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Nitric acid, 60 %
Material Safety Data Sheet
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SECTION 1. IDENTIFICATION OF THE SUBSTANCE AND OF THE COMPANY/UNDERTAKING
1.1 Product identifier
Name of substance Nitric acid, 60 % IUPAC name Nitric acid EC number 231-714-2 CAS number 7697-37-2 REACH registration number 01-2119487297-23-0005 Chemical formula
1.2. Relevant identified uses of the substance or mixture and uses advised
against
1.2.1 Identified uses - Formulation and repackaging - Formulation of mixtures with the use of nitric acid < 70%
- Use in industrial plants - Application of nitric acid < 70% in industrial plants as a semi-manufactured product - Use in industrial plants - Application of nitric acid < 70% in industrial plants as a reactive auxiliary substance (cleaning agent, pH regulator, gaseous emissions treatment, regeneration of ion exchange resins, processing of metals and plastics, surface processing, water treatment) - Common use by professionals - Applications of nitric acid < 70% by professionals (indoor and outdoor use of reactive substances in open systems as cleaning agents, pH regulators, for metal processing) - Consumer use - Applications of products containing nitric acid (< 3%)
1.2.2. Uses advised against 1.3 Details on the supplier of the safety data sheet
Producer Grupa Azoty ZAK S.A.
Address PO Box 163; ul. Mostowa 30A;
47-220 Kędzierzyn-Koźle; Poland
Telephone № (+48 77) 481 20 00 (operator)
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Person responsible for [email protected]
safety data sheet
1.4 Emergency telephone numbers (in Poland)
Company’s Dispatch Office (+48 77) 481-34-01 Emergency system 112 Police 997 Fire Dept. 998 Medical aid 999
SECTION 2: HAZARDS IDENTIFICATION
2.1. Classification of the substance or mixture Classification according to the Regulation (EC) No. 1272/2008 (CLP) Caustic / irritating effect to the skin: Skin Corr.1A (H314: Causes severe skin burns and eye damage) Metals corrosiveness: Met. Corr. 1 (H290: May be corrosive to metals.) Acute toxicity: Acute Tox. 3 (H331: Toxic if inhaled)
2.2. Label elements
GHS05: GHS06: Warning phrase: Danger Hazard statements H314: Causes severe skin burns and eye damage. H290: May be corrosive to metals. H331: Toxic if inhaled. Precautionary statements P210: Keep away from sources of heat, hot surfaces, sparks, open flames and other sources of ignition. Do not smoke. P220: Keep away from clothing and combustible materials. P221: Take any precaution to avoid mixing with combustibles P260: Do not breathe mist/vapours/spray. P280: Wear protective gloves / protective clothing / eye protection / face protection. P310: Immediately call a POISON CENTRE/doctor. P363: Wash contaminated clothing before reuse.
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P390: Absorb spillage to prevent material damage. P301 + P330 + P331: IF SWALLOWED: rinse mouth. DO NOT induce vomiting. P303 + P361 + P353: IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. P305 + P351 + P338: IF THE SUBSTANCE GETS IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P304 + P340: IF INHALED: Remove person to fresh air and keep comfortable for breathing. P404: Store in a closed container. P406: Store in a container with a resistant inner liner.
2.3. Other hazards EUH071: Corrosive to the respiratory tract. SECTION 3. COMPOSITION/INFORMATION ON INGREDIENTS
3.1 Substances
Name of substance EC number CAS number IUPAC name Concentration [%]
Nitric acid 231-714-2 7697-37-2 Nitric acid 57-63
3.2 No data available
SECTION 4. FIRST AID MEASURES
4.1 Description of first aid measures
4.1.1 General advice
Quick action is necessary. Administer first aid and call a doctor immediately. The rescuers must use suitable personal protective equipment. Evacuate the affected person from the place of exposure. Make sure that the eyewash fountains and safety showers are located close to the work stations. Those exposed to the risk of eye contact should be instructed on the need and the method immediately applicable in eye washing, and on the locations and directions for use of eyewash fountains and safety showers.
4.1.2 Inhalation
Evacuate the affected person to fresh air. Arrange the comfortable half-upright position and keep at rest. If not breathing, or when the symptoms of weakness are shown, apply
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artificial respiration. Mouth-to-mouth or mouth-to-nose resuscitation methods may be dangerous. Oxygen may be administered by qualified personnel.
