25632-60-4

Usage

Uses

Used in Fragrance and Flavor Industry:
1-(2,4-dihydroxyphenyl)dodecan-1-one is used as a fragrance ingredient for its sweet, floral, and woody aroma, adding depth and complexity to perfumes, colognes, and other scented products.
Used in Cosmetic and Personal Care Products:
In the cosmetic and personal care industry, 1-(2,4-dihydroxyphenyl)dodecan-1-one is used as a fragrance component, enhancing the sensory experience of products such as lotions, creams, and shampoos.
Used in Antioxidant Applications:
1-(2,4-dihydroxyphenyl)dodecan-1-one is studied for its potential antioxidant properties, which could make it a valuable additive in the food and pharmaceutical industries to extend shelf life and improve product quality.
Used in Antimicrobial Applications:
1-(2,4-dihydroxyphenyl)dodecan-1-one's potential antimicrobial properties suggest that it could be utilized in various applications where controlling the growth of microorganisms is essential, such as in the medical, food preservation, and water treatment industries.

Upstream product

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

Downstream Products

• 143286-97-9 1-(4-Butoxy-2-hydroxy-phenyl)-dodecan-1-one 
• 101002-34-0 1-(2-Hydroxy-4-octyloxy-phenyl)-dodecan-1-one 
• 143286-99-1 1-(4-Decyloxy-2-hydroxy-phenyl)-dodecan-1-one 
• 24305-56-4 4-(n-dodecyl)resorcinol 
• 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 
• 251463-52-2 2,4-diacetoxyphenyl undecyl ketone 

Relevant academic research and scientific papers

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.

ANTIBACTERIAL AGENTS AGAINST DRUG-RESISTANT STAPHYLOCOCCUS AUREUS OR VANCOMYCIN-RESISTANT ENTEROCOCCUS AND ANTIFUNGAL AGENTS COMPRISING STEPHANITIS SVENSONI-DERIVED POLYKETIDE OR SYNTHETIC ANALOGS THEREOF

PROBLEM TO BE SOLVED: To provide antibacterial or antifungal agents comprising a naturally occurring substance or synthetic analogs thereof having high antibacterial activity against methicillin-resistant Staphylococcus aureus or vancomycin-resistant Ente

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

Synthese von 4-Alkoxy-2-hydroxyphenylketoximen als Metallextraktions-Reagenzien

The C-Acylation (Friedel-Crafts reaction) of resorcinol with aluminium chloride, the monoetherification in 4-position of the resulting 2,4-dihydroxyphenylketones, and the preparation of oximes (8, 9, 10, 11) from this ketones were investigated.The compounds obtained are characterized by elemental analysis, and the i.r., u.v. and 1H-n.m.r. spectra are discussed.Solubility data of some oximes are determined in water, octane and toluene.The extraction properties for copper-(II)-and iron-(III)-ions are measured by isotope methods in relation to the extragent structure, the extraction time and the pH-range.