Determine the necessary mass, volume, or concentration for preparing a solution.
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Il benzilideneacetone è utilizzato nell'industria dei profumi per il suo odore di pisello dolce. È uno dei principali costituenti dell'olio essenziale di Monanthotaxis capea.[1] Alcuni studi suggeriscono che, oltre allo skatole e all'androstenone, anche il benzilideneacetone potrebbe essere uno dei composti volatili che contribuiscono allo sviluppo dell'odore di cinghiale nei campioni di grasso
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Classe | Benzene and substituted derivatives |
| Subclass | Styrenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Styrenes |
| Alternative Parents | Enones Acryloyl compounds Ketones Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Styrene - Alpha,beta-unsaturated ketone - Enone - Acryloyl-group - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as styrenes. These are organic compounds containing an ethenylbenzene moiety. |
| External Descriptors | benzylideneacetone |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
| Certificate of Analysis | Jul 03, 2026 | P111783 | |
| Certificate of Analysis | Jan 19, 2026 | P111783 | |
| Certificate of Analysis | Jan 19, 2026 | P111783 | |
| Certificate of Analysis | Aug 15, 2024 | P111783 | |
| Certificate of Analysis | Jul 23, 2024 | P111783 | |
| Certificate of Analysis | Jul 23, 2024 | P111783 | |
| Certificate of Analysis | Jul 23, 2024 | P111783 | |
| Certificate of Analysis | May 06, 2024 | P111783 | |
| Certificate of Analysis | May 06, 2024 | P111783 | |
| Certificate of Analysis | Apr 11, 2022 | P111783 |
| Solubilità | Soluble in alcohol, chloroform, diethyl ether. |
|---|---|
| Sensibilità | Light sensitive. |
| Indice di rifrazione | 1.8536 |
| Punto di infiammabilità (°F) | 123℃ |
| Punto di infiammabilità (°C) | 123℃ |
| Punto di ebollizione (°C) | 260-262°C |
| Punto di fusione (°C) | 39-41°C |
| Peso molecolare | 146.190 g/mol |
| XLogP3 | 2.100 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 146.073 Da |
| Monoisotopic Mass | 146.073 Da |
| Topological Polar Surface Area | 17.100 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 152.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 1 |