6313-88-8

Basic information

• Product Name: 4'-Dodecylacetophenone
• Synonyms: 1-(4-Dodecylphenyl)ethanone;4'-Dodecylacetophenone;Acetophenone, 4'-dodecyl-;Ethanone, 1-(4-dodecylphenyl)-;Nsc 39806;p-Dodecylacetophenone;p-Dodecylphenyl methyl ketone;p-Laurylacetophenone
• CAS NO: 6313-88-8
• Molecular Formula: C₂₀H₃₂O
• Molecular Weight: 288.4675
• Mol File: 6313-88-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 400.6°Cat760mmHg
• Flash Point: 169.1°C
• Appearance: /
• Density: 0.904g/cm³
• Vapor Pressure: 1.26E-06mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: 4'-Dodecylacetophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-Dodecylacetophenone(6313-88-8)
• EPA Substance Registry System: 4'-Dodecylacetophenone(6313-88-8)

Safety Data

• Hazardous Substances Data: 6313-88-8(Hazardous Substances Data)

Usage

General Description

4'-Dodecylacetophenone is a chemical compound with the molecular formula C18H28O. It is a ketone with a dodecyl chain attached to the acetophenone ring. 4'-Dodecylacetophenone is commonly used in organic synthesis as a starting material for the preparation of various chemical compounds, including pharmaceuticals, pesticides, and fragrances. It is also used as a flavoring agent in the food industry. Additionally, 4'-Dodecylacetophenone has been studied for its potential antibacterial and antifungal properties, making it a promising candidate for the development of new antimicrobial agents. Overall, 4'-Dodecylacetophenone has a wide range of applications in various industries due to its versatile chemical properties.

InChI:InChI=1/C20H32O/c1-3-4-5-6-7-8-9-10-11-12-13-19-14-16-20(17-15-19)18(2)21/h14-17H,3-13H2,1-2H3

Upstream product

• 108-24-7 acetic anhydride 
• 123-01-3 1-dodecylbenzene 
• 75-36-5 acetyl chloride 
• 17746-06-4 n-tridecanoyl chloride 
• 6005-99-8 1-phenyltridecan-1-one 
• 638-53-9 tridecanoic acid 

Downstream Products

• 21021-55-6 4-dodecylbenzoic acid 
• 65189-92-6 1-(1-hydroxyethyl)-4-dodecylbenzene 
• 102707-42-6 4-(4-dodecyl-phenyl)-thiazol-2-ylamine 
• 95706-37-9 1-(4-ethyl-phenyl)-dodecane 
• 133633-72-4 p-(n-dodecyl)phenylacetic acid 
• 86849-47-0 bis(p-n dodecyl benzoyl) methane 
• 3663-30-7 N-acetyl-4-n-dodecylaniline 
• 78575-64-1 (4-Dodecyl-phenyl)-oxo-acetaldehyde oxime 
• 75817-94-6 2,6,2',6'-Tetrakis-(4-dodecyl-phenyl)-[4,4']bipyranylidene 
• 75818-00-7 2,6-Bis-(4-dodecyl-phenyl)-pyranylium; perchlorate 
• 53097-38-4 methyl 3-(4-dodecylphenyl)-3-oxopropanoate 
• 66218-69-7 p-(n-dodecyl)styrene 
• 94763-54-9 1-Amino-2-n-dodecyl-5-ethylbenzol 
• 5519-35-7 p-(n-dodecyl)benzyl alcohol 

Relevant articles and documents

Ultrafast relaxation processes of triarylpyrylium cations

The time evolution of the fluorescence and the photoinduced absorption spectra of four triarylpyrylium cations, differing in the number of dodecyl chains attached to the chromophore, was studied by means of femtosecond fluorescence upconversion and picose

Synthesis, insecticidal evaluation of novel 1,3,4-thiadiazole chrysanthemamide derivatives formed by an EDCI/HOBt condensation

A series of novel pesticides with two components derived from a 1,3,4-thiadiazole and chrysanthemic acid were synthesised via an EDCI/HOBt condensation. These 1,3,4-thiadiazole chrysanthemamides were identified by IR, 1H NMR and elemental analyses. Their insecticidal activity was also evaluated.

One-step synthesis of novel flavylium salts containing alkyl side chains in their 3-, 4′-, 5- or 6-positions and their photophysical properties in micellar media

A one-step preparation of several flavylium salts containing alkyl side chains in their 3-, 4′-, 5- or 6-positions is described. Flavylium salts with alkyl side chains in positions 3 or 4′ were isolated from reactions between 2,4-dihydroxybenzaldehyde and