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Supelco

15-Acetyldeoxynivalenol

reference material

Synonym(s):

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

Empirical Formula (Hill Notation):
C17H22O7
CAS Number:
Molecular Weight:
338.35
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

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

InChI key

IDGRYIRJIFKTAN-HTJQZXIKSA-N

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General description

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

Application

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).
  • Milk samples by liquid chromatography combined with tandem mass spectrometry (LC-MS/MS).

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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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)
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)
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)
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
Nadia Ponts et al.
FEBS letters, 581(3), 443-447 (2007-01-26)
Effect of exogenous H(2)O(2) and catalase was tested in liquid cultures of the deoxynivalenol and 15-acetyldeoxynivalenol-producing fungus Fusarium graminearum. Accordingly to previous results, H(2)O(2) supplementation of the culture medium leads to increased toxin production. This study indicates that this event

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