As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
Cas:110-80-5
Min.Order:1 Kilogram
FOB Price: $3.0
Type:Lab/Research institutions
inquiryWelcome to Simagchem, your partner in China as a premier supply of bulk specialty chemicals for industry and life science. We introduce experienced quality product and exceptional JIT service with instant market intelligence in China to benefit our
Cas:110-80-5
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inquiryProduct description: Product name 2-Ethoxyethanol CAS number 110-80-5 Assay ≥99.5% Appearance Colorless transparent liquid Capacity 2000mt/year Application Solvent, leather c
Cas:110-80-5
Min.Order:1 Kilogram
FOB Price: $12.0
Type:Lab/Research institutions
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Type:Trading Company
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inquiryECS ECS is usually used as solvent for nitrocellulose, acetate fiber, synthetic resin, paint. It is used as coloring agent, stabilizer of emulsion, printing ink and vitamin B12 refine solvent in leather industry. And it is used as painting diluen
Cas:110-80-5
Min.Order:1 Kilogram
FOB Price: $1.4 / 2.0
Type:Manufacturers
inquiryThe above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
Cas:110-80-5
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Min.Order:5 Kiloliter
FOB Price: $1.2 / 5.0
Type:Manufacturers
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Min.Order:1 Metric Ton
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Type:Lab/Research institutions
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Cas:110-80-5
Min.Order:0 Metric Ton
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Type:Lab/Research institutions
inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:110-80-5
Min.Order:10 Gram
FOB Price: $100.0
Type:Lab/Research institutions
inquirysupplier in China Appearance:colourless liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as a solvent, nitro celluloid, varnish lea
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Min.Order:1 Metric Ton
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Type:Lab/Research institutions
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Cas:110-80-5
Min.Order:1 Kilogram
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Type:Lab/Research institutions
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Hebei Lead Bio-Chemicals Co., Ltd. established in 2006, devolved in resurching, manufacturing and supplying of pharmaceuticals,food ingredients, cosmetics,health care products, Chinese herb, plant extracts and some fine chemicals,is one of leading gr
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Jinhua huayi chemical co., ltd. is dedicated to the development, production and marketing of chemicals. On the basis of equality and mutual benefit, and under the principle of customer first, credit first, quality first, we are ready to join hands
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
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Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
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Cas:110-80-5
Min.Order:1 Kilogram
FOB Price: $112.0
Type:Trading Company
inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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sell high purity of 2-Ethoxyethanol Application:sell high purity of 2-Ethoxyethanol
Hangzhou ZeErRui Chemical Co., Ltd. located in Lingang industrial areas, our plant covers an area of 6000 square meters.ZeErRui dedicated to the development, production and marketing of chemicals. We have earned ourselves a good reputation at home an
Cas:110-80-5
Min.Order:0
Negotiable
Type:Lab/Research institutions
inquirylow price and high purityAppearance:solid or liquid Storage:in sealed air resistant place Package:As customer require Application:Pharma;Industry;Agricultural Transportation:by sea or by airplane Port:any port in China
