Skip to Content
Merck
CN
All Photos(1)

Documents

Safety Information

Z0417

Sigma-Aldrich

β-Zearalanol

~98% (HPLC)

Sign Into View Organizational & Contract Pricing

Synonym(s):
2,4-Dihydroxy-6-(6β,10-dihydroxyundecyl]benzoic acid μ-lactone
Empirical Formula (Hill Notation):
C18H26O5
CAS Number:
Molecular Weight:
322.40
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.77

sterility

non-sterile

Quality Level

Assay

~98% (HPLC)

form

powder

drug control

regulated under CDSA - not available from Sigma-Aldrich Canada

availability

not available in Canada

solubility

methanol: 19.60-20.40 mg/mL, clear, colorless to faintly yellow

shipped in

ambient

storage temp.

−20°C

SMILES string

C[C@H]1CCC[C@@H](O)CCCCCc2cc(O)cc(O)c2C(=O)O1

InChI

1S/C18H26O5/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/h10-12,14,19-21H,2-9H2,1H3/t12-,14-/m0/s1

InChI key

DWTTZBARDOXEAM-JSGCOSHPSA-N

Gene Information

rat ... Ar(24208)

Pictograms

Health hazardCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Repr. 2 - Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

监管及禁止进口产品

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

F Di Carlo et al.
Il Farmaco; edizione scientifica, 35(5), 425-429 (1980-05-01)
The interference of two weak estrogens (P-1496 and P-1560) on the binding of estradiol with uterine estrogen receptors is comparatively studied. Both P-1496 and P-1560 decrease the estradiol binding capacity, but P-1560 is less effective than P-1496. Since P-1496 is
F M Launay et al.
Food additives and contaminants, 21(9), 833-839 (2005-01-26)
There is currently little information concerning the prevalence of zeranol and taleranol in animal urine following metabolism of the naturally occurring Fusarium spp. toxins. An epidemiological study is described which involves four European Union control laboratories in which 8008 urine
Marianne Erbs et al.
Journal of AOAC International, 90(4), 1197-1202 (2007-09-01)
Immunoaffinity extraction has become increasingly important as a sample preparation and cleanup method in mycotoxin analysis. In this study, the antibody specificities of 3 commercial immunoaffinity columns (IACs) targeting zearalenone (ZON) were compared for alpha-zearalenol, beta-zearalenol, zearalanone, alpha-zearalanol, and beta-zearalanol.
D J Everett et al.
Journal of toxicology and environmental health, 20(4), 435-443 (1987-01-01)
Uterotrophic response in sexually immature female rats has been used to rank the relative estrogenic potencies of six resorcylic acid lactones (RALs) and to compare their activities with that of 17 beta-estradiol. On oral administration, the estrogenic potency relative to
T M Chichila et al.
Journal of analytical toxicology, 12(6), 310-318 (1988-11-01)
Bovine tissues, including liver, muscle, kidney, bile, serum, and urine, have been quantified by selected ion monitoring capillary gas chromatography/mass spectrometry to establish the distribution of the anabolic drug, zeranol, and its metabolites, taleranol and zearalanone, after administration of zeranol

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