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115-10-6

Basic Information
CAS No.: 115-10-6
Name: Methane, 1,1'-oxybis-
Article Data: 562
Cas Database
Molecular Structure:
Molecular Structure of 115-10-6 (Methane, 1,1'-oxybis-)
Formula: C2H6O
Molecular Weight: 46.069
Synonyms: Ether, dimethyl(7CI);DME;Demeon D;Dimethyl oxide;Dymel A;Methoxymethane;Wood ether;Dimethylether (7CI);Methane, oxybis- (9CI);Methyl ether (6CI,8CI);
EINECS: 204-065-8
Density: 0.678 g/cm3
Melting Point: -141 °C(lit.)
Boiling Point: -24.8 °C(lit.)
Flash Point: -41°C
Solubility: Soluble in water
Appearance: colourless gas
Hazard Symbols: ExtremelyF++
Risk Codes: 12
Safety: 9-16-33
Transport Information: UN 1033
PSA: 9.23000
LogP: 0.26260
Synthetic route
38222-83-2

2,6-di-tert-butyl-4-methylpyridine

278172-59-1

methyltriphenylbismuthonium tetrafluoroborate

A

67-56-1

methanol

B

115-10-6

Dimethyl ether

C

160142-36-9

2,6-di-tert-butyl-4-methylpyridinium tetrafluoroborate

D

603-33-8

triphenylbismuthane

Conditions
ConditionsYield
With H2O In chloroform-d1 water was added to mixt. (Ph3BiMe)(BF4) and 2,6-di-tert-butyl-4-methylpyridine in CDCl3 and mixt. was allowed to stand at room temp. for 33 h; detn. by NMR;A 30%
B 16%
C 100%
D 100%
67-56-1

methanol

38222-83-2

2,6-di-tert-butyl-4-methylpyridine

278172-59-1

methyltriphenylbismuthonium tetrafluoroborate

A

115-10-6

Dimethyl ether

B

160142-36-9

2,6-di-tert-butyl-4-methylpyridinium tetrafluoroborate

C

603-33-8

triphenylbismuthane

Conditions
ConditionsYield
In chloroform-d1 alcohol was added to mixt. (Ph3BiMe)(BF4) and 2,6-di-tert-butyl-4-methylpyridine in CDCl3 and allowed to react at 23°C for 4-7 h; detn. by NMR;A 69%
B 100%
C 100%

C4H10O2*C10H15(1-)*C24BF20(1-)*Si(2+)

A

123-91-1

1,4-dioxane

B

110-71-4

1,2-dimethoxyethane

C

115-10-6

Dimethyl ether

D

Cp*Si(1+)* B(C6F5)4(1-)

Conditions
ConditionsYield
In dichloromethane-d2 for 120h;A n/a
B n/a
C n/a
D 100%
67-56-1

methanol

115-10-6

Dimethyl ether

Conditions
ConditionsYield
NaPZSM-5 In water at 250℃; under 7600.51 Torr; Product distribution / selectivity;99%
50 to 70 meshes; silica-alumina catalyst; Aldrich at 225 - 350℃; for 4h;96%
ZSM-5 zeolite on β-silicon carbide at 400℃; under 760.051 Torr; for 18h; Product distribution / selectivity; Inert atmosphere;90%
4291-05-8, 62248-83-3

N-sulfinylmethylamine

420-37-1

trimethoxonium tetrafluoroborate

A

115-10-6

Dimethyl ether

B

65149-75-9

N-Methyl-N-sulfinylmethanaminium tetrafluoroborate

Conditions
ConditionsYield
at 15℃; for 3h;A n/a
B 99%
67-56-1

methanol

108-29-2

5-methyl-dihydro-furan-2-one

A

115-10-6

Dimethyl ether

B

624-24-8

methyl valerate

Conditions
ConditionsYield
With water at 255℃; for 23.8333h; Catalytic behavior; Concentration; Time; Reagent/catalyst; Inert atmosphere; Gas phase; chemoselective reaction;A 52.7%
B 98.6%
67-56-1

methanol

A

50-00-0

formaldehyd

B

115-10-6

Dimethyl ether

Conditions
ConditionsYield
molybdenum(VI) oxide In gas at 290 - 350℃; under 750.06 Torr; Thermodynamic data; Product distribution; structure sensitive oxidation with orthorhomb. or microcrystalline MoO3, further temperatures, activation energy EA;A 95%
B 5%
With oxygen; aluminophosphate zeolite at 300℃; Product distribution; temperature, without oxygen, effect of catalysts;
With oxygen; vanadia at 300 - 600℃; Product distribution; further catalysts;
756-79-6

dimethyl methane phosphonate

A

34557-54-5

methane

B

676-96-0

Trimethylphosphine oxide

C

115-10-6

Dimethyl ether

D

magnesium bis(methyl methylphosphonate)

