110-80-5

Basic information

• Product Name: 2-Ethoxyethanol
• Synonyms: GLYCOL ETHER EE;ETHYLENE GLYCOL MONOETHYL ETHER;ETHYLENE GLYCOL ETHYL ETHER;ETHYL GLYCOL;ETHYL CELLOSOLVE;CELLOSOLVE;CELLOSOLVE(R);CELLOSOLVE SOLVENT
• CAS NO: 110-80-5
• Molecular Formula: C₄H₁₀O₂
• Molecular Weight: 90.12
• EINECS: 203-804-1
• Product Categories: Industrial/Fine Chemicals;Ethylene Glycols & Monofunctional Ethylene Glycols;Monofunctional Ethylene Glycols;solvent,waterproofing agent
• Mol File: 110-80-5.mol
• Article Data: 41

Chemical Properties

• Melting Point: -100 °C
• Boiling Point: 135 °C(lit.)
• Flash Point: 107.6 °F
• Appearance: Clear, colorless/Liquid
• Density: 0.93 g/mL at 25 °C(lit.)
• Vapor Density: 3.1 (vs air)
• Vapor Pressure: 3.8 mm Hg ( 20 °C)
• Refractive Index: n20/D 1.407(lit.)
• Storage Temp.: Flammables area
• Solubility: water: miscible
• PKA: 14.44±0.10(Predicted)
• Explosive Limit: 1.8-15.7%(V)
• Water Solubility: miscible
• Stability: Stable. Readily forms explosive mixtures with air - note the wide explosion range. Vapour may travel considerable distance to a
• Merck: 14,3750
• BRN: 1098271
• CAS DataBase Reference: 2-Ethoxyethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Ethoxyethanol(110-80-5)
• EPA Substance Registry System: 2-Ethoxyethanol(110-80-5)

Safety Data

• Hazard Codes: T
• Statements: 60-61-10-20/21/22-20/22
• Safety Statements: 53-45
• RIDADR: UN 1171 3/PG 3
• WGK Germany: 1
• RTECS: KK8050000
• TSCA: Yes
• HazardClass: 3
• PackingGroup: III
• Hazardous Substances Data: 110-80-5(Hazardous Substances Data)

Usage

Chemical Description

2-ethoxyethanol is a solvent used in organic synthesis.

InChI:InChI=1/C4H10O.C2H6O2/c1-3-5-4-2;3-1-2-4/h3-4H2,1-2H3;3-4H,1-2H2

Synthetic route

2-(2-Chloroethoxy)ethanol (628-89-7) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide for 3h; Catalytic behavior; Irradiation;	94%

oxirane (75-21-8) + ethanol (64-17-5) → 2-ethoxy-ethanol (110-80-5) + ethylene glycol (107-21-1)

Conditions	Yield
at 149.84℃; under 22502.3 Torr; for 3h; Inert atmosphere;	A 79.3% B 21.4%

oxirane (75-21-8) + ethanol (64-17-5) + carbon dioxide (124-38-9) → [1,3]-dioxolan-2-one (96-49-1) + 2-ethoxy-ethanol (110-80-5) + ethylene glycol (107-21-1)

Conditions	Yield
With lanthanum(III) oxide; potassium iodide at 149.84℃; under 22502.3 Torr; for 3h;	A 77.3% B 14.1% C 6.8%

oxirane (75-21-8) + ethanol (64-17-5) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With carbon dioxide at 149.84℃; under 22502.3 Torr; for 3h;	47.2%
in Gegenwart aktivierten Hydrosilicaten;
With hydrogen fluoride at 81℃;

oxirane (75-21-8) + ethanol (64-17-5) + carbon dioxide (124-38-9) → [1,3]-dioxolan-2-one (96-49-1) + 2-ethoxy-ethanol (110-80-5) + ethylene glycol (107-21-1) + Diethyl carbonate (105-58-8)

