≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normale Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
l'1,2-diidro Esemestano è un composto correlato dell'Esemestano.
| Pubchem Sid | 504767289 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504767289 |
| Sorrisi canonici | CC12CCC3C(C1CCC2=O)CC(=C)C4=CC(=O)CCC34C |
| IUPAC Name | (8R,9S,10R,13S,14S)-10,13-dimethyl-6-methylidene-1,2,7,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthrene-3,17-dione |
| InChIKey | KQRGETZTRARSMA-DAELLWKTSA-N |
| INCHI | 1S/C20H26O2/c1-12-10-14-15-4-5-18(22)20(15,3)9-7-16(14)19(2)8-6-13(21)11-17(12)19/h11,14-16H,1,4-10H2,2-3H3/t14-,15-,16-,19+,20-/m0/s1 |
| Isomeri SMILES | C[C@]12CC[C@H]3[C@H]([C@@H]1CCC2=O)CC(=C)C4=CC(=O)CC[C@]34C |
| Peso molecolare | 298.42 |
| Reaxy-Rn | 2003088 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2003088&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Classe | Steroids and steroid derivatives |
| Subclass | Androstane steroids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Androgens and derivatives |
| Alternative Parents | 3-oxo delta-4-steroids 17-oxosteroids Delta-4-steroids Cyclohexenones Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic homopolycyclic compounds |
| Substituents | Androgen-skeleton - Oxosteroid - 17-oxosteroid - 3-oxosteroid - 3-oxo-delta-4-steroid - Delta-4-steroid - Cyclohexenone - Cyclic ketone - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as androgens and derivatives. These are 3-hydroxylated C19 steroid hormones. They are known to favor the development of masculine characteristics. They also show profound effects on scalp and body hair in humans. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 J2221550 | Certificate of Analysis | Aug 15, 2025 | D330735 |
| J2221161 | Certificate of Analysis | Aug 11, 2025 | D330735 |
| J2221163 | Certificate of Analysis | Aug 11, 2025 | D330735 |
| J2221164 | Certificate of Analysis | Aug 11, 2025 | D330735 |
| J2221167 | Certificate of Analysis | Aug 11, 2025 | D330735 |
| A2411477 | Certificate of Analysis | Aug 22, 2022 | D330735 |
| A2411478 | Certificate of Analysis | Aug 22, 2022 | D330735 |
| A2411479 | Certificate of Analysis | Aug 22, 2022 | D330735 |
| A2411480 | Certificate of Analysis | Aug 22, 2022 | D330735 |
| Punto di fusione (°C) | 164 °C |
|---|---|
| Peso molecolare | 298.400 g/mol |
| XLogP3 | 2.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 298.193 Da |
| Monoisotopic Mass | 298.193 Da |
| Topological Polar Surface Area | 34.100 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 613.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 5 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
