Basic information description Chemical properties Uses First aid Protective measures Medical Surveillance Storage waste disposal Safety Supplier Related
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Oxalic acid

Basic information description Chemical properties Uses First aid Protective measures Medical Surveillance Storage waste disposal Safety Supplier Related

Oxalic acid Basic information

Product Name:
Oxalic acid
Synonyms:
  • OXALATE ION CHROMATOGRAPHY STANDARD
  • PH STANDARD SOLUTION OXALATE BUFFER
  • BETZ 0295
  • ETHANEDIOIC ACID
  • DICARBOXYLIC ACID C2
  • DI-CARBOXYLIC ACID
  • Kleesαure
  • Kyselina stavelova
CAS:
144-62-7
MF:
C2H2O4
MW:
90.03
EINECS:
205-634-3
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  • Pharmaceutical intermediates
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Mol File:
144-62-7.mol
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Oxalic acid Chemical Properties

Melting point:
189.5 °C (dec.)(lit.)
Boiling point:
365.1°C (estimate)
Density 
0.99 g/mL at 25 °C
vapor density 
4.4 (vs air)
vapor pressure 
<0.01 mm Hg ( 20 °C)
refractive index 
1.4261 (estimate)
Flash point:
101-157°C
storage temp. 
Store below +30°C.
solubility 
water: soluble108g/L at 25°C
form 
Liquid
pka
1.23(at 25℃)
color 
White
PH
1 (100g/l, H2O, 20℃)
PH Range
6 - 8 at 25 °C
Water Solubility 
90 g/L (20 ºC)
Sublimation 
101-157 ºC
Merck 
14,6911
BRN 
385686
Henry's Law Constant
1.43 at pH 4 (quoted, Gaffney et al., 1987)
Exposure limits
NIOSH REL: TWA 1, STEL 2, IDLH 500; OSHA PEL: TWA 1; ACGIH TLV: TWA 1, STEL 2 (adopted).
Stability:
Stable, but moisture sensitive. Incompatible with metals.
InChIKey
MUBZPKHOEPUJKR-UHFFFAOYSA-N
CAS DataBase Reference
144-62-7(CAS DataBase Reference)
NIST Chemistry Reference
Oxalic acid(144-62-7)
EPA Substance Registry System
Oxalic acid (144-62-7)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
21/22-63-34-41
Safety Statements 
24/25-23-36/37/39-27-26-39-37-36-36/37
RIDADR 
UN 3261 8/PG 3
WGK Germany 
1
RTECS 
RO2450000
TSCA 
Yes
HazardClass 
8
PackingGroup 
III
HS Code 
29171110
Hazardous Substances Data
144-62-7(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 375 mg/kg

MSDS

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Oxalic acid Usage And Synthesis

description

Oxalic acid is a strong dicarboxylic acid occurring in many plants and vegetables, usually as its calcium or potassium salts. Oxalic acid is the only possible compound in which two carboxyl groups are joined directly; for this reason oxalic acid is one of the strongest organic acids. Unlike other carboxylic acids (except formic acid), it is readily oxidized; this makes it useful as a reducing agent for photography, bleaching, and ink removal. Oxalic acid is usually prepared by heating sodium formate with sodium hydroxide to form sodium oxalate, which is converted to calcium oxalate and treated with sulfuric acid to obtain free oxalic acid.
concentrations of oxalic acid are pretty low in most plants and plant-based foods, but there’s enough in spinach, chard and beet greens to interfere with the absorption of the calcium these plants also contain.
It is produced in the body by metabolism of glyoxylic acid or ascorbic acid. It is not metabolized but excreted in the urine. It is used as an analytical reagent and general reducing agent.Oxalic acid is a natural acaricide used for treatment against varroa mites in colonies with no/low brood, packages, or swarms. Vaporized oxalic acid is used by some beekeepers as an insecticide against the parasitic Varroa mite.