4.1.3 Skin
Wash out with water. Take off the contaminated clothing and flush the affected skin with plenty of water for at least 15 minutes. In case of chemical burns, seek medical attention immediately. Do not use soap and/or any neutralising agents.
4.1.4 Eyes
Immediately flush eyes with the eye-wash solution or with plenty of water for at least 15 minutes. Avoid using a strong water jet because of the risk of mechanical corneal damage. Keep the eyelids open when flushing. Do not rub the eyes.
4.1.5 Ingestion
Do not induce vomiting. If the affected person is conscious, rinse mouth with water and give milk to drink. Do not give any neutralising (alkaline) agents. Provide medical attention immediately.
4.2 Most important symptoms and effects, both acute and delayed
Poisoning, skin burns, eye damage, respiratory irritation.
4.3 Indication of any immediate medical attention and special treatment needed
No data available.
SECTION 5. FIRE-FIGHTING MEASURES
5.1 Extinguishing media
Nitric acid is not combustible. If a fire breaks out, however, use the best available fire extinguishing media: water or CO2. Extinguishing media which must not be used for safety reasons: do not use chemical extinguishers and fire foam; do not try putting out the fire with steam or sand.
5.2 Special hazards arising from the substance or mixture
Nitric acid is not combustible but it is an oxidiser, hence it may react with numerous flammable materials to produce a fire and to release toxic fumes (nitrogen oxides). Its contact with a strong reducer may result in an explosion. It reacts with most metals and
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hydrogen is released in the process. Hydrogen/air mixtures are explosive. Dangerous products of decomposition and combustion: nitrogen oxides.
5.3 Advice for fire-fighters
5.3.1 Special protective equipment
Use self-contained breathing apparatus and full acid-resistant fire-fighting clothing.
5.3.2 Precautions for fire-fighting
Cool tanks with water spray if exposed to high temperature or flames. Prevent fire water from entering the environment.
SECTION 6. ACCIDENTAL RELEASE MEASURES
6.1 Personal precautions, protective equipment and emergency procedures
6.1.1 Personal precautions
Those involved in clean-up of a major spillage should wear protective clothing and isolating breathing apparatus. Avoid any eye contact and inhalation of vapours. Keep unnecessary personnel away.
6.1.2 Precautions for emergency responders
Refer to section 8.
6.2 Environmental precautions
Prevent further leaking if that is possible and safe to do. Prevent product entry to sewage systems and water courses. Protect drain inlets. Notify relevant authorities in case of accidental pollution of water bodies or sewage systems. Dilute acid with water and/or neutralise it with soda or sodium carbonate before discharging it to a sewage treatment plant or to the aquatic environment.
6.3 Methods and material for containment and cleaning up
6.3.1 Methods for containment
Stop the liquid escape as soon as possible. Ventilate the spill area if required. In case of a large spill, contain the spilled material and pump the liquid for recovery or disposal.
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6.3.2 Methods for cleaning up
Dilute small spills with water and neutralise them carefully with soda and/or ground limestone. In case of need, cover/absorb large spills with sand or dry earth. Do not use any organic compounds, sawdust, etc. Collect the soaked sorption material with the use of suitable tools and place in a properly labelled container. Pump bulk volumes of spilled product to properly labelled containers.
6.4 Reference to other sections
Refer also to sections 8 and 13 in this MSDS.
SECTION 7. HANDLING AND STORAGE
7.1 Precautions for safe handling
7.1.1 Advice on safe handling
Avoid any contact with skin and eyes. Do not breathe vapours. Provide sufficient ventilation. Wear protective gloves and chemical safety goggles or face shield when transferring small volumes. When leakages or splashes can reasonably be expected, use full personal protective equipment. When diluting, ALWAYS add acid to water and NEVER add water to acid. Do not eat and do not drink when handling the product. Avoid any direct contact with the substance, avoid inhalation of vapours, and observe rules of good personal hygiene.
7.1.2 Advice on protection against fire and explosion
Do not smoke in the room where the product is handled. Keep all incompatible substances away (refer to section 10: Stability and Reactivity).
