ETHYL OXALATE
ETHYL OXALATE
Ethyl oxalate is a chemical intermediate used in the manufacture of API and various dyes.
Ethyl oxalate can be used as a solvent for a number of synthetic and natural resins.
Ethyl oxalate is also used as a cost effective additive based in the dye-sensitized solar cells (DSSCs).
CAS Number: 95-92-1
EC Number: 202-464-1
Chemical Formula: C2H5OOCCOOC2H5
Molar Mass: 146.14 g/mol
Synonyms Diethyl oxalate, 95-92-1, Ethyl oxalate, Ethanedioic acid, diethyl ester, Diethyl ethanedioate, diethyloxalate, Oxalic acid, diethyl ester, Oxalic ether, Oxalic Acid Diethyl Ester, Diethylester kyseliny stavelove, Ethanedioic acid, 1,2-diethyl ester, Diethyl ester of oxalic acid, 860M3ZWF6J, Diethyl oxalate, 99%, diethyl ethane-1,2-dioate, Ethyl oxalate (VAN), HSDB 2131, EINECS 202-464-1, UN2525, Diethylester kyseliny stavelove [Czech], BRN 0606350, diethyl ethaneioate, Oxalic acid diethyl, diethyl ethane-dioate, oxalic acid diethylester, 1,2-diethyl ethanedioate, Diethyl oxalate, >=99%, 4-02-00-01848 (Beilstein Handbook Reference), Ethanedioic acid diethyl ester, CHEMBL3183226, Diethyl oxalate, analytical standard, Ethyl oxalate [UN2525] [Poison], MCULE-5264218494, UN 2525, CAS-95-92-1, Diethyl oxalate, purum, >=99.0% (GC), FT-0645510, 5-pentyl-5-tetrahydropyran-2-yl-imidazolidine-2,4-dione, ETHANEDIOIC ACID,DIETHYL ESTER (DIETHYLOXALATE), F1908-0115, Z940713540, AKOS BBS-00004457, Ethanedioic acid diethyl ester, ETHYL OXALATE, Diethyl oxalate, DIETHYL ETHANEDIOATE, RARECHEM AL BI 0114, OXALIC ACID DIETHYL ESTER, C2H5OCOCOOC2H5, Ceftriaxone Impurity 2, Oxalic acid diethyl ester Oxalic acid diethyl ester Oxalic acid diethyl ester, DIethlyoxalate, Ceftriaxone Impurity 5, Ceftriaxone Impurity 11, Diethyl ester of oxalic acid, Diethyl ester, oxalic acid, Diethylester kyseliny stavelove, diethylesterkyselinystavelove, dlethyloxalate, Oxalic ether, oxalicether, Diethyl oxate, Diethyl oxalate, STANDARD FOR GC, Diethyl oxalate, 99+%, DiethyloxalateForSynthesis, diethyl ethaneioate, Diethyl oxalate, 98.0% MIN, Diethyl oxalate, 99.0% MIN, Diethyloxaiate, Oxalsurediethylester, Diαthyloxalat, oxalic acid diethylester Diethyl oxalate, Diethyl oxalate pure, GKSW, Diethyl oxalate, 99% 1KG, Diethyl oxalate, 99% 2.5KG, Diethyl oxalate, 99% 25GR, Diethyl oxalate, 99% 500GR, Dithyl oxalate, Diethyl oxalate purum, >=99.0% (GC), Diethyl oxalate [for SpectrophotoMetry], Diethyl oxalat, Diethyleoxalate, Ethanedioicacid, 1,2-diethyl ester, DiethylOxalate>, DiethylOxalate[forSpectrophotometry]>, Diethyl oxalate fandachem, Diethyl oxalate (DEOX), Diethyl oxalate ISO 9001：2015 REACH, 95-92-1, Diethyl oxalate, 95-92-1, Ethyl oxalate, Ethanedioic acid, diethyl ester, Diethyl ethanedioate, diethyloxalate, Oxalic acid, diethyl ester, Oxalic ether, Oxalic Acid Diethyl Ester, NSC 8851, UNII-860M3ZWF6J, Diethylester kyseliny stavelove, MFCD00009119, Diethyl ester of oxalic acid, 860M3ZWF6J, Ethanedioic acid, 1,2-diethyl ester, Ethyl oxalate (VAN), HSDB 2131, EINECS 202-464-1, UN2525, BRN 0606350, diethyl ethaneioate, Oxalic acid diethyl, diethyl ethane-dioate, oxalic acid diethylester, 1,2-diethyl ethanedioate, C2H5OCOCOOC2H5, Diethyl oxalate, >=99%, EC 202-464-1, SCHEMBL7262, WLN: 2OVVO2, DSSTox_CID_24472, DSSTox_RID_80254, DSSTox_GSID_44472, 4-02-00-01848 , CHEMBL3183226, DTXSID2044472, NSC8851, AMY37179, NSC-8851, ZINC1648270, Diethyl oxalate, analytical standard, Tox21_302109, BBL011413, STL146519, AKOS000120214, Ethyl oxalate , MCULE-5264218494, UN 2525, CAS-95-92-1, NCGC00255767-01, AS-14315BP-13324, K733, Diethyl oxalate, purum, >=99.0% (GC), FT-0645510, O0078, O0120Q904612, J-802189, Q-200981, 5-pentyl-5-tetrahydropyran-2-yl-imidazolidine-2,4-dione, ETHANEDIOIC ACID,DIETHYL ESTER (DIETHYLOXALATE), F1908-0115, Z940713540
Due to Ethyl oxalate chemical characteristic, Ethyl oxalate (DEOX) is miscible with alcohols, ether and other common organic solvents.
