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K2126

Sigma-Aldrich

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

≥98.00% (TLC), powder

Synonyme(s) :

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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About This Item

Formule empirique (notation de Hill):
C20H25NO5
Numéro CAS:
35048-47-6
Poids moléculaire :
359.42
Numéro Beilstein :
2484202
Numéro MDL:
MFCD00056459
Code UNSPSC :
51111800
ID de substance PubChem :
329817132
Nomenclature NACRES :
NA.77

product name

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

Source biologique

synthetic (organic)

Niveau de qualité

200

Pureté

≥98.00% (TLC)

Forme

powder

Solubilité

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

Conditions d'expédition

ambient

Température de stockage

2-8°C

Chaîne 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

Clé InChI

AWARIMYXKAIIGO-UYGYUSPXSA-N

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Description générale

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

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
F Mao et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 26(8), 611-614 (1991-01-01)
According to the character of structure and activity of the test reagents I-IV, two new reagents V and VI for detecting estrogen receptor of human mammary cancer cells were synthesized. This simplifies the route of synthesis and increases activity. Key
May L Chiu et al.
Biotechnology and applied biochemistry, 58(1), 75-82 (2011-03-31)
A convenient homogeneous enzyme immunoassay for estradiol is described. Unlike heterogeneous immunoassays, which require time-consuming separation steps or expensive automated systems, homogeneous immunoassays, wherein all reagents are freely suspended in bulk solution, can be simple and fast without costly instrumentation.
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
C M Furnival et al.
The British journal of surgery, 70(8), 457-459 (1983-08-01)
The performance of a fluorescent cytochemical oestrogen receptor (ER) assay has been compared with an established dextran-coated charcoal ER assay in 85 cases of primary breast cancer. Both assays were performed on tissue samples from the same tumour, by independent
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