25632-60-4

Basic information

• Product Name: 1-(2,4-dihydroxyphenyl)dodecan-1-one
• CAS NO: 25632-60-4
• Molecular Formula: C₁₈H₂₈O₃
• Molecular Weight: 292.4131
• Mol File: 25632-60-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 438.5°C at 760 mmHg
• Flash Point: 233.1°C
• Density: 1.033g/cm³
• Vapor Pressure: 2.67E-08mmHg at 25°C
• Refractive Index: 1.522
• CAS DataBase Reference: 1-(2,4-dihydroxyphenyl)dodecan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,4-dihydroxyphenyl)dodecan-1-one(25632-60-4)
• EPA Substance Registry System: 1-(2,4-dihydroxyphenyl)dodecan-1-one(25632-60-4)

Safety Data

• Hazardous Substances Data: 25632-60-4(Hazardous Substances Data)

Usage

General Description

1-(2,4-dihydroxyphenyl)dodecan-1-one is a chemical compound consisting of a dodecan-1-one backbone with a 2,4-dihydroxyphenyl group attached to the first carbon. Also known as 2,4-dihydroxyphenyl lauric ketone, this compound is commonly used in the fragrance and flavor industry due to its sweet, floral, and woody aroma. It is also used in cosmetic and personal care products as a fragrance ingredient. Additionally, 1-(2,4-dihydroxyphenyl)dodecan-1-one has been studied for its potential antioxidant and antimicrobial properties, making it a potentially valuable compound for various industrial and medicinal applications.

Upstream product

• 645-66-9 lauric anhydride 
• 108-46-3 recorcinol 
• 143-07-7 lauric acid 
• 112-16-3 n-dodecanoyl chloride 

Downstream Products

• 52066-81-6 Tridodecylresorcin 
• 52066-95-2 1.3-Didodecyl-2.4-dimethoxybenzol 
• 52066-80-5 2.4-Didodecylresorcin 
• 52066-94-1 1-Dodecyl-2.4-dimethoxybenzol 
• 101002-27-1 4-decyloxy-2-hydroxylaurophenone 
• 101002-21-5 4-octyloxy-2-hydroxylaurophenone oxime 
• 143286-67-3 1-(2-Hydroxy-4-pentyloxy-phenyl)-dodecan-1-one oxime 
• 143286-66-2 1-(4-Butoxy-2-hydroxy-phenyl)-dodecan-1-one oxime 
• 143286-65-1 1-(2-Hydroxy-4-methoxy-phenyl)-dodecan-1-one oxime 
• 24305-56-4 4-(n-dodecyl)resorcinol 
• 251463-52-2 2,4-diacetoxyphenyl undecyl ketone 
• 143286-99-1 1-(4-Decyloxy-2-hydroxy-phenyl)-dodecan-1-one 
• 101002-34-0 1-(2-Hydroxy-4-octyloxy-phenyl)-dodecan-1-one 
• 143286-96-8 2-hydroxy-4-methoxyphenyl undecyl ketone 

Relevant articles and documents

Synthesis and evaluation of aromatic methoxime derivatives against five postharvest phytopathogenic fungi of fruits. Main structure–activity relationships

The antifungal activity of a library of twenty-four aromatic methoximes was examined against five representative postharvest phytopathogenic fungi. The panel included Penicillium digitatum, Penicillium italicum, Rhizopus stolonifer, Botrytis cinerea and Monilinia fructicola, all of which cause relevant economic losses worldwide as a result of affecting harvested fruits. The minimum inhibitory concentrations and minimum fungicidal concentrations of each compound were defined and the main structure–activity relationships were determined. Although other congeners were more potent, drug likeliness considerations pointed to the methoxime derived from 2,4-dihydroxypropiophenone as the compound with the most suitable profile. The morphology of the colonies of the fungal strains treated with the methoxime was examined microscopically and the compound was also tested in freshly harvested peaches and oranges, exhibiting promising control profiles in both fruits, similar to those of the commercial agents Imazalil and Carbendazim.

Lipase-catalysed regio- and enantioselective deacetylation of 2,4-diacetoxyphenyl alkyl ketones

Porcine pancreatic lipase in tetrahydrofuran catalyses the deacetylation of 2,4-diacetoxyphenyl alkyl ketones in a highly regioselective fashion. The strategy of regioselective deacetylation of diacetoxyphenyl alkyl ketones has also resulted in the enanti