Chemical properties

Oxalic acid is widely distributed in the plant in nature, most existing in the form of oxalic acid salt. C.W. Scheele had for the first time manufactured oxalate in 1776.
Oxalate is the strongest acid among the dicarboxylic acid. Besides having the general properties of the carboxylic acid, it also has reducing property and can quantitatively reduce the seven valence manganese to bivalent manganese. This property is often used for quantitative analysis of potassium permanganate.
5 C2H2O4 + 2 KMnO4 + 3 H2SO4 →K2SO4 + 2 MNSO4 + 8H2O + 10 CO2;
Oxalic acid can also reduce the trivalent iron into bivalent iron. Because of the high solubility of the bivalent iron in the water, we can apply this principle to remove rust on the clothes.
Oxalic acid can react with phosphorus pentachloride to generate phosphorus oxychloride. C2H2O4 + PCl5 → POCl3 + CO + CO2 + 2 HCL.
Oxalic acid can react with many metals to produce oxalic acid salt. In addition to the alkali metal salt and bivalent iron salts with the rest of the oxalic acid salt being poorly soluble in water. Some metal salt, although is poorly soluble in water, can generate complex that is soluble in water.
Fe2 (C2O4) 3 + 3 K2C2O4 + 6 H2O →2 K3 [Fe (C2O4) 3] • 6 H2O.
Upon heating, alkali metal and alkaline earth metal oxalic acid salt can lose carbon monoxide and form carbonates with carbonate continuing to be subject to heating to be further decomposed into oxide and carbon dioxide. The oxalic acid salt of nickel, cobalt and silver can finally produce metal instead of nonmetal oxide.
The decomposing products of the oxalate are carbon dioxide, carbon monoxide and water.
Oxalate and oxalic acid salt are toxic. Mice, through oral administration, has LD50 of 2000~4000 mg/kg.
The above information is edited by the chemicalbook of Dai Xiongfeng.

Uses

1. Oxalic acid can be mainly used as reducing agent and bleaching agent, mordant for dyeing and printing industry, also used in refining rare metal, the synthesis of various oxalate ester amide, oxalate and grass, etc.
2. Used as analytical reagent.
3. Used as laboratory reagents, chromatography analysis reagent, dye intermediates and standard material.
4. Oxalic acid is mainly used for producing drugs such as antibiotics and borneol and solvent for extracting the rare metal, reducing agent and dye, tanning agent, etc. In addition, oxalic acid can also be used for the synthesis of various kinds of oxalate ester, oxalate, and oxamide with diethyl oxalate, sodium oxalate and calcium oxalate having the largest yield. Oxalate can also be used for the production of cobalt-molybdenum-alumina catalyst, cleaning of metal and marble as well as the bleaching of textiles.

First aid

This kind of chemical, in case of contact with eyes and skin, should be quickly rinsed with plenty of water; Upon inhaling of large amount, we should immediately move the victim away from the scene to fresh air place; if necessary, apply artificial respiration; if be swallowed, immediately give medical injection with plenty of water for rapid gastric lavage and apply symptomatic treatment.

Protective measures

Upon productive operation, we must wear protective work cloth in order to prevent the skin repeatedly or long-term contact. Wear protective glasses to prevent eye contact. For the nitrogen oxide gas produced during the production process, measures should be taken to absorb before discharge. Work clothes if contaminated, should be replaced every day. Permeable work clothes, if getting wet, should be taken off quickly.

Medical Surveillance

During employment and regular physical examination, we should check the skin, respiratory tract, and kidney function. If there is growing oxalic acid salt crystal in the urine, it is helpful to ascertain the oral poisoning. We should pay attention to follow-up. The determination of blood calcium and blood oxalic acid salt content is also suitable for this purpose.

Storage

We should hold it with glass bottle, cask, multi-layer paper bag or metal barrel to prevent mechanical damage. It should be placed in cool, ventilated, dry place for sealed storage. It is best to use the open warehouse and should be placed far away from any places that have potential risk of serious fire. It should be stored separately from antioxidant.

waste disposal

Pre-processing includes chemical reaction with limestone or calcium oxide to generate calcium oxalate. It can be then subject to calcination and can put into particle collection device to collect for reuse.

Chemical Properties

white crystalline powder

Chemical Properties

Oxalic acid is a colorless, odorless powder, or granular solid. The anhydrous form (COOH)2 is an odorless, white solid; the solution is a colorless liquid.

Physical properties

Colorless and odorless rhombic crystals. Hygroscopic.

Uses

Oxalic acid is made by the action of nitric acid on sugars, starch, or cellulose. This highly poisonous colorless crystal is soluble in water, alcohol, and ether. It was used to make ferric oxalate, as a preservative for pyrogallic acid developers, as a sensitizer for platinum papers, and to reduce the density of cyanotype prints.

Uses

An impurity of oxaliplatin which is a coordination complex that is used in cancer chemotherapy. A reducing agent and its conjugate base, known as oxalate (C2O42?), is a useful chelating agent for metal cations.

Uses

Oxalic acid was used: · in the synthesis of hemicellulose hydrolysates of yellow poplars; · in the synthesis of three-dimensionally ordered macroporous metal oxides or carbonates via templating with polystyrene spheres; · as supporting electrolyte in the electrochemical synthesis of polyaniline-polypyrrole composite coatings.