Conditions	Yield
With sodium ethanolate; potassium bromide at 423℃; under 22502.3 Torr; for 3h;	A 44.4% B 6.5% C 39.2% D 29.6%
With sodium ethanolate at 149.84℃; under 22502.3 Torr; for 3h;	A 19.1% B 42.6% C 16.8% D 11.6%
With potassium ethoxide at 149.84℃; under 22502.3 Torr; for 3h;	A 33.1% B 28.3% C 21.6% D 12.8%

oxirane (75-21-8) + ethanol (64-17-5) → 2-ethoxy-ethanol (110-80-5) + ethoxyethoxyethanol (111-90-0)

Conditions	Yield
With sulfuric acid at 100 - 130℃; im Autoklaven;
With toluene-4-sulfonic acid at 100 - 130℃;
With 2,3-Dimethylaniline at 100 - 130℃;
With sulfuric acid at 80 - 100℃;
With metal oxide at 100 - 130℃;

oxirane (75-21-8) + sodium ethanolate (141-52-6) → 2-ethoxy-ethanol (110-80-5)

oxirane (75-21-8) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With nickel; barium(II) oxide at 130 - 150℃; Hydrogenation.unter Druck;

ethyl 2-ethoxyethanoate (817-95-8) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With lithium aluminium tetrahydride; diethyl ether

1-ethoxy-2-trityloxy-ethane (4673-60-3) → 2-ethoxy-ethanol (110-80-5) + monoethylene glycol diethyl ether (629-14-1) + triphenylmethane (519-73-3) + acetaldehyde (75-07-0)

Conditions	Yield
at 325 - 330℃;

sodium 2-hydroxyethoxide (7388-28-5, 10604-71-4, 24768-69-2, 26915-75-3, 50856-01-4, 92004-30-3) + ethyl iodide (75-03-6) → 2-ethoxy-ethanol (110-80-5)

ethyl iodide (75-03-6) + ethylene glycol (107-21-1) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With sodium

ethyl bromide (74-96-4) + 2-chloro-ethanol (107-07-3) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With sodium hydroxide

diethyl sulfate (64-67-5) + 2-chloro-ethanol (107-07-3) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With sodium hydroxide

sodium ethanolate (141-52-6) + 2-chloro-ethanol (107-07-3) → 2-ethoxy-ethanol (110-80-5)

2-methyl-1,3-dioxolane (497-26-7) + triethylaluminum (97-93-8) → 2-ethoxy-ethanol (110-80-5) + 2-(1-Methylpropoxy)ethanol (7795-91-7)

Conditions	Yield
With diethylaluminium hydride In hexane; kerosene for 50h; Heating;	A 0.01 mol B 0.03 mol

2-methyl-1,3-dioxolane (497-26-7) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With triethylaluminum; diethylaluminium hydride In hexane; kerosene for 25h; Heating;	0.02 mol

2-methyl-1,3-dioxolane (497-26-7) → 2-ethoxy-ethanol (110-80-5) + ethanol (64-17-5) + ethane (74-84-0) + monoethylene glycol diethyl ether (629-14-1) + acetic acid (64-19-7) + ethyl acetate (141-78-6)

Conditions	Yield
With hydrogen; Pt-Cab-O-Sil at 300℃; Product distribution; Mechanism; var. of catalyst, temp.;

2-methyl-1,3-dioxolane (497-26-7) → 2-ethoxy-ethanol (110-80-5) + ethyl acetate (141-78-6)

Conditions	Yield
With hydrogen; Pt on Cab-O-Sil at 200℃; Product distribution; Mechanism; var. of H2 coverage, temp.;

2-ethoxyethyl nitrite (41051-51-8) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With 2,2-dimethyl-propanol-1 In chloroform at 26℃; Equilibrium constant; Mechanism; var. alcohols;
With hydrogenchloride; sodium perchlorate at 25℃; Rate constant; acetate buffer pH 2;
With tris-(2-chloro-ethyl)-amine In 1,4-dioxane; water at 25℃; Rate constant; Thermodynamic data; ΔH(excit.), ΔS(excit.), solvent isotope effect (kH/kD);

sulfuric acid mono-(2-ethoxy-ethyl ester) (34253-67-3) → 2-ethoxy-ethanol (110-80-5)

