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(S,E)-Zearalenone

Base Information Edit
  • Chemical Name:(S,E)-Zearalenone
  • CAS No.:17924-92-4
  • Molecular Formula:C18H22O5
  • Molecular Weight:318.37
  • Hs Code.:29322090
  • Nikkaji Number:J108.495J
  • Metabolomics Workbench ID:45078
  • ChEMBL ID:CHEMBL1397216
  • Mol file:17924-92-4.mol
(S,E)-Zearalenone

Synonyms:(S,E)-Zearalenone;Toxin, fusarium;7645-23-0;fusarium toxin;(12E)-16,18-dihydroxy-4-methyl-3-oxabicyclo[12.4.0]octadeca-1(14),12,15,17-tetraene-2,8-dione;Mycotoxin F-2;rac Zearalenone-d6;1H-2-Benzoxacyclotetradecin-1-one, 3,4,5,6,7,8,9,10-octahydro-14,16-dihydroxy-3-methyl-7-oxo-, (E)-;(E)-3,4,5,6,7,8,9,10-Octahydro-14,16-dihydroxy-3-methyl-7-oxo-1H-2-benzoxacyclotetradecin-1-one;Mycotoxin F 2;SCHEMBL588841;SCHEMBL588842;6-(10-Hydroxy-6-oxo-trans-1-undecenyl)-.beta.-resorcylic acid lactone;CHEMBL1397216;CHEBI:125462;CHEBI:175078;MBMQEIFVQACCCH-XVNBXDOJSA-N;(11S)-11-methyl-15,17-bis(oxidanyl)-12-oxabicyclo[12.4.0]octadeca-1(18),2,14,16-tetraene-7,13-dione;(E)-3,4,5,6,9,10-Hexahydro-14,16-dihydroxy-3-methyl-1H-2-benzoxacyclotetradecin-1,7(8H)-dione;1H-2-Benzoxacyclotetradecin-1,7(8H)-dione, 3,4,5,6,9,10-hexahydro-14,16-dihydroxy-3-methyl-, (E)-;FeS;NCGC00095344-01;NCGC00095344-03;AB01209588-01;BRD-A94796533-001-01-1;14,16-dihydroxy-3-methyl-3,4,5,6,7,8,9,10-octahydro-1H-2-benzoxacyclotetradecine-1,7-dione;14,16-Dihydroxy-3-methyl-3,4,5,6,9,10-hexahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione-, [S-(E)]-

Suppliers and Price of (S,E)-Zearalenone
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • Zearalenone
  • 10mg
  • $ 262.00
  • TRC
  • Zearalenone
  • 50mg
  • $ 65.00
  • TRC
  • Zearalenone
  • 25mg
  • $ 55.00
  • TRC
  • Zearalenone
  • 10mg
  • $ 45.00
  • Tocris
  • Zearalenone
  • 10
  • $ 82.00
  • Tocris
  • Zearalenone
  • 50
  • $ 345.00
  • Sigma-Aldrich
  • Zearalenone fungal mycotoxin
  • 25mg
  • $ 274.00
  • Sigma-Aldrich
  • Zearalenone fungal mycotoxin
  • 10mg
  • $ 140.00
  • Sigma-Aldrich
  • Zearalenone solution certified reference material, 50?μg/mL in acetonitrile, ampule of 1?mL
  • 1 mL
  • $ 86.60
  • Sigma-Aldrich
  • Zearalenone solution certified reference material, 50 μg/mL in acetonitrile, ampule of 1 mL
  • crm46916
  • $ 83.90
Total 103 raw suppliers
Chemical Property of (S,E)-Zearalenone Edit
Chemical Property:
  • Appearance/Colour:Crystalline solid 
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:164-165 °C 
  • Refractive Index:1.539 
  • Boiling Point:600.4 °C at 760 mmHg 
  • PKA:7.58±0.40(Predicted) 
  • Flash Point:219.5 °C 
  • PSA:83.83000 
  • Density:1.168 g/cm3 
  • LogP:3.57960 
  • Storage Temp.:−20°C 
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:0
  • Exact Mass:318.14672380
  • Heavy Atom Count:23
  • Complexity:445
Purity/Quality:

99% *data from raw suppliers

Zearalenone *data from reagent suppliers

Safty Information:
  • Pictogram(s): CorrosiveC, HarmfulXn, Flammable
  • Hazard Codes:C,Xn,F 
  • Statements: 34-62-63-36-20/21/22-11 
  • Safety Statements: 26-36/37/39-45-36-16-36/37 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC1CCCC(=O)CCCC=CC2=C(C(=CC(=C2)O)O)C(=O)O1
  • Isomeric SMILES:CC1CCCC(=O)CCC/C=C/C2=C(C(=CC(=C2)O)O)C(=O)O1
  • Recent EU Clinical Trials:Study evaluation of 2nd hormone line response by -[18F]fluoro-17β-?stradiol (FES) PET/CT in metastatic breast cancer patients
  • Uses Zearalenone is a resorcylic acid lactone produced by a number of Fusarium sp.. Zearalenone acts as a non-steroidal estrogen, binding to estrogen receptor and is uterotropic. Zearalenone induces reproductive problems in animals and, in some animal models, is thought to be a primary initiator of hepatic tumours. In vivo, zearalenone undergoes metabolic reduction to the more estrogenic zearalenol. Contamination of grains, notably maize, by Fusarium species gives rise to high levels of zearalenone and is regarded as an important food quality issue for both humans and animal health. A phytoestrogenic mycotoxin and ER activator Estrogenic mycotoxin produced by Fusarium fungi commonly found in grains. One of a group of compounds known as resorcylic acid lactones
Technology Process of (S,E)-Zearalenone

There total 73 articles about (S,E)-Zearalenone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogenchloride; In tetrahydrofuran; at 25 ℃; for 216h;
DOI:10.1021/jo00008a053
Guidance literature:
With aluminium(III) iodide; tetra-(n-butyl)ammonium iodide; In benzene; at 10 ℃;
DOI:10.1055/s-0030-1260058
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