Fentanyl

Fentanyl structural formula

CAS Number437-38-7
Molecular FormulaC22H28N2O
Molecular Weight336.480
InChI KeyPJMPHNIQZUBGLI-UHFFFAOYSA-N
LogP4.05
Synonyms
  • Fentanyl
  • N-Phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide
  • Propanamide, N-phenyl-N-[1-(2-phenylethyl)-4-piperidinyl]-
  • 437-38-7
  • 5-22-08-00049
  • Propanamide, N-phenyl-N-[1-(2-phenylethyl)-4-piperidinyl]-
  • 1-Phenethyl-4-(N-phenylpropionamido)piperidine
  • 1-Phenethyl-4-N-propionylanilinopiperidine
  • Durogesic
  • Fentanest
  • Fentanil
  • fentanila
  • Fentora
  • N-[1-(2-Phenylethyl)-4-piperidinyl]propionanilide
  • Phentanyl
  • Propionanilide, N-(1-phenethyl-4-piperidyl)-
  • Sublimase
  • BRN 0494484
  • EINECS 207-113-6
  • Fentanylum
  • N-(1-Phenethyl-4-piperidinyl)-N-phenylpropionamide
  • N-Phenyl-N-(1-(2-phenylethyl)-4-piperidinyl)propanamide
  • Sentonil
  • Duragesic-100
  • Duragesic-12
  • Duragesic-25
  • Duragesic-50
  • Duragesic-75
  • Fentanyl-100
  • Fentanyl-12
  • Fentanyl-25
  • Fentanyl-50
  • Fentanyl-75
  • UNII-UF599785JZ
  • Matrifen
  • Fentanyl Transdermal System
  • Fentanyl buccal
  • Durotep MT
  • Lazanda
  • N-(1-Phenethyl-piperidin-4-yl)-N-phenyl-propionamide
  • N-(1-phenethyl-4-piperidinyl)-N-phenylpropionamide
  • N-(1-phenethyl-4-piperidyl)propionanilide
  • N-(1-phenethylpiperidin-4-yl)-N-phenylpropionamide
  • N-phenethyl-4-(N-propionylanilino)piperidine
  • N-phenyl-N-(1-(2-phenylethyl)-4-piperidinyl)propanamide

Applications:

HPLC Determination of Fentanyl on Primesep 200 Column

March 29, 2019

HPLC Determination of Fentanyl

 

Condition
Column Primesep 200, 4.6×150 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 60/40%
Buffer H3PO4 – 0.1 %
Flow Rate 1.0 ml/min
Detection UV, 200 nm

 

Description
Class of compounds
 Narcotic, Drug, Basic, Hydrophobic, Ionizable, Zwitterionic
Analyzing Compounds Fentanyl

 

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.

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Application Analytes:
Fentanyl
Fentanyl citrate
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 Fentanyl on Newcrom R1 HPLC column

May 16, 2018
Separation of Fentanyl on Newcrom R1 HPLC column

Fentanyl 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.

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Application Analytes:
Fentanyl
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.