Dimethyl Ether
Your Professional Difluoroethane Manufacturer in China
Jiangsu July Chemical Co.,Ltd is located in Jiangyin city, Wuxi, Jiangsu Province. It owns two industrial-grade gas of Dimethyl Ether& LPG stations, our mainly products include Dimethyl Ether, LPG, Methanol, R152a, R134a, Ethylene glycol and so on.
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Dimethyl ether (DME) is a synthetically produced alternative to diesel for use in specially designed compression ignition diesel engines. Under normal atmospheric conditions, DME is a colorless gas. It is used extensively in the chemical industry and as an aerosol propellant. Dimethyl ether requires about 75 pounds per square inch (psi) of pressure to be in liquid form. Because of this, DME's handling requirements are similar to those of propane-both must be kept in pressurized storage tanks at an ambient temperature.
Product Specification
|
CAS Number |
115-10-6 |
|
Abbreviations |
DME |
|
Beilstein Reference |
1730743 |
|
ECHA InfoCard |
100.003.696 |
|
EC Number |
204-065-8 |
|
RTECS number |
PM4780000 |
|
Chemical formula |
C2H6O |
|
Molar mass |
46.069 g·mol−1 |
|
Appearance |
Colorless gas |
|
Odor |
Ethereal |
|
Density |
2.1146 kg m−3 (gas, 0 °C, 1013 mbar) 0.735 g/mL (liquid, −25 °C) |
|
Melting point |
−141 °C; −222 °F; 132 K |
|
Boiling point |
−24 °C; −11 °F; 249 K |
|
Solubility in water |
71 g/L (at 20 °C (68 °F)) |
|
Vapor pressure |
592.8 kPa |
|
Preferred IUPAC name |
Methoxymethane |
|
Other Names |
Dimethyl ether[1] R-E170 Demeon Dimethyl oxide Dymel A Methyl ether Methyl oxide Mether Wood ether |
Comparison of Fuel Properties
Utilization
Substitute for diesel fuel; transportation fuel; power generation fuel; domestic gas.
Relevant Fuel Regulations
EN590 (diesel fuel).
Main Feedstocks
Forest products, agricultural by-products, organic waste, energy crops, black liquor.
Scale of Production
Demonstration scale.
DME is primarily produced by converting natural gas, organic waste or biomass to synthesis gas (syngas). The syngas is then converted into DME via a two-step synthesis, first to methanol in the presence of catalyst (usually copper-based), and then by subsequent methanol dehydration in the presence of a different catalyst (for example, silica-alumina) into DME.
The following reactions occur:
2H2+ CO ⇄CH3OH
2CH 3OH ⇄CH3OCH3 + H2O
CO+H 2O ⇄CO2+H2
Alternatively, DME can be produced through direct synthesis using a dual-catalyst system which permits both methanol synthesis and dehydration in the same process unit, with no intermediate methanol separation, a procedure that, by eliminating the intermediate methanol synthesis stage, the licensors claim promises efficiency advantages and cost benefits.Both the one-step and two-step processes are commercially available.DME can also be converted itself into olefins and synthetic hydrocarbons.
Chemical Composition and Characteristics
With the ether bond connecting two methyl groups (-CH3) to an oxygen atom (-O-), DME has the chemical formula CH3OCH3. Several distinctive traits distinguish it
Gaseous at Ambient Conditions
DME is a gas at normal pressure and ambient temperature, making it appropriate for various gaseous applications.
Non-toxic and Colorless
When burnt, DME does not release any hazardous pollutants and is non-toxic. Its adaptability is additionally increased because it has no color or smell.
High Energy Density
The high energy density of DME makes it a desirable fuel option for various applications.
Application of Dimethyl Ether

01
Alternative Fuel
DME has drawn interest as a cleaner substitute for LPG (liquefied petroleum gas) and diesel. It may be utilized in compression-ignition diesel engines to reduce particulate matter and greenhouse gas emissions.

02
Aerosol Propellant
DME is used in aerosol goods, including deodorants, hairsprays, and insect repellents as fuel.

03
Chemical Feedstock
DME is a feedstock utilized to synthesize several chemicals, such as acetic acid, dimethyl sulfate, and others.

04
Refrigeration
It may be utilized as a refrigerant in the cooling sector, especially in certain heat pump applications.
Advantages of Dimethyl Ether
DME is produced by a process of catalytic dehydration of methanol that gives water as a by-product. Thanks to this process, a minimum purity of 99.9%, a maximum methanol content of 1 ppm and 100 ppm of pure water are guaranteed, as well as a stable pressure. This results in the security that we will always know with what type of gas purity we are going to work, unlike other propellants, mixtures of different gases and origins that do not guarantee the previous parameter.
DME is miscible in water. By using from 6% to 34% weight of DME it is possible to form a single liquid phase with water: stable, homogeneous, and transparent. For other amounts of DME, phase separation is formed, although just adding 6% by weight of ethyl alcohol prevents such formation. The water formulation is positive for several reasons. Water is cheap, non-flammable, it is not a VOC (volatile organic component), and it is a great solvent. On the other hand, it is colourless, odourless, and ecologically accepted. The addition of certain amounts of water reduces the flammability of certain products (and even in some cases cancels it), increases the solubility of certain active principles and reduces the total cost of the formulation and in formulations where the use of perfumes is required, facilitates its development.
Its great solvent power is remarkable and very practical in certain formulations. A theoretical value of this parameter is its solubility value. These values are calculated considering, among various factors, the heat of vaporization and the molar volume. Propane and butane have solubility values between 5.8 and 6.6. The DME presents a value of 7.3. A more recognized value to illustrate solvent power is the Kauri Butanol number. This value is obtained by using a 20% standard solution of a Kauri resin and titrating it with a solvent or a propellant. The number of millilitres required to achieve the cloud point at 20°C is defined as the Kauri Butanol number. Propane and butane have values between 15 and 20. The DME is markedly higher, around 91. A practical way to demonstrate this solvent power of DME is its influence on the “cloud point”. DME lowers the “cloud point” of aerosol formulations, which is particularly important in hair spray formulations where most of the most common polymers are compatible with DME. DME increases the solvent power of formulations; This makes it an excellent component for hairspray, spray paints and some technical products such as spray polyurethane foams, adhesives.
DME can be used in multiple ways:
●As the sole propellant.
●Mixed with the most common hydrocarbons, minimizing their major disadvantages (solvent power, miscibility with water).
●Mixed with co2, being the best solvent for this product.
●Mixed with the new generation of hfcs such as 134a, 152a, 365 fa, 227.
To reduce the emission of VOCs (volatile organic components) of current formulations, it is necessary to replace some of its components with others that are not considered VOCs.
The ideal substitute in most cases is WATER, as it is colourless, odourless, non-flammable, non-toxic, non-VOC, compatible with the skin, inexpensive, and a good solvent.
Hazards




