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CEFADROXIL

CEFADROXIL Suppliers list
Company Name: Shaanxi TNJONE Pharmaceutical Co., Ltd
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Products Intro: Product Name:Cefadroxil Monohydrate
CAS:50370-12-2
Purity:99% Package:1Kg
Company Name: Hangzhou FandaChem Co.,Ltd.
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Email: FandaChem@Gmail.com
Products Intro: Product Name:Cefadroxil;BL-S 578
CAS:50370-12-2
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Products Intro: Product Name:CEFADROXIL
CAS:50370-12-2
Purity:99% Package:3KG;3USD
Company Name: Chongqing Chemdad Co., Ltd
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Products Intro: Product Name:CEFADROXIL
CAS:50370-12-2
Purity:0.98 Package:1kg,2kg,5kg,10kg,25kg
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:cefadroxil
CAS:50370-12-2
Purity:0.99 Package:1kg

CEFADROXIL manufacturers

  • Cefadroxil
  • Cefadroxil pictures
  • $36.00 / 100mg
  • 2024-11-05
  • CAS:50370-12-2
  • Min. Order:
  • Purity: 98.91%
  • Supply Ability: 10g
  • Cefadroxil
  • Cefadroxil pictures
  • $36.00 / 100mg
  • 2024-11-05
  • CAS:50370-12-2
  • Min. Order:
  • Purity: 98.91%
  • Supply Ability: 10g
  • Cefprozil Impurity B
  • Cefprozil Impurity B pictures
  • $0.00 / 10mg
  • 2024-04-10
  • CAS:50370-12-2
  • Min. Order: 10mg
  • Purity: 90%+
  • Supply Ability: 10g
CEFADROXIL Basic information
Product Name:CEFADROXIL
Synonyms:(6R,7R)-7-[(R)-2-AMINO-2-(4-HYDROXY-PHENYL)-ACETYLAMINO]-3-METHYL-8-OXO-5-THIA-1-AZA-BICYCLO[4.2.0]OCT-2-ENE-2-CARBOXYLIC ACID;CEFAMOX;(6r-(6-alpha,7-beta(r*)))-l)acetyl)amino)-3-methyl-8-oxo;P-HYDROXYCEPHALEXINE;5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylicacid,7-((amino(4-hydroxypheny;bidocef;bl-s578;oracefal
CAS:50370-12-2
MF:C16H17N3O5S
MW:363.39
EINECS:256-555-6
Product Categories:Active Pharmaceutical Ingredients;Alphabetic;C;CA - CGForensic and Veterinary Standards;Drugs&Metabolites;Neat Compounds;cephalosporins
Mol File:50370-12-2.mol
CEFADROXIL Structure
CEFADROXIL Chemical Properties
Melting point 197°C (rough estimate)
Boiling point 238°C (rough estimate)
density 1.59
refractive index 1.6390 (estimate)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
solubility Water:9.17(Max Conc. mg/mL);25.23(Max Conc. mM)
pka3.12±0.50(Predicted)
form powder or crystals
color White to off-white
InChIKeyBOEGTKLJZSQCCD-UEKVPHQBSA-N
CAS DataBase Reference50370-12-2
Safety Information
Hazard Codes Xn
Risk Statements 36/37/38-42/43
Safety Statements 26-36
WGK Germany 2
RTECS XI0337000
MSDS Information
ProviderLanguage
SigmaAldrich English
CEFADROXIL Usage And Synthesis
DescriptionCephadroxil is an orally administered antibiotic, which is very similar to cephalexin. After oral administration, its peak serum level is slightly lower than that of cephalexin, but it is excreted more slowly. Therefore, it can be used for oral administration at 8- or 12-hourly intervals (Buck and Price, 1977; Pfeffer et al., 1977). Cephadroxil is still available in a number of European countries (for example, Spain, Belgium, Luxembourg, Portugal, and Finland, among others).
Chemical PropertiesCefadroxil is a light orange colored powder. It is a cephalosporin antibiotic and is used for the treatment of bacterial infections. Cefadroxil is stable under recommended storage conditions. Cefadroxil is not considered hazardous when handled under normal medical conditions and with good housekeeping
OriginatorOracefal,Bristol,France,1977
UsesAntibacterial;Bacterial transpeptidase inhibitor
DefinitionChEBI: A cephalosporin bearing methyl and (2R)-2-amino-2-(4-hydroxyphenyl)acetamido groups at positions 3 and 7, respectively, of the cephem skeleton.
Manufacturing Process1.8 g of sodium N-(1-methoxycarbonyl-1-propen-2-yl)-D(-)-α-amino-(4- hydroxyphenyl)acetate was suspended in 10 ml of acetone, and one droplet of N-methylmorpholine was added thereto, and the mixture was cooled to -15°C.There was added 0.85 g of ethyl chlorocarbonate thereto, and the mixture was reacted at -13°C to -10°C for 30 minutes, and then the reaction solution was cooled to -20°C.
On the other hand, 1 g of 7-amino-3-methyl-3-cephem-4-carboxylic acid was suspended in 20 ml of methanol, and 1.4 g of triethylamine was added thereto to be dissolved, and 0.4 ml of acetic acid was further added thereto. This solution was cooled to -20°C and the mixed acid anhydride prepared previously was added thereto. After the mixture was reacted at -20°C for 1 hour, the temperature of the reaction mixture was raised to 0°C over a period of 1 hour, and the mixture was reacted for 3 hours at the same temperature.
After the reaction, 1 ml of water was added to the reaction mixture, and the mixture was adjusted to a pH of 1.0 with concentrated hydrochloric acid while being cooled, and then stirred for 30 minutes, The insoluble matters were filtered off, and the filtrate was adjusted to a pH of 5.5 with triethylamine. This solution was concentrated under reduced pressure, and the residue was diluted with 20 ml of acetone to precipitate white crystals. The crystals were collected by filtration and washed with ethanol to obtain 1.46 g of white crystals of 7-[D(-)-α-amino-(4-hydroxyphenyl)acetamido]-3-methyl-3- cephem-4-carboxylic acid having a decomposition point of 197°C.
Therapeutic FunctionAntibacterial
Health HazardExposures to cefadroxil cause certain common side effects. These include nausea, vomiting, stomach disorders, rashes, itching, unusual tiredness or weakness, yellowing of the skin or eyes, red, swollen, or blistered skin, unusual bruising or bleeding, sore throat, respiratory distress, tightness in the chest, swelling of the mouth, face, lips, or tongue, decreased urination, dark urine, vaginal itching, odor, or discharge, fever, chills, joint pain, and seizures. Prolonged or long-term use of cefadroxil should be avoided.
PrecautionsCefadroxil should be used only under proper medical health care since it has properties of penicillin allergy, renal function, gastrointestinal tract damage. Pregnant women and breast-feeding women should avoid exposure to cefadroxil.
CEFADROXIL Preparation Products And Raw materials
Raw materials7-Amino-3-methyl-3-cephem-4-carboxylic acid-->Ethyl chloroformate
Preparation Products3-Hydroxy-4-Methyl-2(5H)-thiophenone
Tag:CEFADROXIL(50370-12-2) Related Product Information
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