1168-52-1

Usage

Uses

Used in Dietary Supplements:
2,3-Dimethyl-5-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl]-2,5-cyclohexadiene-1,4-dione is used as a dietary supplement for its essential role in maintaining healthy skin, hair, and nails. It provides various health benefits, such as boosting the immune system, reducing the risk of heart disease, and supporting eye health.
Used in Cosmetic Products:
In the cosmetic industry, 2,3-Dimethyl-5-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl]-2,5-cyclohexadiene-1,4-dione is used as an antioxidant and anti-inflammatory agent for its ability to protect the skin from oxidative damage and reduce inflammation. This contributes to improved skin health and appearance.
Used in Pharmaceutical Products:
2,3-Dimethyl-5-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl]-2,5-cyclohexadiene-1,4-dione is utilized in pharmaceutical products as an antioxidant and anti-inflammatory agent. Its properties help protect cells from oxidative damage and reduce inflammation, making it beneficial for various health conditions and treatments.
Used in Food Industry:
In the food industry, 2,3-Dimethyl-5-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl]-2,5-cyclohexadiene-1,4-dione is used as a natural antioxidant to extend the shelf life of food products and maintain their freshness. Its presence helps prevent the oxidation of fats and oils, ensuring the quality and safety of the products.

Upstream product

• 608-43-5 2,3-dimethyl-1,4-dihydroxybenzene 
• 526-86-3 2,3-dimethyl-1,4-benzoquinone 
• 110107-11-4 2,3-Dimethyl-5-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienyl)-benzene-1,4-diol 

Relevant academic research and scientific papers

Synthesis of plastoquinone derivatives with different structures of the side chain

Two schemes for the synthesis of plastoquinone derivatives with ω-substituted alkyl side chains have been developed, based on radical alkylation of 2,3-dimethyl-1,4-benzoquinone with ω-substituted carboxylic and/or dicarboxylic acids in the presence of S2O82- and Ag+.In Scheme 1, radical alkylation of 2,3-dimethyl-1,4-benzoquinone with 11-bromoundecanoic acid, in the presence of (NH4)2S2O8 and AgNO3, gave 2,3-dimethyl-5-(10-bromodecyl)-1,4-benzoquinone, which, after hydration, gave 2,3-dimethyl-5-(10-hydroxydecyl)-1,4-benzoquinone.Esterification of 2,3-dimethyl-5-(10-hydroxydecyl)-1,4-benzoquinone with different acyl chlorides gave 2,3-dimethyl-5-(10-acyloxydecyl)-1,4-benzoquinone.In Scheme 2, radical alkylation of 2,3-dimethyl-1,4-benzoquinone with adipic acid, in the presence of K2S2O8 and AgNO3, gave 2,3-dimethyl-5-(4-carboxybutyl)-1,4-benzoquinone, which was converted to 2,3-dimethyl-5--1,4-benzoquinone by esterification with different alcohols in the presence of dicyclohexylcarbodiimide. 2,3-Dimethyl-5-(8-carboxyoctyl)-1,4-benzoquinone and 2,3-dimethyl-5--1,4-benzoquinone were similarly synthesized from 2,3-dimethyl-1,4-benzoquinone and sebacic acid.Plastoquinone derivatives having different kinds of double bonds in the side chain with and without a 6-methyl group were synthesized from 2,3,5-trimethyl-1,4-benzoquinone and 2,3-dimethyl-1,4-benzoquinone by successive reactions with (1) NaBH4; (2) KHSO4, different kinds of allylic alcohols; (3) Ag2O.The allylic alcohols were prepared from their corresponding aldehydes by reduction with NaBH4. 2,3,6-Trimethyl-1,4-benzoquinone by radical methylation with acetic acids in the presence of K2S2O8 + AgNO3.