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Usage

Uses

Used in Traditional Medicine:
6-Hydroxy-2,6-dimethyl-2,7-octadieic acid is used as a traditional medicine ingredient for its potential therapeutic properties. It is known for its anti-inflammatory and anti-allergic effects, making it a valuable component in the treatment of various health conditions.
Used in Aromatherapy:
In the aromatherapy industry, 6-Hydroxy-2,6-dimethyl-2,7-octadieic acid is used as a natural aroma compound for its characteristic scent. It is extracted from plants in the Lamiaceae family and utilized in various aromatherapy products to provide a pleasant and soothing fragrance.
Used in Flavoring Agents:
6-Hydroxy-2,6-dimethyl-2,7-octadieic acid is used as a flavoring agent in the food and beverage industry. Its unique aroma and flavor profile make it a desirable ingredient in the creation of various food products, enhancing taste and aroma.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, 6-Hydroxy-2,6-dimethyl-2,7-octadieic acid is used as a natural ingredient for its potential anti-inflammatory and anti-allergic properties. It can be incorporated into skincare products, hair care products, and other personal care formulations to provide soothing and beneficial effects for the users.
Used in Pharmaceutical Development:
6-Hydroxy-2,6-dimethyl-2,7-octadieic acid is used as a potential pharmaceutical candidate for its therapeutic properties. Researchers are studying its anti-inflammatory and anti-allergic effects to develop new drugs and treatments for various health conditions.
Used in Agricultural Applications:
In agriculture, 6-Hydroxy-2,6-dimethyl-2,7-octadieic acid can be used as a natural pest repellent or as a component in the development of plant growth regulators. Its unique chemical properties may offer potential benefits in enhancing crop growth and protection against pests.

InChI:InChI=1/C10H16O3/c1-4-10(3,13)7-5-6-8(2)9(11)12/h4,6,13H,1,5,7H2,2-3H3,(H,11,12)/b8-6+

Upstream product

• 1370004-83-3 9-(6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-β-D-glucopyranosyloxy)guaiacylglycerol 
• 1370004-84-4 9-(6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-β-D-glucopyranosyloxy)syringoylglycerol 
• 1384485-03-3 6-O-[(2E,6S)-2,6-dimethyl-6-hydroxy-2,7-octadienoyl]-(α-β)-D-glucopyranose 
• 83905-61-7 phlebotrichin 
• 92751-87-6 (6S)-2-trans-6-α-L-arabinopyranosyloxy-2,6-dimethyl-2,7-octadienoic acid 
• 110065-68-4 gymnocladus saponin F₁ 

Relevant academic research and scientific papers

α-Glucosidic hydroquinone derivatives from Viburnum erosum

Six undescribed compounds (1–6) were isolated from the leaves of Viburnum erosum along with four known compounds 7–10. The structures were determined by NMR and MS spectroscopic analyses, and their absolute configurations were established by chemical and

New CuCl2-induced glucoside esters and other constituents from Portucala oleracea

Two new glucoside esters 1 and 2 were produced as stress metabolites in the fresh leaves of Portulaca oleracea, in response to abiotic stress elicitation by CuCl2. A new sugar ester (3) and two known compounds (4 and 5) were also isolated. Their structures were established by spectroscopic means. The antioxidative activities of stress metabolites and the related isolates were evaluated by DPPH assay. The results showed that new stress-driven adducts of monolignans and monoterpenes with a glucose bridge exhibited much stronger antioxidative activities than other compounds.

Studies on the Constituents of Leguminous Plants. X. The Structures of New Triterpenoid Saponins from the Fruits of Gymnocladus chinensis BAILLON

Four new triterpenoid saponins, gymnocladus saponins F2 (1), F1 (2), E (3) and D1 (4), were isolated from the fruits of Gymnocladus chinensis BAILLON.On the basis of chemical and physicochemical evidence, they were characterized structurally as 3,28-bisglycosides of 2β,23-dihydroxyacacic acid having a glycosyl monoterpene carboxylate as an acyl moiety.