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Z2000

Sigma-Aldrich

β-Zearalenol

≥98%

Synonym(s):

beta-Zearalenol, 2,4-Dihydroxy-6-(6β,10-dihydroxy-trans-1-undecenyl)benzoic acid μ-lactone

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About This Item

Empirical Formula (Hill Notation):
C18H24O5
CAS Number:
71030-11-0
Molecular Weight:
320.38
MDL number:
MFCD00151078
UNSPSC Code:
12352100
PubChem Substance ID:
24902174
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

Assay

≥98%

form

powder

storage temp.

−20°C

SMILES string

C[C@H]1CCC[C@@H](O)CCC\C=C\c2cc(O)cc(O)c2C(=O)O1

InChI

1S/C18H24O5/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/h3,7,10-12,14,19-21H,2,4-6,8-9H2,1H3/b7-3+/t12-,14-/m0/s1

InChI key

FPQFYIAXQDXNOR-PMRAARRBSA-N

Gene Information

rat ... Ar(24208)

Related Categories

Application

Reactant involved in biological studies including:
  • Synthesis of amino glycoside nucleotides
  • Enzymatic synthesis of glucuronides of zearalenone
  • Derivatization of Zearalenone

Pictograms

Health hazardCorrosion
GHS08,GHS05

Signal Word

Danger

Hazard Statements

H314,H361d

Hazard Classifications

Repr. 2 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000369124
0000324198
0000369124
0000329410
0000243766

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Lian Li et al.
Animals : an open access journal from MDPI, 10(1) (2020-01-17)
Zearalenone (ZEA) and T-2 are the most common mycotoxins in grains and can enter the animal and human food-chain and cause many health disorders. To elucidate the toxic response profile, we stimulated bovine granulosa cells (GCs) with β-zearalenol or HT-2.
A Vulić et al.
Journal of analytical toxicology, 43(2), 126-133 (2018-10-09)
Metabolic transformation of zearalenone (ZEA), a mycotoxin which can contaminate both food and feed, results in the formation of five metabolites, one of them being zeranol (α-ZAL), which can be abused in farm animals as a growth promoter. To the

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