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35073-27-9

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35073-27-9 Usage

General Description

2-methylbutyl formate is a chemical compound with the molecular formula C6H12O2. It is an ester, specifically the ester of 2-methyl-1-butanol and formic acid. This clear, colorless liquid has a fruity odor and is commonly used as a flavoring agent in the food and beverage industry, especially in the production of artificial fruit flavors. It is also used as a fragrance in perfumes and cosmetics. Additionally, 2-methylbutyl formate has insecticidal properties and is used in the formulation of insect repellents. It is important to handle this chemical with caution, as it may cause irritation to the eyes, skin, and respiratory system upon exposure.

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

35073-27-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name formic acid-(2-methyl-butyl ester)

1.2 Other means of identification

Product number -
Other names Ameisensaeure-(2-methyl-butylester)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:35073-27-9 SDS

35073-27-9Downstream Products

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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