Ethyl oxalate is slightly soluble in water.
Ethyl oxalate is a Diester of ethyl alcohol and oxalic acid.
Ethyl oxalate appears as a colorless liquid.
Ethyl oxalate is slightly denser than water and insoluble in water.
Ethyl oxalate undergoes transesterification with phenol in the liquid phase over very efficient MoO3/TiO2 solid-acid sol-gel catalysts to form diphenyl oxalate.
Ethyl oxalate undergoes Claisen condensation with active methylene group of ketosteroids to form glyoxalyl derivatives.
Ethyl oxalate undergoes hydrogenation in the presence of high copper contented mesoporous Cu/SBA-15 catalysts to yield ethylene glycol.
Form of Ethyl oxalate is liquid.
A sustainable process based on carbon monoxide (CO) coupling reaction has been considered as an alternative method for DEO
Ethyl oxalate appears as a colorless liquid.
Ethyl oxalate is slightly soluble in water.
Ethyl oxalate is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 tonnes per annum.
Ethyl oxalate is used in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Ethyl oxalate is a chemical intermediate used in the manufacture of API and various dyes.
Ethyl oxalate can be used as a solvent for a number of synthetic and natural resins.
Ethyl oxalate is also used as a cost effective additive based in the dye-sensitized solar cells (DSSCs)
Ethyl oxalate may have a promising industrial application for coal to ethylene glycol production.
Ethyl oxalate is a clear colorless liquid with characteristic.
Ethyl oxalyl Chloride is manufactured by hydrolysis of Ethyl oxalate with Potassium Carbonate.
Ethyl oxalate is a chemical used to pre-treat wood chips in order to refine and prepare them for further processing (such as obtaining wood pulp).
Ethyl oxalate is also used as a starting material to synthesize Ethylene glycol (E890140) by means of catalytic hydrogenation.
Ethyl oxalate is a chemical intermediate used in the manufacture of API and various dyes.
Applications of Ethyl Oxalate:
Ethyl oxalate is used to prepare active pharmaceutical ingredients (API), plastics and dyestuff intermediates.
Ethyl oxalate is also used as a solvent for cellulose esters, ethers, resins, perfumes and lacquers for electronics.
Ethyl oxalate is involved in the transesterification reaction with phenol to get dipheny oxalate.
Ethyl oxalate is also involved in the Claisen condensation ketosteroids to prepare glyoxalyl derivatives.
Further, Ethyl oxalate is used to prepare sym-1,4-diphenyl-1,4-dihydro-1,2,4,5-polytetrazine.
In addition to this, Ethyl oxalate is utilized in the microemulsion synthesis of zinc oxide nanoparticles.
Ethyl oxalate was used in microemulsion synthesis of ZnO nanoparticles.
Uses of Ethyl Oxalate:
Ethyl oxalate is used especially for production of pesticides and also as a starting material of so-called oxalate syntheses used in many areas, such as in pharmaceutical industry (production of steroids, barbiturates), in dyeing industry (Tartrazin dyestuff) and other specialised chemicals and in PU and plastic industry.
Ethyl oxalate is used to make pharmaceuticals, plastics, dyes, and dyestuff intermediates.
