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Merck
모든 사진(1)

문서

46573

Supelco

Estrone

VETRANAL®, analytical standard

동의어(들):

1,3,5(10)-Estratrien-3-ol-17-one, 3-Hydroxy-1,3,5(10)-estratrien-17-one, Folliculin

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모든 사진(1)

About This Item

실험식(Hill 표기법):
C18H22O2
CAS Number:
53-16-7
Molecular Weight:
270.37
Beilstein:
1915077
EC Number:
200-164-5
MDL number:
MFCD00003620
UNSPSC 코드:
41116107
PubChem Substance ID:
329757214

Grade

analytical standard

Quality Level

200

제품 라인

VETRANAL®

유통기한

limited shelf life, expiry date on the label

기술

HPLC: suitable
gas chromatography (GC): suitable

mp

258-260 °C (lit.)

응용 분야

pharmaceutical (small molecule)

형식

neat

SMILES string

C[C@]12CC[C@H]3[C@@H](CCc4cc(O)ccc34)[C@@H]1CCC2=O

InChI

1S/C18H22O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-16,19H,2,4,6-9H2,1H3/t14-,15-,16+,18+/m1/s1

InChI key

DNXHEGUUPJUMQT-CBZIJGRNSA-N

유전자 정보

human ... ESR1(2099)

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

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

추천 제품

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

법적 정보

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

픽토그램

Health hazard
GHS08

신호어

Danger

유해 및 위험 성명서

H351,H360FD,H362

Hazard Classifications

Carc. 2 - Lact. - Repr. 1A

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type P2 (EN 143) respirator cartridges

Choose from one of the most recent versions:

시험 성적서(COA)

Lot/Batch Number
BCCG6639
BCCB6518
SZBE205XV
SZE8123XV
SZBB265XV

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

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이미 열람한 고객

Slide 1 of 5

1 of 5

Estriol ≥97%

Sigma-Aldrich

E1253

Estriol

Estrone 3-sulfate sodium salt contains ~35% Tris as stabilizer

Sigma-Aldrich

E0251

Estrone 3-sulfate sodium salt

Picrotin European Pharmacopoeia (EP) Reference Standard

Y0001508

Picrotin

17α-Ethynylestradiol ≥98%

Sigma-Aldrich

E4876

17α-Ethynylestradiol

Ethinyl Estradiol Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1480

Ethinyl Estradiol

Annamaria Lilienkampf et al.
Journal of medicinal chemistry, 52(21), 6660-6671 (2009-10-15)
Many breast tumors are hormone-dependent, and estrogens, especially estradiol (E2), have a pivotal role in their growth and development. 17beta-Hydroxysteroid dehydrogenase type 1 (17beta-HSD1) is a key enzyme in the biosynthesis of female sex steroids, catalyzing the NADPH-dependent reduction of
Emma M Ferguson et al.
Water research, 47(4), 1604-1615 (2013-01-12)
Estuaries are often the final repositories for aquatic pollutants but how estuarine hydrology influences the availability of marine- and freshwater-derived pollutants is not well understood, particularly for micro-pollutants such as endocrine disrupting chemicals. To address this knowledge gap, this study
Juilee Rege et al.
The Journal of clinical endocrinology and metabolism, 98(3), 1182-1188 (2013-02-07)
A broad analysis of adrenal gland-derived 19-carbon (C19) steroids has not been reported. This is the first study that uses liquid chromatography-tandem mass spectrometry to quantify 9 C19 steroids (androgens and their precursors), estrone, and estradiol in the adrenal vein
Shanshan Zhao et al.
Breast cancer research : BCR, 16(2), R30-R30 (2014-03-29)
Paradoxically, a breast cancer risk reduction with conjugated equine estrogens (CEE) and a risk elevation with CEE plus medroxyprogesterone acetate (CEE + MPA) were observed in the Women's Health Initiative (WHI) randomized controlled trials. The effects of hormone therapy on serum sex
Yannick Laplante et al.
Bioorganic & medicinal chemistry, 16(4), 1849-1860 (2007-11-24)
Estrogens play an important role in the development of breast cancer. Inhibiting 17beta-hydroxysteroid dehydrogenase type 1 (17beta-HSD1)--the enzyme responsible for the last step in the biosynthesis of the most potent estrogen, estradiol (E2)--would thus allow hindering the growth of estrogen-sensitive
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LC-MS Analysis of Hormones in Tap Water

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수돗물내 호르몬의 LC-MS 분석

Milli-Q® 초순수 시스템은 실험실 수돗물 내 호르몬을 포함하여 유기 오염물질이 없는 정제수를 제공하므로 가장 민감한 LC-MS/MS 분석에 적합합니다.

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