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Merck
CN

32749

Supelco

β-雌二醇 3-甲醚 溶液

VETRANAL®, 100 μg/mL in acetonitrile, 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

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关于此项目

经验公式(希尔记法):
C19H26O2
化学文摘社编号:
分子量:
286.41
EC 号:
UNSPSC代码:
41116107
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等级

analytical standard

产品线

VETRANAL®

保质期

limited shelf life, expiry date on the label

浓度

100 μg/mL in acetonitrile

技术

HPLC: suitable
gas chromatography (GC): suitable

包装形式

single component solution

储存温度

2-8°C

SMILES字符串

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

InChI key

ULAADVBNYHGIBP-GFEQUFNTSA-N

应用

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

法律信息

VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

FlameExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

35.6 °F - closed cup

闪点(°C)

2.0 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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)
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

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