7.1.3 Advice on the protection of the environment
Refer to section 8: Environmental exposure controls.
7.2 Conditions for safe storage, including any incompatibilities
7.2.1 Technical measures/storage conditions
Store in original, properly labelled and tightly closed containers, in cool, dry and well-ventilated storage rooms. Provide forced-flow ventilation and the floor which is acid-proof, which does not absorb water/liquids and which is easy to clean flushing. The floor should slope towards the drain inlets. Keep all flammable materials away. Protect
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against direct sunlight, heat and water/humidity. Protect the containers against corrosion and physical damage.
7.3. Specific end use(s)
- Formulation and repackaging - Formulation of mixtures with the use of nitric acid < 70%: Exposure scenario 2 - Use in industrial plants - Application of nitric acid < 70% in industrial plants as a semi-manufactured product: Exposure scenario 3 - Use in industrial plants - Application of nitric acid < 70% in industrial plants as a reactive auxiliary substance (cleaning agent, pH regulator, gaseous emissions treatment, regeneration of ion exchange resins, processing of metals and plastics, surface processing, water treatment): Exposure scenario 4 - Common use by professionals - Applications of nitric acid < 70% by professionals (indoor and outdoor use of reactive substances in open systems as cleaning agents, pH regulators, for metal processing): Exposure scenario 5 - Consumer use - Applications of products containing nitric acid (< 3%): Exposure scenario 6
SECTION 8. EXPOSURE CONTROLS / PERSONAL PROTECTION
8.1 Control parameters
8.1.1 OEL(s) for Poland
MAC 1.4 mg/m3 MAC (STEL) 2.6 mg/m3 MAC(C) not established BLV not established
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8.1.2 Derived No Effect Levels (DNELs) – Workers
Acute toxicity / short term exposure (systemic effect)
No systemic exposure and absorption of nitric acid is expected. It may be absorbed locally in case of ingestion, inhalation and/or skin contact. After its absorption, nitric acid is generally distributed throughout the organism in the form of nitrate which makes a basic component in organisms, and its life is naturally controlled in human organisms.
Acute / short-term exposure (local effect) – inhalation
DNEL = 2.6 mg/m3 (1 ppm). 7.3. Specific end use(s) - Formulation and repackaging - Formulation of mixtures with the use of nitric acid < 70%: Exposure scenario 2 - Use in industrial plants - Application of nitric acid < 70% in industrial plants as a semi-manufactured product: Exposure scenario 3 - Use in industrial plants - Application of nitric acid < 70% in industrial plants as a reactive auxiliary substance (cleaning agent, pH regulator, gaseous emissions treatment, regeneration of ion exchange resins, processing of metals and plastics, surface processing, water treatment): Exposure scenario 4 - Common use by professionals - Applications of nitric acid < 70% by professionals (indoor and outdoor use of reactive substances in open systems as cleaning agents, pH regulators, for metal processing): Exposure scenario 5 - Consumer use - Applications of products containing nitric acid (< 3%): Exposure scenario 6
7.3. Specific end use(s) - Formulation and repackaging - Formulation of mixtures with the use of nitric acid < 70%: Exposure scenario 2 - Use in industrial plants - Application of nitric acid < 70% in industrial plants as a semi-manufactured product: Exposure scenario 3 - Use in industrial plants - Application of nitric acid < 70% in industrial plants as a reactive auxiliary substance (cleaning agent, pH regulator, gaseous emissions treatment, regeneration of ion exchange resins, processing of metals and plastics, surface processing, water treatment): Exposure scenario 4 - Common use by professionals - Applications of nitric acid < 70% by professionals (indoor and outdoor use of reactive substances in open systems as cleaning agents, pH regulators, for metal processing): Exposure scenario 5 - Consumer use - Applications of products containing nitric acid (< 3%): Exposure scenario 6
Acute / short-term exposure (local effect) – dermal
In accordance with the Regulation (EC)№ 1272/2008 Annex VI, Table 3.1, the specific concentration limit for HNO3 equals to 20 % for corrosion. Irritation may be expected within the concentrations of 5-20 %.
