: HY-A0088A.
Cefotaxime-d3
Broad spectrum third generation cephalosporin antibiotic. Group: Biochemicals. Alternative Names: (6R, 7R) -3-[ (Acetyloxy) methyl]-7-[[ (2Z) -2- (2-amino-4-thiazolyl) -2- (methoxyimino) acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid-d3; Cefotax-d3; HR 756-d3; Pretor-d3; Tolycar-d3. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences.
Worldwide
Cefotaxime Impurity 25
Cefotaxime Impurity 25. Uses: For analytical and research use. Group: Impurity standards. CAS No. 134203-90-0. Molecular formula: C34H42ClN5O10S2. Mole weight: 780.31. Catalog: APB134203900.
Cefotaxime Impurity 6
Cefotaxime Impurity 6. Uses: For analytical and research use. Group: Impurity standards. CAS No. 123238-79-9. Molecular formula: C14H13N5O5S2. Mole weight: 395.41. Catalog: APB123238799.
Cefotaxime Impurity B
An impurity of Cefotaxime sodium. Synonyms: (6R,7R)-7-[[(2Z)-2-(2-Amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; Deacetylcefotaxime; Desacetylcefotaxime. Grades: > 95%. CAS No. 66340-28-1. Molecular formula: C14H15N5O6S2. Mole weight: 413.43.
Cefotaxime Impurity D Sodium Salt
An impurity of Cefotaxime. Synonyms: 5-Thia-1-azabicyclo[4.2.0]?oct-2-ene-2-carboxylic acid, 3-[ (acetyloxy)?methyl]?-7-[[ (2-amino-4-thiazolyl)? (methoxyimino)?acetyl]?amino]?-8-oxo-, monosodium salt, [6R-[6α,?7β(E)?]?]?- (9CI). Grades: > 95%. CAS No. 65715-12-0. Molecular formula: C16H16N5O7S2. Na. Mole weight: 454.46 22.99.
Cefotaxime Related Compound E
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Cefotaxime sodium
Broad spectrum third generation cephalosporin antibiotic. The name Cefotaxime applies to the isomer having a syn-methoxy imino group. Uses: Designed for use in research and industrial production. Additional or Alternative Names: hr756;Cefotaxime Na;sodium cefotaxime;Tolycar;FIR-756. Product Category: Inhibitors. Appearance: White to pale yellow crystalline powder. CAS No. 64485-93-4. Molecular formula: C16H16N5NaO7S2. Mole weight: 477.45. Purity: 0.9925. Density: 1.8 g/cm³. Product ID: ACM64485934. Alfa Chemistry ISO 9001:2015 Certified.
Cefotaxime sodium
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharma & vet compounds & metabolitespharma & vet compounds & metabolitesapi standardseuropean pharmacopoeia (ph. eur.)pharmaceutical toxicologypharmacopoeial standards. Alternative Names: Sodium (6R,7R)-3-[(acetyloxy)methyl]-7-[[(2Z)-2-(2-aminothiazol-4-yl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate, Cefotax, HR 756, Pretor, Tolycar,(6R,7R)-3-[(Acetyloxy)methyl]-7-[[(2Z)-2-(2-amino-4-thiazolyl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Sodium Salt, Cefotaxime sodium.
Cefotaxime sodium
Cefotaxime (Cefotaxim) sodium, a β-lactamase stable cephalosporin and a third-generation cephalosporin antibiotic, possesses broad-spectrum antibiotic activity against numerous Gram-positive and Gram-negative bacteria [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Cefotaxim sodium; HR-756 sodium. CAS No. 64485-93-4. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g; 5 g. Product ID: HY-A0088.
Cefotaxime Sodium
(6R,7R,Z)-3-(acetoxymethyl)-7-(2-(2-aminothiazol-4-yl)-2-(methoxyimino)-acetamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid. Possible carcinogen. Packaged under nitrogen. CAS No. 63527-52-6. Product ID: 8-04257. Molecular formula: C16H17N6O7S2. Mole weight: 455.4.
Cefotaxime sodium salt
100g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N5O7S2 ·Na. CAS No. 64485-93-4. Prepack ID 50013891-100g. Molecular Weight 478.46. See USA prepack pricing.
Cefotaxime sodium salt
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N5O7S2 ·Na. CAS No. 64485-93-4. Prepack ID 50013891-1g. Molecular Weight 478.46. See USA prepack pricing.
