E9875
Estrone 3-methyl ether
synthetic (organic), ≥97% (HPLC), Synthetic estrogen, powder
别名:
3-Methoxy-1,3,5(10)-estratrien-17-one
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关于此项目
经验公式（希尔记法）:
C19H24O2
化学文摘社编号:
分子量:
284.39
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
51111800
EC Number:
216-613-3
MDL number:
产品名称
Estrone 3-methyl ether, ≥97% (HPLC)
InChI key
BCWWDWHFBMPLFQ-VXNCWWDNSA-N
InChI
1S/C19H24O2/c1-19-10-9-15-14-6-4-13(21-2)11-12(14)3-5-16(15)17(19)7-8-18(19)20/h4,6,11,15-17H,3,5,7-10H2,1-2H3/t15-,16-,17+,19+/m1/s1
SMILES string
COc1ccc2C3CCC4(C)C(CCC4=O)C3CCc2c1
biological source
synthetic (organic)
sterility
non-sterile
assay
≥97% (HPLC)
form
powder
solubility
chloroform: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow
shipped in
ambient
storage temp.
room temp
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Ewa Kozłowska et al.
Scientific reports, 9(1), 10734-10734 (2019-07-26)
Estrone, estradiol, ethynylestradiol and estrone 3-methyl ether underwent a biotransformation process in the submerged culture of Isaria fumosorosea KCh J2. Estrone was transformed into seven metabolites, four of which were glycosylated. Estradiol was selectively glycosylated at C-3 and then transformed
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