Air & Water Reactions
Highly flammable. Upon standing and exposure to air (oxygen) tendency to form explosive peroxides. When ethers containing peroxides are heated (distilled) they can detonate.
Fire Hazard
Behavior in Fire: Containers may explode. Vapors are heavier than air and may travel long distance to a source of ignition and flash back.
Health Hazard
Inhalation produces some anesthesia (but less than that of ethyl ether), blurring of vision, headache, intoxication, loss of consciousness. Liquid or concentrated vapor irritates eyes. Contact of liquid with skin may cause frostbite.
Reactivity Profile
DIMETHYL ETHER is a colorless, highly flammable gas (b. p. -24°C), slightly toxic. Very dangerous fire and explosion hazard when exposed to flame, sparks, heat or strong oxidizers. Violent reaction with aluminum hydride, lithium aluminum hydride. Upon standing and exposure to air (oxygen) tendency to form explosive peroxides. When ethers containing peroxides are heated (distilled) they can detonate.
Precautionary Statement
General
●If medical advice is needed, have product container or label at hand.
●Keep out of reach of children.
●Read carefully and follow all instructions.
Prevention
●Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
●Wear protective gloves/ protective clothing/eye protection/face protection.
●Avoid breathing gas.
●Do not get in eyes, on skin, or on clothing.
Response
●Leaking gas fire: Do not extinguish, unless leak can be stopped safely.
●If exposed or concerned, get medical advice.
●IF INHALED: Remove person to fresh air and keep comfortable for breathing.
●IF ON SKIN: Thaw frosted parts with lukewarm water. Do not rub affected area. Get immediate medical advice/attention.
●Eliminate all ignition sources if safe to do so.
Storage
●Protect from sunlight. Store in a well-ventilated place.
●Store locked up.
●Ether needs to be stored in a flammable storage cabinet when not in use.
●Ether can form peroxides over time when exposed to oxygen and sunlight. Labs should follow the Peroxidizable Materials guideline found here.
●Ether should be stored in a cool place, preferably in an explosion-proof refrigerator. Under no circumstances can ether be stored in a refrigerator that is not explosion-proof.
Disposal
●Dispose of contents/ container to an approved facility in.
●Accordance with local, regional, national and international regulations.
Main Hazard
●This substance is an extremely flammable gas.
Other Hazards
●An asphyxiant at high concentrations-oxygen depletion can be fatal.

●Prior to working with Dimethyl Ether you should be trained on its proper handling and storage.
●Dimethyl Ether is not compatible with OZONE; OXIDIZING AGENTS (such as PERCHLORATES, PEROXIDES, PERMANGANATES, CHLORATES, NITRATES, CHLORINE, BROMINE and FLUORINE); STRONG ACIDS (such as HYDROCHLORIC, SULFURIC and NITRIC); and HALOGENS.
●Store in tightly closed containers in a cool, well-ventilated area, and prevent AIR from entering container.
●Sources of ignition, such as smoking and open flames, are prohibited where Dimethyl Ether is used, handled, or stored.
●Metal containers involving the transfer of Dimethyl Ether should be grounded and bonded.
●Use only non-sparking tools and equipment, especially when opening and closing containers of Dimethyl Ether.
●Peroxide formation may occur in containers that have been opened and remain in storage for more than six months. Peroxides can be detonated by friction, impact or heating.
Ultimate FAQ Guide to Dimethyl Ether
Q: What are the benefits of using DME?
Q: What are the disadvantages of dimethyl ether?
Q: What is the common use of dimethyl ether?
Q: Is dimethyl ether good for the environment?
Q: How is dimethyl ether made?
Q: What are the advantages and disadvantages of ether?
Q: Is dimethyl ether a good solvent?
Q: Is dimethyl ether explosive?
Q: Is dimethyl ether stronger than ethanol?
Q: Can you drink dimethyl ether?
Q: What is the main advantage of producing DME from syngas?
Q: Is dimethyl ether soluble in water?
Q: Why is dimethyl ether volatile?
Q: What are the benefits of ether?
Q: Is dimethyl ether volatile?
Q: Why is diethyl ether a good solvent?
Q: Why is diethyl ether bad?
Q: Is dimethyl ether an alcohol?
Q: What is the difference between methanol and dimethyl ether?
Q: What is the main advantage of DME?