Cefotaxime sodium salt
5g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H17N5O7S2 ·Na. CAS No. 64485-93-4. Prepack ID 50013891-5g. Molecular Weight 478.46. See USA prepack pricing.
Cefotaxime sodium salt, 916-964ug/mg (HPLC) USP
Cefotaxime inhibits synthesis of bacterial cell walls and used for Agrobacterium. Group: Biochemicals. Alternative Names: (6R, 7R, Z) -3- (acetoxymethyl) -7- (2- (2-aminothiazol-4-yl) -2- (methoxyimino) acetamido) -8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid. Grades: USP. CAS No. 64485-93-4. Pack Sizes: 1g, 10g, 25g. US Biological Life Sciences.
Worldwide
Cefotaxime, Sodium Salt, High Purity, Cell Culture-Tested
Potent beta-lactamase-resistant antibiotic of cephalosporin class. Active against Gram-positive and Gram-negative organisms, including Gram-negative anaerobes. Inhibits cell wall synthesis. Group: Biochemicals. Alternative Names: (6R, 7R) -3-[ (Acetyloxy) methyl]-7-[[ (2Z) -2- (2-amino-4-thiazolyl) -2- (methoxyimino) acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic Acid Sodium Salt; Cefotax; HR 756; Pretor; Tolycar. Grades: Cell Culture Grade. CAS No. 64485-93-4. Pack Sizes: 1g, 5g. US Biological Life Sciences.
Worldwide
Cefoteta, Disodium
Cefoteta, Disodium. Group: Biochemicals. Grades: Highly Purified. CAS No. 74356-00-6. Pack Sizes: 250mg, 500mg, 1g, 2g, 5g. US Biological Life Sciences.
Worldwide
Cefotetan
Cefotetan is a semisynthetic cephamycin antibiotic that exerts its bactericidal effects by inhibition of cell-wall synthesis [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 69712-56-7. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg. Product ID: HY-N6670.
Cefotetan
100mg Pack Size. Group: Antibiotics, Bioactive Small Molecules, Research Organics & Inorganics. Formula: C17H17N7O8S4. CAS No. 69712-56-7. Prepack ID 90005452-100mg. Molecular Weight 575.62. See USA prepack pricing.
Cefotetan
It is produced by the strain of Semisynthetic Cephamycins compounds. The disodium salt of Cefotetan is used in preparation for injection. The antimicrobial activity of Cefotetan corresponds to the second generation of cephalosporins. Synonyms: Cefotetanum; Cefotan; (6R,7S)-7-(4-(Carbamoylcarboxymethylene)-1,3-dithiethane-2-carboxamido)-7-methoxy-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid; Apacef. Grades: 95%. CAS No. 69712-56-7. Molecular formula: C17H17N7O8S4. Mole weight: 575.62.
Cefotetan
An antibiotic related to Cephalosporin, used in the treatment of bacterial infections. Group: Biochemicals. Alternative Names: (6R,7S)-7-[[[4-(2-Amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; Apacef. Grades: Highly Purified. CAS No. 69712-56-7. Pack Sizes: 10mg, 100mg, 250mg. US Biological Life Sciences.
Worldwide
Cefotetan
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standardspharmaceutical toxicology. Alternative Names: Apacef, 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, [6R-(6?,7?)]-,5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, (6R,7S)-, Cefotetan, 1,3-Dithietane, 5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid deriv.
Cefotetan disodium
Cefotetan is a second-generation cephalosporin. It can bind to penicillin-binding proteins and disrupts the cell wall synthesis. Cefotetan is active against some strains of β-lactamase producing bacteria. Cefotetan shows anti-microbial activity against Gram-positive and Gram-negative bacteria and it is more efficacious against Gram-negative and anaerobic bacteria. Uses: Antibacterial. Synonyms: ICI156834; ICI 156834; ICI-156834; YM 09330; YM09330; YM-09330; Yamatetan; Cefotan; Apatef; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, sodium salt (1:2), (6R,7S)-; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, disodium salt, (6R,7S)-; 5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 7-[[[4-(2-amino-1-carboxy-2-oxoethylidene)-1,3-dithietan-2-yl]carbonyl]amino]-7-methoxy-3-[[(1-methyl-1H-tetrazol-5-yl)thio]methyl]-8-oxo-, disodium salt, [6R-(6α,7α)]-; Cefotetan sodium; Ceftenon; Cepan Darvilen. Grades: 98%. CAS No. 74356-00-6. Molecular formula: C17H15N7Na2O8S4. Mole weight: 619.59.
