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32943

Supelco

Deoxynivalenol

reference material

Synonym(s):

3α,7α,15-Trihydroxy-12,13-epoxytrichothec-9-en-8-one, Vomitoxin

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About This Item

Empirical Formula (Hill Notation):
C15H20O6
CAS Number:
Molecular Weight:
296.32
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard
reference material

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

neat

storage temp.

−20°C

SMILES string

[H][C@]12O[C@]3([H])[C@H](O)C[C@@](C)([C@]34CO4)[C@@]1(CO)[C@H](O)C(=O)C(C)=C2

InChI

1S/C15H20O6/c1-7-3-9-14(5-16,11(19)10(7)18)13(2)4-8(17)12(21-9)15(13)6-20-15/h3,8-9,11-12,16-17,19H,4-6H2,1-2H3/t8-,9-,11-,12-,13-,14-,15+/m1/s1

InChI key

LINOMUASTDIRTM-QGRHZQQGSA-N

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General description

Deoxynivalenol belongs to the class of type B trichothecene mycotoxins typically produced by the species of Fusarium genus.[1] It is cytotoxic and is known to hinder the macromolecular synthesis.[2]

Application

Deoxynivalenol may be used as a reference standard for the determination of the analyte in:
  • Cereals by high performance liquid chromatography-mass spectrometry (HPLC-MS),[1] ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS)[3] and HPLC-MS/MS.[4]
  • Biological fluidsby HPLC coupled to diode array detector (DAD)[5]and LC-MS/MS.[6]
  • Eggs by HPLC with ultraviolet (UV) detection.[7]

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Skull and crossbones

signalword

Danger

hcodes

Hazard Classifications

Acute Tox. 2 Oral

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Masked mycotoxins: determination of a deoxynivalenol glucoside in artificially and naturally contaminated wheat by liquid chromatography- tandem mass spectrometry.
Berthiller F, et al.
Journal of Agricultural and Food Chemistry, 53(9), 3421-3425 (2005)
Analysis of deoxynivalenol and de-epoxy-deoxynivalenol in animal tissues by liquid chromatography after clean-up with an immunoaffinity column.
Valenta H, et al.
Mycotoxin Research, 19(1), 51-51 (2003)
Study on the transmission of deoxynivalenol and de-epoxy-deoxynivalenol into eggs of laying hens using a high-performance liquid chromatography-ultraviolet method with clean-up by immunoaffinity columns.
Valenta H and Danicke S
Molecular Nutrition And Food Research, 49(8), 779-785 (2005)
Quantitative determination of T-2 toxin, HT-2 toxin, deoxynivalenol and deepoxy-deoxynivalenol in animal body fluids using LC-MS/MS detection.
De Baere S, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 879(24), 2403-2415 (2011)
Determination of nivalenol and deoxynivalenol in wheat using liquid chromatography-mass spectrometry with negative ion atmospheric pressure chemical ionisation.
Razzazi-Fazeli E, et al.
Journal of Chromatography A, 854(1-2), 45-55 (1999)

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