144-62-7

  • Product NameOxalic acid
  • Molecular FormulaC2H2O4
  • Molecular Weight90.0355
  • Purity99%
  • AppearanceOdorless white solid
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Product Details

Quick Details

  • CasNo: 144-62-7
  • Molecular Formula: C2H2O4
  • Appearance: Odorless white solid
  • Purity: 99%

Wholesale Factory Supply High Purity Oxalic acid 144-62-7 Fast Delivery

  • Molecular Formula:C2H2O4
  • Molecular Weight:90.0355
  • Appearance/Colour:Odorless white solid 
  • Vapor Pressure:2.51E-06mmHg at 25°C 
  • Melting Point:189-191 °C 
  • Boiling Point:365.099 °C at 760 mmHg 
  • PKA:1.38±0.54(Predicted) 
  • Flash Point:188.79 °C 
  • PSA:74.60000 
  • Density:1.772 g/cm3 
  • LogP:-0.84440 
  • IDLH: 500 mg/m3See: 144627  

Oxalic acid(Cas 144-62-7) Usage

EXPOSURE ROUTES

inhalation, ingestion, skin and/or eye contact

FIRST AID

(See procedures) Eye:Irrigate immediately Skin:Water flush promptly Breathing:Respiratory support Swallow:Medical attention immediately

InChI:InChI=1/C2H2O4/c3-1(4)2(5)6/h(H,3,4)(H,5,6)/p-2

144-62-7 Relevant articles

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Acetone is a significant pollutant in co...

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Kudernatsch

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Atomically mixed Fe-group nanoalloys: Catalyst design for the selective electrooxidation of ethylene glycol to oxalic acid

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Frankel et al.

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Biocatalytic Production of Glyoxylic Acid

Seip, John E.,Fager, Susan K.,Gavagan, John E.,Gosser, Lawrence W.,Anton, David L.,DiCosimo, Robert

, p. 2253 - 2259 (1993)

The production of glyoxylic acid from gl...

Ozonation of azo dye Acid Black 1 under the suppression effect by chloride ion

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The aim of this study is to determine th...

OXIDATION OF 4-METHYL-4-(2-HYDROXYMETHYL)-1,3-DIOXANE TO 2-HYDROXY-2-METHYLGLUTARIC ACID

Devekki, A. B.,Egor'kov, A. N.,Blanshtein, I. B.,Devekki, A. V.,Idlis, G. S.

, p. 1066 (1988)

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Leung, Lam-Wing H.,Weaver, Michael J.

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The application of real-time FTIR spectr...

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Adams et al.

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Overberger,Hoyt

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THE STRUCTURE OF THEOBROMURIC ACID

Poje, M.,Palkovic, A.

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Rao

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Oxidation of coals in liquid phases. X. Mechanism of the cleavage of benzenecarboxylic acids to oxalic acid and carbon dioxide by the base-catalyzed oxygen-oxidation

Ichinose,Okuwaki

, p. 159 - 165 (1990)

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Clemo,Raper

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OZONIZATION OF ORGANIC COMPOUNDS - 5. AROMATIC COMPOUNDS.

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Juettner,Smith,Howard

, p. 236 (1937)

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Oxidation of glyoxal initiated by ?OH in oxygenated aqueous solution

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, p. 2889 - 2891 (1997)

The kinetics and mechanism of the oxidat...

Base-free selective oxidation of glycerol with 3% H2O 2 catalyzed by sulphonato-salen-chromium(III) intercalated LDH

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A MgAl layered-double hydroxides (LDH) i...

Engaging thieno[2,3-b]indole-2,3-dione for the efficient synthesis of spiro[indoline-3,4′-thiopyrano[2,3-b]indole] by reaction with N-substituted isatilidenes

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A simple and efficient method, proceedin...

Catalytic ozonation of 4-chlorophenol and 4-phenolsulfonic acid by CeO2 films

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Ceria films (CeO2(f)) were deposited on ...

Identification of 3,4-dihydroxy-2-oxo-butanal (L-threosone) as an intermediate compound in oxidative degradation of dehydro-L-ascorbic acid and 2,3-diketo-L-gulonic acid in a deuterium oxide phosphate buffer.

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Electroreduction of Carbon Dioxide Catalyzed by Iron-Sulfur Clusters 2-

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, p. 6834 - 6836 (1982)

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VOLUBOLIN, A 4-PHENYL-2H-1-BENZOPYRAN-2ONE FROM DALBERGIA VOLUBILIS

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, p. 2625 - 2626 (1983)

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Baker

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Degradation and toxicity changes in aqueous solutions of chloroacetic acids by Fenton-like treatment using zero-valent iron

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Andreasch

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Electrochemical Strategy for the Simultaneous Production of Cyclohexanone and Benzoquinone by the Reaction of Phenol and Water

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Cyclohexanone and benzoquinone are impor...

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Paragraph 0064-0065, (2021/03/17)

The invention discloses a preparation me...

Electro-oxidation of glycerol into formic acid by nickel-copper electrocatalysts

Shen, Yi,Zhang, Jiali

, (2021/09/11)

Herein, non-precious metallic nickel-cop...

144-62-7 Process route

2-Amino-5-methylbenzenesulfonic acid
88-44-8

2-Amino-5-methylbenzenesulfonic acid

2,6-dinitro-p-cresol
609-93-8

2,6-dinitro-p-cresol

oxalic acid
144-62-7,97993-78-7

oxalic acid

Conditions
Conditions Yield
ethyl N-(4-nitrophenyl)oxamate
5416-11-5

ethyl N-(4-nitrophenyl)oxamate

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

ethanol
64-17-5

ethanol

oxalic acid
144-62-7,97993-78-7

oxalic acid

4-nitro-aniline
100-01-6,104810-17-5

4-nitro-aniline

Conditions
Conditions Yield

144-62-7 Upstream products

  • 67-56-1
    67-56-1

    methanol

  • 56-23-5
    56-23-5

    tetrachloromethane

  • 6578-78-5
    6578-78-5

    1,1-bis(3,4-dimethylphenyl)ethylene

  • 859773-30-1
    859773-30-1

    3,4-di-tert-butyl-1,1,6,6-tetraphenyl-hexa-1,2,4,5-tetraene

144-62-7 Downstream products

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    553-90-2

    Dimethyl oxalate

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    74515-24-5

    2.3.5-trimethyl-6-((7R:11R)-trans-phytyl)-hydroquinone

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    113455-77-9

    O-Methyl-11,12-didehydro-retinol

  • 31604-39-4
    31604-39-4

    2-(4-nitrophenyl)isoindoline-1,3-dione

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