Skin irritation, Category 2
Serious eye damage, Category 1
H315 Causes skin irritation
H318 Causes serious eye damage
P264 Wash ... thoroughly after handling.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P302+P352 IF ON SKIN: Wash with plenty of water/...
P321 Specific treatment (see ... on this label).
P332+P317 If skin irritation occurs: Get medical help.
P362+P364 Take off contaminated clothing and wash it before reuse.
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.
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Fresh air, rest. Refer for medical attention.
Remove contaminated clothes. Rinse skin with plenty of water or shower.
First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.
Rinse mouth. Do NOT induce vomiting. Give nothing to drink. Refer for medical attention .
Inhalation of mist causes coughing and irritation of mucous membranes. Ingestion, even of diluted preparations, has a corrosive effect on the esophagus and stomach. Contact with more concentrated solutions can cause severe burns of skin or eye. (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 if 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.
Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Excerpt from ERG Guide 153 [Substances - Toxic and/or Corrosive (Combustible)]: Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Those substances designated with a (P) may polymerize explosively when heated or involved in a fire. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form. (ERG, 2016)
Use water spray, powder, alcohol-resistant foam, carbon dioxide.
Collect leaking and spilled liquid in sealable containers as far as possible. Cautiously neutralize spilled liquid with weak alkaline solution such as disodium carbonate. Then wash away with plenty of water.
Collect leaking and spilled liquid in sealable containers as far as possible. Cautiously neutralize spilled liquid with weak alkaline solution such as disodium carbonate. Then wash away with plenty of water.
ACCIDENTAL RELEASE MEASURES: Personal precautions, protective equipment and emergency procedures: Use personal protective equipment. Avoid breathing vapors, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas; Environmental precautions: Do not let product enter drains; Methods and materials for containment and cleaning up: Soak up with inert absorbent material and dispose of as hazardous waste. Keep in suitable, closed containers for disposal.
NO open flames. 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 bases.Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Hygroscopic.
no data available
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 safety goggles or face shield.
Protective gloves.
Use local exhaust or breathing protection.
no data available
Liquid. Viscous.
Colourless.
Odorless
< -80 °C. Atm. press.:Ca. 1 atm. Remarks:VIscous solutions do not solidify.
122 °C. Atm. press.:15 mm Hg. Remarks:Crystalline lactic acid.;122 °C. Atm. press.:1 atm. Remarks:Temperature at which a 88% aqueous solution starts to boil. DUring boiling, temperature will increase due to changing composition of solution (evaporation of water).
Combustible.
no data available
>= 74 °C. Atm. press.:1 atm.
400 °C. Atm. press.:>= 1 011.4 - <= 1 018.9 hPa.
no data available
The pH of a 10 wt% aqueous solution of lactic acid is 1.75
cP = 18.4. Temperature:25.0°C. Remarks:80 % w/w solution of lactic acid.
In water: 86.1 % w/w. Temperature:20 °C. pH:>= 0 - <= 14. Remarks:Lactic acid is soluble in water in all ratios. Solubility is not dependent on pH. pH of the solution will depend on the concentration, but at higher concentrations an ever larger fraction of the lactic acid will form oligomers.;93 % w/w. Temperature:35 °C. pH:>= 0 - <= 14. Remarks:Lactic acid is soluble in water in all ratios. Solubility is not dependent on pH. pH of the solution will depend on the concentration, but at higher concentrations an ever larger fraction of the lactic acid will form oligomers..Methanol.;Ethanol.;N-propanol.
log Pow = -0.72 - -0.65. Remarks:Results taken from experimental database (-0.72) and KowWin estimate (-0.65), temperature and pH.
0.004 hPa. Temperature:20 °C.
1.19 g/cm3. Temperature:25 °C.;1.2 g/cm3. Temperature:25 °C.
no data available
no data available
The substance is a medium strong acid.
Stable under recommended storage conditions.
LACTIC ACID is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in it to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. Slowly corrodes most metals (USCG, 1999).
no data available
Incompatible materials: Bases, Oxidizing agents, Reducing agents
When heated to decompositionit emits acrid smoke and irritating fumes.
no data available
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The substance is corrosive to the eyes. The substance is irritating to the skin and respiratory tract. Corrosive on ingestion.
no data available
No indication can be given about the rate at which a harmful concentration of this substance in the air is reached on evaporation at 20°C.
AEROBIC: Lactic acid reached 22% of its theoretical BOD in 5 days using a sewage inoculum(1). In a closed bottle screening test, lactic acid, present at 2 mg/L, reached 12, 67, and 88% of its theoretical BOD after 5, 15, and 30 days, respectively, using an activated sludge inoculum(2). Lactic acid reached 59% of its theoretical BOD in 5 days using a sludge inoculum and the Warburg screening test(3). Lactic acid, present at 500 mg/L, reached 27.5, 29.4, and 33.3% of its theoretical BOD in 6, 12, and 24 hours, respectively, using an activated sludge inoculum at 2500 mg/L(4). Lactic acid was found to be easily biodegradable by biological sewage treatment(5). Lactic acid, present at 100 mg/L, reached 76% of its theoretical BOD in 2 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test which classified the compound as readily biodegradable(6).
An estimated BCF of 3 was calculated for lactic acid(SRC), using a log Kow of -0.72(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).
Experimental Koc values for lactic acid on a clastic mud (3.5% organic carbon) and a lateritic muddy sand (1.3% organic carbon) were 5.7 and <0.08, respectively(1). Utilizing an HPLC method, the Koc of lactic acid (93% aqueous solution) on soil and sewage sludge at neutral pH and pH 2 was <20.9(2). According to a classification scheme(3), these Koc values suggest that lactic acid is expected to have very high mobility in soil. The pKa of lactic acid is 3.86(4), indicating that this compound will exist partially to almost entirely in anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(5).
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