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17226-69-6

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17226-69-6 Usage

Physical state

Colorless liquid

Odor

Slightly sweet

Common uses

Solvent, reagent in organic synthesis, production of pharmaceuticals and agrochemicals, synthesis of fine chemicals and flavors

Reactivity

Highly reactive

Oxidizing ability

Powerful oxidizing agent

Applications in chemical reactions

Oxidation of alkenes and alcohols, preparation of peroxycarboxylic acids

Importance

Versatile and important compound in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 17226-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,2 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17226-69:
(7*1)+(6*7)+(5*2)+(4*2)+(3*6)+(2*6)+(1*9)=106
106 % 10 = 6
So 17226-69-6 is a valid CAS Registry Number.

17226-69-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dimethyl-4-(propan-2-yloxymethyl)-1,3-dioxolane

1.2 Other means of identification

Product number -
Other names 2,2-dimethyl-4-[(propan-2-yloxy)methyl]-1,3-dioxolane

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:17226-69-6 SDS

17226-69-6Downstream Products

17226-69-6Relevant articles and documents

Catalytic Hydrogenolysis of Solketal on Bifunctional Catalysts with Production of High Octane Components of Motor Fuels

Goncharova, A. V.,Knyazeva, M. I.,Maksimov, A. L.,Ni, D. S.,Ramazanov, D. N.,Samoilov, V. O.

, p. 108 - 117 (2020/03/27)

The possibility of implementing the concept of converting bioglycerin into a blend of oxygenates, potentially applicable as components of gasoline by ketalization with acetone (T = 30°C–40°C, atmospheric pressure), accompanied by mild hydrogenolysis of ketal [T = 100°C–140°C, p(H2) = 2 MPa] to obtain a mixture of of glycerol and solketal isopropyl ethers was demonstrated. Results showed that the preferred method of conversion was the separate performing of ketalization and hydrogenolysis, since when these stages are combined, the side reaction of the formation of free isopropyl alcohol was highly selective. The regularities in the influence of the composition of the catalytic system (Pd/C + para-toluenesulfonic acid) on its activity were observed in the reaction of catalytic hydrogenation of solketal to a mixture of glycerol and solketal isopropyl ethers (optimal ratio of Pd/para-toluenesulfonic acid = 0.811 mol). The addition of 4%–5% glycerol to raw materials increased the yield of target hydrogenation products from 25% to 36%. Using a flow unit, the catalytic hydrogenation of solketal was optimized. In the optimal mode [T = 170°C, p(H2) = 4 MPa, v = 0.5 h?1, H2/feedstock = 660 nL L?1], the conversion of solketal to a mixture of target products (glycerol monoisopropyl ether, glycerol diisopropyl ethers, and solketal isopropyl ether) reached 98%. The possibility of carrying out the reaction on heterogeneous bifunctional catalysts of the Pd/sulfonated coal type was shown.

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