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

91635-41-5

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91635-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91635-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,6,3 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 91635-41:
(7*9)+(6*1)+(5*6)+(4*3)+(3*5)+(2*4)+(1*1)=135
135 % 10 = 5
So 91635-41-5 is a valid CAS Registry Number.

91635-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethoxydecane

1.2 Other means of identification

Product number -
Other names 3-ethoxy-decane

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:91635-41-5 SDS

91635-41-5Downstream Products

91635-41-5Relevant academic research and scientific papers

Selective synthesis of 2-ethoxy alkanes through ethoxylation of 1-alkenes with bioethanol over zeolite beta catalyst in a liquid phase continuous process

Radhakrishnan, Sambhu,Franken, Joris,Martens, Johan A.

, p. 1475 - 1479 (2012)

1-Hexene was ethoxylated with ethanol and ethanol-water mixtures mimicking bioethanol in a liquid phase, continuous flow process over a fixed bed of zeolite beta catalyst at a reaction temperature of 423 K and a pressure of 6 MPa. The selectivity for ethoxy alkanes on a hexene basis exceeded 90%. GC-MS, 1H & 13C-NMR and 13C DEPT NMR confirmed the main reaction products to be 2-ethoxy hexane and 3-ethoxy hexane in molar ratio 20:1. Side products were diethyl ether from ethanol and dodecenes and hexanol from 1-hexene. Under optimized reaction conditions, the catalyst was stable for at least 14 hours on-stream. The 2-ethoxylation activity of 1-alkenes by zeolite beta was confirmed in reactions with 1-octene and 1-decene. 1-Alkenes can be synthesized out of biomass via conversion into synthesis gas and the Fischer-Tropsch process. The here presented ethoxylation process could contribute green chemicals to the diesel pool and presents a pathway for synthesis of high boiling solvents.

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