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Diglyme

CAS No.
111-96-6
Chemical Name:
Diglyme
Synonyms
DIGLYME;2-METHOXYETHYL ETHER;DEDM;BIS(2-METHOXYETHYL) ETHER;1-Methoxy-2-(2-methoxyethoxy)ethane;DIMETHYLDIGLYCOL;iglyme;Di(2-Methoxyethyl) ether;glyme2;DIYGLME
CBNumber:
CB4302276
Molecular Formula:
C6H14O3
Molecular Weight:
134.17
MDL Number:
MFCD00008503
MOL File:
111-96-6.mol
MSDS File:
SDS
Last updated:2023-12-06 09:36:59

Diglyme Properties

Melting point -64 °C (lit.)
Boiling point 162 °C (lit.)
Density 0.944 g/mL at 20 °C (lit.) 0.939 g/mL at 25 °C (lit.)
vapor density 4.6 (vs air)
vapor pressure 3 mm Hg ( 20 °C)
refractive index n20/D 1.408(lit.)
Flash point 134.6 °F
storage temp. Store below +30°C.
solubility Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly)
form Liquid
color ≤10(APHA)
Odor Mild ethereal.
Relative polarity 0.244
explosive limit 1.4-17.4%(V)
Evaporation Rate 0.36
Viscosity 1.14 mPa s 20 C
Water Solubility Miscible
Sensitive Hygroscopic
λmax λ: 225 nm Amax: 1.00
λ: 240 nm Amax: 0.50
λ: 260 nm Amax: 0.20
λ: 280 nm Amax: 0.08
λ: 320-400 nm Amax: 0.01
Merck 14,3165
BRN 1736101
Dielectric constant 7.2999999999999998
Stability Stable. Combustible. Incompatible with strong oxidizing agents. May be air or light sensitive.
InChIKey SBZXBUIDTXKZTM-UHFFFAOYSA-N
LogP -0.36 at 25℃
CAS DataBase Reference 111-96-6(CAS DataBase Reference)
EWG's Food Scores 2-5
FDA UNII M4BH3X0MVZ
NIST Chemistry Reference Ethane, 1,1'-oxybis[2-methoxy-(111-96-6)
EPA Substance Registry System Diethylene glycol dimethyl ether (111-96-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS08
Signal word  Danger
Hazard statements  H226-H360FD
Precautionary statements  P202-P210-P233-P240-P241-P308+P313
Hazard Codes  T
Risk Statements  60-61-10-19
Safety Statements  53-45
RIDADR  UN 3271 3/PG 3
WGK Germany  1
RTECS  KN3339000
3-10-23
Autoignition Temperature 370 °F
TSCA  Yes
HazardClass  3
PackingGroup  III
HS Code  29091990
Toxicity LD50 orally in Rabbit: 4760 mg/kg
NFPA 704
2
1 1

Diglyme price More Price(37)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 8.02934 Diethylene glycol dimethyl ether (stabilised) for synthesis 111-96-6 250ML $47.8 2024-03-01 Buy
Sigma-Aldrich 8.02934 Diethylene glycol dimethyl ether (stabilised) for synthesis 111-96-6 1L $160 2024-03-01 Buy
Sigma-Aldrich 8.02934 Diethylene glycol dimethyl ether (stabilised) for synthesis 111-96-6 2.5L $352 2024-03-01 Buy
Sigma-Aldrich M14102 Diethylene glycol dimethyl ether ReagentPlus?, 99% 111-96-6 20L $1290 2023-06-20 Buy
Sigma-Aldrich 04143 Diethylene glycol dimethyl ether analytical standard 111-96-6 1mL $28.5 2022-05-15 Buy
Product number Packaging Price Buy
8.02934 250ML $47.8 Buy
8.02934 1L $160 Buy
8.02934 2.5L $352 Buy
M14102 20L $1290 Buy
04143 1mL $28.5 Buy

Diglyme Chemical Properties,Uses,Production

Description

Bis (2-methoxyethyl) ether, also known as diglyme, is a linear aliphatic diether widely used as a solvent and present as a clear liquid at room temperature with a mild ether odor. The compound is notknown to occur in nature. It is synthesized from ethylene oxide and methanol in the presence of either acidic or basic catalysts. The reaction is based on the classic Williamson ether synthesis. It can also be produced from diethylene glycol and dimethyl sulfate. In June 2012, ECHA proposed addition of diglyme to the REACH very high concern list.

Chemical Properties

Diethylene glycol dimethyl ether is a clear, water-white neutral liquid of faint, pleasant odor. This ether may be used as a solvent for alkali metal hydrides for use in such reactions as reduction, alkylation and condensation. It may also be used as a lacquer solvent.

