Tetracycline

Tetracycline structural formula

CAS Number60-54-8
Molecular FormulaC22H24N2O8
Molecular Weight444.440
InChI KeyOFVLGDICTFRJMM-WESIUVDSSA-N
LogP-1.30
Synonyms
  • Tetracycline
  • (4S,4aS,5aS,6S,12aS)-4-(Dimethylamino)-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide
  • 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, (4S,4aS,5aS,6S,12aS)-
  • 60-54-8
  • 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, (4S,4aS,5aS,6S,12aS)-
  • (-)-Tetracycline
  • 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-
  • 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, [4S-(4α,4aα,5aα,6β,12aα)]-
  • 6-Methyl-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-1,11-dioxo-2-naphthacenecarboxamide
  • Abramycin
  • Achromycin
  • Acromicina
  • Actisite
  • Agromicina
  • Akne-Pyodron
  • Akne-Pyodron Kur
  • Ambramicina
  • Ambramycin
  • Apo-Tetra
  • Arcanacycline
  • Biocycline
  • Bio-Tetra
  • Britaciclina
  • Calociclina
  • Ciclibion
  • Cyclomycin
  • Deschlorobiomycin
  • Dispatetrin
  • Economycin
  • Enterocycline
  • Florocycline
  • Gammatet
  • Kinciclina
  • Latycin
  • Limecycline
  • Medocycline
  • Mericycline
  • Micycline
  • Neocycline
  • Novo-Tetra
  • NSC 108579
  • Nu-Tetra
  • Omegamycin
  • Orlycycline
  • Panmycin
  • Polycycline
  • Quimocyclin N
  • Quimpe Antibiotico
  • Resteclin
  • Robitet Robicaps
  • Roviciclina
  • Sagittacin N
  • Servitet
  • Spaciclina
  • Steclin V
  • Sumycin syrup
  • Tetra Hubber
  • Tetrabioptal
  • tetraciclina
  • Tetracitro S
  • Tetra-Co
  • Tetracyclin
  • Tetradecin
  • Tetrafil
  • Tetrafosammina
  • Tetralan
  • Tetralen
  • Tetramig
  • Tetramykoin
  • Tetra-Proter
  • Tetraseptine
  • Triphacycline
  • Veracin
  • Vetacyclinum
  • Cefracycline suspension
  • Copharlan
  • Democracin
  • 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,1 0,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide
  • EINECS 200-481-9
  • Lexacycline
  • 6-Methyl-1,11-dioxy-2-naphthacenecarboxamide
  • Polyotic
  • SK-Tetracycline
  • Solvocin
  • Tetracycline I
  • Tetracycline II
  • Tetraverine
  • Tsiklomistsin
  • Tetracyclinum
  • UNII-F8VB5M810T
  • (4S,4aS,5aS,12aS)-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide
  • Deschlorobiomycin
  • Liquamycin
  • Tetrazyklin
  • Tsiklomitsin
  • tetracycline zwitterion
  • 6591-49-7
  • 929020-51-9
  • 1172112-85-4

Applications:

HPLC Method For Analysis Of  Tetracycline on Primesep 100 Column

August 9, 2021

Separation type: Liquid Chromatography Mixed-mode

 

 

High Performance Liquid Chromatography (HPLC) Method for Analysis of Tetracycline

Tetracycline is a broad spectrum antibiotic, that is, it is active against many different types of bacteria. It is effective against Chlamydia psittaci, Neisseria gonorrhoeae, Haemophilus influenzae, Streptococcus pneumoniae, Mycoplasma pneumoniae, Chlamydia trachomatis, and others. Tetracycline prevents the growth of bacteria by preventing the bacteria from manufacturing proteins they need to survive. Tetracycline can be retained on the Primesep 100 mixed-mode column using an isocratic analytical method with a simple mobile phase of water, acetonitrile (MeCN, ACN), and sulphuric acid (H2SO4) buffer. The analysis method can be UV detected at 200 nm.

 

Condition

Column Primesep 100, 4.6×150 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 50/50%
Buffer H2SO4 – 0.5%
Flow Rate 1.0 ml/min
Detection UV, 200 nm

 

Description

Class of Compounds
Drug, Antibiotics
Analyzing Compounds Tetracycline

 

Application Column

Primesep 100

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

Select options
Application Analytes:
Tetracycline
Tetracycline hydrochloride
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

Separation of Antibiotics in Mixed-mode chromatography

May 11, 2015

 

A complex mixture of sulphonamide, macrolide, tetracycline and fluoroquinolone antibiotics were separated in one run using mixed-mode chromatography with LC/MS -compatible conditions. All compounds are separated based on reversed-phase and/or ion-exchange mechanism. Method can be used for analysis of various classes of antibiotics and related impurities in different sample matrices (blood, urine, soil, waste water).

 

Condition

Column Obelisc R, 2.1×150 mm, 5 µm, 100A
Mobile Phase Gradient MeCN – 0-25%, 6 min, 25-70% 14 min
Buffer Gradient Formic Acid – 0.05%-0.3%, 10 min, 14 min hold
Flow Rate 1.0 ml/min
Detection UV, 270 nm

 

Description

Class of Compounds
 Antibiotic, Drug, Hydrophobic, Ionizable
Analyzing Compounds Sulphanilamide, Sulphaguanidine, Oxytetracycline, Marbofloxacin, Sulphadiazine, Chlortetracycline, Nofloxacin, Spiramycin, Cefalonium, Tylosin, Josamycin, Sulphamethoxazole, Dapsone, Sulphaquinoxalline, Flumequine

 

Application Column

Obelisc R

SIELC has developed the Obelisc™ columns, which are mixed-mode and utilize Liquid Separation Cell technology (LiSC™). These cost-effective columns are the first of their kind to be commercially available and can replace multiple HPLC columns, including reversed-phase (RP), AQ-type reversed-phase, polar-embedded group RP columns, normal-phase, cation-exchange, anion-exchange, ion-exclusion, and HILIC (Hydrophilic Interaction Liquid Chromatography) columns. By controlling just three orthogonal method parameters - buffer concentration, buffer pH, and organic modifier concentration - users can adjust the column properties with pinpoint precision to separate complex mixtures.

Select options
Application Analytes:
Carboxymethylcysteine
Chlortetracycline
Dapsone
Flumequine
Josamycin
Marbofloxacin
Norfloxacin
Oxytetracycline
Spiramycin
Sulfamethoxazole
Sulfonamides
Sulphadiazine
Sulphaguanidine
Sulphanilamide
Sulphaquinoxaline
Tetracycline
Tylosin

Application Detection:
ELSD Detection
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Separation of Tetracyclines

November 21, 2010


Tetracyclines are a group of broad spectrum of antibiotics. Structure can be described as derivatives of polycyclic naphthacene carboxamide. Tetracyclines are hydrophilic and basic compounds due to the presence of hydroxyls and amino group. Mixture of tetracyclines and their impurities were separated based on weak reversed-phase and strong cation-exchange mechanisms on a Primesep 200 mixed-mode HPLC column. Elution of compounds was monitored by UV.

Application Column

Primesep 200

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

Select options
Application Analytes:
Tetracycline

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.