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Long-term exposure (systemic effects) – dermal and inhalation
No systemic exposure and absorption of nitric acid is expected. It may be absorbed locally in case of ingestion, inhalation and/or skin contact. After its absorption, nitric acid is generally distributed throughout the organism in the form of nitrate which makes a basic component in organisms, and its life is naturally controlled in human organisms.
Long-term exposure (local effects) – inhalation
DNEL for long-term local exposure = 1.3 mg/m3 (0.5 ppm).
Long-term exposure (local effects) – dermal
In accordance with the Regulation № 1272/2008 (CLP), Annex VI, Table 3.1, the specific concentration limit for HNO3 equals to 20 % for corrosion. Irritation may be expected within the concentrations of 5-20 %.
8.1.3 Derived No Effect Levels (DNELs) – general population
Acute / short-term exposure (systemic effect) – dermal and inhalation
No systemic exposure and absorption of nitric acid is expected. It may be absorbed locally in case of ingestion, inhalation and/or skin contact. After its absorption, nitric acid is generally distributed throughout the organism in the form of nitrate which makes a basic component in organisms, and its life is naturally controlled in human organisms.
Acute / short-term exposure (local effect) – inhalation
DNEL = 1.3 mg/m3.
Acute / short-term exposure (local effect) – dermal
In accordance with the Regulation № 1272/2008 (EC), Annex VI, Table 3.1, the specific concentration limit for HNO3 equals to 20 % for corrosion. Irritation may be expected within the concentrations of 5-20 %.
Long-term exposure (systemic effects) – dermal, inhalation and oral
No systemic exposure and absorption of nitric acid is expected. It may be absorbed locally in case of ingestion, inhalation and/or skin contact. After its absorption, nitric acid is generally distributed throughout the organism in the form of nitrate which
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makes a basic component in organisms, and its life is naturally controlled in human organisms.
Long-term exposure (local effects) – inhalation
DNEL = 0.65 mg/m3.
Long-term exposure (local effects) – dermal
In accordance with the Regulation № 1272/2008 (CLP), Annex VI, Table 3.1, the specific concentration limit for HNO3 equals to 20 % for corrosion. Irritation may be expected within the concentrations of 5-20 %.
8.1.4 Predicted No Effect Concentration (PNEC)
PNEC – aqua
Nitric acid is a strong acid which will dissociate in water to produce ions H+ and NO3–. The protons may affect the pH value of the aqueous medium which entails toxic effects for aquatic organisms.
PNEC – sediment
PNEC data for nitric acid are not critical since it is a substance which will dissociate in water to produce ions: H+ and NO3–. High water solubility of nitric acid is indicative of its predominant presence in the aquatic compartment – acid will not be absorbed on the surface of sediment particles.
PNEC – soil
After it is applied to soil, nitric acid will penetrate through its bed, according to soil viscosity. When going through soil, nitric acid will dissolve chemical compounds which are contained in soil, in particular it will dissolve carbonates. Leaching acids out of soil will be controlled by the water content in that specific soil. Nitrates produced by nitric acid are absorbed by plants, or they are processed by denitrification organisms which produce nitrogen or dinitrogen monoxide.
PNEC – STP
The hazard for the sewage treatment plant (process) connected with the presence of nitric acid results predominantly from the increase in the concentration of H+ ions which are released from dissociation (change in pH). Since the STP parameters, like pH, are subjected to regular monitoring and adjustment, the PNEC value for nitric acid is of low significance in the case of STP.
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PNEC – oral
Nitric acid has no bioaccumulation potential. It is an inorganic compound which is water-miscible and perfectly water-soluble. Nitric acid will dissociate in water to produce H+ and NO3–, hence bioaccumulation of nitric acid is not critical.
8.2 Exposure controls
8.2.1 Appropriate engineering controls
Use local ventilation systems where necessary. Provide safety showers and eyewash fountains in all places where skin and/or eye contact may be expected.
8.2.2 Individual protection measures
EYE AND FACE PROTECTION Chemical safety goggles in accordance with EN 166, or face shield in accordance with EN 402 (required).
HAND PROTECTION In case of possible dermal contact, use impervious protective gloves which are resistant to chemicals, in accordance with EN 374 (required), and which are made of butyl rubber, PVC or fluorinated elastomer (PTFE).
SKIN AND BODY PROTECTION Protective clothing which is resistant to chemicals (EN 14605) and chemical-resistant boots.
