Serious eye damage, Category 1
Danger
H318 Causes serious eye damage
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P305+P354+P338 IF IN EYES: Immediately rinse with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P317 Get medical help.
none
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no data available
Fresh air, rest. Half-upright position. Refer immediately for medical attention.
Remove contaminated clothes. Rinse skin with plenty of water or shower for at least 15 minutes. Refer for medical attention .
Rinse with plenty of water (remove contact lenses if easily possible). Refer immediately for medical attention.
Rinse mouth. Do NOT induce vomiting. Refer immediately for medical attention.
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. (USCG, 1999)
Treatment should be rapidly instituted by giving a dilute solution of calcium lactate, lime water, finely pulverized chalk, plaster, and/or milk to supply large amounts of calcium to inactivate oxalate by forming an insoluble calcium salt in the stomach. Gastric lavage is controversial, since this may compound an already severe corrosive lesion in the esophagus or stomach. However, if used, gastric lavage should be done with limewater (calcium hydroxide). Intravenous gluconate or calcium chloride solutions should be given to prevent hypocalcemic tetany; in severe cases parathyroid extract also has been given. ... Additionally, acute renal failure should be anticipated, and careful fluid management is necessary. Oxalates
Use water spray, dry chem, "alc resistant" foam, or carbon dioxide. dust may be reduced with water spray. aqueous solution must be contained for disposal. use water to keep fire-exposed containers cool. water may cause foaming of molten material. oxalic acid dihydrate
Special Hazards of Combustion Products: Generates poisonous gases (USCG, 1999)
Wear self-contained breathing apparatus for firefighting if necessary.
HEALTH | 0 | Poses no health hazard, no precautions necessary and would offer no hazard beyond that of ordinary combustible materials | |
FIRE | 0 | Materials that will not burn under typical fire conditions, including intrinsically noncombustible materials such as concrete, stone, and sand. Materials that will not burn in air when exposed to a temperature of 820 °C (1,500 °F) for a period of 5 minutes.(e.g. Carbon tetrachloride) | |
REACT | 0 | Normally stable, even under fire exposure conditions, and is not reactive with water (e.g. helium,N2) | |
SPEC. HAZ. |
Avoid dust formation. Avoid breathing mist, gas or vapours.Avoid contacting with skin and eye. Use personal protective equipment.Wear chemical impermeable gloves. Ensure adequate ventilation.Remove all sources of ignition. Evacuate personnel to safe areas.Keep people away from and upwind of spill/leak.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance, protective gloves and safety goggles. Sweep spilled substance into covered plastic containers. If appropriate, moisten first to prevent dusting. Wash away remainder with plenty of water.
Cover with soda ash or sodium bicarbonate. Mix and add water. Neutralize and drain into a drain with sufficient water.
Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.
Separated from strong oxidants and food and feedstuffs. Dry. Well closed.STORE IN COOL, DRY, WELL-VENTILATED LOCATION. OXALIC ACID DIHYDRATE
Component | Carboxylic acids, di-, C4-6 |
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CAS No. | 68603-87-2 |
Recommended Exposure Limit: 10 Hr Time-Weighted Avg: 1 mg/cu m. Recommended Exposure Limit: 15 Min Short-Term Exposure Limit: 2 mg/cu m. |
no data available
Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear tightly fitting safety goggles with side-shields conforming to EN 166(EU) or NIOSH (US).
Wear fire/flame resistant and impervious clothing. Handle with gloves. Gloves must be inspected prior to use. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it.
If the exposure limits are exceeded, irritation or other symptoms are experienced, use a full-face respirator.
no data available
Oxalic acid is an odorless white solid. Sinks and mixes with water. (USCG, 1999)
ANHYDROUS OXALIC ACID, CRYSTALLIZED FROM GLACIAL ACETIC ACID IS ORTHORHOMBIC, CRYSTALS BEING PYRAMIDAL OR ELONGATED OCTAHEDRA
Odorless.
189.5°C (dec.)(lit.)
302.894°C at 760 mmHg
Combustible Solid
no data available
151.212°C
Not flammable (USCG, 1999)
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50 to 100 mg/mL at 75° F (NTP, 1992)
-0.81
0.99 g/mL at 25°C
4.3 (NTP, 1992) (Relative to Air)
no data available
Decomposes on contact with hot surfaces or flames. This produces formic acid and carbon monoxide. The solution in water is a medium strong acid. Reacts violently with strong oxidants. This generates fire and explosion hazard. Reacts with some silver compounds. This produces explosive silver oxalate. Attacks some forms of plastic.