Ethyl oxalate is also used as a solvent for cellulose esters, ethers, resins, perfumes, and lacquers for electronics.
Ethyl oxalate is a chemical used to pre-treat wood chips in order to refine and prepare them for further processing (such as obtaining wood pulp).
Ethyl oxalate is also used as a starting material to synthesize Ethylene glycol (E890140) by means of catalytic hydrogenation.
Ethyl oxalate uses and applications include:
Solvent for cellulose esters and ethers, many natural and synthetic resins, paint stripping;
radio-tube cathode fixing lacquers;
perfumes;
chelating agent;
cleaner for polymeric residues;
pigment dispersant;
intermediate for organic synthesis, pharmaceuticals, barbiturates (CNS depressants), dyes;
in food packaging adhesives
Suggested storage of Ethyl Oxalate:
Moisture-sensitive
Use and Manufacturing:
Manufacture of phenobarbital,
Ethylbenzyl malonate,
Triethylamine, & similar chemicals;
Manufacture of plastics,
Dyestuff intermediates;
Solvent for cellulose esters
Organic syntheses,
Esp in mfr of pharmaceuticals;
Solvent for ethers & resins
Olvent for perfumes & for natural & synthetic resins (cellulose esters);
Agent in radio tube cathode fixing lacquers; c
Hem int for pharmaceuticals,
Plastics & dyes.
Widespread uses by professional workers:
Ethyl oxalate is used in the following products: laboratory chemicals and polymers.
Ethyl oxalate is used in the following areas: building & construction work.
Other release to the environment of Ethyl oxalate is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners), outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).
Uses at industrial sites:
Ethyl oxalate is used in the following products: polymers and laboratory chemicals.
Ethyl oxalate has an industrial use resulting in manufacture of another substance (use of intermediates).
Ethyl oxalate is used in the following areas: building & construction work, formulation of mixtures and/or re-packaging and scientific research and development.
Ethyl oxalate is used for the manufacture of: chemicals.
Release to the environment of Ethyl oxalate can occur from industrial use: in the production of articles, for thermoplastic manufacture, of substances in closed systems with minimal release and as an intermediate step in further manufacturing of another substance (use of intermediates).
Other Industry Uses:
Intermediates
Processing aids, not otherwise listed
Agro chemical pesticide
Consumer Uses:
Apparel and footwear care products
Agro chemical pesticide
Other Uses:
Chelating:
Reacts and forms complexes with metal ions that could affect the stability and / or appearance of cosmetic products.
Hair conditioner:
Leaves hair easy to comb, soft, soft and shiny and / or confers volume, lightness and shine.
Masking:
Reduces or inhibits the odor or basic taste of the product.
Plasticiser:
Softens and softens another substance that otherwise could not easily be deformed, dispersed or worked.
Solvent:
Dissolves other substances.
Potential Uses:
Chelating agents, hair conditioning, plasticisers, solvents
Ethyl oxalate is used as a solvent for paint stripping and resins.
Ethyl oxalate is used as cleaner for polymeric residues.
Ethyl oxalate is used as pigment dispersant.
There are some specialty application of Ethyl oxalate as a solvent in nitrocellulose lacquers.
Ethyl oxalate is a chemical intermediate used in the manufacture of API and various dyes.
Ethyl oxalate can be used as a solvent for a number of synthetic and natural resins.
Ethyl oxalate is also used as a cost effective additive based in the dye-sensitized solar cells (DSSCs).
Ethyl oxalate is an important intermediate in chemical industry, especially in pharmaceutical industry, which can be utilized for the synthesis of high value drugs, dyestuff and as the useful solvent for spices.
Ethyl oxalate is used in microemulsion synthesis of ZnO nanoparticles.
Ethyl oxalate is used in the synthesis of sym-1,4-diphenyl-1,4-dihydro-1,2,4,5-polytetrazine.
Ethyl oxalate can be used in Pharma & Life Science, Agriculture, Plastics, Cosmetics & Personal Care.
Ethyl oxalate can be applied as Agrochemicals.
Ethyl oxalate is widely used in fine chemical industry.
Ethyl oxalate can be added to unmodified vegetable oils in any ratio.
As heating oil, use can be made of a mixture which, as main component, consists of vegetable oils and up to 50% by volume Ethyl oxalate.
Ethyl oxalate is used as a solvent for plastics and in the manufacture of perfumes and pharmaceuticals.
As heating oil use can be made of a mixture which originates from the refining of crude oil and is admixed with up to 25% by volume Ethyl oxalate.
