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IRMM315

4-Deoxynivalenol in acetonitrile

IRMM®, certified reference material

Synonyme(s) :

Deoxynivalenol solution

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About This Item

Formule empirique (notation de Hill):
C15H20O6
Numéro CAS:
51481-10-8
Poids moléculaire :
296.32
Numéro CE :
200-835-2
Numéro MDL:
MFCD09039270
Code UNSPSC :
41116107
ID de substance PubChem :
329815693
Nomenclature NACRES :
NA.24

Qualité

certified reference material

Agence

IRMM®

Fabricant/nom de marque

JRC

Application(s)

general analytical

Format

matrix material

Température de stockage

2-8°C

Chaîne SMILES 

CC1=C[C@H]2O[C@@H]3[C@H](O)C[C@@](C)([C@]34CO4)[C@@]2(CO)[C@H](O)C1=O

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

Clé InChI

LINOMUASTDIRTM-QGRHZQQGSA-N

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Description générale

Check out our entire range of trichothecene type mycotoxin reference materials

Remarque sur l'analyse

For more information please see:
IRMM315

Informations légales

IRMM is a registered trademark of European Commission

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

35.6 °F - closed cup

Point d'éclair (°C)

2.0 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number

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Dirk Rohweder et al.
Archives of animal nutrition, 67(1), 37-47 (2013-01-23)
Fusarium infections do not only affect the grain, but also the rest of the plant, which result in contamination of plants with the mycotoxin deoxynivalenol (DON). The bioavailability of DON may be influenced by the matrix due to the differences
Joelma Lucioli et al.
Toxicon : official journal of the International Society on Toxinology, 66, 31-36 (2013-02-14)
Trichothecenes induce changes in the intestinal barrier function through decreased expression of cell junction proteins and apoptosis of enterocytes. The mitogen activated protein kinases (MAPK) play an important role in the signaling pathways of cell turnover and differentiation. Using ex
Patricia M Cano et al.
PloS one, 8(1), e53647-e53647 (2013-01-18)
Deoxynivalenol (DON) is a mycotoxin produced by Fusarium species which is commonly found in temperate regions worldwide as a natural contaminant of cereals. It is of great concern not only in terms of economic losses but also in terms of
Stephen N Wegulo
Toxins, 4(11), 1157-1180 (2012-12-04)
Deoxynivalenol (DON) is a mycotoxin produced by the plant pathogenic fungi Fusarium graminearum and F. culmorum. These and other closely related fungi cause a disease known as Fusarium head blight (FHB) in small grain cereals. Other mycotoxins produced by FHB-causing
Yuqin Li et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 30(2), 356-364 (2012-12-05)
The mechanism of interaction between deoxynivalenol (DON) and human serum albumin (HSA) was studied using spectroscopic methods including fluorescence spectra, UV-VIS, Fourier transform infrared (FT-IR) and circular dichroism (CD). The quenching mechanism was investigated in terms of the association constants
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