Oxalic acid can be dehydrated by careful drying @ 100 deg c, but losses occur through sublimation oxalic acid dihydrate
OXALIC ACID is hygroscopic and sensitive to heat. This compound may react violently with furfuryl alcohol, silver, sodium, perchlorate, sodium hypochlorite, strong oxidizers, sodium chlorite, acid chlorides, metals and alkali metals. (NTP, 1992). 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 gases, and inert CO2 gas [Von Bentzinger, R. et al., Praxis Naturwiss. Chem., 1987, 36(8), 41-42].
no data available
Reacts with strong alkalies, strong oxidizing materials, chlorites, and hypochlorites. Oxalic acid dihydrate
Decomp products incl carbon monoxide & formic acid.
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Six tests at oxalic acid initial concns of 3.3 to 10 ppm exhibited 75 to 202 %BODT over an incubation period of 5 days in an aerobic screening study using sewage inoculum(1). A 78 and 55.5 %BODT for oxalic acid was measured under aerobic conditions over a period of 5 days in screening tests at 20 deg C using sewage inoculum(2). Oxalic acid at initial concns of 0.00375, 0.0375, and 0.375 ppm exhibited 95, 99, and 100% degradation, respectively, in an aerobic screening study at 25 deg C using sewage inoculum(3). In another screening study using sewage inoculum, 68 and 64 %BODT were measured for oxalic acid at initial concns of 10 and 20 ppm, respectively, over a 5 day incubation period(4). An 89 %BODT was measured for oxalic acid (10 ppm initial concn) in an aerobic screening study using sewage inoculum at 19.5-20.5 deg C over an incubation period of 5 days(5).
Based on an average experimental water solubility of 220,000 mg/L at 25 deg C(1) and a regression derived equation(2), the BCF for oxalic acid can be estimated to be approximately 0.6(SRC) and therefore should not be expected to bioconcentrate in aquatic organisms(SRC).
Based on an average experimental water solubility of 220,000 mg/L at 25 deg C(1) and a regression derived equation(2), the Koc for undissociated oxalic acid can be estimated to be approximately 5. This Koc value indicates that oxalic acid will have very high mobility in soil(3); therefore, adsorption to soil and sediment may not be an important fate process. Based on pKa1 and pKa2 values of 1.25 and 4.28(4) respectively, oxalic acid will exist primarily as the oxalate ion under environmental conditions (pH 5-9). No experimental data are available to determine whether the oxalate ion will adsorb to sediment or soil more strongly than its estimated Koc value indicates(SRC).
no data available
The material can be disposed of by removal to a licensed chemical destruction plant or by controlled incineration with flue gas scrubbing. Do not contaminate water, foodstuffs, feed or seed by storage or disposal. Do not discharge to sewer systems.
Containers can be triply rinsed (or equivalent) and offered for recycling or reconditioning. Alternatively, the packaging can be punctured to make it unusable for other purposes and then be disposed of in a sanitary landfill. Controlled incineration with flue gas scrubbing is possible for combustible packaging materials.
ADR/RID: Not dangerous goods. (For reference only, please check.)
IMDG: Not dangerous goods. (For reference only, please check.)
IATA: Not dangerous goods. (For reference only, please check.)
ADR/RID: Not dangerous goods. (For reference only, please check.)
IMDG: Not dangerous goods. (For reference only, please check.)
IATA: Not dangerous goods. (For reference only, please check.)
ADR/RID: Not dangerous goods. (For reference only, please check.)
IMDG: Not dangerous goods. (For reference only, please check.)
IATA: Not dangerous goods. (For reference only, please check.)
ADR/RID: Not dangerous goods. (For reference only, please check.)
IMDG: Not dangerous goods. (For reference only, please check.)
IATA: Not dangerous goods. (For reference only, please check.)
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available
The information in this MSDS is only applicable to the specified product, unless otherwise specified, it is not applicable to the mixture of this product and other substances. This MSDS only provides information on the safety of the product for those who have received the appropriate professional training for the user of the product. Users of this MSDS must make independent judgments on the applicability of this SDS. The authors of this MSDS will not be held responsible for any harm caused by the use of this MSDS.