6281-40-9 Usage
Uses
Used in Flavor Industry:
3-Phenylpropyl hexanoate is used as a flavoring agent for its sweet, fruity taste, which is particularly reminiscent of peach and pineapple. It is commonly utilized in the creation of various food and beverage products to enhance their flavor profiles and provide a pleasant sensory experience for consumers.
Used in Fragrance Industry:
In the fragrance industry, 3-Phenylpropyl hexanoate is used as a fixative agent to help stabilize and prolong the scent of perfumes and other fragrance products. Its sweet, fruity, green odor adds a unique and appealing dimension to the overall fragrance, making it a valuable component in the formulation of various perfumes, colognes, and other scented products.
Used in Cosmetics and Personal Care Products:
3-Phenylpropyl hexanoate is also employed in the cosmetics and personal care industry, where it serves as an ingredient in the development of products such as lotions, creams, and shampoos. Its pleasant scent and flavor-enhancing properties contribute to the overall sensory experience of these products, making them more appealing to consumers.
Used in the Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 3-Phenylpropyl hexanoate may also find applications in the pharmaceutical industry, potentially serving as a flavoring agent for medications or as a component in the development of drug delivery systems due to its unique chemical properties and pleasant sensory characteristics.
Preparation
By esterification of phenylpropyl alcohol with n-hexanoic acid.
Check Digit Verification of cas no
The CAS Registry Mumber 6281-40-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,8 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6281-40:
(6*6)+(5*2)+(4*8)+(3*1)+(2*4)+(1*0)=89
89 % 10 = 9
So 6281-40-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O2/c1-2-3-5-12-15(16)17-13-8-11-14-9-6-4-7-10-14/h4,6-7,9-10H,2-3,5,8,11-13H2,1H3
6281-40-9Relevant academic research and scientific papers
Highly efficient esterification of carboxylic acids with alcohols by montmorillonite enwrapped titanium as a heterogeneous acid catalyst
Kawabata, Tomonori,Mizugaki, Tomoo,Ebitani, Kohki,Kaneda, Kiyotomi
, p. 9205 - 9208 (2007/10/03)
Montmorillonite-enwrapped titanium catalyst was found to efficiently promote the esterification of carboxylic acids with alcohols. In comparison to other catalysts reported to date, this heterogeneous catalyst offers a remarkably simple workup procedure, and is reusable without any appreciable loss in its activity and selectivity.
An Efficient Esterification Reaction between Equimolar Amounts of Free Carboxylic Acids and Alcohols by the Combined Use of Octamethylcyclotetrasiloxane and a Catalytic Amount of Titanium(IV) Chloride Tris(trifluoromethanesulfonate)
Izumi, Jun,Shiina, Isamu,Mukaiyama, Teruaki
, p. 141 - 142 (2007/10/02)
Various carboxylic esters are prepared in good to high yields from equimolar amounts of free carboxylic acids and alcohols by the combined use of octamethylcyclotetrasiloxane and a catalytic amount of TiCl(OTf)3.
A Novel Transesterification of Thioesters with Alcohols by an Electrochemical Activation
Yamaguchi, Masahiko,Tsukamoto, Yukiharu,Minami, Toru
, p. 1223 - 1226 (2007/10/02)
Esters were synthesized from thioesters and alcohols in high yields by an electrochemical activation.Different results were obtained by the use of n-Bu4N+ I- and LiBF4 as the electrolyte.
