35073-27-9 Usage
Description
2-methylbutyl formate is a chemical compound with the molecular formula C6H12O2, belonging to the ester class as the ester of 2-methyl-1-butanol and formic acid. This clear, colorless liquid is characterized by its fruity odor and is widely recognized for its applications across various industries.
Uses
Used in Food and Beverage Industry:
2-methylbutyl formate is used as a flavoring agent for imparting artificial fruit flavors to food and beverages, enhancing the sensory experience of consumers.
Used in Perfumery and Cosmetics Industry:
In the realm of perfumes and cosmetics, 2-methylbutyl formate serves as a fragrance ingredient, adding a pleasant and fruity scent to these products, thereby increasing their appeal to users.
Used in Pest Control Industry:
Leveraging its insecticidal properties, 2-methylbutyl formate is used in the formulation of insect repellents, providing a means to deter and control insect populations that may be harmful or bothersome.
It is crucial to handle 2-methylbutyl formate with care due to its potential to cause irritation to the eyes, skin, and respiratory system upon exposure, ensuring safety in its application across different sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 35073-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,7 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35073-27:
(7*3)+(6*5)+(5*0)+(4*7)+(3*3)+(2*2)+(1*7)=99
99 % 10 = 9
So 35073-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O2/c1-3-6(2)4-8-5-7/h5-6H,3-4H2,1-2H3
35073-27-9Relevant articles and documents
ETHERIFICATION PROCESS
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Page/Page column 24; 25, (2019/05/10)
The present invention relates to a process for preparing ethers, particularly unsymmetrical ethers, and preferably ethers suitable for use as base stocks for lubricant compositions. In particular, the process involves the reaction of an α,β-unsaturated aldehyde with a trihydrocarbyl orthoester to form an α,β-unsaturated acetal and conversion of the α,β- unsaturated acetal to an ether through hydrogenation and hydrogenolysis.
General Method for the Formylation of Alcohols with Dimethylformamide: An Extension of the Vilsmeier-Haack Reaction
Barluenga, Jose,Campos, Pedro J.,Gonzales-Nunez, Elena,Asensio, Gregorio
, p. 426 - 428 (2007/10/02)
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