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% |
Conditions | Yield |
---|---|
at 149.84℃; under 22502.3 Torr; for 3h; Inert atmosphere; | A 79.3% B 21.4% |
oxirane
ethanol
carbon dioxide
A
[1,3]-dioxolan-2-one
B
2-ethoxy-ethanol
C
ethylene glycol
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% |
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
ethanol
carbon dioxide
A
[1,3]-dioxolan-2-one
B
2-ethoxy-ethanol
C
ethylene glycol
D
Diethyl carbonate
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% |
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℃; |
Conditions | Yield |
---|---|
With nickel; barium(II) oxide at 130 - 150℃; Hydrogenation.unter Druck; |
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
1-ethoxy-2-trityloxy-ethane
A
2-ethoxy-ethanol
B
monoethylene glycol diethyl ether
C
triphenylmethane
D
acetaldehyde
Conditions | Yield |
---|---|
at 325 - 330℃; |
sodium 2-hydroxyethoxide
ethyl iodide
2-ethoxy-ethanol
Conditions | Yield |
---|---|
With sodium |
Conditions | Yield |
---|---|
With sodium hydroxide |
Conditions | Yield |
---|---|
With sodium hydroxide |
2-methyl-1,3-dioxolane
triethylaluminum
A
2-ethoxy-ethanol
B
2-(1-Methylpropoxy)ethanol
Conditions | Yield |
---|---|
With diethylaluminium hydride In hexane; kerosene for 50h; Heating; | A 0.01 mol B 0.03 mol |
Conditions | Yield |
---|---|
With triethylaluminum; diethylaluminium hydride In hexane; kerosene for 25h; Heating; | 0.02 mol |
2-methyl-1,3-dioxolane
A
2-ethoxy-ethanol
B
ethanol
C
ethane
D
monoethylene glycol diethyl ether
E
acetic acid
F
ethyl acetate
Conditions | Yield |
---|---|
With hydrogen; Pt-Cab-O-Sil at 300℃; Product distribution; Mechanism; var. of catalyst, temp.; |
Conditions | Yield |
---|---|
With hydrogen; Pt on Cab-O-Sil at 200℃; Product distribution; Mechanism; var. of H2 coverage, temp.; |
2-ethoxyethyl nitrite
2-ethoxy-ethanol
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)
2-ethoxy-ethanol
Conditions | Yield |
---|---|
With sulfuric acid at 32.5℃; Equilibrium constant; |
ethylene glycol sec-butyl ethyl ether
A
1-butylene
B
2-ethoxy-ethanol
C
(Z)-2-Butene
D
trans-2-Butene
Conditions | Yield |
---|---|
KU-23 sulfonated cation-exchange resins at 130℃; Equilibrium constant; other temperature;; |
carbon monoxide
A
methanol
B
2-ethoxy-ethanol
C
2-methoxy-ethanol
D
ethylene glycol
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
benzyl-methyl-amine
A
2-ethoxy-ethanol
B
Benzylmethylnitrosamin
Conditions | Yield |
---|---|
In 1,4-dioxane; water at 25℃; Rate constant; |
2-ethoxyethyl nitrite
3-hydroxy-dl-proline
A
2-ethoxy-ethanol
B
N-nitrosohydroxyproline
Conditions | Yield |
---|---|
In 1,4-dioxane; water at 25℃; Rate constant; Thermodynamic data; ΔH(excit.), ΔS(excit.), solvent isotope effect (kH/kD); |
piperazine
2-ethoxyethyl nitrite
A
2-ethoxy-ethanol
B
N-nitrosopiperazine
Conditions | Yield |
---|---|
With sodium docusate In 2,2,4-trimethylpentane; water Rate constant; |
2-ethoxyethyl nitrite
malononitrile
A
2-ethoxy-ethanol
B
2-(hydroxyimino)malononitrile
Conditions | Yield |
---|---|
With sodium hydroxide at 25℃; Rate constant; |
uridine 3'-(2-ethoxyethyl) phosphate
A
2-ethoxy-ethanol
B
uridine-3'-phosphate
Conditions | Yield |
---|---|
With zinc(II) nitrate; sodium nitrate at 90℃; pH=5.6; Kinetics; Hydrolysis; |
2-ethoxy-ethanol
p-toluenesulfonyl chloride
2-ethoxyethyl p-toluenesulfonate
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
N-(2,6-dimethylphenyl)alanine
2-ethoxyethyl N-(2,6-dimethylphenyl)alaninate
Conditions | Yield |
---|---|
With thionyl chloride | 100% |
2-ethoxy-ethanol
4-chloro-3-[(2-methanesulfonyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carbonyl)amino]benzoic acid methyl ester
