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Deoxynivalenol

MSDSSample CoA
 
Source: Deoxynivalenol is derived from Fusarium sp.
SynonymsRd toxin, Vomitoxin, deoxynivalenol,
4-Deoxynivalenol, Dehydronivalenol, 4-Desoxynivalenol,
Description: Deoxynivalenol (DON , Vomitoxin) is a type B trichothecene. It occurs in grains such as wheat, barley, oats, rye, and maize, rice, sorghum. Deoxynivalenol (DON ) is produced by numerous strains of Fusarium and some other fungi. Deoxynivalenol (DON )  poisonings occur both in humans and farm animals.
Deoxynivalenol (DON ) is highly toxic, producing a wide range of immunological disturbances and is particularly noted for inducing feed refusal and emesis in pigs, hence the alternative name vomitoxin
Deoxynivalenol (DON ) usually co-occures with other Fusarium toxins, such as Zearalenone, Nivalenol and its derivates,  as well as the group of fumonisins.
CAS number: 51481-10-8
Merck index: 13,10092
Molecular weight: 296.3
Structure:

Deoxynivalenol (vomitoxin, DON)

 

Molecular Formula: C15H20O6
Solubility
information:
Deoxynivalenol (DON ) is soluble in common polar organic solvents as acetonitrile, methanol and ethyl acetate, slightly soluble in water.
Specifications 
Appearance: White crystalline solid.
Purity: At least 98% by TLC
λmax: 
Melting point151-153°C
Solubility 
StorageStore as supplied, at 4°C.
Acetonitrile solution of Deoxynivalenol (DON) has been reported stable for 24 month at room temperature. (Widestrand J.; Pettersson H., Food Addit Contam. 2001 Nov;18(11):987-92),
Classification trichothecene mycotoxin
ApplicationsThe main toxic effect of Deoxynivalenol (DON ) is inhibition of protein synthesis via binding to the ribosome.
Warningsdeoxynivalenol - vomitoxin - is toxicToxic mycotoxin. LD50 = 46 mg/kg (oral, mice). DON has not been reported as  having carcinogenic, teratogenic or mutagenic properties.
Classificationtrichothecene mycotoxin
Related products
  Zearalenone   Fumonisin_B1    DON     3-acetyl-DON

 For Research use only. Not for Human or Drug use
GMP/API grade available on request

No genetically modified organisms are used.
PublicationsPestka J, Zhou HR.
Toll-Like Receptor Priming Sensitizes Macrophages to Proinflammatory Cytokine Gene Induction by deoxynivalenol (DON)   and Other Toxicants.
Toxicol Sci. 2006 May 9
 Quarta A, Mita G, Haidukowski M, Logrieco A, Mule G, Visconti A.
Multiplex PCR assay for the identification of nivalenol, 3- and 15-acetyl-deoxynivalenol (15ADON)   chemotypes in Fusarium.
FEMS Microbiol Lett. 2006 Jun;259(1):7-13.
 Hajjaji A, El Otmani M, Bouya D, Bouseta A, Mathieu F, Collin S, Lebrihi A.
Occurrence of mycotoxins: ochratoxin A, deoxynivalenol (DON)   and toxigenic fungi in Moroccan wheat grains: impact of ecological factors on the growth and ochratoxin A production.
Mol Nutr Food Res. 2006 May 5
 Ngundi MM, Qadri SA, Wallace EV, Moore MH, Lassman ME, Shriver-Lake LC, Ligler FS, Taitt CR.
Detection of deoxynivalenol (DON)   in foods and indoor air using an array biosensor.
Environ Sci Technol. 2006 Apr 1;40(7):2352-6.
 Ponts N, Pinson-Gadais L, Verdal-Bonnin MN, Barreau C, Richard-Forget F.
Accumulation of deoxynivalenol (DON)   and its 15-acetylated form is significantly modulated by oxidative stress in liquid cultures of Fusarium graminearum.
FEMS Microbiol Lett. 2006 May;258(1):102-7
 Sugita-Konsihi Y, Tanaka T, Tabata S, Nakajima M, Nouno M, Nakaie Y, Chonan T, Aoyagi M, Kibune N, Mizuno K, Ishikuro E, Kanamaru N, Minamisawa M, Aita N, Kushiro M, Tanaka K, Takatori K.
Validation of an HPLC analytical method coupled to a multifunctional clean-up column for the determination of deoxynivalenol (DON) .
Mycopathologia. 2006 Apr;161(4):239-43
 Bretz M, Beyer M, Cramer B, Humpf HU.
Stable isotope dilution analysis of the Fusarium mycotoxins deoxynivalenol (DON)   and 3-acetyldeoxynivalenol (DON) .
Mol Nutr Food Res. 2006 Mar;50(3):251-60
 Cetin Y, Bullerman LB.
Confirmation of reduced toxicity of deoxynivalenol (DON)   in extrusion-processed corn grits by the MTT bioassay.
J Agric Food Chem. 2006 Mar 8;54(5):1949-55.
 Goyarts T, Danicke S, Tiemann U, Rothkotter HJ.
Effect of the Fusarium toxin deoxynivalenol (DON) on IgA, IgM and IgG concentrations and proliferation of porcine blood lymphocytes.
Toxicol In Vitro. 2006 Feb 8
 Lemmens M, Scholz U, Berthiller F, Dall'Asta C, Koutnik A, Schuhmacher R, Adam G, Buerstmayr H, Mesterhazy A, Krska R, Ruckenbauer P.
The ability to detoxify the mycotoxin deoxynivalenol (DON)   colocalizes with a major quantitative trait locus for Fusarium head blight resistance in wheat.
Mol Plant Microbe Interact. 2005 Dec;18(12):1318-24
 Sergent T, Parys M, Garsou S, Pussemier L, Schneider YJ, Larondelle Y.
deoxynivalenol (DON)   transport across human intestinal Caco-2 cells and its effects on cellular metabolism at realistic intestinal concentrations.
Toxicol Lett. 2006 Jul 1;164(2):167-76. Epub 2006 Jan 25.
 Jia Q, Zhou HR, Shi Y, Pestka JJ.
Docosahexaenoic acid consumption inhibits deoxynivalenol (DON) -induced CREB/ATF1 activation and IL-6 gene transcription in mouse macrophages.
J Nutr. 2006 Feb;136(2):366-72.
 Awad WA, Bohm J, Razzazi-Fazeli E, Zentek J.
Effects of feeding deoxynivalenol (DON)   contaminated wheat on growth performance, organ weights and histological parameters of the intestine of broiler chickens.
J Anim Physiol Anim Nutr (Berl). 2006 Feb;90(1-2):32-7.
 Gouze ME, Laffitte J, Dedieu G, Galinier A, Thouvenot JP, Oswald IP, Galtier P.
Individual and combined effects of low oral doses of deoxynivalenol (DON)  and nivalenol in mice.
Cell Mol Biol (Noisy-le-grand). 2005 Nov 4;51 Suppl:OL809-17
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Standard solutions

 Deoxynivalenol solution




Deoxynivalenol
(DON , Vomitoxin)
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