Saltar al contenido
Merck

D3253

Supelco

Dienestrol

Sinónimos:

3,4-Bis(4-hydroxyphenyl)-2,4-hexadiene

Iniciar sesiónpara Ver la Fijación de precios por contrato y de la organización


About This Item

Fórmula empírica (notación de Hill):
C18H18O2
Número de CAS:
Peso molecular:
266.33
Beilstein/REAXYS Number:
2053694
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
veterinary

SMILES string

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 key

NFDFQCUYFHCNBW-SCGPFSFSSA-N

¿Está buscando productos similares? Visita Guía de comparación de productos

Biochem/physiol Actions

Synthetic estrogenic compound closely related to diethylstilbestrol

pictograms

Health hazard

signalword

Danger

Hazard Classifications

Carc. 1B - Repr. 2

Storage Class

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

wgk_germany

WGK 3

ppe

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


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

¿Ya tiene este producto?

Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

Visite la Librería de documentos

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

Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.

Póngase en contacto con el Servicio técnico