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2,3-Diisopropoxy-1-propanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63716-05-2

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63716-05-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63716-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,1 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63716-05:
(7*6)+(6*3)+(5*7)+(4*1)+(3*6)+(2*0)+(1*5)=122
122 % 10 = 2
So 63716-05-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H20O3/c1-7(2)11-6-9(5-10)12-8(3)4/h7-10H,5-6H2,1-4H3

63716-05-2SDS

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 1,2-Diisopropyl glycerol diether

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:63716-05-2 SDS

63716-05-2Downstream Products

63716-05-2Relevant academic research and scientific papers

Glycerol Isopropyl Ethers: Direct Synthesis from Alcohols and Synthesis by the Reduction of Solketal

Samoilov, Vadim O.,Onishchenko, Maria O.,Ramazanov, Dzhamalutdin N.,Maximov, Anton L.

, p. 2839 - 2849 (2017/07/28)

The catalytic reduction of solketal ((2,2-dimethyl-1,3-dioxolan-4-yl)methanol) over bifunctional heterogeneous palladium catalysts is proposed as an alternative to the synthesis of glycerol isopropyl ethers by the etherification of glycerol. The direct synthesis of glycerol isopropyl ethers from isopropanol and glycerol requires severe conditions (T=130–150 °C, p(H2)=20–35 bar) and a large excess of isopropanol to reach a considerable yield. The main reaction products in the catalytic reduction of solketal are glycerol mono- and di-isopropyl ethers and solketal isopropyl ether. Solketal conversion over Al-HMS-supported palladium catalysts (T=120 °C and p(H2)=20 bar) affords a mixture of ethers with a high degree of conversion (87 %), 78 % selectivity, and excellent regioselectivity between isomeric ethers. Zeolite-BEA-supported palladium catalysts also exhibit high activity but much lower selectivity because of intense acetone aldol condensation. The effects of Si/Al ratios in BEA zeolites and Al-HMS aluminosilicates and the amounts of supported palladium (1 and 2 wt %) on the properties of the catalysts at different reaction temperatures and hydrogen pressures are considered.

Thermodynamic characteristics of the sorption of glycerol ethers on stationary phase OV-101

Zhabina,Krasnykh,Levanova

, p. 1590 - 1593 (2014/10/16)

Retention characteristics, temperature dependences of the retention characteristics, and thermodynamic characteristics of sorption on the nonpolar OV-101 phase are determined for 33 glycerol mono-, di-, and triethers with linear and branched monobasic alc

POLYOL ETHERS AND PROCESS FOR MAKING THEM

-

Page/Page column 10, (2010/03/31)

New polyol ether compounds and a process for their preparation. The process comprises reacting a polyol, a carbonyl compound, and hydrogen in the presence of hydrogenation catalyst, to provide the polyol ether. The molar ratio of polyol to carbonyl compound in the process is greater than 5:1.

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