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Merck

K2126

Sigma-Aldrich

β-Estradiol-6-one 6-(O-carboxymethyloxime)

≥98.00% (TLC), powder

Sinónimos:

β-Estradiol-6-(O-carboxymethyl)oxime, 1,3,5(10)-Estratriene-3,17β-diol-6-one6-(O-carboxymethyloxime), 3,17β-Dihydroxy-1,3,5(10)-estratriene 6-(O-carboxymethyl)oxime, 6-Ketoestradiol 6-(O-carboxymethyloxime)

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5 MG
MXP 3,965.00
50 MG
MXP 20,805.00

MXP 3,965.00


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5 MG
MXP 3,965.00
50 MG
MXP 20,805.00

About This Item

Fórmula empírica (notación de Hill):
C20H25NO5
Número de CAS:
Peso molecular:
359.42
Beilstein:
2484202
Número MDL:
Código UNSPSC:
51111800
ID de la sustancia en PubChem:
NACRES:
NA.77

MXP 3,965.00


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Nombre del producto

β-Estradiol-6-one 6-(O-carboxymethyloxime),

origen biológico

synthetic (organic)

Nivel de calidad

Ensayo

≥98.00% (TLC)

Formulario

powder

solubilidad

ethanol: 19.60-20.40 mg/mL, clear, colorless to faintly yellow

Condiciones de envío

ambient

temp. de almacenamiento

2-8°C

cadena SMILES

C[C@]12CC[C@H]3[C@@H](C\C(=N\OCC(O)=O)c4cc(O)ccc34)[C@@H]1CC[C@@H]2O

InChI

1S/C20H25NO5/c1-20-7-6-13-12-3-2-11(22)8-15(12)17(21-26-10-19(24)25)9-14(13)16(20)4-5-18(20)23/h2-3,8,13-14,16,18,22-23H,4-7,9-10H2,1H3,(H,24,25)/b21-17-/t13-,14-,16+,18+,20+/m1/s1

Clave InChI

AWARIMYXKAIIGO-UYGYUSPXSA-N

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Descripción general

β-Estradiol-6-one 6-(O-carboxymethyloxime) is a derivative of 17β-estradiol.[1]

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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C J Meijer et al.
Virchows Archiv. B, Cell pathology including molecular pathology, 40(1), 27-37 (1982-01-01)
The present study defines criteria for determining the presence of estrogen-receptors in human breast carcinomas demonstrated by a histochemical assay using 17 beta-estradiol-carboxy-methyl-oxim-bovine serum albumen-FITC. The criteria were: 1) the percentage of cells showing fluorescence; 2) the intensity of the
M Malawer et al.
Journal of surgical oncology, 25(3), 148-152 (1984-03-01)
Hormonal receptors of giant cell tumors (GCTs) have not been previously reported. Five cases of GCT of bone were analyzed for estrogen and progesterone binding. Frozen sections were studied by a histochemical method, using 17-beta-6-CMOBSA-FITC and 11-alpha-hydroxyprogesterone-HS-BSA-TMRITC. Cytoplasmic fluorescence with
Markus Lacorn et al.
Journal of immunological methods, 297(1-2), 225-236 (2005-03-22)
17beta-estradiol (E2) concentrations are in the low pg/ml range in plasma. To develop a sensitive enzyme immunoassay (EIA) for E2-determination a highly specific antibody raised against a 6-carboxymethyl (CMO)-E2-bovine serum albumine conjugate was used. Based on 6-CMO-E2 and 6-amino-E2, four
Mingzhe Liu et al.
Journal of bioscience and bioengineering, 111(5), 564-568 (2011-02-01)
Antibodies were covalently conjugated with poly(ethylene glycol) (PEG) and the properties of the PEGylated antibodies in organic media were investigated. Two types of monoclonal antibody were used in this study. One was a monoclonal antibody (abzyme) that was prepared against
M Bourtourault et al.
Research communications in chemical pathology and pharmacology, 72(3), 273-284 (1991-06-01)
Female rats were immunized with mixed 17 beta-estradiol-6-carboxymethyloxime-bovine serum albumin and testosterone-3-carboxymethyloxime-bovine serum albumin. All the animals produced antibodies against the 2 haptens and were better immunized against 17 beta-estradiol than against testosterone. Nevertheless the disappearance of cyclic ovarian function

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