Conditions	Yield
With sulfuric acid at 32.5℃; Equilibrium constant;

ethylene glycol sec-butyl ethyl ether (77078-19-4) → 1-butylene (106-98-9) + 2-ethoxy-ethanol (110-80-5) + (Z)-2-Butene (590-18-1) + trans-2-Butene (624-64-6)

Conditions	Yield
KU-23 sulfonated cation-exchange resins at 130℃; Equilibrium constant; other temperature;;

carbon monoxide (201230-82-2) → methanol (67-56-1) + 2-ethoxy-ethanol (110-80-5) + 2-methoxy-ethanol (109-86-4) + ethylene glycol (107-21-1)

Conditions	Yield
With hydrogen; rhodium(III) acetylacetonate; tris(2,4-pentanedionato)ruthenium(III); tetrabutyl phosphonium bromide at 220℃; under 326800 Torr; Further byproducts given;	A 250 mmol B n/a C n/a D 77.2 mmol

2-ethoxyethyl nitrite (41051-51-8) + benzyl-methyl-amine (103-67-3) → 2-ethoxy-ethanol (110-80-5) + Benzylmethylnitrosamin (937-40-6)

Conditions	Yield
In 1,4-dioxane; water at 25℃; Rate constant;

2-ethoxyethyl nitrite (41051-51-8) + 3-hydroxy-dl-proline (51-35-4) → 2-ethoxy-ethanol (110-80-5) + N-nitrosohydroxyproline (2443-30-3)

Conditions	Yield
In 1,4-dioxane; water at 25℃; Rate constant; Thermodynamic data; ΔH(excit.), ΔS(excit.), solvent isotope effect (kH/kD);

piperazine (110-85-0) + 2-ethoxyethyl nitrite (41051-51-8) → 2-ethoxy-ethanol (110-80-5) + N-nitrosopiperazine (5632-47-3)

Conditions	Yield
With sodium docusate In 2,2,4-trimethylpentane; water Rate constant;

2-ethoxyethyl nitrite (41051-51-8) + malononitrile (109-77-3) → 2-ethoxy-ethanol (110-80-5) + 2-(hydroxyimino)malononitrile (36568-05-5)

Conditions	Yield
With sodium hydroxide at 25℃; Rate constant;

uridine 3'-(2-ethoxyethyl) phosphate (201601-90-3) → 2-ethoxy-ethanol (110-80-5) + uridine-3'-phosphate (84-53-7)

Conditions	Yield
With zinc(II) nitrate; sodium nitrate at 90℃; pH=5.6; Kinetics; Hydrolysis;

2-ethoxy-ethanol (110-80-5) + p-toluenesulfonyl chloride (98-59-9) → 2-ethoxyethyl p-toluenesulfonate (17178-11-9)

Conditions	Yield
With pyridine at 0℃;	100%
With sodium hydroxide In tetrahydrofuran; water	85%
With triethylamine In dichloromethane at 20℃; for 4h;	81.1%

2-ethoxy-ethanol (110-80-5) + N-(2,6-dimethylphenyl)alanine (67617-64-5) → 2-ethoxyethyl N-(2,6-dimethylphenyl)alaninate (712327-18-9)

Conditions	Yield
With thionyl chloride	100%

2-ethoxy-ethanol (110-80-5) + 4-chloro-3-[(2-methanesulfonyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carbonyl)amino]benzoic acid methyl ester (1386979-21-0) → 4-Chloro-3-{[2-(2-ethoxy-ethoxy)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carbonyl]-amino}-benzoic acid (1386980-79-5)

