60826-15-5

Usage

Uses

Used in Flavor and Fragrance Industry:
3-Hydroxynonyl acetate is used as a flavoring agent for its fruity, waxy, and floral taste characteristics at 10 ppm. It adds a unique and pleasant taste to food and beverage products.
3-Hydroxynonyl acetate is also used as a fragrance ingredient for its herbaceous, fruity, warm, and ethereal odor. It is ideal for creating captivating and long-lasting scents in perfumes, cosmetics, and personal care products.
Used in Aromatherapy:
3-Hydroxynonyl acetate is used as an aromatherapeutic essential oil for its sweet, green apple skin scent with an aldehydic background. It can help promote relaxation, reduce stress, and create a calming atmosphere.
Used in Perfumery:
3-Hydroxynonyl acetate is used as a fixative in perfumery for its ability to extend the longevity of fragrances. Its unique aroma characteristics can add depth and complexity to perfume compositions, making them more appealing and long-lasting.

InChI:InChI=1/C11H22O2/c1-4-6-7-8-9-11(5-2)13-10(3)12/h11H,4-9H2,1-3H3

Upstream product

• 185019-15-2 nonan-3-ol 
• 141-78-6 ethyl acetate 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Relevant academic research and scientific papers

Ethyl acetate as an acetyl surrogate for the iodine catalyzed acetylation of alcohols

The use of readily available ethyl acetate in the presence of iodine as an alternative acetylating agent is reported. Amines and phenols were unreactive under the examined reaction conditions, indicating that the method is highly chemoselective.

An algorithm for the deconvolution of mass spectrosopic patterns in isotope labeling studies. Evaluation for the hydrogen-deuterium exchange reaction in ketones

(Graph Presented) An easy to use computerized algorithm for the determination of the amount of each labeled species differing in the number of incorporated isotope labels based on mass spectroscopic data is described and evaluated. Employing this algorithm, the microwave-assisted synthesis of various α-labeled deuterium ketones via hydrogen-deuterium exchange with deuterium oxide was optimized with respect to time, temperature, and degree of labeling. For thermally stable ketones the exchange of α-protons was achieved at 180°C within 40-200 min. Compared to reflux conditions, the microwave-assisted protocol led to a reduction of the required reaction time from 75-94 h to 40-200 min. The α-labeled deuterium ketones were reduced by biocatalytic hydrogen transfer to the corresponding enantiopure chiral alcohols and the deconvolution algorithm validated by regression analysis of a mixture of labeled and unlabeled ketones/alcohols.