Conditions | Yield |
---|---|
In water-d2 Irradiation; |
Conditions | Yield |
---|---|
With hydrogen; nickel at 30℃; under 735.06 Torr; for 0.5h; Product distribution; |
succinic acid monomethyl ester sodium salt
sodium succinate
Conditions | Yield |
---|---|
With sodium hydroxide In methanol; water at 20℃; Rate constant; Thermodynamic data; ΔH(excit.), ΔS(excit.); various solvents; | |
With sodium hydroxide at 25℃; Kinetics; Further Variations:; Temperatures; Solvents; Hydrolysis; |
succinic acid monopropyl ester sodium salt
sodium succinate
Conditions | Yield |
---|---|
With sodium hydroxide In water; acetone at 30℃; Rate constant; various solvents; |
sodium glycolate
sodium succinate
magnesium succinate
sodium succinate
Conditions | Yield |
---|---|
With sodium hydroxide In water for 1h; pH=12.4; | |
With sodium hydroxide In water for 1h; pH=12.4; Product distribution / selectivity; |
calcium succinate
sodium succinate
Conditions | Yield |
---|---|
With sodium carbonate In water for 1h; pH=10.5; | |
With sodium carbonate In water for 1h; pH=10.5; Product distribution / selectivity; |
Conditions | Yield |
---|---|
With hydrogenchloride; iron(II) ammonium sulfate; pseudomonas sp.AK1 γ-butyrobetaine hydroxylase; potassium chloride; γ-butyrobetaine hydrochloride In water-d2 pH=7.5; Kinetics; Reagent/catalyst; Enzymatic reaction; |
Conditions | Yield |
---|---|
In water |
Conditions | Yield |
---|---|
With water; sodium hydroxide for 0.00277778h; pH=12.8; | >= 95 %Spectr. |
Conditions | Yield |
---|---|
With water; sodium hydroxide for 0.00555556h; pH=13; | >= 95 %Spectr. |
sodium succinate
Conditions | Yield |
---|---|
With hydrogen; sodium hydroxide In methanol; water at 29.84℃; Kinetics; Catalytic behavior; Solvent; |
Conditions | Yield |
---|---|
With lanthanum(III) chloride at 116℃; for 19h; Product distribution; also with other alcohols; variation of reaction time, temperature and proportion of reagents; | A 3% B 95% |
Conditions | Yield |
---|---|
In methanol; water a MeOH soln. of 2,2'-bipyridine added dropwise to a MeOH soln. of Cu salt with stirring for 15 min, an aq. soln. of disodium succinate added slowly, refluxed for 2 h; cooled, filtered, kept in a CaCl2-desiccator for days; elem. anal.; | 90% |
Conditions | Yield |
---|---|
In ethanol under N2 atm. disodium dicarboxylate was added to EtOH soln. (n-Bu)3SnCland stirred for 15 h at 40°C; soln. was filtered and evapd., residue was recrystd. from EtOH; elem. anal.; | 85.5% |
Conditions | Yield |
---|---|
In methanol; water a MeOH soln. of 1,10-phenanthroline added dropwise to a MeOH soln. of Cusalt with stirring for 15 min, an aq. soln. of disodium succinate added slowly, refluxed for 2 h; cooled, filtered, kept in a CaCl2-desiccator for days; elem. anal.; | 85% |
Conditions | Yield |
---|---|
In water High Pressure; a soln. of Na salt added to a soln. of Pr salt with stirring, heated at 175°C; crystd. overnight by cooling to room temp.; elem. anal.; | 82% |
methanol
water
sodium succinate
sodium hydroxide
zinc(II) chloride
Conditions | Yield |
---|---|
Stage #1: methanol; N,N'-bis[2-carboxybenzomethyl]-N,N'-bis[2-pyridylmethyl]-1,3-diaminopropan-2-ol; sodium hydroxide; zinc(II) chloride for 1h; Reflux; Stage #2: water; sodium succinate for 1h; Reflux; | 82% |
sodium succinate
1-chloromethylbenzindol-2(1H)-one (CMBI)
A
BIM hydrogen succinate
B
Succinic acid bis-(2-oxo-2H-benzo[cd]indol-1-ylmethyl) ester
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 100℃; for 0.333333h; | A n/a B 80% |
[fac-Mn(CO)3(1,2-bis(diphenylphosphino)ethane)(OH2)]BF4
sodium succinate
Conditions | Yield |
---|---|
In chloroform; water (Ar); sodium succinate dissolved in water; to CHCl3 soln. of (CO)3(dppe)Mn(OH2)BF4 equimolar quantity of new ligand added dropwise; stirring continued for 10-20 min; CHCl3 soln. separated; washed with water; dried and evaporated; resulting solids washed with hexane; dried in vacuo; | 80% |
Conditions | Yield |
---|---|
In water High Pressure; a soln. of Na salt added to a soln. of Gd salt with stirring for 10 min,heated for 24 h at 175°C; crystd. overnight by cooling to room temp.; elem. anal.; | 80% |
Conditions | Yield |
---|---|
In water High Pressure; a soln. of Na salt added to a soln. of Sm salt with stirring, heated at 175°C; crystd. overnight by cooling to room temp.; elem. anal.; | 80% |
Conditions | Yield |
---|---|