Conditions	Yield
Stage #1: 2-ethoxy-ethanol With sodium hydride In N,N-dimethyl-formamide; mineral oil at 20℃; for 0.5h; Stage #2: 4-chloro-3-[(2-methanesulfonyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carbonyl)amino]benzoic acid methyl ester In N,N-dimethyl-formamide; mineral oil at 20℃; for 18h;	100%

2-ethoxy-ethanol (110-80-5) + methyl 6-(2,6-difluoro-4-hydroxyphenyl)-5-fluoropyridine-2-carboxylate (1355011-30-1) → methyl 6-(4-(2-ethoxyethoxy)-2,6-difluorophenyl)-5-fluoropicolinate (1395998-01-2)

Conditions	Yield
Stage #1: 2-ethoxy-ethanol With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃; for 0.166667h; Stage #2: methyl 6-(2,6-difluoro-4-hydroxyphenyl)-5-fluoropyridine-2-carboxylate In tetrahydrofuran	100%

2-ethoxy-ethanol (110-80-5) + vinyl acetate (108-05-4) → 2-ethoxyethyl acetate (111-15-9)

Conditions	Yield
With dilithium tetra(tert-butyl)zincate In toluene at 0℃; for 1h; Inert atmosphere;	100%

2-ethoxy-ethanol (110-80-5) + diisopropoxidobis(2,4-pentanedionato)zirconium(IV) → zirconium (OCH2CH2OCH2CH3)2-bis(acetylacetonate)

Conditions	Yield
In benzene byproducts: (CH3)2CHOH; performed in a moisture free environment; benzene soln. of Zr(acac)2(OiPr)2 added to a benzene suspension of the organic ligand; refluxed for 4h; solvent removed under reduced pressure; purified by recrystallization from a mixture of dichloromethane and n-hexane; elem. anal.;	99%

2-ethoxy-ethanol (110-80-5) + titanium tetrachloride (7550-45-0) → TiCl3(2-ethoxyethanol-H) (1378027-13-4)

Conditions	Yield
In toluene under an inert atm.; to a soln. of TiCl4 (8.51 mmol) in toluene was added a toluene soln. of a ligand (8.51 mmol); stirring for 3 h; supernatant was decanted and the solid washed with petroleum spirits; the residue was dried under vac.; elem. anal.;	99%

2-ethoxy-ethanol (110-80-5) + bis(N-phenylsalicylideneiminato)aluminium(III)di(μ-isopropoxo)di(isopropoxo) aluminium(III) (443286-95-1) → [(N-phenylsalicylideneiminato)2Al(III)(μ-O(i-Pr))2Al(III)(O(i-Pr))(OCH2CH2OC2H5)] (443286-98-4)

Conditions	Yield
In benzene byproducts: (CH3)2CHOH; under anhyd. conditions; mixt. was refluxed for 4 h, 1:1 molar ratio of Al complex and ligand; solvent was removed; elem. anal.;	98.9%

2-ethoxy-ethanol (110-80-5) + cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV) (23329-69-3, 454677-87-3) + 2-methoxy-ethanol (109-86-4) → 2-ethoxyethanolato-2-methoxyethanolato-bis(8-quinolinato)titanium(IV)

Conditions	Yield
In toluene at 100 - 120℃; Reflux;	98.3%

2-ethoxy-ethanol (110-80-5) + bis(N-phenylsalicylideneiminato)aluminium(III)di(μ-isopropoxo)di(isopropoxo) aluminium(III) (443286-95-1) → [(N-phenylsalicylideneiminato)2Al(III)(μ-O(i-Pr))2Al(III)(OCH2CH2OC2H5)2] (443286-99-5)

Conditions	Yield
In benzene byproducts: (CH3)2CHOH; under anhyd. conditions; mixt. was refluxed for 4 h, 1:2 molar ratio of Al complex and ligand; solvent was removed; elem. anal.;	98.2%

