Skip to Content
Merck
All Photos(1)

Key Documents

34126

Supelco

Zearalenone solution

100 μg/mL in acetonitrile, analytical standard

Synonym(s):

ZON

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C18H22O5
CAS Number:
Molecular Weight:
318.36
EC Number:
MDL number:
UNSPSC Code:
85151701
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
food and beverages
personal care

format

single component solution

storage temp.

−20°C

SMILES string

OC1=C(C(O[C@@H](C)CCC2)=O)C(/C=C/CCCC2=O)=CC(O)=C1

InChI

1S/C18H22O5/c1-12-6-5-9-14(19)8-4-2-3-7-13-10-15(20)11-16(21)17(13)18(22)23-12/h3,7,10-12,20-21H,2,4-6,8-9H2,1H3/b7-3+/t12-/m0/s1

InChI key

MBMQEIFVQACCCH-QBODLPLBSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Certan Vial
Zearalenone is a mycotoxin produced byFusarium graminearum, culmorum crookwellense and roseum in food of plant origin. It is an endocrine disrupter since it binds to the estrogen receptors and interacts with the steroidogenic enzymes.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Zearalenone solution may be used as a reference standard for the analysis of zearalenone content in fish samples using high-performance liquid chromatography (HPLC) with fluorescence detection.
Zearalenone solution may be used as analytical reference standard for the estimation of the analyte in biological samples and food products using various chromtography techniques.

related product

Product No.
Description
Pricing

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Levels of zearalenone and its metabolites in sun-dried kapenta fish and water of Lake Kariba in Zambia?A preliminary study.
Gonkowski S, et al.
The Science of the Total Environment, 637, 1046-1050 (2018)
Determination of zearalenone and its metabolites in urine, plasma and faeces of horses by HPLC-APCI-MS.
Songsermsakul P, et al.
Journal of Chromatography. B, Biomedical Sciences and Applications, 843(2), 252-261 (2006)
Development of a liquid chromatography/time-of-flight mass spectrometric method for the simultaneous determination of trichothecenes, zearalenone and aflatoxins in foodstuffs
Tanaka H, et al.
Rapid Communications in Mass Spectrometry, 20(9), 1422-1428 (2006)
Feng Gao et al.
Mutation research, 755(1), 6-10 (2013-05-07)
Mycotoxins are considered to be significant contaminants of food and animal feed. Zearalenone (ZEA) is a hepatotoxic mycotoxin with estrogenic and anabolic activity found in cereal grains worldwide. ZEA affects hematological and immunological parameters in humans and rodents. The compound
Yuquan Xu et al.
Applied and environmental microbiology, 79(6), 2038-2047 (2013-01-22)
10,11-Dehydrocurvularin is a prevalent fungal phytotoxin with heat shock response and immune-modulatory activities. It features a dihydroxyphenylacetic acid lactone polyketide framework with structural similarities to resorcylic acid lactones like radicicol or zearalenone. A genomic locus was identified from the dehydrocurvularin

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service