Uses

Bis (2-methoxyethyl) ether, due to being chemically inert and possessing excellent solvent properties, is mainly used as a solvent and an anhydrous reaction medium for organometallic synthesis. It is also used as a solubilizer.

Uses

Solvent; it is used as reaction medium for Grignard and similar synthesis.

Uses

Diethylene glycol dimethyl ether is used as a solvent in organic reactions due to its stability towards higher pH and its high boiling point. It is particularly involved in reactions utilizing organometallic reagents such as Grignard reactions and metal hydride reductions. It is also a solvent for hydroboration reactions with diborane.

Definition

ChEBI: A polyether that is the dimethyl ether derivative of diethylene glycol.

General Description

Colorless watery liquid with a pleasant odor. Floats and mixes with water.

Air & Water Reactions

Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick, 1979 p.151-154, 164]. A mixture of liquid air and diethyl ether exploded spontaneously, [MCA Case History 616(1960)]. Water soluble.

Reactivity Profile

A violent explosion occurred when lithium aluminum hydride was being used to dry 2-Methoxyethyl ether. The ignition may have occurred due to the presence of large amounts of water or perhaps peroxide formed in the ether. About 75% of the ether had been removed when the explosion occurred, [MCA Case History 1494 (1968)].

Health Hazard

INGESTION (severe cases): nausea, vomiting, abdominal cramps, weakness progressing to coma.

Fire Hazard

2-Methoxyethyl ether is combustible.

Flammability and Explosibility

Flammable

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Synthesis

265 g (2.5 mol) of diethylene glycol, 320 g (10.0 mol) of methanol, and 14.3 g (0.0125 equivalents) of NAFION 1100 EW Polymer (H+ form) were charged to a one-liter autoclave. After sealing and pressure testing, the contents of the autoclave were agitated, and the autoclave was pressurized to 100 psi with nitrogen. After 5 minutes of agitation, the autoclave was depressurized. This process was repeated two more times to ensure complete deoxygenation. After deoxygenation, the autoclave was heated to a temperature of 198 ℃, and the contents of the autoclave were agitated at 1900 rpm for 5 hours at temperature (198-200 ℃). A pressure of 810 psi was obtained. After 5 hours, the autoclave was cooled and sampled. By analysis, a total of 77.2% by weight of the diethylene glycol (1.93 moles) was converted in the reaction, producing 0.335 mol of Diglyme. The co-product includes 1,4 dioxane and the intermediate diethylene glycol monomethyl ether.Diethylene Glycol Dimethyl Ether

Environmental Fate

The metabolite 2-methoxyacetic acid, which is generated from 2-methroxyethanol by the reaction of alcohol dehydrogenase, may be important for the toxic effects. It can undergo activation to methoxyacetyl coenzyme A and enter the Krebs cycle or fatty acid biosynthesis. Several metabolites of 2-methoxyethanol, such as 2-methoxy-N-acetyl glycine, have been identified that support this pathway. Thus, 2-methoxyacetic acid may interfere with essential metabolic pathways of the cell, and it was hypothesized that this causes the testicular lesions and malformations in experimental animals.

Purification Methods

Dry diglyme with NaOH pellets or CaH2, then reflux with, and distil (under reduced pressure) it from Na, CaH2, LiAlH4, NaBH4 or NaH. These operations are carried out under N2. The amine-like odour of diglyme has been removed by shaking with a weakly acidic ion-exchange resin (Amberlite IR-120) before drying and distilling. Addition of 0.01% NaBH4 to the distillate inhibits peroxidation. Purify it also as for dioxane. It has been passed through a 12-in column of molecular sieves to remove water and peroxides. [Beilstein 1 IV 2393.]

Properties and Applications

Diglyme is also known as Diethylene Glycol Dimethyl Ether. The IUPAC name of this compound is 1-Methoxy-2-(2-methoxyethoxy)ethane. This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups. In addition, it is an aprotic polar solvent with a high boiling point that is stable at high pH levels. Therefore, it is a suitable solvent for organic reactions conducted under strongly alkaline conditions[1]. Some researchers have already used diglyme as a physical absorbent of CO2.