Cefotetan disodium salt
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C17H15N7Na2O8S4. CAS No. 74356-00-6. Prepack ID 18528286-1g. Molecular Weight 619.59. See USA prepack pricing.
Cefotetan free acid 99+%
An antibiotic related to Cephalosporin, used in the treatment of bacterial infections. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1g, 5g. US Biological Life Sciences.
Worldwide
Cefotiam
A semi-synthetic cephalosporin antibiotic. Antibacterial. Group: Biochemicals. Alternative Names: (6R,7R)-. Grades: Highly Purified. CAS No. 95789-30-3. Pack Sizes: 10mg. US Biological Life Sciences.
Worldwide
Cefotiam
It is produced by the strain of Semisynthetic second generation cephalosporin. Cefotiam is active against a broad spectrum of both Gram positive and Gram negative bacteria. Cefotiam binds to penicillin-binding proteins (PBPs), transpeptidases that are responsible for crosslinking of peptidoglycan. By preventing crosslinking of peptidoglycan, cell wall integrity is lost and cell wall synthesis is halted. Synonyms: Cefotiamum; Ceradon; Ceradolan; Haloapor; 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(((2-amino-4-thiazolyl)acetyl)amino)-3-(((1-(2-(dimethylamino)ethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-, (6R-trans)-. Grades: ≥ 95%. CAS No. 61622-34-2. Molecular formula: C18H23N9O4S3. Mole weight: 525.63.
Cefotiam dihydrochloride
Cefotiam dihydrochloride. Group: Biochemicals. Alternative Names: (6R, 7R) -7-[[2- (2-Amino-4-thiazolyl) acetyl]amino]-3-[[[1-[2- (dimethylamino) ethyl]-1H-tetrazol-5-yl]thio]methyl]-8-oxo-5-thia-1-azabicyclo[4. 2. 0]oct-2-ene-2-carboxylic acid hydrochloride; Abbott 48999; Spizef. Grades: Highly Purified. CAS No. 66309-69-1. Pack Sizes: 50mg, 100mg, 250mg, 500mg, 1g. Molecular Formula: C18H25Cl2N9O4S3. US Biological Life Sciences.
Worldwide
Cefotiam Dihydrochloride
Cefotiam hydrochloride is a third generation beta-lactam cephalosporin antibiotic for treatment of severe infections caused by susceptible bacteria. Uses: A third generation beta-lactam cephalosporin antibiotic. Synonyms: Halospor; Pansporin; Pansporine; Spizef; Cefotiam (Hydrochloride). Grades: ≥95%. CAS No. 66309-69-1. Molecular formula: C18H25Cl2N9O4S3. Mole weight: 598.53.
Cefotiam dihydrochloride 98+%
Cefotiam dihydrochloride 98+%. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 100mg, 250mg, 1g, 5g. US Biological Life Sciences.
Cefotiam hexetil hydrochloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 95789-30-3. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences.
Worldwide
Cefotiam Hexetil Hydrochloride
Cefotiam Hexetil Hydrochloride. CAS No: 95789-30-3
Sarchem Laboratories New Jersey NJ
Cefotiam hydrochloride
100mg Pack Size. Group: Antibiotics, Building Blocks, Diagnostic Raw Materials. Formula: C18H23N9O4S3. CAS No. 66309-69-1. Prepack ID 89991046-100mg. Molecular Weight 562.09. See USA prepack pricing.
Cefotiam hydrochloride
Cefotiam (SCE-963) hydrochloride is a parenteral cephalosporin antibiotic. Cefotiam hydrochloride has broad-spectrum activity against Gram-positive and Gram-negative bacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SCE-963 hydrochloride. CAS No. 66309-69-1. Pack Sizes: 5 mg; 10 mg; 50 mg. Product ID: HY-B0734A.
Cefotiam hydrochloride
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Cefovecin Sodium is an antibiotic of the cephalosporin class. It is used for the treatment of skin infections caused by Pasturella multocida in cats, and Staphylococcus intermedius/S. canis in dogs. Cefovecin Sodium is the first single-dose injectable antibiotic for dogs and cats. Uses: The treatment of skin conditions in dogs and cats. Synonyms: UNII-DL8Q24959P; DL8Q24959P; C13142. Grades: 95%. CAS No. 141195-77-9. Molecular formula: C17H18N5NaO6S2. Mole weight: 475.47.
