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IRMM315

4-Deoxynivalenol in acetonitrile

IRMM®, certified reference material

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Synonym(s):
Deoxynivalenol solution, 3α,7α,15-Trihydroxy-12,13-epoxytrichothec-9-en-8-one, DON, Vomitoxin
Empirical Formula (Hill Notation):
C15H20O6
CAS Number:
Molecular Weight:
296.32
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material

agency

IRMM®

manufacturer/tradename

JRC

application(s)

general analytical

format

matrix material

storage temp.

2-8°C

SMILES string

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

InChI key

LINOMUASTDIRTM-QGRHZQQGSA-N

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This Item
CRM4691134124SML1664
vibrant-m

IRMM315

4-Deoxynivalenol in acetonitrile

vibrant-m

CRM46911

Deoxynivalenol solution

vibrant-m

34124

Deoxynivalenol solution

application(s)

general analytical

application(s)

cleaning products
cosmetics
food and beverages
personal care

application(s)

cleaning products
cosmetics
food and beverages
personal care

application(s)

-

storage temp.

2-8°C

storage temp.

-10 to -25°C

storage temp.

−20°C

storage temp.

−20°C

grade

certified reference material

grade

certified reference material, TraceCERT®

grade

analytical standard

grade

-

manufacturer/tradename

JRC

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

-

agency

IRMM®

agency

-

agency

-

agency

-

General description

Analysis Note

For more information please see:
IRMM315

Legal Information

IRMM is a registered trademark of European Commission

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

35.6 °F - closed cup

flash_point_c

2.0 °C - closed cup


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Brenna M Flannery et al.
Toxicology, 304, 192-198 (2013-01-10)
Consumption of the trichothecene deoxynivalenol (DON) suppresses growth in experimental animals - an adverse effect that was used to establish the tolerable daily intake for this toxin. DON ingestion has been recently found to suppress plasma insulin-like growth factor acid-labile
Amal Halawa et al.
Archives of animal nutrition, 67(2), 134-146 (2013-03-26)
Deoxynivalenol (DON) is one of the most important trichothecenes, due to its worldwide distribution and common contamination of animal feed. It mainly affects the gastrointestinal tract and the immune system with a high susceptibility for swine. Lipopolysaccharides (LPS) are endotoxins
Sven Dänicke et al.
Toxicology letters, 220(2), 172-180 (2013-04-23)
The systemic effects of the Fusarium toxin deoxynivalenol (DON) and of bacterial lipopolysaccharides (LPS) were studied in male castrated pigs (40.4 ± 3.7 kg) infused intravenously with either DON or LPS alone (100 μg DON/kg/h, 7.5 μg/LPS/kg/h), or together (100
Silvia W Gratz et al.
Applied and environmental microbiology, 79(6), 1821-1825 (2013-01-15)
Deoxynivalenol (DON) is a potent mycotoxin produced by Fusarium molds and affects intestinal nutrient absorption and barrier function in experimental and farm animals. Free DON and the plant metabolite DON-3-β-d-glucoside (D3G) are frequently found in wheat and maize. D3G is
Joice Sifuentes dos Santos et al.
Food chemistry, 138(1), 90-95 (2012-12-26)
The occurrence of deoxynivalenol (DON) was evaluated in 113 wheat samples from the northern and central/southwestern regions of Paraná State, Brazil during the 2008 and 2009 growing seasons, and this rate of occurrence was used to estimate the DON dietary

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