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Z0417

β-Zearalanol

~98% (HPLC), nonsteroidal estrogen, powder

Synonym(s):

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

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$60.70

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$223.00

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About This Item

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

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Product Name

β-Zearalanol, ~98% (HPLC)

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

sterility

non-sterile

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

Quality Level

Gene Information

rat ... Ar(24208)

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1 of 4

This Item
Z0166A7755Z0167
assay

~98% (HPLC)

assay

≥98% (HPLC)

assay

≥98% (TLC)

assay

≥98% (TLC)

form

powder

form

powder

form

powder

form

powder

drug control

regulated under CDSA - not available from Sigma-Aldrich Canada

drug control

-

drug control

-

drug control

-

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

storage temp.

−20°C

storage temp.

−20°C

storage temp.

room temp

storage temp.

−20°C

solubility

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

solubility

methanol: 9.80-10.20 mg/mL, clear, colorless to faintly yellow

solubility

methanol: 19.60-20.40 mg/mL, clear, colorless

solubility

methanol: 9.80-10.20 mg/mL, clear, colorless

pictograms

Health hazardCorrosion

signalword

Danger

Hazard Classifications

Repr. 2 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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B H Migdalof et al.
Xenobiotica; the fate of foreign compounds in biological systems, 13(4), 209-221 (1983-04-01)
The disposition of [3H]zeranol has been studied in the female Wistar rat, New Zealand rabbit, beagle dog, rhesus monkey and man. The blood elimination half-life of total radioactivity in rabbit was 26 h, monkey 18 h and man 22 h.
Erika Pfeiffer et al.
Molecular nutrition & food research, 54(10), 1468-1476 (2010-04-17)
Glucuronidation constitutes an important pathway in the phase II metabolism of the mycotoxin zearalenone (ZEN) and the growth promotor α-zearalanol (α-ZAL, zeranol), but the enzymology of their formation is yet unknown. In the present study, ZEN, α-ZAL and four of
Alberto Sánchez Arribas et al.
Electrophoresis, 30(3), 499-506 (2009-01-22)
A simple analytical scheme for the screening and quantification of zearalenone and its metabolites, alpha-zearalenol and beta-zearalenol, is reported. Extracts from maize flour samples were collected by supercritical fluid extraction and afterwards, they were analyzed by CE with amperometric detection.
H Malekinejad et al.
Veterinary research communications, 30(4), 445-453 (2006-02-28)
The enzymes 3alpha- and 3beta-hydroxysteroid dehydrogenase (3alpha- and 3beta-HSD) play a pivotal role in synthesis of various steroid hormones including oestradiol and testosterone. The structure of the mycotoxin zearalenone resembles many characteristics of steroids and binds to oestrogen receptors as
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)

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