Cefoxitin
It is produced by the strain of Semisynthetic Cephamycins compounds. Cefoxitin has antimicrobial activity equivalent to second-generation cephalosporins and is highly stable to β-lactamase. Synonyms: (6R-cis)-3-[[(Aminocarbonyl)oxy]methyl]-7-methoxy-8-oxo-7-[(2-thienylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid; Cephoxitin; CEPHOXITIN; Cefoxitina; Cefoxitine; Cefoxitinum; Rephoxitin; Mefoxitin. Grades: ≥98.0%. CAS No. 35607-66-0. Molecular formula: C16H17N3O7S2. Mole weight: 427.45.
Cefoxitin
Cefoxitin, a β-lactam antibiotic, is a broad-spectrum, second-generation cephalosporin. Cefoxitin has a broad spectrum antibacterial activity which includes anaerobic as well as Gram-positive and Gram-negative aerobic bacteria [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 35607-66-0. Pack Sizes: 10 mM * 1 mL; 100 mg. Product ID: HY-B1825.
Cefoxitin
United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards.
Cefoxitin EP Impurity C (Cefalotin Impurity D)
Cefoxitin EP Impurity C (Cefalotin Impurity D). Uses: For analytical and research use. Group: Impurity standards. CAS No. 10590-10-0. Molecular formula: C14H12N2O4S2. Mole weight: 336.39. Catalog: APB10590100.
Cefoxitin sodium
Cefoxitin is derived from cephamycin C, a semi-synthetic, broad-spectrum cepha antibiotic often grouped with the second-generation cephalosporins. Uses: Antibacterial. Synonyms: MK-306; MK 306; MK306; (6R,7S)-3-[[(Aminocarbonyl)oxy]methyl]-7-methoxy-8-oxo-7-[(2-thienylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic Acid Sodium Salt. Grades: ≥95%. CAS No. 33564-30-6. Molecular formula: C16H16N3NaO7S2. Mole weight: 449.43.
Cefoxitin sodium
Cefoxitin sodium (MK-306) is a cephamycin antibiotic, often grouped with the second generation cephalosporins, acts by interfering with cell wall synthesis, its activity spectrum includes a broad range of gram-negative and gram-positive bacteria. Uses: Scientific research. Group: Signaling pathways. Alternative Names: MK-306. CAS No. 33564-30-6. Pack Sizes: 10 mM * 1 mL; 250 mg. Product ID: HY-B1117.
Cefoxitin Sodium
Cefoxitin sodium is a cephalosporin antibiotic, which is produced by Streptomyceslactamdurans. It is a new class of antibiotics prepared by semi-synthesis. Its parent nucleus is similar to cephalosporin, and its antibacterial properties are similar. It is also traditionally included in the second generation of cephalosporins. CAS No. 33564-30-6. Product ID: PAP-0067. Molecular formula: C16H18N3NaO7S2. Category: Antibiotic. Product Keywords: Antibacterial, Anti-inflammatory and Antiviral Series; Cefoxitin Sodium; PAP-0067; Antibiotic; C16H18N3NaO7S2; 33564-30-6. Appearance: Neat. Standard: USP/EP. Color: White. EC Number: 251-574-6. Physical State: neat. Solubility: Very soluble in water, sparingly soluble in alcohol. Storage: 2-8°C. Applications: Strong antibacterial action, with high anti-β-lactamase properties. The antibacterial spectrum includes Escherichia coli, pneumobacter, indole-positive Proteus and Serratia, Klebsiella, influenzae, Salmonella, shigella, etc. Staphylococcus Chemicalbook and a variety of streptococcus also have a good effect. It is mainly used for respiratory tract infection, endocarditis, peritonitis, pyelonephritis, urinary tract infection, septicemia, bone, joint, skin and soft tissue infection caused by sensitive bacteria. Boiling Point: 843°C. Melting Point: >160°C.
Cefoxitin sodium salt
Cefoxitin sodium salt. Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 250mg, 1g, 5g. US Biological Life Sciences.
Worldwide
Cefoxitin sodium salt
1g Pack Size. Group: Antibiotics, Bioactive Small Molecules. Formula: C16H16N3NaO7S2. CAS No. 33564-30-6. Prepack ID 40351828-1g. Molecular Weight 449.44. See USA prepack pricing.