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462-95-3

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462-95-3 Usage

Chemical Properties

colourless liquid

Uses

Different sources of media describe the Uses of 462-95-3 differently. You can refer to the following data:
1. Diethoxymethane (DEM) is offered by Eastman Chemical Company as a cost-effective replacement solvent for monoglyme (1,2- dimethoxyethane) and methylal. The DEM diether is stable under alkaline conditions, but can be cleaved by strong acids. Diethoxymethane can be used as a chemical intermediate in many organic synthesis reactions. Diethoxymethane is useful as a solvent in lithium batteries with nonaqueous electrolytes, as a solvent for polymeric materials, and as a fuel additive. As a chemical intermediate DEM can act as an ethoxymethylating reagent for alcohols and phenols and serve as a source for formaldehyde in organic synthesis.
2. Diethoxymethane may be used as a substitute solvent to dichloromethane and toluene in the O-alkylation of different phenols in the presence of phase transfer catalysts (PTCs).

Synthesis Reference(s)

Synthetic Communications, 25, p. 3939, 1995 DOI: 10.1080/00397919508011470

General Description

A colorless volatile liquid with an agreeable odor. Less dense than water. Flash point below 10°F. Vapors heavier than air. May be narcotic in high concentrations. Used as a solvent and in the manufacture of cosmetics.

Air & Water Reactions

Highly flammable. Soluble in water.

Reactivity Profile

DIETHOXYMETHANE, an acetal, is incompatible with strong oxidizing agents and acids. Breaks down to formaldehyde and ethanol in acidic solutions.

Health Hazard

Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control may cause pollution.

Fire Hazard

HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Flammability and Explosibility

Highlyflammable

Safety Profile

Moderately toxic by ingestion. Flammable when exposed to heat or flame; can react vigorously with oxidizers. When heated to decomposition it emits acrid smoke and irritating fumes.

Check Digit Verification of cas no

The CAS Registry Mumber 462-95-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 462-95:
(5*4)+(4*6)+(3*2)+(2*9)+(1*5)=73
73 % 10 = 3
So 462-95-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H12O2/c1-3-6-5-7-4-2/h3-5H2,1-2H3

462-95-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (B23134)  Diethoxymethane, 99%, stab. with 100ppm BHT   

  • 462-95-3

  • 25ml

  • 328.0CNY

  • Detail
  • Alfa Aesar

  • (B23134)  Diethoxymethane, 99%, stab. with 100ppm BHT   

  • 462-95-3

  • 100ml

  • 351.0CNY

  • Detail
  • Alfa Aesar

  • (B23134)  Diethoxymethane, 99%, stab. with 100ppm BHT   

  • 462-95-3

  • 500ml

  • 1049.0CNY

  • Detail
  • Sigma-Aldrich

  • (538280)  Diethoxymethane  99.7%, contains 50-150 ppm BHT as stabilizer

  • 462-95-3

  • 538280-500ML

  • 1,388.79CNY

  • Detail
  • Sigma-Aldrich

  • (538280)  Diethoxymethane  99.7%, contains 50-150 ppm BHT as stabilizer

  • 462-95-3

  • 538280-2.5L

  • 2,325.96CNY

  • Detail
  • Aldrich

  • (47675)  Formaldehydediethylacetal  absolute, over molecular sieve (H2O ≤0.01%), ≥99.0% (GC)

  • 462-95-3

  • 47675-100ML-F

  • 195.39CNY

  • Detail
  • Aldrich

  • (47675)  Formaldehydediethylacetal  absolute, over molecular sieve (H2O ≤0.01%), ≥99.0% (GC)

  • 462-95-3

  • 47675-500ML-F

  • 790.92CNY

  • Detail

462-95-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethoxymethane

1.2 Other means of identification

Product number -
Other names Ethane, 1,1‘-[methylenebis(oxy)]bis-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:462-95-3 SDS

462-95-3Relevant articles and documents

Thumm,B.A.,Tryon,S.

, p. 2999 - 3002 (1964)

Molera et al.

, (1977)

Enhanced Hydrogenation of Carbon Dioxide to Methanol by a Ruthenium Complex with a Charged Outer-Coordination Sphere

Erickson, Jeremy D.,Linehan, John C.,Preston, Andrew Z.,Wiedner, Eric S.

, p. 7419 - 7423 (2020/07/21)

We report the hydrogenation of CO2 to MeOH by a Ru(triphos) catalyst containing a cationic tetraalkylammonium moiety in the outer coordination sphere. This catalyst affords higher TON and TOF values for MeOH than isostructural catalysts with neutral phosphine ligands. Kinetic data from operando NMR spectroscopy studies indicate the improvement in MeOH production arises from a 12-fold enhancement in the rate of hydrogenation of the transient formaldehyde intermediate. These results provide insight into the catalyst characteristics that promote MeOH formation.

Effect of the Nature of the Catalyst on Catalytic Activity and Selectivity in the Formaldehyde Hydrogenation

Tarasov

, p. 1670 - 1674 (2018/09/13)

The effect the nature of the carrier and supported metal on the activity and selectivity of the catalyst in the reaction of formaldehyde hydrogenation to methanol is studied. The formation of such oxygenates as ethanol, formic acid, and diethyl formal is observed. It is found that ethanol forms on Fe-containing alloyed catalyst, while formic acid forms on the catalysts containing Au. Thermodynamic calculations are performed for a series of side reactions that confirm the formation of the resulting oxygenates.

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