Definition

ChEBI: An alpha,omega-dicarboxylic acid that is ethane substituted by carboxyl groups at positions 1 and 2.

Definition

A white crystalline organic acid that occurs naturally in rhubarb, sorrel, and other plants of the genus Oxalis. It is slightly soluble in water, highly toxic, and used in dyeing and as a chemical reagent.

Production Methods

Many industrial processes have been employed for the manufacture of oxalic acid since it was first synthesized. The following processes are in use worldwide: oxidation of carbohydrates, the ethylene glycol process, the propylene process, the dialkyl oxalate process, and the sodium formate process. Sodium formate process is no longer economical in the leading industrial countries, except for China.
Nitric acid oxidation is used where carbohydrates, ethylene glycol, and propylene are the starting materials. The dialkyl oxalate process is the newest, where dialkyl oxalate is synthesized from carbon monoxide and alcohol, then hydrolyzed to oxalic acid. This process has been developed by UBE Industries in Japan.Many attempts have been made to synthesize oxalic acid by electrochemical reduction of carbon dioxide in either aqueous or nonaqueous electrolytes.

Reactions

The reactions of oxalic acid, including the formation of normal and acid salts and esters, are typical of the dicarboxylic acids class. Oxalic acid, however, does not form an anhydride.
On rapid heating, oxalic acid decomposes to formic acid, carbon monoxide, carbon dioxide, and water. In aqueous solution, it is decomposed by uv, x-ray, or γ -radiation with the liberation of carbon dioxide. Photodecomposition also occurs in the presence of uranyl salts.
Oxalic acid is a mild reducing agent, and is oxidized by potassium permanganate in acid solution to give carbon dioxide and water. Oxalic acid is catalytically reduced by hydrogen in the presence of ruthenium catalyst to ethylene glycol, and electronically reduced to glyoxylic acid.
Oxalic acid reacts with various metals to form metal salts, which are quite important as the derivatives of oxalic acid. It also reacts easily with alcohols to give esters.

General Description

Odorless white solid. Sinks and mixes with water.

Air & Water Reactions

Water soluble. Hygroscopic

Reactivity Profile

Oxalic acid is hygroscopic and sensitive to heat. Oxalic acid may react violently with furfuryl alcohol, silver, sodium, perchlorate, sodium hypochlorite, strong oxidizers, sodium chlorite, acid chlorides, metals and alkali metals. . The heating of mixtures of Oxalic acid and urea has lead to explosions. This is due to the rapid generation of the gases, CO2, CO, and NH3, [Praxis Naturwiss. Chem., 1987, 36(8), 41-42]. Oxalic acid and urea react at high temperatures to form toxic and flammable ammonia and carbon monoxide gasses, and inert CO2 gas [Von Bentzinger, R. et al., Praxis Naturwiss. Chem., 1987, 36(8), 41-42].

Health Hazard

As dust or as a solution, can cause severe burns of eyes, skin, or mucous membranes. Ingestion of 5 grams has caused death with symptoms of nausea, shock, collapse, and convulsions coming on rapidly. Repeated or prolonged skin exposure can cause dermatitis and slow-healing ulcers.

Fire Hazard

Special Hazards of Combustion Products: Generates poisonous gases

Agricultural Uses

Oxalic acid, (COOH)2, also called ethanedioic acid, is a white, crystalline solid, slightly soluble in water. It is a naturally occurring highly oxidized organic compound with significant chelating activity. It is strongly acidic and poisonous, produced by many plants like sorrel (sourwood), the leaf blades of rhubarb, bark of eucalyptus and many plant roots. In plant cells and tissues, oxalic acid gets accumulated as either sodium, potassium or calcium oxalate, of which the latter occurs as crystals. In turn, salts of oxalic acids enter the bodies of animals and human beings, causing pathological disorders, depending upon the amount consumed. Many species of fungi like Aspergillus, Penicillium, Mucor, as well as some lichens and slime moulds produce calcium oxalate crystals. Upon the death of these microorganisms, plants and animals, the salts get released into the soil, causing some amount of toxicity. However, oxalate-degrading microbes, called Oxalobacter formigenes, decrease oxalate absorption in animals and humans.
Oxalic acid is the first of a series of dicarboxylic acids. It is used (a) as a bleaching agent for stains like rust or ink, (b) in textile and leather production, and (c) as monoglyceryl oxalate in the production of ally1 alcohol and formic acid.

