所有图片(1)
About This Item
经验公式（希尔记法）:
C18H26O5
CAS号:
分子量:
322.40
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
推荐产品
无菌性
non-sterile
质量水平
方案
~98% (HPLC)
表单
powder
药品控制
regulated under CDSA - not available from Sigma-Aldrich Canada
存货情况
not available in Canada
溶解性
methanol: 19.60-20.40 mg/mL, clear, colorless to faintly yellow
运输
ambient
储存温度
−20°C
SMILES字符串
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
基因信息
rat ... Ar(24208)
警示用语：
Danger
危险声明
危险分类
Repr. 2 - Skin Corr. 1B
储存分类代码
8A - Combustible corrosive hazardous materials
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
监管及禁止进口产品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
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.
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
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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