In ethanol; water addn. of ethanolic soln. of bipyridine to aq. soln. of succinate salt toaq. soln. of copper compd., heating to 90°C; filtration, keeping at room temp. for 5 d with slow evapn., isolation ofcrystals, washing with cold water and ether, drying in open air, elem. anal.; | 80% |
sodium succinate
benzoyl chloride
A
benzoic acid anhydride
B
benzoic acid
Conditions | Yield |
---|---|
With Pyridine 1-oxide hydrochloride In dichloromethane; water at 18℃; Rate constant; | A 19% B 79% |
Conditions | Yield |
---|---|
In water 1 equiv. of ligand in H2O added to Zn complex in H2O; crystd. for several days, filtered, elem. anal., XRD, TGA; | 78% |
Conditions | Yield |
---|---|
In methanol; water a MeOH soln. of 2,2'-bipyridine added dropwise to a MeOH soln. of Cu salt with stirring for 15 min, an aq. soln. of disodium succinate added slowly, refluxed for 2 h; cooled, filtered, kept in a CaCl2-desiccator for 7 d; elem. anal.; | 78% |
Conditions | Yield |
---|---|
In water High Pressure; a soln. of Na salt added to a soln. of Nd salt with stirring, heated at 175°C; crystd. overnight by cooling to room temp.; elem. anal.; | 78% |
Conditions | Yield |
---|---|
In methanol; water 1 equiv. of Cu-salt in H2O was dropwise added to MeOH soln. of biimidazole-compd., 1 equiv. of aq. soln. of the Na-salt was added, reflux for 12h; cooling to room temp., soln. was filtered, filtrate was kept in a desiccator over CaCl2, crystn. for a few weeks, elem. anal.; | 78% |
Conditions | Yield |
---|---|
Stage #1: methanol; copper(II) choride dihydrate; N,N'-bis[2-carboxybenzomethyl]-N,N'-bis[2-pyridylmethyl]-1,3-diaminopropan-2-ol; sodium hydroxide at 20℃; for 1h; Stage #2: sodium succinate for 1h; | 78% |
Conditions | Yield |
---|---|
In methanol | 76% |
Conditions | Yield |
---|---|
In methanol; water a MeOH soln. of 1,10-phenanthroline added dropwise to an aq. soln. of Cusalt with stirring for 15 min, an aq. soln. of disodium succinate added slowly, refluxed for 20 min; cooled, filtered, kept in a CaCl2-desiccator for 4 d; elem. anal.; | 75% |
Conditions | Yield |
---|---|
In water High Pressure; a soln. of Na salt added to a soln. of Eu salt with stirring, heated at 175°C; crystd. overnight by cooling to room temp.; elem. anal.; | 75% |
Conditions | Yield |
---|---|
In methanol | 74% |
Conditions | Yield |
---|---|
In methanol | 71% |
Conditions | Yield |
---|---|
In water High Pressure; a soln. of Na salt added to a soln. of Dy salt with stirring, heated at 175°C; crystd. overnight by cooling to room temp.; elem. anal.; | 70% |
Conditions | Yield |
---|---|
In methanol; water at 20℃; | 70% |
Conditions | Yield |
---|---|
With lanthanum(III) chloride In water for 10.25h; Heating; | 69.6% |
Conditions | Yield |
---|---|
In methanol | 69% |
The Sodium succinate is an organic compound with the formula C4H4Na2O4. The IUPAC name of this chemical is disodium butanedioate. With the CAS registry number 150-90-3, it is also named as Monosodium Succinate. The product's classification code is Drug / Therapeutic Agent. Besides, it is a white crystalline powder, which should be stored in a closed place. It is mainly used as a flavoring agent.
Physical properties about Sodium succinate are: (1)ACD/LogP: -0.59; (2)ACD/LogD (pH 5.5): -2.15; (3)ACD/LogD (pH 7.4): -5.13; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 1; (7)ACD/KOC (pH 7.4): 1; (8)#H bond acceptors: 4; (9)#H bond donors: 2; (10)#Freely Rotating Bonds: 3; (11)Polar Surface Area: 74.6 Å2; (12)Flash Point: 110.9 °C; (13)Enthalpy of Vaporization: 52.09 kJ/mol; (14)Boiling Point: 236.1 °C at 760 mmHg; (15)Vapour Pressure: 0.0165 mmHg at 25°C.
Preparation: this chemical can be prepared by succinic acid and sodium hydroxide. The reaction temperature is 120 °C.
When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. When you are using it, wear suitable protective clothing and avoid contact with skin and eyes. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
(1)SMILES: [Na+].[Na+].[O-]C(=O)CCC([O-])=O
(2)InChI: InChI=1/C4H6O4.2Na/c5-3(6)1-2-4(7)8;;/h1-2H2,(H,5,6)(H,7,8);;/q;2*+1/p-2
(3)InChIKey: ZDQYSKICYIVCPN-NUQVWONBAU
(4)Std. InChI: InChI=1S/C4H6O4.2Na/c5-3(6)1-2-4(7)8;;/h1-2H2,(H,5,6)(H,7,8);;/q;2*+1/p-2
(5)Std. InChIKey: ZDQYSKICYIVCPN-UHFFFAOYSA-L
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intravenous | 4500mg/kg (4500mg/kg) | "Merck Index; an Encyclopedia of Chemicals, Drugs, and Biologicals", 11th ed., Rahway, NJ 07065, Merck & Co., Inc. 1989Vol. 11, Pg. 1368, 1989. |
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View