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Z0417

Sigma-Aldrich

β-Zearalanol

~98% (HPLC)

Synonym(s):

2,4-Dihydroxy-6-(6β,10-dihydroxyundecyl]benzoic acid μ-lactone

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About This Item

Empirical Formula (Hill Notation):
C18H26O5
CAS Number:
42422-68-4
Molecular Weight:
322.40
MDL number:
MFCD00151077
UNSPSC Code:
12352200
PubChem Substance ID:
24902165
NACRES:
NA.77

sterility

non-sterile

Quality Level

200

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
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 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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Zearalenones: characterization of the estrogenic potencies and receptor interactions of a series of fungal beta-resorcylic acid lactones.
B S Katzenellenbogen et al.
Endocrinology, 105(1), 33-40 (1979-07-01)
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
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