Bis(2-methoxy ethyl)ether (CAS 111-96-6) — formula C6H14O3, molecular weight 134.17; category organic chemicals.
| CAS Number | 111-96-6 |
|---|---|
| Molecular Formula | C6H14O3 |
| Molecular Weight | 134.17 |
| Melting Point | -90 °F (NTP, 1992) |
| Boiling Point | 162 °C |
| LogP | -0.4 |
| Applications | Uses: Used as a solvent and chemical intermediate, [Merck Index] Used in the coating industry and in photolithography to make semiconductor chips, Also used in adhesives, sealants, and automotive care products, [Reference #1], Semiconductor Manufacturing [Category: Industry], Painting (Solvents) [Category: Paint], Working with Glues and Adhesives [Category: Other], Solvent, reaction medium for Grignard and similar syntheses., Diethylene glycol dimethyl ether is used as a solvent in chemical reactions involving metals and organometallic compounds., Solubilizer, Used in production of plastics., Industry Uses: Solvent, Intermediate, Plasticizer, Not Known or Reasonably Ascertainable, Consumer Uses: Plasticizer, Monomers, Household Products: Cosmetics product ingredient: Bis(2-methoxyethyl) ether (Dimethoxydiglycol, Diethylene glycol monomethyl ether (2-(2-methoxyethoxy)ethanol, Methoxydiglycol), Reason for Listing: Listed by the European Union as a Category 1B reproductive toxicant in Annex VI to Regulation (EC) 1272, 2008., Potential Health Impacts: Reproductive Toxicity, Product count: 33, Methods of Manufacturing: Ethylene glycol ethers are produced by reacting ethylene oxide with alcohols in the presence of either acidic or basic catalysts. Temperature, pressure, mole ratios of reactants, and catalysts are chosen to yield the desired product mix., Diethylene glycol + dimethyl sulfate (ether formation), Ethylene glycol monoethers are usually produced by reaction of ethylene oxide with the appropriate alcohol. A mixture of homologues is obtained ... The glycol monoethers can be converted to diethers by alkylation with common alkylating agents, such as dimethyl sulfate or alkyl halides ( Williamson synthesis). Glycol dimethyl ethers are formed by treatment of dimethyl ether with ethylene oxide., Ethers, Formulations, Preparations: Grade: Technical, U.S. Production: 2023: 850, 000 - <1, 000, 000 lb, 2022: 1, 000 - <5, 2021: 550, 2020: 550, (1972) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1975) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1982) 4.72X10+10 g, Diethylene glycol ethers, (2006) 1, 612 million lb annual capacity, Glycol ethers, For more U.S. Production (Complete) data for DIETHYLENE GLYCOL DIMETHYL ETHER (6 total), please visit the HSDB record page., U.S. Imports: (1984) 9.43X10+9 g, Diethylene glycol esters, ethers, etc, General Manufacturing Information: Electrical Equipment, Appliance, and Component Manufacturing, All Other Basic Organic Chemical Manufacturing, Plastics Material and Resin Manufacturing, Fabricated Metal Product Manufacturing, All Other Chemical Product and Preparation Manufacturing, Ethane, 1, 1'-oxybis[2-methoxy-: ACTIVE, Diglyme can be effectively used as an odor-attractant solvent without reducing the attractiveness of the chemical additive, eg, decanoic acid, trimethylammonium decanoate, and trimethylamine. Odorants dissolved in diglyme can be added to aqueous solutions, such as coyote urine. Also, diglyme has a low freezing point so its use as an odor solvent increases the temperature range in which an odor can be effectively used. |
| Category | Organic Chemicals |
