885-98-3

Usage

Uses

Used in Fragrance Industry:
2,5-dimethylbenzene-1,4-diyl diacetate is utilized as a fixative in perfumes, helping to prolong the scent's longevity on the skin. It also serves as a base note, providing a rich, deep foundation to the overall fragrance profile.
Used in Food Industry:
As a flavoring agent, 2,5-dimethylbenzene-1,4-diyl diacetate enhances the taste of food products, adding a subtle sweetness and complexity to the flavor profile.
Used in Pharmaceutical Industry:
2,5-dimethylbenzene-1,4-diyl diacetate has potential applications in the pharmaceutical sector, where its chemical properties may be harnessed for the development of new drugs or as an intermediate in the synthesis of existing medications.
Used in Agricultural Industry:
2,5-dimethylbenzene-1,4-diyl diacetate's potential applications in agriculture suggest that it could be used in the development of new agrochemicals or as a component in pest control strategies, taking advantage of its chemical properties to improve crop protection and yield.

Upstream product

• 615-90-7 2,5-dimethylhydroquinone 
• 108-24-7 acetic anhydride 
• 137-18-8 2,5-Dimethyl-1,4-benzoquinone 
• 64-19-7 acetic acid 
• 106-42-3 para-xylene 

Downstream Products

• 5253-07-6 2,5-dimethyl-3,6-dinitro-1,4-benzoquinone 
• 7059-65-6 2.5-Dimethyl-3-acetylamino-6-nitro-hydrochinondiacetat 
• 7059-64-5 2.5-Dimethyl-3-amino-6-nitro-hydrochinon 
• 6995-66-0 2-Acetoxymethyl-5-methyl-3,6-dinitro-hydrochinon-diacetat 
• 6995-65-9 2-Methoxymethyl-5-methyl-3,6-dinitro-hydrochinondimethylaether 
• 7059-66-7 2-Methoxymethyl-5-methyl-3,6-dinitro-hydrochinon 
• 6995-64-8 2,5-Dimethyl-3,6-dinitro-hydrochinon-dimethylether 
• 6995-70-6 2,5-Dimethyl-3,6-dinitro-hydrochinon-diacetat 
• 5253-06-5 2,5-Dimethyl-3,6-dinitro-hydrochinon 

Relevant academic research and scientific papers

OXYGENATION OF AROMATIC AND ALIPHATIC HYDROCARBONS BY A NEW REAGENT SYSTEM, Fe(CH3CN)6(2+)-H2O2-Ac2O: AN EFFECTIVE MODEL REAGENT FOR MONO-OXYGENASE

Reactions of aromatic and aliphatic hydrocarbons with a new system, Fe(CH3CN)6(2+) - H2O2 - Ac2O in CH3CN, gave oxygenation products with fairly high reaction efficiency ( Tables I and II )compared to known to reagent systems used as enzyme models for mono-oxygenases.Investigations of the mechanism of these reactions indicated the involvement of either complex C.FeIV(OH)(OAc)(2+), or complex D, FeIV(OAc)(2+), dependig on the organic substrate.Keywords-oxygenation; aromatic hydrocarbon; aliphatic hydrocarbon; hexakisacetonitrile iron(II) perchlorate; hydrogen peroxide; enzyme model; mono-oxygenase