Acute toxicity - Category 4, Oral
Acute toxicity - Category 4, Dermal
Skin corrosion, Sub-category 1A
H302 Harmful if swallowed
H312 Harmful in contact with skin
H314 Causes severe skin burns and eye damage
P264 Wash ... thoroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P260 Do not breathe dust/fume/gas/mist/vapours/spray.
P301+P317 IF SWALLOWED: Get medical help.
P330 Rinse mouth.
P302+P352 IF ON SKIN: Wash with plenty of water/...
P317 Get medical help.
P321 Specific treatment (see ... on this label).
P362+P364 Take off contaminated clothing and wash it before reuse.
P301+P330+P331 IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P363 Wash contaminated clothing before reuse.
P304+P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing.
P316 Get emergency medical help immediately.
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P405 Store locked up.
P501 Dispose of contents/container to an appropriate treatment and disposal facility in accordance with applicable laws and regulations, and product characteristics at time of disposal.
no data available
Fresh air, rest. Half-upright position. Refer for medical attention.
First rinse with plenty of water for at least 15 minutes, then remove contaminated clothes and rinse again.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Rest. Refer for medical attention .
INHALATION: Severe irritation to respiratory tract. EYES: Short contact can cause severe damage. SKIN: Causes severe irritation and burns. Ingestion: High hazard - may cause death or permanent injury on short exposure to small quantities. OTHER: May affect blood pressure temporarily. (USCG, 1999)
Immediate first aid: Ensure that adequate decontamination has been carried out. If patient is not breathing, start artificial respiration, preferably with a demand-valve resuscitator, bag-valve-mask device, or pocket mask, as trained. Perform CPR as necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on left side (head-down position, if possible) to maintain an open airway and prevent aspiration. Keep patient quiet and maintain normal body temperature. Obtain medical attention. Organic acids and related compounds
Use dry chemical, carbon dioxide, or alcohol foam extinguishers. Vapors are heavier than air and will collect in low areas. Vapors may travel long distances to ignition sources and flashback. Vapors in confined area may explode in fire. Storage containers and parts of containers may rocket great distances, in many directions. If materials or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Notify local health and fire officials and pollution control agencies. From a secure, explosion-proof location, use water spray to cool exposed containers. If cooling streams are ineffective (venting sound increases in volume and pitch, tank discolors, or shows any signs of deforming), withdraw immediately to a secure position. If employees are expected to fight fires, they must be trained and equipped.
Special Hazards of Combustion Products: Vapor forms explosive mixtures with air. Thermal decomposition produces carbon monoxide and carbon dioxide. Behavior in Fire: Vapors form explosive mixtures with air. Sealed containers may rupture explosively at elevated temperatures (polymerization). (USCG, 1999)
Use AFFF, alcohol-resistant foam, powder, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
Collect leaking and spilled liquid in sealable plastic containers as far as possible. Cautiously neutralize remainder with aqueous sodium carbonate or lime. Then wash away with plenty of water. Do NOT absorb in saw-dust or other combustible absorbents. Personal protection: complete protective clothing including self-contained breathing apparatus.
Collect leaking and spilled liquid in sealable plastic containers as far as possible. Cautiously neutralize remainder with aqueous sodium carbonate or lime. Then wash away with plenty of water. Do NOT absorb in saw-dust or other combustible absorbents. Personal protection: complete protective clothing including self-contained breathing apparatus.
Evacuate and restrict persons not wearing protective equipment from area of spill or leak until cleanup is complete. Remove all ignition sources. Establish forced ventilation to keep levels below explosive limit. Absorb liquids in vermiculite, dry sand, earth, or a similar non-organic materials and deposit in sealed containers. Using caution, neutralize remainder with aqueous sodium carbonate or lime. Then wash away with plenty of water. Keep this chemical out of a confined space, such as a sewer, because of the possibility of an explosion, unless the sewer is designed to prevent the build-up of explosive concentrations. It may be necessary to contain and dispose of this chemical as a hazardous waste. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Contact your Department of Environmental Protection or your regional office of the federal EPA for specific recommendations. If employees are required to clean-up spills, they must be properly trained and equipped.
NO open flames. Above 77°C use a closed system and ventilation. 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. Cool. Keep in the dark. Keep in a well-ventilated room. Store only if stabilized.Prior to working with this chemical you should be trained on its proper handling and storage. Before entering confined space where this chemical may be present, check to make sure that an explosive concentration does not exist. Store in tightly closed containers in a cool, well ventilated area away from oxidizers (such as perchlorates, peroxides, permanganates, chlorates and nitrates). Methacrylic acid should be stored at temperatures below 15 degrees C. Sources of ignition such as smoking and open flames are prohibited where Methacrylic acid is handled, used, or stored. Wherever Methacrylic acid is used, handled, manufactured, or stored, use explosion-proof electrical equipment and fittings.
