32749
β-雌二醇 3-甲醚 溶液
100 μg/mL in acetonitrile, VETRANAL®, analytical standard
别名:
1,3,5(10)-雌三烯-3,17β-二醇 3-甲醚, 17β-羟基-3-甲氧基-1,3,5(10)-雌三烯
InChI key
ULAADVBNYHGIBP-GFEQUFNTSA-N
SMILES string
C[C@]12CCC3C(CCc4cc(C=O)ccc34)C1CC[C@@H]2O
InChI
1S/C19H26O2/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/h4,6,11,15-18,20H,3,5,7-10H2,1-2H3/t15-,16-,17+,18+,19+/m1/s1
grade
analytical standard
product line
VETRANAL®
shelf life
limited shelf life, expiry date on the label
concentration
100 μg/mL in acetonitrile
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
format
single component solution
storage temp.
2-8°C
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
35.6 °F - closed cup
flash_point_c
2.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Structural derivatives of tamoxifen and oestradiol 3-methyl ether as potential alkylating antioestrogens.
V C Jordan et al.
European journal of cancer, 17(2), 193-200 (1981-02-01)
J S Williamson et al.
Applied and environmental microbiology, 55(11), 3029-3031 (1989-11-01)
Aspergillus alliaceus UI 315 was examined for its ability to metabolize 3-methoxy-17 beta-estradiol. Preparative-scale incubations with this substrate afforded good yields of 6 beta-hydroxy-17 beta-estradiol, 4-hydroxy-17 beta-estradiol, and 4,6 beta-dihydroxy-17 beta-estradiol, which were identified by high-pressure liquid chromatography, 1H and
M Edery et al.
Steroids, 35(4), 381-388 (1980-04-01)
Adrenal gland homogenates from four different strains of mice were incubated with (4-14C)-pregnenolone and a NADPH generating system. Although quantitative differences between high and low mammary tumor strains occured, all mice synthesized estrone. The highest aromatase activity was found 2
Lucie Havlíková et al.
Journal of chromatography. A, 1119(1-2), 216-223 (2006-02-10)
A novel HPLC method for simultaneous determination of estradiol and its seven degradation products in topical gel was developed. Zorbax SB-CN (150 mm x 4.6 mm, 5 microm) analytical column and mobile phase composed of acetonitrile, phosphoric acid 0.085%, and
D M Stresser et al.
Biochemical pharmacology, 55(11), 1861-1871 (1998-08-26)
This study demonstrates interplay among human hepatic cytochrome P450 (CYP) isoforms in transforming aromatic compounds from being prosubstrates of CYP3A4 into phenolic substrates. Incubation of methoxychlor with CYP2C19 yields the phenolic monodemethylated derivative (mono-OH-M). Additionally, CYP2C19 catalyzes the ortho-hydroxylation of
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