Estrone, 99%

Name: Estrone, 99% | 53-16-7
Brand: J&K Chemical
SKU: JK438013_5_G
Price: 96.9 USD
Availability: OutOfStock

Cat. No JK438013_5_G

Vendor: J&K Chemical

Product Information

Product Name

Estrone, 99%

Brand Name

J&K

Product Number

438013

CAS

53-16-7

Molecular Formula

C18H22O2

Molecular Weight

270.37

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

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

PubChem CID

5870

IUPAC Name

(8R,9S,13S,14S)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopentaaphenanthren-17-one

InChI Key

DNXHEGUUPJUMQT-CBZIJGRNSA-N

SMILES

CC@12CCC@H3C@H(C@@H1CCC2=O)CCC4=C3C=CC(=C4)O

Properties

Melting Point

258-261

Safety Information

GHS Symbols

Signal Word

Danger

Hazard Statement

H350

H360

Precautionary Statement

P203

P280

P318

P405

P501

References Data Source From Pubchem

Revisiting the dual role of androgens and oestrogens in mammalian sex differentiation with a focus on genitalia

Publication Name: Nature reviews. Urology

Publication Date: 2026-03-04

DOI: 10.1038/s41585-026-01132-z

Gastrointestinal cancers in women: The role of sex hormones

Publication Name: Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology

Publication Date: 2026-03-04

DOI: 10.1007/s12664-026-01976-8

Sexual dimorphism in keratoconus: transcriptomic and hormonal mechanisms underlying stromal remodelling

Publication Name: Eye and vision (London, England)

Publication Date: 2026-03-03

DOI: 10.1186/s40662-026-00478-0

Preparation of meta-cyclophanes via stereospecific ring-expansion rearrangement

Publication Name: Nature Synthesis

Publication Date: 2026-03-02

DOI: 10.1038/s44160-026-01016-5

Lipidomic alterations in oysters caused by environmentally relevant exposure to microplastics and estrogenic endocrine disrupting chemicals

Publication Name: Ecotoxicology (London, England)

Publication Date: 2026-02-28

DOI: 10.1007/s10646-026-03055-2

Estrone, 99%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Revisiting the dual role of androgens and oestrogens in mammalian sex differentiation with a focus on genitalia

Gastrointestinal cancers in women: The role of sex hormones

Sexual dimorphism in keratoconus: transcriptomic and hormonal mechanisms underlying stromal remodelling

Preparation of meta-cyclophanes via stereospecific ring-expansion rearrangement

Lipidomic alterations in oysters caused by environmentally relevant exposure to microplastics and estrogenic endocrine disrupting chemicals

Estrone, 99%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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Estrone, 99%

Product Information

General Information

Properties

Safety Information

References Data Source From Pubchem

Revisiting the dual role of androgens and oestrogens in mammalian sex differentiation with a focus on genitalia

Gastrointestinal cancers in women: The role of sex hormones

Sexual dimorphism in keratoconus: transcriptomic and hormonal mechanisms underlying stromal remodelling

Preparation of meta-cyclophanes via stereospecific ring-expansion rearrangement

Lipidomic alterations in oysters caused by environmentally relevant exposure to microplastics and estrogenic endocrine disrupting chemicals

Estrone, 99%

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2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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