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BETA-ZEARALENOL

CAS No.
71030-11-0
Chemical Name:
BETA-ZEARALENOL
Synonyms
β-Zearalenol;(3S,7S,11E)-;B-zearalenol;Zearalenol-β;BETA-ZEARALENOL;Zearalenol, beta-;13C18-β-Zearalenol;β-Zearalenol solution;Zearalenol-β in Acetonitrile;beta Zearalenol from Giberella zeae
CBNumber:
CB7691214
Molecular Formula:
C18H24O5
Molecular Weight:
320.38
MDL Number:
MFCD00151078
MOL File:
71030-11-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 02:37:03

BETA-ZEARALENOL Properties

Melting point 137-139°C
Flash point 2℃
storage temp. 2-8°C
solubility Acetone: Slightly Soluble; Methanol: Slightly Soluble
form powder
color White to off-white
BRN 3653579
Stability Light Sensitive
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
InChIKey FPQFYIAXQDXNOR-PMRAARRBSA-N
SMILES C[C@H]1CCC[C@@H](O)CCC\C=C\c2cc(O)cc(O)c2C(=O)O1
FDA UNII 35E809PP7O
UNSPSC Code 85151701
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Health Hazard (GHS08)
GHS05,GHS08
Signal word  Danger
Hazard statements  H314-H361d
Precautionary statements  P201-P260-P280-P301+P330+P331-P303+P361+P353-P305+P351+P338
Hazard Codes  Xn,N,F
Risk Statements  20/21/22-40-52/53-68/20/21/22-50-36-22-11
Safety Statements  36/37-61-36-16
RIDADR  UN 3077 9 / PGIII
WGK Germany  3
HS Code  29322090
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Repr. 2
Skin Corr. 1B

BETA-ZEARALENOL price More Price(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Z2000 β-Zearalenol ≥98% 71030-11-0 5mg $250 2026-04-30 Buy
Sigma-Aldrich 35409 β-Zearalenol solution 10μg/mL in acetonitrile, analytical standard 71030-11-0 1ml $935 2026-04-30 Buy
Cayman Chemical 19460 β-Zearalenol ≥98% 71030-11-0 500μg $53 2026-04-30 Buy
Cayman Chemical 19460 β-Zearalenol ≥98% 71030-11-0 1mg $79 2026-04-30 Buy
Cayman Chemical 19460 β-Zearalenol ≥98% 71030-11-0 5mg $129 2026-04-30 Buy
Product number Packaging Price Buy
Z2000 5mg $250 Buy
35409 1ml $935 Buy
19460 500μg $53 Buy
19460 1mg $79 Buy
19460 5mg $129 Buy

BETA-ZEARALENOL Chemical Properties, Uses, Production

Description

β-Zearalenol is a hepatic metabolite of zearalenone , a mycotoxin produced by fungi in food and animal feeds. It is a less potent agonist of estrogen receptors than the parent compound. However, β-zearalenol has pronounced effects on uterotropic activity and sperm acrosome reaction.

Chemical Properties

White Solid

Uses

Reactant involved in biological studies including:• ;Synthesis of amino glycoside nucleotides1• ;Enzymatic synthesis of glucuronides of zearalenone2• ;Derivatization of Zearalenone3,4,5

Uses

β-Zearalenol is a mycotoxin produced by several species of Fusarium. β-Zearalenol exhibits pronounced estrogenic activity, like other zearalenones. Contamination of grains by Fusarium species, notably maize, gives rise to high levels of zearalenol and is regarded as an important food quality issue for both human and animal health.

Uses

The more active Zearalenone (Z270500) metabolite.

Definition

ChEBI: Beta-Zearalenol is a macrolide.

References

[1] Y UENO  F T. alpha-Zearalenol, a major hepatic metabolite in rats of zearalenone, an estrogenic mycotoxin of Fusarium species.[J]. Journal of biochemistry, 1981, 89 2: 563-571. DOI: 10.1093/oxfordjournals.jbchem.a133232
[2] JOSé-MANUEL MOLINA-MOLINA . Assessment of estrogenic and anti-androgenic activities of the mycotoxin zearalenone and its metabolites using in vitro receptor-specific bioassays[J]. Food and Chemical Toxicology, 2014, 74: Pages 233-239. DOI: 10.1016/j.fct.2014.10.008
[3] ANGELA FILANNINO. Dose-response effects of estrogenic mycotoxins (zearalenone, alpha- and beta-zearalenol) on motility, hyperactivation and the acrosome reaction of stallion sperm.[J]. Reproductive Biology and Endocrinology, 2011, 9: 134. DOI: 10.1186/1477-7827-9-134
[4] DANIELA E. MARIN . Effects of zearalenone and its derivatives on the innate immune response of swine[J]. Toxicon, 2010, 56 6: Pages 956-963. DOI: 10.1016/j.toxicon.2010.06.020

BETA-ZEARALENOL Preparation Products And Raw materials

Raw materials

Preparation Products

BETA-ZEARALENOL Suppliers

Global Suppliers ( 87)
Supplier Tel Email Country ProdList Advantage
ShangHai ZskBio CO., LTD 021-58056897 15399714481 info@zsklab.com China 7539 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32273 50
Guangzhou Isun Pharmaceutical Co., Ltd 020-39119399 18927568969 isunpharm@qq.com China 4773 55
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51389 80
Alta Scientific Co., Ltd. 022-6537-8550 15522853686 sales@altasci.com.cn China 4508 55
Shanghai YuanYe Biotechnology Co., Ltd. 15026964105 2881489226@qq.com China 89667 60
Qingdao IniKem BioPharmaTech Co.,Ltd 0532-58268781 18561687109 sales@inikem.com China 299 55
Shanghai SuperLan Chemcial Technique Centre 0-2022843681 15618226720 chaolaichem@foxmail.com China 9996 58
Lynnchem 86-(0)29-85992781 17792393971 info@lynnchem.com China 4578 58
2,4-DIHYDROXY-6-[6BETA,10-DIHYDROXY-TRANS-1-UNDECENYL]BENZOIC ACID MICRO-LACTONE BETA-ZEARALENOL B-zearalenol (3S,7S,11E)-3,4,5,6,7,8,9,10-Octahydro-7,14,16-trihydroxy-3-methyl-1H-2-benzoxacyclotetradecin-1-one 1H-2-Benzoxacyclotetradecin-1-one, 3,4,5,6,7,8,9,10-octahydro-7,14,16-trihydroxy-3-methyl-, (3S-(3R*,7R*,11E))- 1H-2-Benzoxacyclotetradecin-1-one, 3,4,5,6,7,8,9,10-octahydro-7,14,16-trihydroxy-3-methyl-, (3S,7S,11E)- (3S,7S,11E)- (-)-beta-Zearalenol, beta-Trans-Zearalenol Zearalenol, beta- beta Zearalenol from Giberella zeae beta-Zearalenol 10.0 μg/ml Acetonitrile Zearalenol-β Zearalenol-β in Acetonitrile β-Zearalenol solution beta-Zearalenol 100 μg/mL in Acetonitrile 13C18-β-Zearalenol β-Zearalenol 71030-11-0 C18H24O5 Carbonyl Compounds Building Blocks Lactones Organic Building Blocks Chiral Reagents Heterocycles Intermediates & Fine Chemicals Metabolites & Impurities Pharmaceuticals Bioactive Small Molecules Building Blocks Carbonyl Compounds Cell Biology Chemical Synthesis Lactones Organic Building Blocks Z