Doxycycline

Doxycycline structural formula

CAS Number564-25-0
Molecular FormulaC22H24N2O8
Molecular Weight444.441
InChI KeyJBIWCJUYHHGXTC-AKNGSSGZSA-N
LogP-0.0200
Synonyms
  • Doxycycline
  • (4S,4aR,5S,5aR,6R,12aS)-4-(Dimethylamino)-3,5,10,12,12a-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-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, (4S,4aR,5S,5aR,6R,12aS)-
  • 564-25-0
  • DOX
  • DOXY
  • 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, (4S,4aR,5S,5aR,6R,12aS)-
  • 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-
  • 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, [4S-(4?,4a?,5?,5a?,6?,12a?)]-
  • 4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide
  • 5-Hydroxy-?-6-deoxytetracycline
  • 6-Deoxy-5-hydroxytetracycline
  • 6-Deoxyoxytetracycline
  • Dentistar
  • Deoxycycline
  • Deoxymykoin
  • doxiciclina
  • Doximal
  • Doxinyl
  • Doxivetin
  • Doxycen
  • Doxycyclin
  • Doxytetracycline
  • Hydramycin
  • Liviatin
  • Medeomycin
  • Monodox
  • Oxytetracycline, 6-deoxy-
  • Pulmodox
  • Ronaxan
  • Tolexine
  • Vibramycin
  • Vibramycine
  • Vibranos SF
  • Vibraveineuse
  • Vibravenos
  • ?-6-Deoxy-5-hydroxytetracycline
  • ?-6-Deoxyoxytetracycline
  • ?-Doxycycline
  • Azudoxat
  • alpha-6-Deoxy-5-hydroxytetracycline
  • alpha-6-Deoxyoxytetracycline
  • 6-alpha-Deoxy-5-oxytetracycline
  • 6-Deoxytetracycline
  • Doxitard
  • Doxy-Caps
  • Doxy-Puren
  • Doxy-Tabs
  • EINECS 209-271-1
  • 5-Hydroxy-alpha-6-deoxytetracycline
  • Investin
  • alpha-Doxycycline
  • Doxychel
  • Dossiciclina
  • Doxycyclinum
  • UNII-334895S862
  • Doxysol
  • 6alpha-deoxy-5-oxytetracycline
  • doxycycline (anhydrous)

Applications:

HPLC Method For Analysis Of Ivermectin and Doxycycline on Primesep 100 Column

August 31, 2021

Separation type: Liquid Chromatography Mixed-mode


HPLC.cloud
View on hplc.cloud

 

High Performance Liquid Chromatography (HPLC) Method for Analysis of Ivermectin and Doxycycline

vIvermectin is an anti-parasitic drug that is often used to treat or prevent parasites in animals and humans. Ivermectin and Doxycycline can be retained and separated 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 250 nm.

 

Ivermectin and Doxycycline can be retained and separated 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 250 nm.

Condition
Column Primesep 100, 4.6×150 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 65/35%
Buffer H2SO4
Flow Rate 1.0 ml/min
Detection UV, 250 nm

 

Description
Class of Compounds
 Drug, Antibiotics
Analyzing Compounds Ivermectin,  Doxycycline

 

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:
Doxycycline
Ivermectin B1a
Ivermectin B1b
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 Doxycycline on Newcrom R1 HPLC column

February 16, 2018
Separation of Doxycycline on Newcrom C18 HPLC column

Doxycycline can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains an acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particles columns available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation impurities in preparative separation. It also suitable for pharmacokinetics.

Application Column

Newcrom R1

The Newcrom columns are a family of reverse-phase-based columns. Newcrom A, AH, B, and BH are all mixed-mode columns with either positive or negative ion-pairing groups attached to either short (25 Å) or long (100 Å) ligand chains. Newcrom R1 is a special reverse-phase column with low silanol activity.

Select options
Application Analytes:
Doxycycline
The result was obtained by a proprietary SIELC algorithm. It may deviate from the actual experimental data. The experimental data are available upon request. Contact us by e-mail: support@sielc.com or by phone: 847-229-2629.