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6153-56-6

Basic Information
CAS No.: 6153-56-6
Name: Oxalic acid dihydrate
Molecular Structure:
Molecular Structure of 6153-56-6 (Oxalic acid dihydrate)
Formula: C2H6O6
Molecular Weight: 126.06
Synonyms: Ethanedioicacid, dihydrate (9CI);Oxalic acid, dihydrate (8CI);
EINECS: 205-634-3
Density: 1.65 g/cm3
Melting Point: 104-106 °C(lit.)
Boiling Point: 108-109°C
Flash Point: 157°C
Solubility: 138 g/L (20 °C) in water
Appearance: white crystals
Hazard Symbols: HarmfulXn, CorrosiveC
Risk Codes: 21/22
Safety: 24/25
Transport Information: UN 3261 8/PG 3
PSA: 93.06000
LogP: -0.97300
Synthetic route
62-76-0

sodium oxalate

6153-56-6

oxalic acid dihydrate

Conditions
ConditionsYield
With hydrogenchloride; water at 80℃; for 1h; Product distribution / selectivity;56%
cis-{Pt(PMe3)2(OH)2}*nH2O (n=2-3)

cis-{Pt(PMe3)2(OH)2}*nH2O (n=2-3)

6153-56-6

oxalic acid dihydrate

94929-01-8

{Pt(PMe3)2(ox)}

Conditions
ConditionsYield
In not given100%
553-26-4

4,4'-bipyridine

iron(II) bromide hexahydrate

6153-56-6

oxalic acid dihydrate

226401-77-0

(2).infin.[Fe(oxalate)(4,4'-bipyridine)]

Conditions
ConditionsYield
In water byproducts: HBr, H2O; molar ratio Fe:oxalate:bipy:H2O=1:1:1:444, digestion bomb, 170°C,7 d; washing (water, Me2CO), drying in air;99%
553-26-4

4,4'-bipyridine

cobalt(II) bromide hexahydrate

6153-56-6

oxalic acid dihydrate

226401-78-1

(2).infin.[Co(oxalate)(4,4'-bipyridine)]

Conditions
ConditionsYield
In water byproducts: HBr, H2O; molar ratio Co:oxalate:bipy:H2O=1:1:1:444, digestion bomb, 170°C,7 d;99%
7209-38-3

1,4-bis(3-aminopropyl)piperazine

iron(III) chloride hexahydrate

86119-84-8, 7664-38-2

phosphoric acid

6153-56-6

oxalic acid dihydrate

H3NC3H6NHC4H8NHC3H6NH3(4+)*3Fe(3+)*2C2O4(2-)*3HPO4(2-)*PO4(3-)*100H2O=C10H28N4[Fe3(C2O4)2(HPO4)3(PO4)(H2O)]*99H2O

Conditions
ConditionsYield
In water High Pressure; mixt. of FeCl3*6H2O, H2C2O4*2H2O, H3PO4, 1,4-bis(3-aminopropyl)piperazine, and water (pH 4.6) heated at 120°C for 3 d in Teflon-lined stainless-steel Parr acid digestion bomb, slow cooling at 5°C/h to room temp.;99%
65-23-6

5-hydroxy-6-methyl-3,4-pyridinedimethanol

11113-50-1

boric acid

6153-56-6

oxalic acid dihydrate

[B(oxalato)(pyridoxine(-H))]

Conditions
ConditionsYield
In toluene byproducts: H2O; boric acid, pyridoxine and oxalic acid*2H2O in 1:1:1 molar ratio refluxed in toluene during 6 h under continuous sepn. of react. water; filtered; dried at 120°C; elem. anal.;99%
6153-56-6

oxalic acid dihydrate

34851-41-7

tetrabutyl ammonium methoxide

33081-83-3

bis(tetrabutylammonium)oxalate

Conditions
ConditionsYield
In methanol for 4h;98%

indium(III) oxide

86119-84-8, 7664-38-2

phosphoric acid

6153-56-6

oxalic acid dihydrate

110-60-1

1,4-diaminobutane

(1,4-diaminobutane(+2H))0.5*In(HPO4)(H2PO4)(oxalate)0.5

Conditions
ConditionsYield
In water at 150℃; for 168h; Autoclave;95%
6153-56-6

oxalic acid dihydrate

75719-86-7

2,3,4,6-tetra-O-benzyl-1-O-(N-benzyloxycarbonylglycylglycylglycyl)-α-D-glucopyranose

