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34131

Supelco

Nivalenol solution

100 μg/mL in acetonitrile, analytical standard

Sinônimo(s):

3α,4β,7α, 15-Tetrahydroxy-12,13-epoxytrichothec-9-en-8-one, NIV

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About This Item

Fórmula empírica (Notação de Hill):
C15H20O7
Número CAS:
23282-20-4
Peso molecular:
312.32
Número CE:
200-835-2
Número MDL:
MFCD00133673
Código UNSPSC:
85151701
ID de substância PubChem:
329754837
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

prazo de validade

limited shelf life, expiry date on the label

concentração

100 μg/mL in acetonitrile

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

aplicação(ões)

cleaning products
cosmetics
food and beverages
personal care

Formato

single component solution

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

[H][C@]12O[C@]3([H])[C@H](O)[C@@H](O)[C@@](C)([C@]34CO4)[C@@]1(CO)[C@H](O)C(=O)C(C)=C2

InChI

1S/C15H20O7/c1-6-3-7-14(4-16,11(20)8(6)17)13(2)10(19)9(18)12(22-7)15(13)5-21-15/h3,7,9-12,16,18-20H,4-5H2,1-2H3/t7-,9-,10-,11-,12-,13-,14-,15+/m1/s1

chave InChI

UKOTXHQERFPCBU-XBXCNEFVSA-N

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Descrição geral

Certan Vial
Nivalenol is a potential trichothecene mycotoxin, produced by Fusarium nivale., Genotoxicity of nivalenol is evaluated by alkaline single-cell gel electrophoresis assay.
Nivalenol is a secondary metabolite produced by Fusarium species, which is a plant pathogenic fungus of wheat and other cereals.

Aplicação

Nivalenol was used as standard to investigate in vitro mycotoxin binding of deoxynivalenol and nivalenol by adsorbent materials (activated carbon).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogramas

FlameExclamation mark
GHS02,GHS07

Palavra indicadora

Danger

Classificações de perigo

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

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

35.6 °F - closed cup

Ponto de fulgor (°C)

2 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análise (COA)

Lot/Batch Number
BCCJ3937
BCCH9883
BCCH4034
BCCG5948
BCCG2756

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HT-2 Toxin solution 100 μg/mL in acetonitrile, analytical standard

Supelco

34136

HT-2 Toxin solution

Deoxynivalenol

Sigma-Aldrich

D0156

Deoxynivalenol

Diacetoxyscirpenol solution ~100 μg/mL in acetonitrile, analytical standard

Supelco

34137

Diacetoxyscirpenol solution

T2-Toxin solution 100 μg/mL in acetonitrile, analytical standard

Supelco

34071

T2-Toxin solution

15-O-Acetyl-4-deoxynivalenol from Fusarium graminearum

Sigma-Aldrich

A1556

15-O-Acetyl-4-deoxynivalenol from Fusarium graminearum

Determination of nivalenol and deoxynivalenol by liquid chromatography/atmospheric pressure photoionization mass spectrometry
Tanaka H, et al.
Rapid Communications in Mass Spectrometry, 23(19), 3119-3124 (2009)
S Tsuda et al.
Mutation research, 415(3), 191-200 (1998-08-26)
We tested the genotoxicity of nivalenol (NIV), a potent toxic trichothecene from Fusarium nivale, in cultured CHO cells and in several mouse organs and tissues (liver, kidney, thymus, bone marrow and mucosa of stomach, jejunum, and colon) using the alkaline
Giuseppina Avantaggiato et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 42(5), 817-824 (2004-03-30)
In vitro screening of 14 adsorbent materials, including some commercial products used to detoxify Fusarium-mycotoxins, were tested in the pH range of 3-8 for deoxynivalenol (DON)- and nivalenol (NIV)-binding ability. Only activated carbon showed to be effective with binding capacities
Alaleh Zoghi et al.
Mini reviews in medicinal chemistry, 14(1), 84-98 (2013-12-18)
Removal of toxic metals and toxins using microbial biomass has been introduced as an inexpensive, new promising method on top of conventional methods for decontamination of food, raw material and concentrated. In this article the potential application of lactic acid
Matias Pasquali et al.
Electrophoresis, 34(4), 505-509 (2012-11-23)
Fusarium graminearum is widely studied as a model for toxin production among plant pathogenic fungi. A 2D DIGE reference map for the nivalenol-producing strain 453 was established. Based on a whole protein extract, all reproducible spots were systematically picked and
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