RESPIRATORY PROTECTION Use suitable respiratory protection items when the exposure level exceeds or may exceed the allowable values, and as appropriate for the actual exposure which may be experienced: face mask with type E (EN 14387) or with type B filter, or self-contained breathing apparatus.
HYGIENE MEASURES Do not eat, do not drink and do not smoke when handling the product. Wash hands after handling the product, before breaks for
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eating, smoking, going to a lavatory, etc. 8.2.3 Environmental exposure controls
Notify relevant authorities when the substance is discharged to atmosphere, water reservoir(s) and/or sewage system.
Production and commercial use of nitric acid may be potentially connected with emissions to water bodies and with local increase in the concentration of nitrate ions, through reduced pH value in the aqueous environment. When pH of the effluent stream is not neutralised, any discharge from the nitric acid plant may result in lower pH value of the water compartment. However, the pH parameter in the sewage stream is usually subjected to regular monitoring, hence any accidental discharge may be neutralised with ease.
SECTION 9. PHYSICAL AND CHEMICAL PROPERTIES
9.1 Information on basic physical and chemical properties
Appearance: colourless liquid at standard temperature (20°C) and pressure conditions (1013 hPa)
Odour: specific, suffocating Odour threshold: no data available pH: no data available Melting/freezing point: 232 K at 1013 hPa Initial boiling point: 356 K at 1013 hPa Boiling range: no data available Flash point: inorganic substance; no need to test for flash point Evaporation rate: no data available Flammability (solid, gas): not combustible Upper/lower explosive limit: no data available Vapour pressure: 6.1E+03 Pa at 293 K Vapour density: no data available
Relative density: 1.513 at 20°C
Water solubility: 5.0E+05 mg/l at 20°C n-Octanol/water partition
coefficient: inorganic substance, no test is required Auto-ignition temperature: not prone to auto-ignition Decomposition temperature: no data available
Viscosity: 0.75 mPa·s at 20°C
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Explosive properties: no hazard of explosion Oxidising properties: strong oxidiser
9.2 Other information
Granulometry: liquid; no test is required Dissociation constant: pKa = –1
SECTION 10. STABILITY AND REACTIVITY
10.1 Reactivity
No data available.
10.2 Chemical stability
The product is thermally stable under normal storage conditions.
10.3 Possibility of hazardous reactions
It may react vigorously with reducing agents, strong bases, organic substances, chlorides and, last but not least, with metals. It is corrosive to concrete.
10.4 Conditions to avoid
Avoid direct heating and any contact with high temperatures in order to prevent any emission of nitric acid vapours and/or any damage to the container.
10.5 Incompatible materials
Flammable materials, organic substances, reducing agents, alkalies, metal powders, hydrogen sulfide, alcohols, chlorates and carbide, carbon steel, monel metal, copper, numerous metals and alloys, flammable liquids and chromic acid.
10.6 Hazardous decomposition products
Fumes may be released upon heating which will contain NOx.
SECTION 11. TOXICOLOGICAL INFORMATION
11.1 Information on toxicological effects
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11.1.1 Metabolism
Nitrates may be reduced to nitrites, both by the gastrointestinal tract bacteria and by the activity of nitrate reductase.
11.1.2 Toxicokinetics
Nitric acid is an inorganic substance, hence some of its physical-chemical properties (e.g. octanol/water partition) have not been defined which reduces the possibility of its qualitative assessment. Nitric acid has no bioaccumulative potential since nitrates will dissolve in water easily and they will be quickly excreted via urine.
11.1.3 Dermal absorption
The absorption factor is equal to 100 % for mouth, respiratory tract and skin. For the route which starts in the mouth, the factor of 50 % is suggested with the heaviest exposure scenario assumed.
11.1.4 Acute toxicity
Oral In accordance with REACH, the acute toxicity study does not need to be conducted when the substance has been classified as corrosive to skin (column 2, Annex VIII, section 8.5).
Inhalation LC50 (inhalation): 1562.5 mg/m³ air
Skin In accordance with REACH, the acute toxicity study does not need to be conducted when the substance has been classified as corrosive to skin (column 2, Annex VIII, section 8.5).