4-Chloro-3-{[2-(2-ethoxy-ethoxy)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidine-6-carbonyl]-amino}-benzoic acid
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
methyl 6-(2,6-difluoro-4-hydroxyphenyl)-5-fluoropyridine-2-carboxylate
methyl 6-(4-(2-ethoxyethoxy)-2,6-difluorophenyl)-5-fluoropicolinate
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% |
Conditions | Yield |
---|---|
With dilithium tetra(tert-butyl)zincate In toluene at 0℃; for 1h; Inert atmosphere; | 100% |
2-ethoxy-ethanol
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% |
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
bis(N-phenylsalicylideneiminato)aluminium(III)di(μ-isopropoxo)di(isopropoxo) aluminium(III)
[(N-phenylsalicylideneiminato)2Al(III)(μ-O(i-Pr))2Al(III)(O(i-Pr))(OCH2CH2OC2H5)]
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
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
2-methoxy-ethanol
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; Reflux; | 98.3% |
2-ethoxy-ethanol
bis(N-phenylsalicylideneiminato)aluminium(III)di(μ-isopropoxo)di(isopropoxo) aluminium(III)
[(N-phenylsalicylideneiminato)2Al(III)(μ-O(i-Pr))2Al(III)(OCH2CH2OC2H5)2]
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
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
1-(2-furyl)ethanone oxime
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; | 98.2% |
2-ethoxy-ethanol
(Ap)Ti(OPri)2
1-(2-furyl)ethanone oxime
C18H21NO6Ti
Conditions | Yield |
---|---|
In toluene Reflux; | 98.1% |
2-ethoxy-ethanol
5,7,3',4'-tetra-O-benzyl-(+)-catechin
(2R,3S,4S)-5,7,3',4'-tetrabenzyloxy-4-(2"-ethoxyethoxy)flavan-3-ol
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 |
Conditions | Yield |
---|---|
In water under 760.051 Torr; for 7h; Heating / reflux; | 98% |
titanium(IV) isopropylate
2-ethoxy-ethanol
tetrakis(2-ethoxyethanolato)titanium(IV)
Conditions | Yield |
---|---|
In benzene for 4h; Reflux; | 98% |
2-ethoxy-ethanol
Ricinoleic acid
ricinoleic acid ethylene glycol ethyl ether ester
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; |
Conditions | Yield |
---|---|
With tetrabutylammonium perchlorate In acetonitrile at 20℃; for 8h; Electrochemical reaction; | 98% |
2-hydroxypyridin
2-ethoxy-ethanol
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; Reflux; | 97.9% |
2-ethoxy-ethanol
2-acetylthiophene oxime
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; Reflux; | 97.9% |
2-ethoxy-ethanol
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
1-pyridin-2-yl-ethanone oxime
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; | 97.9% |
2-ethoxy-ethanol
(Ap)Ti(OPri)2
1-pyridin-2-yl-ethanone oxime
C19H22N2O5Ti
Conditions | Yield |
---|---|
In toluene Reflux; | 97.6% |
2-ethoxy-ethanol
cis-di-2-propanolato-bis(8-quinolinato)-titanium(IV)
Conditions | Yield |
---|---|
In toluene at 100 - 120℃; Reflux; | 97.5% |
2-ethoxy-ethanol
1-chloro-2,4-dinitro-benzene
2,4-dinitro-1-(2-ethoxyethoxy)benzene
Conditions | Yield |
---|---|
With potassium carbonate In water | 97.4% |
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
5,7,3',4'-tetra-O-benzyl-(+)-catechin
(2R,3S)-5,7-Bis-benzyloxy-2-(3,4-bis-benzyloxy-phenyl)-4-(2-ethoxy-ethoxy)-chroman-3-ol
Conditions | Yield |
---|---|
With 2,3-dicyano-5,6-dichloro-p-benzoquinone In dichloromethane at 20℃; for 2h; | 97% |
Conditions | Yield |
---|---|
In benzene for 4h; Reflux; | 97% |
2-ethoxy-ethanol
ethoxyacetaldehyde
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
chloroacetic acid
chloro-acetic acid-(2-ethoxy-ethyl ester)
Conditions | Yield |
---|---|
F-4SK (H form) In toluene at 120℃; for 3h; | 96% |
With toluene |
2-ethoxy-ethanol
8-dioxane-3-cobalt-bis(1,2-dicarbollide)
sodium hydroxide
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% |
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% |
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