TLV: 20 ppm as TWA.MAK: 180 mg/m3, 50 ppm; peak limitation category: I(2); pregnancy risk group: C
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 face shield.
Protective clothing.
Use ventilation (not if powder), local exhaust or breathing protection.
no data available
Liquid.
Clear, colourless.
Acrid, repulsive odor
15.4 - 15.5 °C.
162 °C. Atm. press.:1 013 hPa.
Class IIIA Combustible Liquid: Fl.P. at or above 140°F and below 200°F.
Lower flammable limit: 1.6% by volume; Upper flammable limit: 8.8% by volume
67 °C. Atm. press.:1 013 hPa.
400 °C. Atm. press.:1 013 hPa.
no data available
no data available
dynamic viscosity (in mPa s) = 1.38. Temperature:25.0°C. Remarks:Temperature: unspecified, but we assume it to be room temperature ca. 22 - 25°C.
Miscible with water
log Pow = 0.93. Temperature:22 °C.
0.97 hPa. Temperature:20 °C. Remarks:Calculated using the Clausius-Clapeyron equation; VP=e^-6303.1*1/temp+21.186; temp = 20 °C = 20°C.
1.01 g/cm3. Temperature:20 °C.
>3 (vs air)
no data available
The substance readily polymerizes due to heating or under the influence of light, oxidizing agents such as peroxides, or in the presence of traces of hydrochloric acid. This generates fire or explosion hazard. Attacks metals.
Acrylic acid and methacrylic acid readily polymerize in the presence of light, heat and oxygen, and also under the action of oxidizing agents such as peroxides.
Flammable when exposed to heat, flame, or oxidizers.Vapours are uninhibited and may polymerize, causing blockage of vents.METHACRYLIC ACID reacts with strong oxidizing agents. Presents a storage hazard: violent exothermic polymerizations leading to explosion can occur spontaneously, particularly at low inhibitor or stabilizer concentrations [Anon., CISHC Chem. Safety Summ., 1979, 50, p. 34; Bond, J., Loss Prev. Bull., 1991, 101, p. 1].
no data available
Oxidizers, elevated temperatures, hydrochloric acid [Note: Typically contains 100 ppm of the monomethyl ether of hydroquinone to prevent polymerization].
When heated to decomposition it emits acrid smoke and irritating fumes.
no data available
no data available
no data available
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The substance is corrosive to the eyes, skin and respiratory tract. Corrosive on ingestion. Inhalation of the vapour may cause lung oedema. See Notes.
no data available
A harmful contamination of the air will be reached rather slowly on evaporation of this substance at 20°C.
AEROBIC: Methacrylic acid was rapidly biodegraded in tests using adapted activated sludge inoculum under aerobic conditions(1). Aerobic standard dilution tests using sewage inoculum provided 53% theoretical BOD after 5 days incubation(2), 68% COD after 19 days(3) and 86% theoretical COD after 42 days(3). The BOD5/COD ratio for methacrylic acid was determined to be 0.16, which is indicative of significant potential for biodegradability(4). In a Closed Bottle test, methacrylic acid was determined to be 86% degraded after 28 days and >95% methacrylic acid was degraded in the Zahn-Wellens test, time not specified(5).
An estimated BCF of 3.1 was calculated for methacrylic acid(SRC), using a log Kow of 0.93(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
An average Koc value of 15 has been reported for methacrylic acid(1). According to a classification scheme(2), this Koc value suggests that methacrylic acid is expected to have very high mobility in soil.
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: UN2531 (For reference only, please check.)
IMDG: UN2531 (For reference only, please check.)
IATA: UN2531 (For reference only, please check.)
ADR/RID: METHACRYLIC ACID, STABILIZED (For reference only, please check.)
IMDG: METHACRYLIC ACID, STABILIZED (For reference only, please check.)
IATA: METHACRYLIC ACID, STABILIZED (For reference only, please check.)
ADR/RID: 8 (For reference only, please check.)
IMDG: 8 (For reference only, please check.)
IATA: 8 (For reference only, please check.)
ADR/RID: II (For reference only, please check.)
IMDG: II (For reference only, please check.)
IATA: II (For reference only, please check.)
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available
The symptoms of lung oedema often do not become manifest until a few hours have passed and they are aggravated by physical effort. Rest and medical observation are therefore essential.Immediate administration of an appropriate inhalation therapy by a doctor, or by an authorized person, should be considered.An added stabilizer or inhibitor can influence the toxicological properties of this substance; consult an expert.