Ethyl oxalate is widely utilized at industrial domains to synthesize a variety of significant fine chemicals, such as dyes, pharmaceuticals, solvents, extractants, various intermediates and ethylene glycol (EG).
Ethyl oxalate is necessary to dissolve DMO in anhydrous methanol or heat DMO to liquid state when Ethyl oxalate is applied to the production of ethylene glycol.
Ethyl oxalate is a liquid chemical at room temperature and convenient as raw material for the production of ethylene glycol by hydrogenation.
Benefits of Ethyl Oxalate:
Highly efficient
Highly stable
Contributes to sustainable ethylene glycol production
General Manufacturing Information of Ethyl Oxalate:
Industry Processing Sectors
All other basic organic chemical manufacturing
Pesticide, fertilizer, and other agricultural chemical manufacturing
Plastic material and resin manufacturing
Solubility of Ethyl Oxalate:
Miscible with alcohols, ether and other common organic solvents.
Completely sol ether, alcohol and acetone; slightly sol hot water.
The solubility of dimethyl oxalate is similar, except that Ethyl oxalate is more soluble in water.
The solubilities of the other esters are similar in organic solvents, but they are insoluble in water.
Production of Ethyl Oxalate:
Dimethyl oxalate can be obtained by esterification of oxalic acid with methanol using sulfuric acid as a catalyst:
2CH3OH+(CO2H)2 → (CO2CH3)2+2H2O
Oxidative carbonylation route:
The preparation by oxidative carbonylation has attracted interest because Ethyl oxalate requires only C1 precursors:
4CH3OH+4 CO+O2→ 2 (CO2CH3)2+2H2O
The reaction is catalyzed by Pd2+.
The synthesis gas is mostly obtained from coal or biomass.
The oxidation proceeds via dinitrogen trioxide, which is formed according to (1) of nitrogen monoxide and oxygen and then reacts according to (2) with methanol forming methyl nitrite.
In the next step of dicarbonylation (3) carbon monoxide reacts with methyl nitrite to dimethyl oxalate in the vapor phase at atmospheric pressure and temperatures at 80-120 °C over a palladium catalyst.
This method is lossless with respect to methyl nitrite, which acts practically as a carrier of oxidation equivalents.
However, the water formed must be removed to prevent hydrolysis of the dimethyl oxalate product.
With 1% Pd/α-Al2O3 dimethyl oxalate is produced selectively in a dicarbonylation reaction, under the same conditions with 2% Pd/C dimethyl carbonate is produced by monocarbonylation.
Alternatively, the oxidative carbonylation of methanol can be carried out with high yield and selectivity with 1,4-benzoquinone as an oxidant in the system Pd(OAc)2/PPh3/benzoquinone with mass ratio 1/3/100 at 65 °C and 70 atm CO.
Production Methods of Ethyl Oxalate:
Ethyl oxalate is produced via esterification of ethanol and oxalic acid.
Ethyl oxalateis a preferred solvent for cellulose acetate and nitrate.
Due to Ethyl oxalate’s chemical characteristic, Ethyl oxalate is miscible with alcohols, ether and other common organic solvents.
Reactions of Ethyl Oxalate:
Dimethyl oxalate (and the related diethyl ester) is used in diverse condensation reactions.
For example, Ethyl oxalate condenses with cyclohexanone to give the diketo-ester, a precursor to pimelic acid.
With diamines, the diesters of oxalic acid condense to give cyclic diamides.
Quinoxalinedione is produced by condensation of dimethyloxalate and o-phenylenediamine:
C2O2(OMe)2 + C6H4(NH2)2 → C6H4(NHCO)2 + 2 MeOH
Hydrogenation gives ethylene glycol.
Dimethyl oxalate can be converted into ethylene glycol in high yields (94.7%).
The methanol formed is recycled in the process of oxidative carbonylation.
Other plants with a total annual capacity of more than 1 million tons of ethylene glycol per year are planned.
Decarbonylation gives dimethyl carbonate.
Diphenyl oxalate is obtained by transesterification with phenol in the presence of titanium catalysts, which is again decarbonylated to diphenyl carbonate in the liquid or gas phase.
Dimethyl oxalate can also be used as a methylating agent.
Ethyl oxalate is notably less toxic than other methylating agents such as methyl iodide or dimethyl sulfate.
Handling and Storage of Ethyl Oxalate:
Precautions for safe handling:
Hygiene measures:
Immediately change contaminated clothing.