Conditions
ConditionsYield
With magnesium In neat (no solvent) at 165℃; for 1.5h; Further byproducts given;A n/a
B 4.8 g
C n/a
D 95%
756-79-6

dimethyl methane phosphonate

A

34557-54-5

methane

B

74-84-0

ethane

C

115-10-6

Dimethyl ether

D

monomethyl methylphosphonate lithium salt

Conditions
ConditionsYield
With lithium In neat (no solvent) at 160℃; for 3h; Further byproducts given. Yields of byproduct given;A n/a
B n/a
C n/a
D 95%
756-79-6

dimethyl methane phosphonate

A

34557-54-5

methane

B

74-85-1

ethene

C

115-10-6

Dimethyl ether

D

73750-69-3

sodium methyl methanephosphonate

Conditions
ConditionsYield
With sodium In neat (no solvent) at 95℃; Further byproducts given. Yields of byproduct given;A n/a
B n/a
C n/a
D 94.5%
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Consensus Reports

Reported in EPA TSCA Inventory.

Standards and Recommendations

DFG MAK: 1000 ppm (1900 mg/m3)
DOT Classification:  2.1; Label: Flammable Gas

Specification

The Methyl ether, with the CAS registry number 115-10-6 and EINECS registry number 204-065-8, has the systematic name of dimethyl ether. And the molecular formula of this chemical is C2H6O. The simplest ether is a kind of colourless gas, and belongs to the following product categories: Organics; Ethers (Low Boiling point); Gas Cylinders; Synthetic Organic Chemistry. In addition, when combusted, dimethyl ether produces minimal NOx and CO, though HC and soot formation are significant.

The physical properties of Methyl ether are as following: (1)ACD/LogP: 0.02; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.022; (4)ACD/LogD (pH 7.4): 0.022; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 24.478; (8)ACD/KOC (pH 7.4): 24.478; (9)#H bond acceptors: 1; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 0; (12)Polar Surface Area: 9.23 Å2; (13)Index of Refraction: 1.309; (14)Molar Refractivity: 13.06 cm3; (15)Molar Volume: 67.912 cm3; (16)Polarizability: 5.177×10-24cm3; (17)Surface Tension: 14.012 dyne/cm; (18)Density: 0.678 g/cm3; (19)Enthalpy of Vaporization: 21.51 kJ/mol; (20)Vapour Pressure: 4784.153 mmHg at 25°C.

Preparation of Methyl ether: It can be prepared by converting hydrocarbons sourced from natural gas or coal via gasification to synthesis gas (syngas). Synthesis gas is then converted into methanol in the presence of catalyst (usually copper-based), with subsequent methanol dehydration in the presence of a different catalyst (for example, silica-alumina) resulting in the production of Methyl ether.

Uses of Methyl ether:  It is a useful precursor to other organic compounds and an aerosol propellant. It is also used as fuel in household and industry. In addition, it can also be used as a refrigerant.

You should be cautious while dealing with this chemical. It is a kind of extremely flammable chemical. Therefore, you had better take the following instructions: Keep container in a well-ventilated place; Keep away from sources of ignition - No smoking; Take precautionary measures against static discharges.

You can still convert the following datas into molecular structure:
(1)SMILES: COC
(2)InChI: InChI=1/C2H6O/c1-3-2/h1-2H3
(3)InChIKey: LCGLNKUTAGEVQW-UHFFFAOYAU

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
rat LC50 inhalation 308gm/m3 (308000mg/m3) BEHAVIORAL: GENERAL ANESTHETIC Toxicologist. Vol. 1, Pg. 79, 1981.