Fumonisin b1

CAS Number116355-83-0
Molecular FormulaC34H59NO15
Molecular Weight721.8
InChI KeyUVBUBMSSQKOIBE-DSLOAKGESA-N
LogP-0.5
Synonyms
  • fumonisin b1
  • 116355-83-0
  • fumonisin-B1
  • Macrofusine
  • 3ZZM97XZ32
  • 1,2,3-Propanetricarboxylic acid, 1,1'-[(1S,2R)-1-[(2S,4R,9R,11S,12S)-12-amino-4,9,11-trihydroxy-2-methyltridecyl]-2-[(1R)-1-methylpentyl]-1,2-ethanediyl] ester, (2R,2'R)-
  • fumonisin B(1)
  • FB1
  • (R)-3-Carboxy-pentanedioic acid mono-{(1S,3S,5R,10R,12S,13S)-13-amino-1-[(1R,2R)-1-((R)-3,4-dicarboxy-butyryloxy)-2-methyl-hexyl]-5,10,12-trihydroxy-3-methyl-tetradecyl} ester
  • Fumonisin B1 50 microg/mL in Acetonitrile/Water
  • UNII-3ZZM97XZ32
  • CCRIS 4433
  • HSDB 7077
  • NSC-629151
  • 1,2,3-PROPANETRICARBOXYLIC ACID, 1,1'-((1S,2R)-1-((2S,4R,9R,11S,12S)-12-AMINO-4,9,11-TRIHYDROXY-2-METHYLTRIDECYL)-2-((1R)-1-METHYLPENTYL)-1,2-ETHANEDIYL) ESTER, (2R,2'R)-
  • 1,2,3-Propanetricarboxylic acid, 1,1'-[1-(12-amino-4,9,11-trihydroxy-2-methyltridecyl)-2-(1-methylpentyl)-1,2-ethanediyl] ester, [2S-[1[1R*(S*),2S*(S*),2(S*)],2R*,4S*,9S*,11R*,12R*]]-; Fumonisin B1
  • NSC 629151
  • (2R,2'R)-2,2'-{[(5R,6R,7S,9S,11R,16R,18S,19S)-19-amino-11,16,18-trihydroxy-5,9-dimethylicosane-6,7-diyl]bis[oxy(2-oxoethane-2,1-diyl)]}dibutanedioic acid
  • FUMONISIN B1 [MI]
  • FUMONISIN B1 [IARC]
  • DTXSID6020644
  • SCHEMBL13555629
  • CHEBI:38221
  • Fumonisin B1, reference material
  • 19 - Fusarium mycotoxins in oats
  • GLXC-25523
  • HY-N6719
  • LMSP01080022
  • AKOS024457430
  • 1,2,3-Propanetricarboxylic acid, 1,1'-(1-(12-amino-4,9,11-trihydroxy-2-methyltridecyl)-2-(1-methylpentyl)-1,2-ethanediyl) ester
  • CS-0029116
  • Q63395324
  • Fumonisin B1 from Fusarium moniliforme, >=98% (HPLC)
  • Fumonisins B1 and B2 Mixture 50 ug/mL in Acetonitrile/Water
  • Fumonisins B1 and B2 Mixture 50 microg/mL in Acetonitrile/Water
  • (2R)-2-[2-[(5R,6R,7S,9S,11R,16R,18S,19S)-19-amino-6-[(3R)-3,4-dicarboxybutanoyl]oxy-11,16,18-trihydroxy-5,9-dimethylicosan-7-yl]oxy-2-oxoethyl]butanedioic acid
  • 1,1'-[(1S,2R)-1-[(2S,4R,9R,11S,12S)-12-Amino-4,9,11-trihydroxy-2-methyltridecyl]-2-[(1R)-1-methylpentyl]-1,2-ethanediyl-1,2,3-(2R,2'R)-propanetricarboxylic acid ester.
  • 1,2,3-Propanetricarboxylic acid, 1,1'-(1-(12-amino-4,9,11-trihydroxy-2-methyltridecyl)-2-(1-methylpentyl)-1,2-ethanediyl)ester

Applications:

HPLC Method for Analysis of Fumonisin B1 on Primesep 100 Column

October 6, 2023

HPLC Method for Analysis of Fumonisin b1 on Primesep 100 by SIELC Technologies

HPLC Method for Analysis of Fumonisin b1 on Primesep 100 Column by SIELC Technologies


 High Performance Liquid Chromatography (HPLC) Method for Analysis of  Fumonisin b1

Fumonisin B1 is a type of mycotoxin produced by Fusarium molds, particularly Fusarium verticillioides and Fusarium proliferatum. These molds commonly infect corn and other crops, and through these, fumonisin B1 can enter the food chain. This toxin is found worldwide, and it’s especially a concern in areas where corn is a staple food.

Fumonisin B1 is a notable mycotoxin due to its stability, widespread occurrence, and potential to cause harm to animals and humans. Monitoring and managing levels of this toxin in food products is essential to safeguard public and animal health.

Fumonisin B1 can be retained, and analyzed on a Primesep 100 mixed-mode stationary phase column using an isocratic analytical method with a simple mobile phase of water, Acetonitrile (MeCN), and a sulfuric acid as a buffer. This analysis method can be detected using UV at 210 nm.

ColumnPrimesep 100, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseMeCN/H2O
BufferH2SO4 -0.1%
Flow Rate1.0 ml/min
DetectionUV 210 nm

Class of Compounds
Drug
Analyzing CompoundsFumonisin b1

Application Column

Primesep 100

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Fumonisin b1
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.