Bis[2-(2-hydroxyethoxy)ethyl] ether

Bis[2-(2-hydroxyethoxy)ethyl] ether Basic information
Product Name:Bis[2-(2-hydroxyethoxy)ethyl] ether
Synonyms:2,2'-Oxydiethylenedixoydiethanol;octane-1,7-diol;Bis[2-(2-hydroxyethoxy)ethyl] ether, Tetra(ethylene glycol), Tetraglycol;2,2'-[Oxybis(2,1-ethanediyloxy)]diethanol;Tetraethylene glycol,Bis[2-(2-hydroxyethoxy)ethyl] ether, Tetra(ethylene glycol), Tetraglycol;Tetraethylene glycol, 99.5%;Tetraethylene glycol, 99.5% 1LT;Tetraethylene glycol, 99.5% 2.5LT
CAS:112-60-7
MF:C8H18O5
MW:194.23
EINECS:203-989-9
Product Categories:Materials Science;Poly(ethylene glycol) and Oligo(ethylene glycol);Ethylene Glycols;Poly(ethylene glycol) and Poly(ethylene oxide);Polymer Science;Polymers;Ethylene Glycols & Monofunctional Ethylene Glycols;peg
Mol File:112-60-7.mol
Bis[2-(2-hydroxyethoxy)ethyl] ether Structure
Bis[2-(2-hydroxyethoxy)ethyl] ether Chemical Properties
Melting point -5.6 °C (lit.)
Boiling point 314 °C (lit.)
density 1.125 g/mL at 25 °C (lit.)
vapor density 6.7 (vs air)
vapor pressure <0.01 mm Hg
refractive index n20/D 1.459(lit.)
Fp 400 °F
storage temp. Store below +30°C.
solubility 1000g/l
pka14.06±0.10(Predicted)
form Liquid
color Clear slightly yellow
PH8.5-9.0 (500g/l, H2O, 20℃)
explosive limit0.5-3.4%(V)
Water Solubility soluble
BRN 1634320
Stability:Stable. Incompatible with strong oxidizing agents, strong bases.
LogP-2 at 25℃
CAS DataBase Reference112-60-7(CAS DataBase Reference)
NIST Chemistry ReferenceEthanol, 2,2'-[oxybis(2,1-ethanediyloxy)]bis-(112-60-7)
EPA Substance Registry SystemTetraethylene glycol (112-60-7)
Safety Information
Risk Statements 36/37/38
Safety Statements 24/25
WGK Germany 2
RTECS XC2100000
Autoignition Temperature340 °C DIN 51794
TSCA Yes
HS Code 29094919
Hazardous Substances Data112-60-7(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: > 18056 mg/kg LD50 dermal Rabbit > 18056 mg/kg
MSDS Information
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Bis[2-(2-hydroxyethoxy)ethyl] ether English
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Bis[2-(2-hydroxyethoxy)ethyl] ether Usage And Synthesis
DescriptionTetraethylene glycol is a polymer consisting of ethylene glycol monomer units and two terminal hydroxyl groups. The hydroxyl groups can react to further derivatize the compound. Ethylene glycol compounds have hydrophilic characteristics. The solubility of the polymer increases as the number of ethylene glycol groups increase.
Chemical PropertiesTetraethylene glycol is a high-boiling, clear liquid of low volatility. hygroscopic. It is completely miscible with water and a wide variety of organic solvents. insoluble in benzene, toluene, or gasoline. Combustible. For certain aliphatic hydrocarbons, it has a very slight affinity. Tetraethylene glycol is used as a coupling agent for blending water-soluble and water-insoluble compounds in such formulations as lubricants, glues, cork and textile products, etc.
UsesSolvent for nitrocellulose, plasticizer, lacquers, coating compositions.
UsesTetraethylene glycol is used as a solvent to dissolve water-insoluble compounds. It is employed as a nitrocellulose solvent, a plasticizer, a natural gas desiccant, a hydraulic fluid and in lacquers and coatings. Furthermore, it is used in the synthesis of tetraethylene glycol methacrylate monomer. It acts as a chemical intermediate and acts as a solvent for the manufacturing of inks and dyes. In addition, it serves as a coupling agent in the production of textile lubricants and formulations.
DefinitionChEBI: Tetraethylene glycol is a poly(ethylene glycol).
Production MethodsTetraethylene glycol is prepared commercially by adding ethylene oxide to ethylene glycol, diethylene glycol, or water in the presence of a suitable catalyst.
General DescriptionColorless to straw-colored liquid with a mild odor. Sinks and mixes with water.
Air & Water ReactionsWater soluble.
Reactivity ProfileBis[2-(2-hydroxyethoxy)ethyl] ether is a ether-alcohol derivative. The ether being relatively unreactive. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert alcohols to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides. May attack some forms of plastics [USCG, 1999].
Health HazardCompound is nonirritating. No symptoms observed by any exposure route.
Flammability and ExplosibilityNonflammable
Safety ProfileMildly toxic by ingestion. A sktn and eye irritant. Combustible when exposed to heat or flame; can react with oxidzing materials. To fight fire, use alcohol foam, water, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.
1,13-BIS(8-QUINOLYL)-1,4,7,10,13-PENTAOXATRIDECANE TOMATINE Tetra(ethylene glycol) diacrylate PENTA(ETHYLENE GLYCOL) DI-P-TOLUENESULFONATE NIGERICIN SODIUM SALT Dicyclohexano-24-crown-8 18-Crown-6 (+)-(18-CROWN-6)-2,3,11,12-TETRACARBOXYLIC ACID N-OCTYLPENTAOXYETHYLENE Benzo-15-crown-5 1,1-DIMETHYLSILA-17-CROWN-6 2-DECYL-1,4,7,10,13,16-HEXAOXACYCLO-OCTADECANE 3,6,9,12,15-pentaoxaheptadecane BIS[(12-CROWN-4)METHYL] DODECYLMETHYLMALONATE Tetraethyleneglycol monooctyl ether HEPTAETHYLENE GLYCOL Tetraethylene glycol dimethacrylate monensin methyl ester

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