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32928

Supelco

15-Acetyldeoxynivalenol

reference material

Sinonimo/i:

15-O-Acetyl-4-deoxynivalenol from Fusarium graminearum, 15-Acetoxy-3α,7α-dihydroxy-12,13-epoxytrichothec-9-en-8-one

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About This Item

Formula empirica (notazione di Hill):
C17H22O7
Numero CAS:
88337-96-6
Peso molecolare:
338.35
Numero MDL:
MFCD00083218
Codice UNSPSC:
85151701
ID PubChem:
329754392
NACRES:
NA.24

Grado

analytical standard
reference material

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

cleaning products
cosmetics
food and beverages
personal care

Formato

neat

Temperatura di conservazione

−20°C

Stringa SMILE

CC(=O)OC[C@]12[C@H](O)C(=O)C(C)=C[C@H]1O[C@@H]3[C@H](O)C[C@@]2(C)[C@]34CO4

InChI

1S/C17H22O7/c1-8-4-11-16(6-22-9(2)18,13(21)12(8)20)15(3)5-10(19)14(24-11)17(15)7-23-17/h4,10-11,13-14,19,21H,5-7H2,1-3H3/t10-,11-,13-,14-,15-,16-,17+/m1/s1
IDGRYIRJIFKTAN-HTJQZXIKSA-N

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Descrizione generale

15-Acetyldeoxynivalenols belong to the class of type B trichothecene mycotoxins, generated by several Fusarium fungi.[1]

Applicazioni

15-Acetyldeoxynivalenol may be used as an analytical reference standard for the determination of the analyte in:
  • Pig urine and maize samples by high performance liquid chromatography-mass spectrometry (HPLC-MS).[2]
  • Milk samples by liquid chromatography combined with tandem mass spectrometry (LC-MS/MS).[3]

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

Pittogrammi

Skull and crossbones
GHS06

Avvertenze

Danger

Indicazioni di pericolo

H300,H311 + H331

Classi di pericolo

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCCG8542
BCCF8385
BCCC8494
BCCB3659
BCBW5613

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HT-2 Toxin ≥98% (HPLC)

Sigma-Aldrich

T4138

HT-2 Toxin

Carnitina acetiltransferasi ammonium sulfate suspension, ≥50 units/mg protein

Sigma-Aldrich

C4899

Carnitina acetiltransferasi

Deoxynivalenol solution certified reference material, 200 μg/mL in ethyl acetate: methanol (95:5), ampule of 1 mL

Supelco

CRM46911

Deoxynivalenol solution

Determination of 12 type A and B trichothecenes in cereals by liquid chromatography- electrospray ionization tandem mass spectrometry.
Klotzel M, et al.
Journal of Agricultural and Food Chemistry, 53(23), 8904-8910 (2005)
Determination of mycotoxins in bovine milk by liquid chromatography tandem mass spectrometry.
S?rensen LK and Elb?k TH
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 820(2), 183-196 (2005)
Simultaneous determination of major B-trichothecenes and the de-epoxy-metabolite of deoxynivalenol in pig urine and maize using high-performance liquid chromatography-mass spectrometry.
Razzazi-Fazeli E, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 796(1), 21-33 (2003)
Sara C Cunha et al.
Journal of separation science, 33(4-5), 600-609 (2010-02-16)
A new analytical method for the rapid and simultaneous determination of five mycotoxins (zearelenone, deoxynivalenol, Fusarenon X, 15-acetyldeoxynivalenol and nivalenol) in breakfast cereals and flours by heart-cutting GC-MS has been developed and validated. Extraction was performed with MeCN, applying a
J Merhej et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 27(5), 710-717 (2010-02-20)
Reducing production of type B trichothecenes by Fusarium graminearum on cereals is necessary to control contamination, prevent yield reduction and protect human and animal health. Thus, an understanding of how trichothecene biosynthesis is induced is essential. The effect of ambient
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