11.1.5 Skin irritation
Nitric acid has been classified as corrosive to skin, cat. 1A (concentration ≥ 20 %), in accordance with the CLP Regulation, Annex VI, table 3.1 (Regulation (EC) 1272/2008 on classification, labelling and packaging of substances and mixtures). Therefore, no in vitro study for skin corrosion/irritation is required. In accordance with the REACH Regulation: the in vivo study does not need to be conducted if the substance is a strong acid (pH < 2) (column 2, Annex VIII, section 8.1.1).
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11.1.6 Eye irritation
Nitric acid has been classified as corrosive to skin, cat. 1A (concentration ≥ 20 %), in accordance with the CLP Regulation, Annex VI, table 3.1 (Regulation (EC) 1272/2008 on classification, labelling and packaging of substances and mixtures). Therefore, no in vitro study for eye irritation is required in accordance with the REACH Regulation (column 2, Annex VII, section 8.2). In accordance with the REACH Regulation: the in vivo study does not need to be conducted if the substance is a strong acid (pH < 2) (column 2, Annex VIII, section 8.1.1).
11.1.7 Respiratory irritation
No data available.
11.1.8 Mutagenicity
Genetic toxicity: not available Based on available tests for nitric acid, and based on numerous tests of sodium nitrate and potassium nitrate, nitric acid is found non-genotoxic.
11.1.9 Carcinogenicity
Oral No essential differences were identified in the occurrence of malignant tumours for the experimental group and control group.
Inhalation Male rat (Wistar) – NOAEC (carcinogenicity): ≥ 49 mg/m3
Skin No data available.
11.1.10 Toxicity for reproduction
11.1.10.1 Fertility
NOAEL: 1500 mg/kg bw/day
11.1.10.2 Developmental toxicity (oral)
NOAEL: 1500 mg/kg bw/day
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SECTION 12. ECOLOGICAL INFORMATION
12.1 Toxicity
12.1.1 Short-term toxicity to fish
Lethal median pH (96 h): 3-3.5 for Macrochirus lepomis Lethal median pH (96 h): about 3.7 for Oncorhynchus mykiss
12.1.2 Long-term toxicity to fish
In accordance with the REACH Regulation, section 1.5 in Annex XI, testing may be omitted.
12.1.3 Toxicity to algae and aquatic plants
In accordance with the REACH Regulation, section 1.5 in Annex XI, testing may be omitted.
12.1.4 Toxicity to soil organisms
Nitric acid is readily water-soluble, hence it will strongly acidify soil and water and it will damage any biological life (it is corrosive).
12.1.5 Toxicity to terrestrial plants
Nitric acid is readily water-soluble, hence it will strongly acidify soil and water and it will damage any biological life (it is corrosive).
12.1.6 Toxicity to terrestrial animals
No data available.
12.1.7 Microbiological activity in sewage treatment systems
In accordance with the REACH Regulation, column 2, Annex VIII, the study does not need to be conducted.
12.1.8 Mammals
No data available.
12.2 Persistence and degradability
12.2.1 Stability
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In accordance with REACH, column 2, on standard information requirements (Annex IX), the study does not need to be conducted if the substance is inorganic.
12.2.2 Hydrolysis
At the concentration of 0.1 mol/l in water, 93 % of nitric acid will undergo ionisation or dissociation. Acidity of nitric acid is about –1.4 pK.
12.2.3 Photo-transformation/photolysis
No data available. No test data are required by REACH.
12.2.4 Biodegradation in water and in sediments
In accordance with the REACH Regulation, column 2, the study does not need to be conducted if the substance is inorganic.
12.2.5 Biodegradation in soil
In accordance with the REACH Regulation, column 2, the study does not need to be conducted if the substance is inorganic.
12.3 Bioaccumulative potential
Nitric acid is readily water-soluble and it will not accumulate in the fatty tissue. Hence, the bioaccumulation studies are not considered critical.
12.4 Mobility in soil
12.4.1 Adsorption/desorption
The screening tests for adsorption/desorption (OECD 121) are not applicable for nitric acid since that substance may not be investigated with the use of the HPLC analytical method – it is inorganic. Moreover, QSAR is not applicable to inorganic substances, either.
12.4.2 Volatilisation
No information is available.
12.4.3 Distribution modelling
No information is available.