2-ethoxy-ethanol (110-80-5) + cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV) (23329-69-3, 454677-87-3) + 1-(2-furyl)ethanone oxime (5007-50-1) → 2-acetylfuranoximato-2-ethoxyethanolato-bis(8-quinolinato)titanium(IV)

Conditions	Yield
In toluene at 100 - 120℃;	98.2%

2-ethoxy-ethanol (110-80-5) + (Ap)Ti(OPri)2 (1445651-86-4) + 1-(2-furyl)ethanone oxime (5007-50-1) → C18H21NO6Ti (1445651-84-2)

Conditions	Yield
In toluene Reflux;	98.1%

2-ethoxy-ethanol (110-80-5) + 5,7,3',4'-tetra-O-benzyl-(+)-catechin (20728-73-8) → (2R,3S,4S)-5,7,3',4'-tetrabenzyloxy-4-(2"-ethoxyethoxy)flavan-3-ol (478796-20-2)

Conditions	Yield
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane at 20℃; for 2h;	98%
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane	98%
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane at 0 - 20℃; Inert atmosphere;	85%
With 2,3-dicyano-5,6-dichloro-p-benzoquinone

2-ethoxy-ethanol (110-80-5) + lutetium(III) acetate → ethoxyethanol adduct of lutetium acetate

Conditions	Yield
In water under 760.051 Torr; for 7h; Heating / reflux;	98%

titanium(IV) isopropylate (546-68-9) + 2-ethoxy-ethanol (110-80-5) → tetrakis(2-ethoxyethanolato)titanium(IV) (71965-15-6)

Conditions	Yield
In benzene for 4h; Reflux;	98%

2-ethoxy-ethanol (110-80-5) + Ricinoleic acid (141-22-0) → ricinoleic acid ethylene glycol ethyl ether ester (10031-89-7)

Conditions	Yield
With sodium hydrogensulfate monohydrate In dichloromethane at 150℃; for 0.416667h; Microwave irradiation; High pressure;	98%
With toluene-4-sulfonic acid In cyclohexane for 5h; Time; Reagent/catalyst; Solvent; Reflux;

2-ethoxy-ethanol (110-80-5) + para-thiocresol (106-45-6) → 2-ethoxyethyl 4-methylbenzenesulfinate

Conditions	Yield
With tetrabutylammonium perchlorate In acetonitrile at 20℃; for 8h; Electrochemical reaction;	98%

2-hydroxypyridin (142-08-5) + 2-ethoxy-ethanol (110-80-5) + cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV) (23329-69-3, 454677-87-3) → 2-ethoxyethanolato-2-pyridineato-bis(8-quinolinato)titanium(IV)

Conditions	Yield
In toluene at 100 - 120℃; Reflux;	97.9%

2-ethoxy-ethanol (110-80-5) + 2-acetylthiophene oxime (1956-45-2, 92313-45-6, 92313-54-7) + cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV) (23329-69-3, 454677-87-3) → 2-acetylthiopheneoximato-2-ethoxyethanolato-bis(8-quinolinato)titanium(IV)

Conditions	Yield
In toluene at 100 - 120℃; Reflux;	97.9%

2-ethoxy-ethanol (110-80-5) + cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV) (23329-69-3, 454677-87-3) + 1-pyridin-2-yl-ethanone oxime (1758-54-9, 79462-42-3, 81563-77-1) → 2-acetylpyridineoximato-2-ethoxyethanolato-bis(8-quinolinato)titanium(IV)

Conditions	Yield
In toluene at 100 - 120℃;	97.9%

2-ethoxy-ethanol (110-80-5) + (Ap)Ti(OPri)2 (1445651-86-4) + 1-pyridin-2-yl-ethanone oxime (1758-54-9, 79462-42-3, 81563-77-1) → C19H22N2O5Ti (1445651-77-3)

Conditions	Yield
In toluene Reflux;	97.6%

2-ethoxy-ethanol (110-80-5) + cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV) (23329-69-3, 454677-87-3) → 2-ethoxyethanolato-2-propanolato-bis(8-quinolinato)titanium(IV)

