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1-butoxyoctane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53839-23-9

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53839-23-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53839-23-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,8,3 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53839-23:
(7*5)+(6*3)+(5*8)+(4*3)+(3*9)+(2*2)+(1*3)=139
139 % 10 = 9
So 53839-23-9 is a valid CAS Registry Number.

53839-23-9SDS

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 1-butoxyoctane

1.2 Other means of identification

Product number -
Other names 1-butoxy-octane

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:53839-23-9 SDS

53839-23-9Downstream Products

53839-23-9Relevant academic research and scientific papers

PROCESS FOR MAKING A COMPOSITION COMPRISING AT LEAST TWO DIFFERENT DIALKYL ETHERS

-

Page/Page column 17, (2009/06/27)

The present invention relates to a process for making a composition comprising at least two different ethers using ethanol, or a combination of ethanol and methanol, as a starting material.

Reductive O- and N-alkylations. Alternative catalytic methods to nucleophilic substitution

Fache, Fabienne,Bethmont, Valerie,Jacquot, Laurent,Lemaire, Marc

, p. 231 - 238 (2007/10/03)

Different amides have been selectively mono-N-alkylated using catalytic heterogeneous palladium and carbonyl compounds as alkylating agents. The same salt free method has been applied to the synthesis of ethers from alcohols. Reaction parameters have been studied in detail and a mechanism is proposed.

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