Apply preventive skin protection.
Wash hands and face after working with substance.
Conditions for safe storage, including any incompatibilities:
Storage conditions:
Tightly closed.
Keep in a well-ventilated place.
Keep locked up or in an area accessible only to qualified or authorized persons.
Stability and Reactivity of Ethyl Oxalate:
Ethyl oxalate is an ester.
Esters react with acids to liberate heat along with alcohols and acids.
Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products.
Heat is also generated by the interaction of esters with caustic solutions.
Flammable hydrogen is generated by mixing esters with alkali metals and hydrides
Chemical stability:
Ethyl oxalate is chemically stable under standard ambient conditions (room temperature).
First Aid Measures of Ethyl Oxalate:
General advice:
First aider needs to protect himself.
If inhaled:
Fresh air.
Call in physician.
In case of skin contact:
Take off immediately all contaminated clothing.
Rinse skin with water/ shower.
Call a physician immediately.
In case of eye contact:
Rinse out with plenty of water.
Remove contact lenses.
If swallowed:
Make victim drink water.
Accidental Release Measures of Ethyl Oxalate:
Environmental precautions:
Do not let product enter drains.
Methods and materials for containment and cleaning up:
Cover drains.
Collect, bind, and pump off spills.
Take up carefully with liquid-absorbent material.
Dispose of properly.
Clean up affected area.
Fire Fighting Measures of Ethyl Oxalate:
Extinguishing media:
Suitable extinguishing media:
Water
Foam
Carbon dioxide (CO2)
Dry powder
Unsuitable extinguishing media:
For Ethyl oxalate no limitations of extinguishing agents are given.
Further information:
Remove container from danger zone and cool with water.
Prevent fire extinguishing water from contaminating surface water or the ground water system.
Exposure Controls/personal Protection of Ethyl Oxalate:
Eye/face protection:
Use tightly fitting safety goggles.
Skin protection:
Full contact
Material: butyl-rubber
Minimum layer thickness: 0,7 mm
Break through time: 480 min
Splash contact:
Material: Nitrile rubber
Minimum layer thickness: 0,4 mm
Break through time: 10 min
Body Protection:
protective clothing
Control of environmental exposure:
Do not let product enter drains.
Identifiers of Ethyl Oxalate:
CAS Number: 553-90-2
ChemSpider: 10649
ECHA InfoCard: 100.008.231
PubChem CID: 11120
UNII: IQ3Q79344S
CompTox Dashboard (EPA): DTXSID9060287
InChIInChI=1S/C4H6O4/c1-7-3(5)4(6)8-2/h1-2H3
Key: LOMVENUNSWAXEN-UHFFFAOYSA-N
InChI=1/C4H6O4/c1-7-3(5)4(6)8-2/h1-2H3
Key: LOMVENUNSWAXEN-UHFFFAOYAF
SMILES: O=C(OC)C(=O)OC
INCI name: Ethyl oxalate
EINECS/ELINCS number: 202-464-1
Classification: Regulated
Restriction in Europe: III/3
EC / List no.: 202-464-1
CAS no.: 95-92-1
Mol. formula: C6H10O4
CAS number: 95-92-1
EC index number: 607-147-00-5
EC number: 202-464-1
Hill Formula: C₆H₁₀O₄
Chemical formula: C₂H₅OOCCOOC₂H₅
Molar Mass: 146.14 g/mol
HS Code: 2917 11 00
Synonym(s): Diethyl ethanedioate, Ethyl oxalate
Linear Formula: C2H5OCOCOOC2H5
CAS Number: 95-92-1
Molecular Weight: 146.14
Beilstein: 606350
EC Number: 202-464-1
MDL number:MFCD00009119
PubChem Substance ID:24848078
NACRES:NA.22
Properties of Ethyl Oxalate:
Physical State: Liquid
Storage: Store at room temperature
Melting Point: -41° C (lit.)
Boiling Point: 185° C (lit.)
Density: 1.08 g/cm3 at 25° C
Formula: C6H10O4
Formula Weight: 146.14
Melting point: -41°
Boiling Point: 184-186°
Flash Point: 75°(167°F)
Density: 1.077
Refractive Index: 1.4100
Storage & Sensitivity:
Moisture Sensitive.
Store under Argon.
Ambient temperatures.
Solubility:
Miscible with alcohols, ether and other common organic solvents.