Conditions	Yield
In toluene at 100 - 120℃; Reflux;	97.5%

2-ethoxy-ethanol (110-80-5) + 1-chloro-2,4-dinitro-benzene (97-00-7) → 2,4-dinitro-1-(2-ethoxyethoxy)benzene (32895-19-5)

Conditions	Yield
With potassium carbonate In water	97.4%

2-ethoxy-ethanol (110-80-5) → 3-oxapentanoic acid (627-03-2)

Conditions	Yield
With sodium persulfate; sodium bis(1,2-dicarbollyl)cobaltate(III); potassium carbonate In water for 8h; pH=7; Irradiation;	97%
With sodium hydroxide; potassium hexacyanoferrate(III) at 30℃; Kinetics; Further Variations:; substrate and reagents concentration dependence; Oxidation;
With Jones reagent In acetone at 20℃;
With sodium hydroxide; cadmium(II) oxide at 225 - 250℃; im Kupferautoklaven;

2-ethoxy-ethanol (110-80-5) + 5,7,3',4'-tetra-O-benzyl-(+)-catechin (20728-73-8) → (2R,3S)-5,7-Bis-benzyloxy-2-(3,4-bis-benzyloxy-phenyl)-4-(2-ethoxy-ethoxy)-chroman-3-ol (882867-43-8)

Conditions	Yield
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane at 20℃; for 2h;	97%

titanium(IV) isopropylate (546-68-9) + 2-ethoxy-ethanol (110-80-5) → titanium(IV)(isopropoxide)(OCH2CH2OEt)3

Conditions	Yield
In benzene for 4h; Reflux;	97%

2-ethoxy-ethanol (110-80-5) → ethoxyacetaldehyde (22056-82-2)

Conditions	Yield
With Dess-Martin periodane In dichloromethane for 1h; Concentration;	96.5%
With bromamine T In hydrogenchloride at 45℃; Thermodynamic data; Rate constant; Mechanism; Ea, ΔH(excit.), ΔS(excit.), ΔG(excit.);
With pyridinium chlorochromate In dimethyl sulfoxide for 6h; Kinetics; Mechanism; Thermodynamic data; Εa, log A, ΔS(excit.), ΔG(excit.);

2-ethoxy-ethanol (110-80-5) + chloroacetic acid (79-11-8) → chloro-acetic acid-(2-ethoxy-ethyl ester) (60682-94-2)

Conditions	Yield
F-4SK (H form) In toluene at 120℃; for 3h;	96%
With toluene

2-ethoxy-ethanol (110-80-5) + 8-dioxane-3-cobalt-bis(1,2-dicarbollide) (188478-29-7) + sodium hydroxide (1310-73-2) → Na(1+)*Co(C2B9H11)C2B9H10(O(CH2CH2O)3CH2CH3)(1-)=NaCo(C2B9H11)C2B9H10(O(CH2CH2O)3CH2CH3)

Conditions	Yield
In 2-ethoxy-ethanol (N2); stirring alcohol with NaOH for 45 min, addn. of cobalt complex, stirring at room temp. for 15 min; evapn., thin layer chromy. (silica gel, CH2Cl2/ethanol 9:1); elem. anal.;	96%

2-ethoxy-ethanol (110-80-5) + cobalt(II) chloride (7646-79-9) → Co4Cl2(OC2H4OC2H5)6 (625838-58-6)

Conditions	Yield
With sodium In 2-ethoxy-ethanol; toluene N2, Na dissolved, CoCl2 added with vigorous stirring, refluxed for 40 min, left for 30 min at room temp.; soln. decanted, left overnight at -30°C, crysts. decanted, dried (vac.);	96%

