75705-48-5

Usage

Uses

Used in Fragrance Industry:
Geranyl propionate is used as a fragrance ingredient for its sweet, floral, and slightly fruity aroma. It is particularly valued for its ability to add depth and complexity to perfumes, colognes, and other scented products, making it a staple in the fragrance industry.
Used in Flavor Industry:
In the flavor industry, geranyl propionate serves as a flavoring agent in the food and beverage sector. Its pleasant and aromatic taste enhances the overall flavor profile of various products, contributing to a more enjoyable consumer experience.
Used in Personal Care Products:
Geranyl propionate is also utilized in the production of personal care products due to its appealing scent and taste. It can be found in a range of products, from lotions and creams to shampoos and conditioners, where it provides a pleasant sensory experience for the user.
Used in Household Cleaners:
(E)-3,7-Dimethyl-2,7-octadien-1-ol propanoate is further employed in the formulation of household cleaners, where it not only contributes to the cleaning efficacy but also leaves a fresh and inviting scent, making the cleaning process more enjoyable for consumers.
Used in Commercial Goods Production:
Geranyl propionate's multifaceted applications extend to the production of various other commercial goods, where its incorporation enhances the sensory appeal and overall consumer experience.

InChI:InChI=1/C13H22O2/c1-5-13(14)15-10-9-12(4)8-6-7-11(2)3/h9H,2,5-8,10H2,1,3-4H3/b12-9+

Upstream product

• 104857-56-9 Propionic acid (E)-3,7-dimethyl-7-(2,2,2-trifluoro-acetoxy)-oct-2-enyl ester 
• 29021-98-5 3-(2-methyl-[1,3]dioxolan-2-yl)-propan-1-ol 
• 79-03-8 propionyl chloride 

Relevant academic research and scientific papers

7-METHYL-3-METHYLENE-7-OCTENAL ACETAL COMPOUND AND METHODS FOR PRODUCING ALDEHYDE COMPOUND AND ESTER COMPOUND USING THE SAME

There are provided methods of efficiently producing compounds that are, for example, sex pheromones of San Jose Scale. For example, there is provided a method for producing a 7-methyl-3-methylene-7-octenyl carboxylate compound (4), the method including the steps of: hydrolyzing a 7-methyl-3-methylene-7-octenal acetal compound (1) to obtain 7-methyl-3-methylene-7-octenal (2); reducing the 7-methyl-3-methylene-7-octenal (2) to obtain 7-methyl-3-methylene-7-octenol (3); and esterifying the 7-methyl-3-methylene-7-octenol (3) to obtain a 7-methyl-3-methylene-7-octenyl carboxylate compound (4).

SYNTHESIS OF THE PHEROMONES, (E)-3,7-DIMETHYL-2,7-OCTADIENYL PROPIONATE, (E)-3,7-DIMETHYL-2-OCTENE-1,8-DIOL AND FRONTALIN FROM A COMMON INTERMEDIATE

Ketal ester 9 has been prepared in five steps from methyl levulinate 4 (scheme 1).The propionate 1, diol 2 and (+/-) frontalin 3 were prepared from ester 9 employing the routes shown in scheme 2,3 and 4 respectively.The branched chain alkenes 13 and 20 were prepared conveniently from the primary alcohols 11 and 10 following the procedure of S.Wolff.Triethyl phosphonopropionate 7 has been prepared by methylating triethylphosphonoacetate with methyl iodide in the presence of sodium hydride.

A SIMPLE METHOD OF ISOMERIZATION OF THE TERMINAL DOUBLE BOND IN A TERPENE CHAIN

The utilisability of the isomerization of the terminal double bond in terpenic compounds with trifluoroacetic acid was investigated.The results obtained were used in the synthesis of the main part of the pheromone of Quadraspidiotus perniciosus COMSTOCK, i.e. (2E)-3,7-dimethyl-2,7-octadien-1-yl propionate.