Toxicity evaluation

Bis (2-methoxyethyl) ether will present as a vapor, when released to air, at a vapor pressure of 2.96 mmHg at 25°C. The vapor phase is easily degraded in the atmosphere by reaction with photochemically produced hydroxyl radicals. The half-life for the reaction is estimated to be 22 h. Bis (2-methoxyethyl) ether does not contain chromophores that will absorb at wavelengths >290 nm and therefore is not expected to be susceptible to direct photolysis by sunlight.
Bis (2-methoxyethyl) ether has very high mobility in soil based on the estimated Koc of 15, when released to soil. It may volatilize from dry soil surfaces based upon its vapor pressure. Aquatic fate: Bis (2-methoxyethyl) ether does not absorb to suspended solids and sediments when released into water. Hydrolysis is not an important environmental matter because bis (2-methoxyethyl) ether does not contain a functional group that can hydrolyze under environmental conditions.

References

[1] Weijia Huang. “An Aprotic Polar Solvent, Diglyme, Combined with Monoethanolamine to Form CO2 Capture Material: Solubility Measurement, Model Correlation, and Effect Evaluation.” Industrial & Engineering Chemistry Research 54 13 (2015): 3430–3437.

553-90-2
96-35-5
111-96-6
Synthesis of Diglyme from Dimethyl oxalate
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View Lastest Price from Diglyme manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
DIETHYLENE GLYCOL DIMETHYL ETHER pictures 2024-03-27 DIETHYLENE GLYCOL DIMETHYL ETHER
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US $0.00-0.00 / kg 190kg 99.5%MIN 3500tons Anhui lixing chemical co.,ltd
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US $100.00 / bag 1bag 99 5000 Hebei Fengqiang Trading Co., LTD
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US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
Poly-Solv β,β’-dimethoxydiethylether DIETHYLENE GLYCOL DIMETHYL ETHER ABS. O. MOL.SIEVE(H2O<0.005% 2-METHOXYETHYL ETHER, 99+%, SPECTROPHOTO -METRIC GRADE 2-METHOXYETHYL ETHER, ANHYDROUS, 99.5% Catafor MS DiethyleneGlycolDimethylEther(Dedm) DiethyleneGlycolDimethylEtherC6H14O3 DimethylDigolForSynthesis METHYL DIGLYMER / BIS-(2-METHOXYETHYL)ETHER 2-Methoxyethyl ether, extra pure, 99% BIS(2-METHOXYETHYL)ETHER,REAGENT 1-(2-Methoxyethoxy)-2-Methoxyethane 1,5-DiMethoxy-3-oxapentane Bis(2-methoxyethyl) Ether Diglyme Dimethylcarbitol DIETHYLENE GLYCOL DIMETHYL ETHER (STABIL Diethylene glycol diMethyl ether, 99.5%, SuperDry, J&KSeal Diethylene glycol diMethyl ether, 99.5%, SuperDry Diethylene glycol diMethyl ether, extra pure Diethylene glycol diMethyl ether, SuperDry, J&KSeal Diethylene glycol dimethyl ether anhydrous, 99.5% Diethylene glycol dimethyl ether ReagentPlus(R), 99% Diethylene glycol dimethyl ether spectrophotometric grade, >=99% Diethylene glycol dimethyl ether Vetec(TM) reagent grade, 98% DIMETHOXYDIGLYCOL Diethylene glycol diMethyl ether, 99.5%, SpcDry, Water≤50 ppM (by K.F.), SpcSeal Bis(2-methoxye Diethylene glycol dimethyl ether≥ 99.9% (Assay) Diethylene Glycol Dimethyl Ether 〔Bis(2-methoxyethyl) Ether〕 Bis(2-Methoxyethyl)Ether (Diethylene Glycol Dimethyl Ether) DIETHYLENE GLYCOL DIMETHYL ETHER, ANHYD& 1,1’-oxybis(2-methoxy)-Ethane 1,1’-oxybis(2-methoxy-ethan 1,1’-oxybis(2-methoxyethane) 1,1’-oxybis[2-methoxy-ethan 1,1’-oxybis[2-methoxyethane] 1,1'-Oxybis(2-methoxy)ethane 1-methoxy-2-(2-methoxy-ethoxy)-ethane 1-methoxy-2-(2-methoxyethoxy)-ethane 2-(2-Methoxyethoxy)-1-methoxyethane 2,2’-oxybis-ethanodimethylether 2,2'-Oxybisethanol dimethyl ether 2,5,8-Trioxanonane 3-oxa-1,5-pentanediol,dimethylether 3-Oxapentane-1,5-dioldimethylether bis(2-methoxyethyl) bis(2-methoyxethyl)ether CH3OCH2CH2OCH2CH2OCH3 Dariloid 100 Diethyl glycol dimethyl ether diethylglycoldimethylether Diglycol methyl ether diglycolmethylether diglyme (diethylene glycol dimethyl ether) Dimethoxydiethylene glycol Dimethyldigycol Dricoid 200 Ethane, 1,1'-oxybis*2-methoxy-