Molecular Weight: 146.14
XLogP3: 0.6
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 4
Rotatable Bond Count: 5
Exact Mass: 146.05790880
Monoisotopic Mass: 146.05790880
Topological Polar Surface Area: 52.6 Ų
Heavy Atom Count: 10
Complexity: 114
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
Assay as Deo by G.C.: 98% Min.
Acidity as Oxalic Acid: 0.10% Max.
Moisture Contents: 0.105 Max.
Relative Density: 1.078 – 1.082
Boiling Range: 181 – 188°C
Appearance: colorless clear liquid (est)
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Specific Gravity: 1.07600 to 1.08200 @ 25.00 °C.
Pounds per Gallon – (est).: 8.953 to 9.003
Refractive Index: 1.40700 to 1.41300 @ 20.00 °C.
Melting Point: -41.00 to -40.00 °C. @ 760.00 mm Hg
Boiling Point: 185.70 °C. @ 760.00 mm Hg
Boiling Point: 113.00 to 114.00 °C. @ 50.00 mm Hg
Vapor Pressure: 0.414000 mmHg @ 25.00 °C.
Vapor Density: 5.03 ( Air = 1 )
Flash Point: 168.00 °F. TCC ( 75.56 °C. )
logP (o/w): 0.560
Appearance Form: liquid
Color: colorless
Odor: aromatic
Odor Threshold: 0,1 ppm
pH: No data available
Melting point/range: -41 °C – lit.
Initial boiling point and boiling range: 185 °C – lit.
Flash point 75 °C – closed cup
Upper explosion limit: 2,67 %(V)
Lower explosion limit: 0,42 %(V)
Vapor pressure 1,33 hPa at 47 °C
Vapor density 5,04 – (Air = 1.0)
Relative density 1,08 at 20 °C
Water solubility at 20 °C
Partition coefficient: n-octanol/water log Pow: 0,56 – (Lit.)
Autoignition temperature: 412 °C at 984 hPa
Decomposition temperature: Distillable in an undecomposed state at normal pressure.
Viscosity Viscosity, kinematic: No data available
Viscosity, dynamic: 2,01 mPa.s at 20 °C
Specifications of Ethyl Oxalate:
Assay (GC, area%): ≥ 98.0 % (a/a)
Density (d 20 °C/ 4 °C): 1.076 – 1.079
Identity (IR): passes test
Names of Ethyl Oxalate:
Regulatory process names:
Diethyl ethanedioate
Diethyl oxalate
Diethyl oxalate
diethyl oxalate
Diethylester kyseliny stavelove
Ethanedioic acid, 1,2-diethyl ester
Ethanedioic acid, diethyl ester
ETHYL OXALATE
Ethyl oxalate
Ethyl oxalate (VAN)
oxalic acid diethylester diethyl oxalate
oxalic acid diethylester; diethyl oxalate
Oxalic acid, diethyl ester
Oxalic ether
Translated names:
acid oxalic dietilester dietil oxalat (ro)
diethylester čťavelové kyseliny diethyl-oxalát (cs)
diethyloxalaat (nl)
diethyloxalat ethyloxalat (da)
Diethyloxalat Oxalsäurediethylester (de)
dietil ester oksalne kisline dietil oksalat (sl)
dietile ossalato etile ossalato (it)
dietylester kyseliny šťaveľovej dietyl-oxalát (sk)
dietyloksalat etyloksalat (no)
dietyloxalat (sv)
Dietyylioksalaatti (fi)
diéthylester de l’acide oxalique; oxalate de diéthyle oxalate d’éthyle (fr)
Oksaalhappe dietüülester Dietüüloksalaat (et)
oksalo rūgšties dietilesteris dietiloksalatas (lt)
oxalato de dietilo oxalato de etilo (pt)
oxalato de dietilo éster dietílico del ácido oxálico (es)
oxálsav-dietil-észter dietil-oxalát (hu)
skābeņskābes dietilesteris dietiloksalāts (lv)
szczawian dietylu ester dietylowy kwasu szczawiowego (pl)
οξαλικός διαιθυλεστέρας (el)
диетилов естер на оксаловата киселина диетил оксалат (bg)
IUPAC names:
DIETHYL OXALATE
Diethyl Oxalate
Diethyl oxalate
diethyl oxalate
Diethyl oxalate
diethyl oxalate
diethylester
Diethyloxalat
Oxalic acid diethylester
oxalic acid diethylester
Trade names:
BRUGGOLEN P22
Other identifiers:
607-147-00-5
95-92-1