Upstream product

• 75-21-8 oxirane 
• 497-26-7 2-methyl-1,3-dioxolane 
• 97-93-8 triethylaluminum 
• 34253-67-3 sulfuric acid mono-(2-ethoxy-ethyl ester) 
• 77078-19-4 ethylene glycol sec-butyl ethyl ether 
• 41051-51-8 2-ethoxyethyl nitrite 
• 51-35-4 3-hydroxy-dl-proline 
• 109-77-3 malononitrile 
• 462-95-3 formaldehyde diethyl acetal 
• 96-49-1 [1,3]-dioxolan-2-one 
• 67-56-1 methanol 
• 64-17-5 ethanol 
• 124-38-9 carbon dioxide 
• 930-68-7 cyclohexenone 

Downstream Products

• 6963-40-2 acetoacetic acid-(2-ethoxyethyl)-ester 
• 111-15-9 2-ethoxyethyl acetate 
• 106-13-8 lauric acid-(2-ethoxy-ethyl ester) 
• 604-63-7 2-benzoyl-benzoic acid-(2-ethoxy-ethyl ester) 
• 624-55-5 glycolic acid-(2-ethoxy-ethyl ester) 
• 617-74-3 lactic acid-(2-ethoxy-ethyl ester) 
• 109-44-4 adipic acid bis-(2-ethoxy-ethyl ester) 
• 624-10-2 decanedioic acid bis-(2-ethoxy-ethyl ester) 
• 74944-83-5 (2,4-dichloro-phenoxy)-acetic acid-(2-ethoxy-ethyl ester) 
• 18407-94-8 Si(Oet-2-Oet)4 
• 371-54-0 fluoro-acetic acid-(2-ethoxy-ethyl ester) 
• 33139-19-4 1-ethoxy-2-(2-chloro-4-nitro-phenoxy)-ethane 
• 2004-70-8 1-methylbuta-1,3-diene 
• 693-86-7 ethenylcyclopropane 

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The densities, ρ, speeds of sound, u and refractive indices, nD of the binary mixtures of 1-butyl-3-methylimidazolium hexafluorophosphate [Bmim][PF6] with 2-methoxyethanol and 2-ethoxyethanol, including those of pure liquids, have been measured over the entire range of composition at 298.15, 30...detailed

Thermophysical properties of 1-butyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imide with 2-Ethoxyethanol (cas 110-80-5) from T = (298.15 to 323.15) K at atmospheric pressure08/23/2019

Density (ρ) and speed of sound (u) data is determined for various binary compositions of 1-butyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imide ([Bmim][NTf2]) and 2-ethoxyethanol (2EE) at different temperatures. The experimental data of density and speed of sound is used to calculate t...detailed

Efficient ITO-free organic light-emitting diodes comprising PEDOT:PSS transparent electrodes optimized with 2-Ethoxyethanol (cas 110-80-5) and post treatment08/21/2019

We demonstrate highly conductive poly (3,4-ethylenedioxythiophene):poly (styrenesulfonate) (PEDOT:PSS) films introduced with a newly investigated solvent 2-ethoxyethanol. The films are optimized by simple solvent post treatment and show enhanced conductivities and reduced sheet resistances. Solv...detailed

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Selective synthesis of dimethoxyethane via directly catalytic etherification of crude ethylene glycol

Etherification of ethylene glycol with methanol provides a sustainable route for the production of widely used dimethoxyethane; dimethoxyethane is a green solvent and reagent that is applied in batteries and used as a potential diesel fuel additive. SAPO-34 zeolite was found to be an efficient and highly selective catalyst for this etherification via a continuous flow experiment. It achieved up to 79.4% selectivity for dimethoxyethane with around 96.7% of conversion. The relationship of the catalyst's structure and the dimethoxyethane selectivity was established via control experiments. The results indicated that the pore structure of SAPO-34 effectively limited the formation of 1,4-dioxane from activated ethylene glycol, enhanced the reaction of the activated methanol with ethylene glycol in priority, and thus resulted in high selectivity for the desired products. The continuous flow technology used in the study could efficiently promote the complete etherification of EG with methanol to maintain high selectivity for dimethoxyethane.

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