10225-39-5 Usage
Uses
Used in Food and Beverage Industry:
2-Butyl-1-phenyl-1,3-butanedione is used as a flavoring agent for imparting a rich, buttery, and creamy taste to various food products and beverages. Its ability to mimic the flavor of dairy products without the use of actual dairy ingredients makes it a popular choice for enhancing the taste profile of a wide range of consumables.
Used in Perfumery and Fragrance Industry:
In the realm of perfumes and colognes, 2-Butyl-1-phenyl-1,3-butanedione serves as a key component in creating complex and appealing scents. Its buttery aroma adds depth and richness to fragrance compositions, contributing to a more luxurious and comforting olfactory experience.
Used in Cosmetics and Personal Care Products:
Beyond its applications in food and fragrances, 2-Butyl-1-phenyl-1,3-butanedione also finds use in the cosmetics and personal care industry. It can be incorporated into products such as lotions, creams, and soaps to provide a pleasant, creamy scent that enhances the sensory experience of using these products.
Used in Aromatherapy:
The soothing and comforting aroma of 2-Butyl-1-phenyl-1,3-butanedione makes it a suitable candidate for use in aromatherapy. It can be used in diffusers or blended with other essential oils to create custom aromatherapy blends designed to promote relaxation and a sense of well-being.
Used in Industrial Applications:
Beyond consumer products, 2-Butyl-1-phenyl-1,3-butanedione may also be utilized in industrial settings for its chemical properties. For instance, it could be employed as a starting material or intermediate in the synthesis of other organic compounds, or as a component in the production of certain types of plastics or coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 10225-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,2 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10225-39:
(7*1)+(6*0)+(5*2)+(4*2)+(3*5)+(2*3)+(1*9)=55
55 % 10 = 5
So 10225-39-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O2/c1-3-4-10-13(11(2)15)14(16)12-8-6-5-7-9-12/h5-9,13H,3-4,10H2,1-2H3
10225-39-5Relevant academic research and scientific papers
Iridium-catalyzed reaction of enones with alcohols affording 1,3-diketones
Obora, Yasushi,Nakamura, Kazuhiro,Hatanaka, Shintaro
supporting information; experimental part, p. 6720 - 6722 (2012/07/17)
An iridium-catalyzed coupling reaction of alcohols with enones has been successfully developed providing access to 1,3-diketones with high selectivity in good yields. This reaction provides an atom-economical route to 1,3-diketones from readily available
Facile syntheses of 2,2-dimethyl-6-(2-oxoalkyl)-1,3-dioxin-4-ones and the corresponding 6-substituted 4-hydroxy-2-pyrones
Katritzky, Alan R.,Wang, Zuoquan,Wang, Mingyi,Hall, C. Dennis,Suzuki, Kazuyuki
, p. 4854 - 4856 (2007/10/03)
A variety of 2,2-dimethyl-6-(2-oxoalkyl)-1,3-dioxin-4-ones 5a-l and the corresponding 6-substituted 4-hydroxy-2-pyrones 3a-l were prepared in high yields under mild reaction conditions by the reaction of 2,2,6-trimethyl-1,3- dioxin-4-one 4 with 1-acylbenz
Convenient, High-Yield Method for the Methylation of 1,3-Diketones
Choudhary, Anil,Baumstark, Alfons L.
, p. 688 - 690 (2007/10/02)
A general method for the facile dimethylation of 1,3-diketones is presented.The method involves the use of readily available, inexpensive reagents and is carried out under mild conditions.Monomethylation may be carried out by slight modification (simplification) of the procedure.Several examples are presented which show that the method is applicable to alkylations with primary halides as well.Isolated yields for monoalkylation are approximately 95percent while those for dialkylation are ca. 90percent.Alkylation is taking place by the reaction of the enolates of 1,3-diketones with alkyl halides.