12.5 Results of PBT and vPvB assessment
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The assessment for PBT and vPvB is not essential and it is not required for inorganic substances.
12.6 Other adverse effects
No data available.
SECTION 13. DISPOSAL CONSIDERATIONS
13.1 Waste treatment methods
Waste disposal must be in compliance with the national and local waste management regulations. The appropriate disposal method should be selected depending on the local conditions and technical possibilities for disposal. Nitric acid may be neutralised with soda, with sodium carbonate or with ground limestone. Diluted solutions may be discharged to a sewage treatment plant capable of removing nitrogen compounds.
Applicable regulations
a) Directive of the European Parliament and of the Council 2008/98/EC of 19 November 2008 on waste and repealing certain Directives (OJ of 2008, vol. 51, L 312, as amended);
b) Act of 14 December 2012 on waste (Journal of Laws of 2013, item 21) along with implementing acts;
c) Act of 11 May 2001 on the obligations of some entrepreneurs with respect to the management of some waste and on the product fee and deposit fee (Journal of Laws of 2001 No. 63, item 639; consolidated text, Journal of Laws of 2007, No. 90, item 607, as amended) along with implementing acts;
d) Act of 13 June 2013 on packaging and packaging waste management (Journal of Laws of 2013, item 888).
SECTION 14. TRANSPORT INFORMATION
14.1 UN number
RID/ADR 2031 – Nitric acid ADN(R) 2031 – Nitric acid IMDG 2031 – Nitric acid ICAO/IATA 2031 – Nitric acid
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14.2 UN proper shipping name
RID/ADR Other than red fuming, with less than 65 % nitric acid ADN(R) Other than red fuming, with less than 65 % nitric acid IMDG Other than red fuming, with less than 65 % nitric acid ICAO/IATA Other than red fuming, with less than 65 % nitric acid
14.3 Transport hazard class(es)
RID/ADR 8 (classification code C1) ADN(R) 8 IMDG 8 ICAO/IATA 8
14.4 Packing group
RID/ADR II; label № 8 (nitric acid < 65 %) ADN(R) II; label № 8 (nitric acid < 65 %) IMDG II; label № 8 (nitric acid < 65 %) (EmS: F-A, S-B (nitric acid
< 65 %)) ICAO/IATA II; label № 8 (nitric acid < 65 %)
14.5 Environmental hazards
No data available.
14.6 Special precautions for user
No data available.
14.7 Transport in bulk according to Annex II of MARPOL 73/78 and the IBC Code
No data available.
SECTION 15. REGULATORY INFORMATION
15.1 Safety, health and environmental regulations/legislation specific for the substance or mixture
EU legislation
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1. Regulation (EC) № 1907/2006, of the European Parliament and of the Council, of 18 December 2006, concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) № 793/93 and Commission Regulation (EC) № 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC (Official Journal of the EU of 2006, Vol. 49, L396, with further amendments).
2. Regulation (EC) № 1272/2008, of the European Parliament and of the Council, of 16 December 2008, on classification, labelling and packaging of substances and mixtures, amending and repealing Directives 67/548/EEC and 1999/45/EC, and amending Regulation (EC) № 1907/2006 (Official Journal of the EU of 2008, Vol. 51, L353).
3. Commission Directives 2000/39/EC of 8 June 2000 and 2006/15/EC of 7 February 2006 establishing the first and second list of indicative occupational exposure limit values.