75719-99-2

1-O-(glycylglycylglycyl)-α-D-glucopyranose mono-oxalate

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In 2-methoxy-ethanol; acetic acid for 24h;92%
6153-56-6

oxalic acid dihydrate

75719-88-9

2,3,4,6-tetra-O-benzyl-1-O-(N-benzyloxycarbonyl-L-phenylalanylglycylglycyl)-β-D-glucopyranose

75720-06-8

1-O-(L-phenylalanylglycylglycyl)-β-D-glucopyranose mono-oxalate

Conditions
ConditionsYield
With hydrogen; palladium on activated charcoal In 2-methoxy-ethanol; acetic acid for 20h;92%
304-88-1

N-phenylbenzohydroxamic acid

11113-50-1

boric acid

6153-56-6

oxalic acid dihydrate

87285-07-2

{C6H5CON(C6H5)O}{O(O)CC(O)O}B

Conditions
ConditionsYield
In benzene heating under reflux for 6 h; evapn. of solvent, crystd. with petroleum ether several times, elem. anal.;92%
6153-56-6

oxalic acid dihydrate

5970-45-6

zinc(II) acetate dihydrate

zinc oxalate dihydrate

Conditions
ConditionsYield
In ethylene glycol byproducts: acetic acid, H2O; oxalic acid added slowly with stirring to soln. of zinc acetate at room temp. for 12 h; filetred, washed (acetone) several times, dried at 120°C; XRD;92%
In methanol byproducts: acetic acid, H2O; oxalic acid added slowly with stirring to soln. of zinc acetate at room temp. for 12 h; filetred, washed (acetone) several times, dried at 120°C; XRD;90%

uranyl nirate hexahydrate

ammonium hydroxide

6153-56-6

oxalic acid dihydrate

ammonium dioxoperoxy(oxalato)uranate(VI) hydrate

Conditions
ConditionsYield
With water; dihydrogen peroxide In water to soln. of UO2(NO3)2*6H2O added soln. of NH4OH with stirring; filtered; to aq. suspn. added C2O4H2*2H2O and stirred for 5 min; excess of 30% H2O2 added and stirred for 15 min; soln. of NH4OH added (pH = 6); ethanol added; centrifuged; washed with ethanol; dried in vacuo; elem. anal.;91%

Cu(acetylacetonate)(triphenylphosphine)2

6153-56-6

oxalic acid dihydrate

{Cu2(μ-C2O4)(PPh3)4}

Conditions
ConditionsYield
In methanol; dichloromethane byproducts: acetylacetone; react. mixt. (molar ratio Cu-complex:oxalic acid = 1:0.5) stirred for 24 h at room temp. in CH2Cl2/MeOH (10:1); filtration, evapn. to dryness; extn. of the residue with CH2Cl2; addn. of Et2O; elem. anal., mol. weight measurement;90%

tetrakis(hydroxylamine)-platinum(II) hydroxide

6153-56-6

oxalic acid dihydrate

trans-tetrahydroxylaminodioxalatoplatinum(IV)

Conditions
ConditionsYield
With dihydrogen peroxide In water addn. of 30% H2O2 to H2C2O4*2H2O in H2O; (Pt(NH2OH)4)(OH)2 was added in portions to the soln.; standing in the dark for 72 h; mechanism discussed;; filtration through a glass filter; the ppt. was washed with cold H2O, acetone, and ether, and dried in air; elem. anal.;;90%
512-56-1

trimethyl phosphite

potassium tetranitroplatinate(IV)

6153-56-6

oxalic acid dihydrate

4K(1+)*Pt4(6+)*4NO2(1-)*C2O4(2-)*4OH(1-)*2(CH3O)3PO=K4{Pt4(NO2)4(C2O4)(OH)4}*2(CH3O)3PO

Conditions
ConditionsYield
In further solvent(s) trimethylphosphate is added to Pt complex, mixt. is carefully heated at 180-200°C until sample dissolves, cooling to room temp., filtn., addn. of oxalic acid under stirring; ppt. is filtered, washed (CHCl3/EtOH), elem. anal.;90%

potassium tetranitroplatinate(IV)

6153-56-6

oxalic acid dihydrate

2K(1+)*Pt(NO2)2(HC2O4)2(2-)=K2{Pt(NO2)2(HC2O4)2}

Conditions
ConditionsYield
With (CH3O)3PO In further solvent(s) trimethylphosphate is added to Pt complex, mixt. is carefully heated at 140-160°C until sample dissolves, cooling to room temp., filtn., addn. of oxalic acid under stirring, react. time 2-5 h; ppt. is filtered, washed (cold H2O/EtOH), elem. anal.;90%

potassium tetranitroplatinate(IV)