Documented applications: Uses: Used as a solvent and chemical intermediate, [Merck Index] Used in the coating industry and in photolithography to make semiconductor chips, Also used in adhesives, sealants, and automotive care products, [Reference #1], Semiconductor Manufacturing [Category: Industry], Painting (Solvents) [Category: Paint], Working with Glues and Adhesives [Category: Other], Solvent, reaction medium for Grignard and similar syntheses., Diethylene glycol dimethyl ether is used as a solvent in chemical reactions involving metals and organometallic compounds., Solubilizer, Used in production of plastics., Industry Uses: Solvent, Intermediate, Plasticizer, Not Known or Reasonably Ascertainable, Consumer Uses: Plasticizer, Monomers, Household Products: Cosmetics product ingredient: Bis(2-methoxyethyl) ether (Dimethoxydiglycol, Diethylene glycol monomethyl ether (2-(2-methoxyethoxy)ethanol, Methoxydiglycol), Reason for Listing: Listed by the European Union as a Category 1B reproductive toxicant in Annex VI to Regulation (EC) 1272, 2008., Potential Health Impacts: Reproductive Toxicity, Product count: 33, Methods of Manufacturing: Ethylene glycol ethers are produced by reacting ethylene oxide with alcohols in the presence of either acidic or basic catalysts. Temperature, pressure, mole ratios of reactants, and catalysts are chosen to yield the desired product mix., Diethylene glycol + dimethyl sulfate (ether formation), Ethylene glycol monoethers are usually produced by reaction of ethylene oxide with the appropriate alcohol. A mixture of homologues is obtained ... The glycol monoethers can be converted to diethers by alkylation with common alkylating agents, such as dimethyl sulfate or alkyl halides ( Williamson synthesis). Glycol dimethyl ethers are formed by treatment of dimethyl ether with ethylene oxide., Ethers, Formulations, Preparations: Grade: Technical, U.S. Production: 2023: 850, 000 - <1, 000, 000 lb, 2022: 1, 000 - <5, 2021: 550, 2020: 550, (1972) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1975) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1982) 4.72X10+10 g, Diethylene glycol ethers, (2006) 1, 612 million lb annual capacity, Glycol ethers, For more U.S. Production (Complete) data for DIETHYLENE GLYCOL DIMETHYL ETHER (6 total), please visit the HSDB record page., U.S. Imports: (1984) 9.43X10+9 g, Diethylene glycol esters, ethers, etc, General Manufacturing Information: Electrical Equipment, Appliance, and Component Manufacturing, All Other Basic Organic Chemical Manufacturing, Plastics Material and Resin Manufacturing, Fabricated Metal Product Manufacturing, All Other Chemical Product and Preparation Manufacturing, Ethane, 1, 1'-oxybis[2-methoxy-: ACTIVE, Diglyme can be effectively used as an odor-attractant solvent without reducing the attractiveness of the chemical additive, eg, decanoic acid, trimethylammonium decanoate, and trimethylamine. Odorants dissolved in diglyme can be added to aqueous solutions, such as coyote urine. Also, diglyme has a low freezing point so its use as an odor solvent increases the temperature range in which an odor can be effectively used..
Bis(2-methoxy ethyl)ether is a carbon-based organic compound with CAS registry number 111-96-6 and molecular formula C6H14O3 (molecular weight 134.17), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 111-96-6
Its molecular formula C6H14O3 comprises 6 C, 14 H, 3 O atoms.
Also known as: Bis(2-methoxy ethyl)ether · 双(2-甲氧基乙基)醚
Category: organic chemicals
The CAS registry number of Bis(2-methoxy ethyl)ether is 111-96-6.
Molecular formula C6H14O3, molecular weight 134.17.
It is also registered under: Bis(2-methoxy ethyl)ether, 双(2-甲氧基乙基)醚.
Recorded applications: Uses: Used as a solvent and chemical intermediate, [Merck Index] Used in the coating industry and in photolithography to make semiconductor chips, Also used in adhesives, sealants, and automotive care products, [Reference #1], Semiconductor Manufacturing [Category: Industry], Painting (Solvents) [Category: Paint], Working with Glues and Adhesives [Category: Other], Solvent, reaction medium for Grignard and similar syntheses., Diethylene glycol dimethyl ether is used as a solvent in chemical reactions involving metals and organometallic compounds., Solubilizer, Used in production of plastics., Industry Uses: Solvent, Intermediate, Plasticizer, Not Known or Reasonably Ascertainable, Consumer Uses: Plasticizer, Monomers, Household Products: Cosmetics product ingredient: Bis(2-methoxyethyl) ether (Dimethoxydiglycol, Diethylene glycol monomethyl ether (2-(2-methoxyethoxy)ethanol, Methoxydiglycol), Reason for Listing: Listed by the European Union as a Category 1B reproductive toxicant in Annex VI to Regulation (EC) 1272, 2008., Potential Health Impacts: Reproductive Toxicity, Product count: 33, Methods of Manufacturing: Ethylene glycol ethers are produced by reacting ethylene oxide with alcohols in the presence of either acidic or basic catalysts. Temperature, pressure, mole ratios of reactants, and catalysts are chosen to yield the desired product mix., Diethylene glycol + dimethyl sulfate (ether formation), Ethylene glycol monoethers are usually produced by reaction of ethylene oxide with the appropriate alcohol. A mixture of homologues is obtained ... The glycol monoethers can be converted to diethers by alkylation with common alkylating agents, such as dimethyl sulfate or alkyl halides ( Williamson synthesis). Glycol dimethyl ethers are formed by treatment of dimethyl ether with ethylene oxide., Ethers, Formulations, Preparations: Grade: Technical, U.S. Production: 2023: 850, 000 - <1, 000, 000 lb, 2022: 1, 000 - <5, 2021: 550, 2020: 550, (1972) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1975) PROBABLY GREATER THAN 4.54X10+5 GRAMS, (1982) 4.72X10+10 g, Diethylene glycol ethers, (2006) 1, 612 million lb annual capacity, Glycol ethers, For more U.S. Production (Complete) data for DIETHYLENE GLYCOL DIMETHYL ETHER (6 total), please visit the HSDB record page., U.S. Imports: (1984) 9.43X10+9 g, Diethylene glycol esters, ethers, etc, General Manufacturing Information: Electrical Equipment, Appliance, and Component Manufacturing, All Other Basic Organic Chemical Manufacturing, Plastics Material and Resin Manufacturing, Fabricated Metal Product Manufacturing, All Other Chemical Product and Preparation Manufacturing, Ethane, 1, 1'-oxybis[2-methoxy-: ACTIVE, Diglyme can be effectively used as an odor-attractant solvent without reducing the attractiveness of the chemical additive, eg, decanoic acid, trimethylammonium decanoate, and trimethylamine. Odorants dissolved in diglyme can be added to aqueous solutions, such as coyote urine. Also, diglyme has a low freezing point so its use as an odor solvent increases the temperature range in which an odor can be effectively used..
Category: Organic Chemicals.
Independent reference data for Bis(2-methoxy ethyl)ether (CAS 111-96-6), compiled from public chemistry databases.
| CAS Registry Number | 111-96-6 |
|---|---|
| PubChem CID | 8150 |
| Molecular formula | C6H14O3 |
| IUPAC name | 1-methoxy-2-(2-methoxyethoxy)ethane |
| UNII (FDA) | M4BH3X0MVZ |
| Molecular Weight | 134.17 |
|---|---|
| XLogP3 | -0.4 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 6 |
| Exact Mass | 134.094294304 |
| Monoisotopic Mass | 134.094294304 |
| Topological Polar Surface Area | 27.7 |
| Heavy Atom Count | 9 |
| Boiling Point | 162 °C |
|---|---|
| Boiling Point | 162 °C @760 [mm Hg] |
| Melting Point | -90 °F (NTP, 1992) |
| Melting Point | -68 °C |
| Flash Point | 153 to 158 °F (NTP, 1992) |
| Flash Point | 153 °F (67 °C) (CLOSED CUP) |
| Flash Point | 51 °C c.c. |
| Density | Sp gr: 0.9451 at 20 °C/20 °C |
| Density | 0.9451 @25 °C |
| Vapor Pressure | 2.96 [mmHg] |
Diglyme; 111-96-6; 1-Methoxy-2-(2-methoxyethoxy)ethane; Bis(2-methoxyethyl) ether; DIETHYLENE GLYCOL DIMETHYL ETHER; 2,5,8-Trioxanonane; Dimethyl carbitol; Di(2-Methoxyethyl) ether; Bis(2-methoxyethyl)ether; Glyme 2; Dimethoxydiglycol; (2-Methoxyethyl) ether; Ether, bis(2-methoxyethyl); Methyldiglyme; Diglycol methyl ether; Diethyl glycol dimethyl ether
| Reported hazard statements | H226, H360 (90.8%), H320, H361, H303, H316, H335, H336 |
|---|
H226: Flammable liquid and vapor [Warning Flammable liquids]
H360FD: May damage fertility; May damage the unborn child [Danger Reproductive toxicity]
Bis(2-methoxy ethyl)ether · CAS 111-96-6 · C6H14O3. UNII M4BH3X0MVZ. Boiling Point: 162 °C; Boiling Point: 162 °C @760 [mm Hg]; Melting Point: -90 °F (NTP, 1992).
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.
中文页面: 双(2-甲氧基乙基)醚