ChemicalBook--->CAS DataBase List--->350820-16-5

350820-16-5

350820-16-5 Structure

350820-16-5 Structure
IdentificationBack Directory
[Name]

ESTRONE-2,4-D2
[CAS]

350820-16-5
[Synonyms]

ESTRONE-2,4-D2
[Molecular Formula]

C18H20D2O2
[MDL Number]

MFCD01074230
[MOL File]

350820-16-5.mol
[Molecular Weight]

272.38
Chemical PropertiesBack Directory
[Melting point ]

259 - 261°C
[storage temp. ]

Refrigerator
[solubility ]

Chloroform (Slightly, Sonicated), Ethanol (Slightly, Sonicated) Methanol (Slightly)
[form ]

Solid
[color ]

White to Off-White
Safety DataBack Directory
[Symbol(GHS) ]


GHS08
[Signal word ]

Danger
[Hazard statements ]

H351-H360-H362
[Precautionary statements ]

P201-P202-P260-P263-P264-P270-P280-P308+P313-P405-P501
Hazard InformationBack Directory
[Description]

Estrone-d2 is intended for use as an internal standard for the quantification of estrone (Item Nos. ISO60165 | 10006485) by GC- or LC-MS. Estrone is one of the three naturally occurring estrogens, the others being estradiol (Item Nos. ISO60155 | 10006315) and estriol (Item Nos. ISO60164 | 10006484). Estrone is synthesized from androstenedione by the aromatase enzyme system in the ovaries and placenta, and is also synthesized from estradiol by 17-hydroxy steroid dehydrogenase in the liver. Serum concentrations of estrone in premenopausal women fluctuate according to the menstrual cycle and becomes the most predominant estrogen in postmenopausal women. The binding affinities of estrone to the estrogen receptors α and β are approximately 60% and 37% relative to estradiol.
[Uses]

Estrone-2,4-d2 (CAS# 350820-16-5) is a useful isotopically labeled research compound. It could potentially be useful as a wetland substrate for the removal of pharmaceutical and personal care products from contaminated water.
[References]

[1] GRUBER C, TSCHUGGUEL W, SCHNEEBERGER C, et al. Production and actions of estrogens.[J]. The New England Journal of Medicine, 2002, 16 1: 0. DOI: 10.1056/nejmra000471
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