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4-ethoxybutyl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60905-39-7

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60905-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60905-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,0 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60905-39:
(7*6)+(6*0)+(5*9)+(4*0)+(3*5)+(2*3)+(1*9)=117
117 % 10 = 7
So 60905-39-7 is a valid CAS Registry Number.

60905-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethoxybutyl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
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:60905-39-7 SDS

60905-39-7Downstream Products

60905-39-7Relevant academic research and scientific papers

A process for the preparation of acetate

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Paragraph 0065; 0066; 0067; 0068, (2017/01/26)

The invention relates to an acetate preparation method. The method comprises the following steps: carrying out a contact reaction of sec-butyl acetate and alcohol in the presence of an ester exchange catalyst under an ester exchange reaction condition, adding products obtained after the contact reaction into a separation tower, controlling the tower top temperature to separate unreacted sec-butyl acetate and sec-butyl alcohol generated after the reaction from the tower top, and carrying out normal-pressure or reduced-pressure flash evaporation to separate acetate generated after the reaction from a tower bottom fraction, wherein the alcohol is alcohol having a general formula of R(OH)n and/or polyol alkylether having at least one hydroxy group, R is a C5-C20 n-valence alkyl group, a C5-C20 n-valence alkenyl group, a C5-C12 n-valence cycloalkyl group or a C7-C20 n-valence aryl group, and n is an integer in a range of 1-5. The method has the advantages of high conversion rate of the alcohol as a reaction raw material, and high acetate selectivity.

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