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重要文件

D3253

Supelco

烯雌酚

同義詞:

3,4-双(4-羟苯基)-2,4-己二烯

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About This Item

經驗公式(希爾表示法):
C18H18O2
CAS號碼:
分子量::
266.33
Beilstein:
2053694
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:

技術

HPLC: suitable
gas chromatography (GC): suitable

應用

forensics and toxicology
veterinary

SMILES 字串

C\C=C(c1ccc(O)cc1)\C(=C\C)c2ccc(O)cc2

InChI

1S/C18H18O2/c1-3-17(13-5-9-15(19)10-6-13)18(4-2)14-7-11-16(20)12-8-14/h3-12,19-20H,1-2H3/b17-3+,18-4+

InChI 密鑰

NFDFQCUYFHCNBW-SCGPFSFSSA-N

尋找類似的產品? 前往 產品比較指南

生化/生理作用

与己烯雌酚密切相关的合成雌激素化合物

象形圖

Health hazard

訊號詞

Danger

危險聲明

危險分類

Carc. 1B - Repr. 2

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 3

個人防護裝備

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


分析證明 (COA)

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K Chae et al.
Steroids, 63(3), 149-157 (1998-04-29)
Diethylstilbestrol (DES) is a well-characterized carcinogen in humans and animals although its mechanisms of carcinogenicity are not yet known. While the estrogenic activity of DES is important, there is evidence that oxidative metabolism also plays an important role for its
E G Silva et al.
Gynecologic oncology, 71(2), 240-246 (1998-11-25)
We have been searching for an animal model for ovarian epithelial neoplasms. Our previous study suggested that by giving intermediate doses of testosterone to guinea pigs it is possible to induce cystadenomas in the ovaries in 6 to 10 months.
G G Kuiper et al.
Endocrinology, 138(3), 863-870 (1997-03-01)
The rat estrogen receptor (ER) exists as two subtypes, ER alpha and ER beta, which differ in the C-terminal ligand binding domain and in the N-terminal transactivation domain. In this study we investigated the messenger RNA expression of both ER
Bárbara Socas-Rodríguez et al.
Analytical and bioanalytical chemistry, 409(18), 4467-4477 (2017-06-07)
Within this study, a new method enabling monitoring of various estrogenic substances potentially occurring in milk and dairy products was proposed. Groups of compounds fairly differing in physico-chemical properties and biological activity were analyzed: four natural estrogens, four synthetic estrogens
Bárbara Socas-Rodríguez et al.
Journal of chromatography. A, 1496, 58-67 (2017-04-02)
In this work, a simple and fast methodology has been validated and applied for the analysis of a group of 22 estrogenic compounds including eight phytoestrogens (i.e. daidzein, enterodiol, glycitein, enterolactone, genistein, formononetin, prunetin, biochanin A), six mycotoxins (β-zearalanol, β-zearalenol

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