National legal regulations
a) Act of 25 February 2011 on chemicals and chemical mixtures (Journal of Laws 2011 No. 63, item 322, as amended) along with implementing acts;
b) Act of 27 April 2001, Environmental Protection Law, (Journal of Laws 2001 No. 62, item 627; consolidated text, Journal of Laws 2013 No. 1232, as amended) along with implementing acts;
c) Act of 18 July 2001, Water Law, (Journal of Laws 2001 No. 115, item 1229; consolidated text, Journal of Laws of 2012, item 145, as amended) along with implementing acts;
d) Act of 14 December 2012 on waste (Journal of Laws of 2013, item 21) along with implementing acts;
e) Act of 11 May 2001 on the obligations of some entrepreneurs with respect to the management of some waste and on the product fee and deposit fee (Journal of Laws 2001 No. 63, item 639; consolidated text, Journal of Laws 2007 No. 90, item 607, as amended) along with implementing acts;
g) Act of 13 June 2013 on packaging and packaging waste management (Journal of Laws of 2013, item 888);
h) Act of 19 August 2011 on road transport of dangerous goods (Journal of Laws 2011 No. 227, item 1367, as amended) along with implementing acts;
i) Act of 6 September 2001 on road transport (Journal of Laws 2001 No. 125, item 1371; consolidated text, Journal of Laws 2007 No. 125, item 874, as amended)
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along with implementing acts; j) Government Declaration dated 28 May 2013 on coming into effect of the
amendments to Annexes A and B of the European Agreement concerning the International Carriage of Dangerous Goods (ADR) made in Geneva on 30 September 1957 (Journal of Laws of 16 July 2013, item 815; it contains the consolidated text.
k) Act of 26 June 1974, Labour Code, (Journal of Laws 1974 No. 24, item 141; consolidated text, Journal of Laws 1998 No. 21, item 94, as amended) along with implementing acts;
l) Act of 30 August 2002 on the compliance assessment system (Journal of Laws 2005 No. 259, item 2173; consolidated text, Journal of Laws 2004 No. 204, item 2087, as amended) along with implementing acts;
m) Act of 24 August 1991 on fire protection (Journal of Laws 1991 No. 81, item 351; consolidated text, Journal of Laws 2002 No. 147, item 1229, as amended) along with implementing acts;
n) Government Declaration dated 29 June 2011 on the amendment of the scope of application of the Convention concerning International Carriage by Rail (COTIF), made in Bern on 9 May 1980 (Journal of Laws 2011 No. 180, item 1073);
o) Government Declaration dated 16 May 2011 on coming into force of the amendments to the Regulations concerning the International Carriage of Dangerous Goods by Rail (RID) which constitute the annex to the Convention concerning International Carriage by Rail (COTIF), made in Bern on 9 May 1980 (Journal of Laws 2011 No. 137, item 805).
15.2 Chemical safety assessment
Chemical safety assessment has been carried out.
SECTION 16. OTHER INFORMATION
16.1. Changes
According to REACH and CLP Regulations.
16.2 A key or legend to abbreviations and acronyms used
DNEL Derived No Effect Level. PNEC Predicted No Effect Concentration.
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NOAEC No Observable Adverse Effect Concentration. NOAEL No Observable Adverse Effect Level. LCx Lethal Concentration x %. LDx Lethal Dose x %. PBT Persistent, Bioaccumulative and Toxic. vPvB Very Persistent and Very Bioaccumulative. EC EC list comprises three earlier European lists of chemicals which have been
put together pursuant to EU legal provisions: EINECS, ELINCS and “No-longer polymers” (NLP) list.
CAS Chemical Abstracts Service. IUPAC International Union of Pure and Applied Chemistry. REACH Registration, Evaluation, Authorisation and restriction of Chemicals. CLP Classification, labelling and packaging of chemical substances and mixtures MAC Maximum Admissible Concentration MAC (STEL) Maximum Admissible Short-Term Concentration
ECx Effective concentration which inhibits the x% growth of the population under investigation
ADR International Agreement concerning the International Carriage of Dangerous Goods by Road
RID Regulations concerning the International Carriage of Dangerous Goods by Rail
UN United Nations MAC(C) Maximum Admissible Ceiling Concentration BLV Biological Limit Value ES Exposure Scenario
16.3 Key literature references and sources for data
1. Nitric acid – registration dossier. 16.4 Advice on training
1. An employer is obliged to inform all the workers who come into contact with nitric acid about risks and personal protection equipment listed in the MSDS
2. The distributor/downstream user is obliged to give the recipient the information contained in the MSDS
16.5 In place of
This Material Safety Data Sheet is NOT any product quality specification, and it may NOT be understood as any guarantee for the product quality or for the product compliance with the client’s requirements for individual applications. The purpose of this MSDS is to provide the guidelines for safe handling of the product (occupational safety and environmental protection), its transport and storage. The figures and data specified herein are based on our current knowledge and on current legislation. The
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clients should verify that information against the provisions of the laws and/or regulations which are valid in their countries and/or companies.