Sodium diethyl oxalacetate

Base Information

Chemical Name:Sodium diethyl oxalacetate
CAS No.:40876-98-0
Deprecated CAS:136978-97-7,49635-95-2,52980-17-3,58333-46-3,63277-17-8,86284-65-3,86387-68-0,125898-38-6,1147385-24-7,1152096-26-8,1164336-01-9,1165931-73-6,1240313-39-6,125699-43-6,77422-95-8,1201639-55-5,1448338-94-0,1639345-30-4,1807940-30-2,1841081-31-9,200116-47-8,2081970-32-1,2097939-23-4,2117722-35-5,2158207-78-2,2268681-26-9,2296713-46-5,2318934-17-5,2486381-24-0,2308574-82-3,1147385-24-7,1152096-26-8,1164336-01-9,1165931-73-6,1201639-55-5,1240313-39-6,125699-43-6,125898-38-6,1448338-94-0,1639345-30-4,1807940-30-2,1841081-31-9,200116-47-8,2081970-32-1,2097939-23-4,2117722-35-5,2158207-78-2,2268681-26-9,2296713-46-5,2308574-82-3,2318934-17-5,2486381-24-0,2649101-98-2,2766124-11-0,49635-95-2,52980-17-3,58333-46-3,63277-17-8,77422-95-8,86284-65-3,86387-68-0
Molecular Formula:C₈H₁₁O₅*Na
Molecular Weight:210.162
Hs Code.:29183000
European Community (EC) Number:255-122-9,610-923-6
UNII:6CA025Y4FG
DSSTox Substance ID:DTXSID2028010
NSC Number:126906
Wikidata:Q27264482
Mol file:40876-98-0.mol

Synonyms:Sodium diethyl oxalacetate;Sodium diethyl oxaloacetate;Diethyl sodiooxalacetate;Diethyl sodium oxalacetate;Sodium diethyl oxobutanedioate;Diethyl oxaloacetate, monosodium salt;Diethyl oxobutanedioate ion(1-) sodium;1,4-diethoxy-1,3,4-trioxobutan-2-ide sodium salt;6CA025Y4FG;DTXSID2028010;NSC-126906;Butanedioic acid, oxo-, diethyl ester, ion(1-), sodium;Butanedioic acid, 2-oxo-, 1,4-diethyl ester, ion(1-), sodium (1:1);Micox;EINECS 255-122-9;NSC 126906;Sodiumdiethyloxalacetate;AI3-04820;NATRUM OXALACETICUM;UNII-6CA025Y4FG;sodium;diethyl 2-oxobutanedioate;JPTKZRPOIUYFTM-UHFFFAOYSA-N;DTXCID701284963;NATRUM OXALACETICUM [HPUS];Tox21_201051;NSC126906;CS-W019382;DIETHYL OXOSUCCINATE SODUIM SALT;PB47442;DIETHYL OXALACETATE, SODIUM SALT;NCGC00258604-01;AS-80947;CAS-40876-98-0;DIETHYL SODIUM OXALACETATE [WHO-DD];NS00030864;Oxalacetic acid, diethyl ester, sodium deriv.;P16485;Butanedioic acid, diethyl ester, ion(1-), sodium;Q27264482

Suppliers and Price of Sodium diethyl oxalacetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

AK Scientific
Diethyl Oxalacetate Sodium Salt
100g
$ 95.00

Alfa Aesar
Diethyl oxalacetate sodium salt, 95%
100g
$ 39.20

Alfa Aesar
Diethyl oxalacetate sodium salt, 95%
500g
$ 130.00

Alichem
Sodium1,4-diethoxy-1,4-dioxobut-2-en-2-olate
500g
$ 162.00

Ambeed
Sodiumdiethyloxalacetate 95%
500g
$ 129.00

Ambeed
Sodiumdiethyloxalacetate 95%
1kg
$ 245.00

Ambeed
Sodiumdiethyloxalacetate 95%
10g
$ 8.00

Ambeed
Sodiumdiethyloxalacetate 95%
25g
$ 10.00

Ambeed
Sodiumdiethyloxalacetate 95%
100g
$ 29.00

American Custom Chemicals Corporation
DIETHYL OXALOACETATE SODIUM SALT 95.00%
500G
$ 4384.70

Total 104 raw suppliers

Chemical Property of Sodium diethyl oxalacetate

Chemical Property:

Appearance/Colour:beige to light orange crystalline powder
Melting Point:188-190 °C
PSA：75.66000
LogP:0.42700
Storage Temp.:2-8°C
Sensitive.:Moisture Sensitive
Water Solubility.:Slightly soluble in water (1.2 g/L) (25°C).
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:7
Exact Mass:210.05041773
Heavy Atom Count:14
Complexity:214

Purity/Quality:

99% ^*data from raw suppliers

Diethyl Oxalacetate Sodium Salt ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:T,Xi
Statements: 45-46-48/20/21/22-36-36/38
Safety Statements: 26-24/25-45-53

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCOC(=O)[CH-]C(=O)C(=O)OCC.[Na+]
Uses Dyes, synthesis. Diethyl oxalacetate sodium salt is used in the preparation of oxaloacetic acid. It is also used as an active pharmaceutical intermediate.

Technology Process of Sodium diethyl oxalacetate

There total 1 articles about Sodium diethyl oxalacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 70.0%