Safety Profile

Poison by subcutaneous route. Moderately toxic by ingestion. A skin and severe eye irritant. Acute oxalic poisoning results from ingestion of a solution of the acid. There is marked corrosion of the mouth, esophagus, and stomach, with symptoms of vomiting, burning abdominal pain, collapse, and sometimes convulsions. Death may follow quickly. The systemic effects are attributed to the removal by the oxalic acid of the calcium in the blood. The renal tubules become obstructed by the insoluble calcium oxalate, and there is profound hdney dlsturbance. The chief effects of inhalation of the dusts or vapor are severe irritation of the eyes and upper respiratory tract, gastrointestinal disturbances, albuminuria, gradual loss of weight, increasing weakness and nervous system complaints, ulceration of the mucous membranes of the nose and throat, epistaxis, headache, irritation, and nervousness. Oxalic acid has a caustic action on the skin and may cause dermatitis; a case of early gangrene of the fingers resembling that caused by phenol has been described. More severe cases may show albuminuria, chronic cough, vomiting, pain in the back, and gradual emaciation and weakness. The skin lesions are characterized by crachng and fissuring of the skin and the development of slow-healing ulcers. The skin may be bluish in color, and the nails brittle and yellow. Violent reaction with furfuryl alcohol, Ag, NaClO3, NaOCl. When heated to decomposition it emits acrid smoke and irritating fumes. See also OXALATES

Potential Exposure

Oxalic acid is used in textile finishing, paint stripping; metal and equipment cleaning; as an intermediate; as an analytic reagent and in the manufacture of dyes, inks, bleaches, and paint removers; varnishes, wood, and metal cleansers; dextrin, cream of tartar, celluloid, oxalates, tartaric acid, purified methyl alcohol, glycerol, and stable hydrogen cyanide. It is also used in the photographic, ceramic, metallurgic, rubber, leather, engraving, pharmaceutical, paper, and lithographic industries.

Source

Oxalic acid occurs naturally in many plants including buckwheat leaves (111,000 ppm), lambsquarter (140,000 to 300,000 ppm), black pepper (4,000 to 34,000 ppm), star fruit (50,000 to 95,800 ppm), purslane (1,679 to 16,790 ppm), nance bark (27,300 ppm), rhubarb 4,400 to 13,360 ppm), tea leaves (2,192 to 10,000 ppm), bitter lettuce (10,000 ppm), spinach (6,580 ppm), cacao (1,520 to 5,000 ppm), bananas (22 to 5,240 ppm), ginger (5,000 ppm in rhizome), cashews (3,184 ppm), almonds (4,073 ppm), taro roots (1,334 ppm), tamarind (1,960 ppm), garden sorrel (3,000 ppm), mustard green leaves (1,287 ppm), peppers (257 to 1,171 ppm), sweet potato roots (1,000 ppm), pumpkins, oats (400 ppm), tomatillo (109 to 536 ppm), various cabbage leaves (59 to 350 ppm), and horseradish (Duke, 1992).
Oxalic acid was identified as a constituent in a variety of composted organic wastes. Detectable concentrations were reported in all 21 composts extracted with water. Concentrations ranged from 0.60 mmol/kg in a straw + dairy cattle manure to 21.89 mmol/kg in straw + wood bark + dairy cattle manure. The overall average concentration was 9.67 mmol/kg (Baziramakenga and Simard, 1998).

Environmental Fate

Biological. Heukelekian and Rand (1955) reported a 5-d BOD value of 0.12 g/g which is 66.7% of the ThOD value of 0.18 g/g.
Chemical/Physical. At temperatures greater than 189.5 °C, decomposes to carbon dioxide, carbon monoxide, formic acid, and water (Windholz et al., 1983). Ozonolysis of oxalic acid in distilled water at 25 °C under acidic conditions (pH 6.3) yielded carbon dioxide (Kuo et al., 1977). Absorbs moisture in air forming the dihydrate (Huntress and Mulliken, 1941).
Reacts with bases forming water soluble salts.

Shipping

UN3261 Corrosive solid, acidic, organic, n.o.s., Hazard class: 8; Labels: 8-Corrosive material, Technical Name Required.

Incompatibilities

The aqueous solution is a medium-strong acid. Compounds of the carboxyl group react with all bases, both inorganic and organic (i.e., amines) releasing substantial heat, water and a salt that may be harmful. Incompatible with arsenic compounds (releases hydrogen cyanide gas), diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides (releasing heat, toxic, and possibly flammable gases), thiosulfates and dithionites (releasing hydrogen sulfate and oxides of sulfur). Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from silver compounds; strong alkalis; chlorites. Contact with some silver compounds forms explosive materials.

Waste Disposal

Pretreatment involves chemical reaction with limestone or calcium oxide forming calcium oxalate. This may then be incinerated utilizing particulate collection equipment to collect calcium oxide for recycling.

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