5975-78-0
5975-78-0 structure
- Name: Zearalanone
- Chemical Name: (S)-Zearalanone
- CAS Number: 5975-78-0
- Molecular Formula: C18H24O5
- Molecular Weight: 320.380
- Catalog: analytical chemistry Standard Food and cosmetics standards
- Create Date: 2018-06-29 22:43:04
- Modify Date: 2026-07-01 17:06:15
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Zearalenone is a nonsteroidal estrogenic mycotoxin produced by Fusarium species, which colonizes several grains. Zearalenone has low acute toxicity and carcinogenicity. Due to its agonistic effect on the estrogen receptor, Zearalenone exhibits distinct estrogenic and anabolic properties in several animal species, resulting in severe effects on the reproductive system[1].
| Name | (S)-Zearalanone |
|---|---|
| Synonyms |
Zanone
Ccris Zealanone (Certified Reference Material) 2,4-Dihydroxy-6-(10-hydroxy-6-oxoundecyl)benzoic acid μ-lactone solution Zealanone Standd (S)-3,4,5,6,9,10,11,12-Octahydro-14,16-dihydroxy-3-methyl-1H-2-benzoxacyclotetradecin-1,7(8H)-dione 1H-2-Benzoxacyclotetradecin-1,7(8H)-dione, 3,4,5,6,9,10,11,12-octahydro-14,16-dihydroxy-3-methyl-, (3S) (S)-Zealanone, P 1502, Zanone (S)-Zealanone beta-Resorcylic acid, 6-(10-hydroxy-6-oxoundecyl)-, mu-lactone 2-[(S)-10-Hydroxy-6-oxoundecyl]-4,6-dihydroxybenzoic acid 1,2-lactone Zealanone 10.0 μg/ml Acetonitrile (S)-Zealanone in Acetonitrile Zealanone solution 2,4-DIHYDROXY-6-[10-HYDROXY-6-OXO-UNDECYL]BENZOIC ACID MICRO-LACTONE (11S)-15,17-dihydroxy-11-methyl-12-oxabicyclo[12.4.0]octadeca-1(18),14,16-triene-7,13-dione (3S)-14,16-Dihydroxy-3-methyl-3,4,5,6,9,10,11,12-octahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione 2,4-Dihydroxy-6-(10-hydroxy-6-oxoundecyl)benzoic acid μ-lactone P-1502 Zealanone in Methanol ZEALANONE Zealanone,2,4-Dihydroxy-6-(10-hydroxy-6-oxoundecyl)benzoic acid μ-lactone 1H-2-Benzoxacyclotetradecin-1,7(8H)-dione, 3,4,5,6,9,10,11,12-octahydro-14,16-dihydroxy-3-methyl-, (S) |
| Description | Zearalenone is a nonsteroidal estrogenic mycotoxin produced by Fusarium species, which colonizes several grains. Zearalenone has low acute toxicity and carcinogenicity. Due to its agonistic effect on the estrogen receptor, Zearalenone exhibits distinct estrogenic and anabolic properties in several animal species, resulting in severe effects on the reproductive system[1]. |
|---|---|
| Related Catalog | |
| Target |
Estrogen receptor |
| References |
| Density | 1.1±0.1 g/cm3 |
|---|---|
| Boiling Point | 576.8±50.0 °C at 760 mmHg |
| Melting Point | 184-186ºC |
| Molecular Formula | C18H24O5 |
| Molecular Weight | 320.380 |
| Flash Point | 209.2±23.6 °C |
| Exact Mass | 320.162384 |
| PSA | 83.83000 |
| LogP | 3.45 |
| Vapour Pressure | 0.0±1.7 mmHg at 25°C |
| Index of Refraction | 1.526 |
| Storage condition | −20°C |
| Symbol |
GHS07, GHS08 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H302-H312-H315-H319-H332-H335-H351 |
| Precautionary Statements | P261-P280-P305 + P351 + P338 |
| Personal Protective Equipment | Eyeshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges |
| Hazard Codes | Xn |
| Risk Phrases | 20/21/22-36/37/38-40 |
| Safety Phrases | 22-26-36 |
| RIDADR | UN 1648 3 / PGII |
| WGK Germany | 3 |
| HS Code | 29322090 |
|
~19%
5975-78-0 |
| Literature: El-Sharkawy, Saleh H.; Abul-Hajj, Yusuf J. Journal of Organic Chemistry, 1988 , vol. 53, # 3 p. 515 - 519 |
| Precursor 1 | |
|---|---|
| DownStream 0 | |