6640-78-4 Usage
Uses
Used in the Cosmetics and Personal Care Industry:
Isobutyl benzoate is utilized as a fragrance ingredient and solvent due to its pleasant scent and ability to dissolve other substances. It enhances the sensory experience of cosmetic products while aiding in the formulation process.
Used as a Flavoring Agent in the Food Industry:
In the food industry, isobutyl benzoate serves as a flavoring agent, imparting a desirable taste to various food products, thereby improving their overall appeal to consumers.
Used as a Plasticizer in the Plastics and Resins Manufacturing Industry:
Isobutyl benzoate is employed as a plasticizer in the production of plastics and resins. It helps to increase the flexibility and workability of these materials, making them more suitable for a range of applications.
Safety Considerations:
While isobutyl benzoate is considered safe and non-toxic when used in controlled amounts, it is important to note that high concentrations can cause irritation to the skin and eyes. Therefore, proper handling and usage guidelines should be followed to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 6640-78-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,4 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6640-78:
(6*6)+(5*6)+(4*4)+(3*0)+(2*7)+(1*8)=104
104 % 10 = 4
So 6640-78-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O2/c1-9(2)8-14-12(13)11-6-4-5-10(3)7-11/h4-7,9H,8H2,1-3H3
6640-78-4Relevant academic research and scientific papers
Hu, Yongke,Li, Bindong
, p. 7301 - 7307 (2017)
A highly efficient palladium-catalyzed approach for the direct oxidative esterification of benzylic alcohols with methanol and long-chain aliphatic alcohols under mild conditions has been achieved. This practical catalyst system exhibits a broad substrate scope and good functional group tolerance. Catalytic amount of Bi(OTf)3 is used as co-catalyst to improve the activity and selectivity of the reactions. A variety of esters are obtained in yields of 43–96%.