6153-56-6

oxalic acid dihydrate

2K(1+)*Pt(NO2)3(HC2O4)(2-)=K2{Pt(NO2)3(HC2O4)}

Conditions
ConditionsYield
With (CH3O)3PO In further solvent(s) trimethylphosphate is added to Pt complex, mixt. is carefully heated at 100-120°C until sample dissolves, cooling to room temp., filtn., addn. of oxalic acid under stirring, react. time 2-5 h; ppt. is filtered, washed (H2O/EtOH), elem. anal.;90%
6153-56-6

oxalic acid dihydrate

866-55-7

dichlorodiethylstannane

2C2H5(1-)*Sn(4+)*(COO)2(2-)*H2O=(C2H5)2Sn(C2O4)*H2O

Conditions
ConditionsYield
In water slow pouring acid soln. to soln. of Sn-compd. (stirring); after 1 h ppt. filtration off; elem. anal.;90%

vanadia

6153-56-6

oxalic acid dihydrate

V2O2(4+)*2OH(1-)*C2O4(2-)*2H2O=V2O2(OH)2(C2O4)*2H2O

Conditions
ConditionsYield
With H3BO3 In water High Pressure; V2O5, H2C2O4*2H2O, H3BO3 and H2O mixed in a molar ratio 1:14:29:151, heated in an autoclave at 155°C for 20 d; cooled to room temp.(5°C/h), filtered, washed (H2O), dried at room temp., elem. anal.;90%
584-13-4

4-amino-1,2,4-triazole

ferrous(II) sulfate heptahydrate

6153-56-6

oxalic acid dihydrate

[Fe(μ-ox)(4-amino-1,2,4-triazole)2]n

Conditions
ConditionsYield
In water soln. (10 ml) of H2C2O4*2H2O (0.2 mmol) added dropwise to soln. (25 ml) of (C2H2N3)NH2 (1.00 mmol) and FeSO4*7H2O (0.2 mmol); ppt. sepd.; washed with cold H2O and Et2O; dried in air; elem. anal.;90%
584-13-4

4-amino-1,2,4-triazole

6153-56-6

oxalic acid dihydrate

7646-85-7

zinc(II) chloride

[Zn(μ-ox)(4-amino-1,2,4-triazole)2]n

Conditions
ConditionsYield
In water soln. (10 ml) of H2C2O4*2H2O (0.2 mmol) added dropwise to soln. (25 ml) of (C2H2N3)NH2 (1.00 mmol) and ZnCl2 (0.40 mmol); ppt. sepd.; washed with cold H2O and Et2O; dried in air; elem. anal.;90%
Raw Materials
62-76-0
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Chemistry

Molecular structure of Ethanedioic acid, dihydrate (CAS NO.6153-56-6) is:

Product Name: Ethanedioic acid, dihydrate
CAS Registry Number: 6153-56-6
IUPAC Name: oxalic acid dihydrate
Molecular Weight: 126.06544 [g/mol]
Molecular Formula: C2H6O6
H-Bond Donor: 4
H-Bond Acceptor: 6 
EINECS: 205-634-3
Melting Point: 104-106 °C(lit.)
Water Solubility: 138 g/L (20 °C)
Sublimation: 157 °C 
Density: 1.65 g/cm3
Flash Point: 188.8 °C
Enthalpy of Vaporization: 67.15 kJ/mol
Boiling Point: 365.1 °C at 760 mmHg
Vapour Pressure: 2.51E-06 mmHg at 25°C
Stability: Stable. Incompatible with bases, acid chlorides, steel, silver, silver compounds, moisture. Avoid contact with metals. 
Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts

Uses

 Ethanedioic acid, dihydrate (CAS NO.6153-56-6) can be used in wood bleaching and brightener, stain remover.

Safety Profile

Safty information about Ethanedioic acid, dihydrate (CAS NO.6153-56-6) is:
Hazard Codes: HarmfulXn, CorrosiveC
Risk Statements: 21/22 
R21/22:Harmful in contact with skin and if swallowed.
Safety Statements: 24/25 
S24/25:Avoid contact with skin and eyes.
RIDADR: UN 3261 8/PG 3
WGK Germany: 1
RTECS: RO2450000
HazardClass: 8
PackingGroup: III
HS Code: 29171100

Specification

 Ethanedioic acid, dihydrate , its cas register number is 6153-56-6. It also can be called Dicarbolic acid dihydrate ; Ethanedioic acid dihydrate .It is a white crystals.