DGT® SolventGlue EC.7

Remove to open air. If the subject stops breathing, administer artificial respiration. Get medical advice/attention immediately.

Remove contaminated clothing. Rinse skin with a shower immediately. Wash contaminated clothing before using it again.

Remove contact lenses, if present. Wash immediately with plenty of water for at least 15 minutes, opening the eyelids fully. If problem persists, seek medical advice.

Get medical advice/attention immediately. Do not induce vomiting. Do not administer anything not explicitly authorised by a doctor.

carbon dioxide, foam, chemical powder. For product loss or leakage that has not caught fire, water spray can be used to disperse flammable vapours and protect those trying to stem the leak.

Do not use jets of water. Water is not effective for putting out fires but can be used to cool containers exposed to flames to prevent explosions.

Excess pressure may form in containers exposed to fire at a risk of explosion. Do not breathe combustion products. Heat may cause the product to polymerise, which could lead to explosion.

Water is not effective for putting out fires but can be used to cool containers exposed to flames to prevent explosions.

Block the leakage if there is no hazard.

The product must not penetrate into the sewer system or come into contact with surface water or ground water.

Absorb the remainder with inert absorbent material.

Materials: inert absorbent material

Keep away from heat, sparks and naked flames; do not smoke or use matches or lighters. Avoid bunching of electrostatic charges. When performing transfer operations involving large containers, connect to an earthing system and wear antistatic footwear. Vigorous stirring and flow through the tubes and equipment may cause the formation and accumulation of electrostatic charges. In order to avoid the risk of fires and explosions, never use compressed air when handling. Open containers with caution as they may be pressurised.

Store only in the original container. Store the containers sealed, in a well ventilated place, away from direct sunlight. Store in a cool and well ventilated place, keep far away from sources of heat, naked flames and sparks and other sources of ignition.

Do not eat, drink or smoke during use.

Keep away from heat, sparks and naked flames; do not smoke or use matches or lighters. Avoid bunching of electrostatic charges.

As the use of adequate technical equipment must always take priority over personal protective equipment, make sure that the workplace is well aired through effective local aspiration.

Protect hands with category III work gloves (see standard EN 374). The following should be considered when choosing work glove material: compatibility, degradation, failure time and permeability. The work gloves' resistance to chemical agents should be checked before use, as it can be unpredictable. The gloves' wear time depends on the duration and type of use.

Wear airtight protective goggles (see standard EN 166).

If the threshold value (e.g. TLV-TWA) is exceeded for the substance or one of the substances present in the product, wear a mask with a type AX filter, whose limit of use will be defined by the manufacturer (see standard EN 14387). In the presence of gases or vapours of various kinds and/or gases or vapours containing particulate (aerosol sprays, fumes, mists, etc.) combined filters are required. Respiratory protection devices must be used if the technical measures adopted are not suitable for restricting the worker's exposure to the threshold values considered. The protection provided by masks is in any case limited. If the substance considered is odourless or its olfactory threshold is higher than the corresponding TLV-TWA and in the case of an emergency, wear open-circuit compressed air breathing apparatus (in compliance with standard EN 137) or external air-intake breathing apparatus (in compliance with standard EN 138). For a correct choice of respiratory protection device, see standard EN 529.

Wear category II professional long-sleeved overalls and safety footwear (see Regulation 2016/425 and standard EN ISO 20344). Wash body with soap and water after removing protective clothing. Consider the appropriateness of providing antistatic clothing in the case of working environments in which there is a risk of explosion.

The emissions generated by manufacturing processes, including those generated by ventilation equipment, should be checked to ensure compliance with environmental standards.

The product is stable in normal conditions of use and storage.

There are no particular risks of reaction with other substances in normal conditions of use. 2-PHENOXYETHANOL: In water at 1% reacts to form a weak acid (pH=6). ETHYL ACETATE: Decomposes slowly into acetic acid and ethanol under the effect of light, air and water. DICHLOROMETHANE: Decomposes at temperatures above 120°C/248°F. With water and alkalis it may form hydrochloric acid and attack aluminium, copper and alloys.

The vapours may also form explosive mixtures with the air. ETHYL ACETATE: Risk of explosion on contact with: alkaline metals, hydrides, oleum. May react violently with: fluorine, strong oxidising agents, chlorosulphuric acid, potassium tert-butoxide. Forms explosive mixtures with: air. ETHANOL: Risk of explosion on contact with: alkaline metals, alkaline oxides, calcium hypochlorite, sulphur monofluoride, acetic anhydride, acids, concentrated hydrogen peroxide, perchlorates, perchloric acid, perchloronitrile, mercury nitrate, nitric acid, silver, silver nitrate, ammonia, silver oxide, ammonia, strong oxidising agents, nitrogen dioxide. May react dangerously with: bromoacetylene, chlorine acetylene, bromine trifluoride, chromium trioxide, chromyl chloride, fluorine, potassium tert-butoxide, lithium hydride, phosphorus trioxide, black platinum, zirconium (IV) chloride, zirconium (IV) iodide. Forms explosive mixtures with: air. DICHLOROMETHANE: Risk of explosion on contact with: alkaline metals, nitric acid, aluminium powder, ethanediamine, aluminium chloride, perchloric acid, dinitrogen pentoxide, sodium nitride, n-nitroso n-methylurea, potassium hydroxide. May react dangerously with: alkaline earth metals, metal powders, sodium amides, potassium tert-butylate. May form explosive mixtures with: air. METHYL METHACRYLATE: May polymerise on contact with: ammonia, organic peroxides, persulphates. Risk of explosion on contact with: dibenzoyl peroxide, diterbutyl peroxide, propionaldehyde. May react dangerously with: strong oxidising agents. Forms explosive mixtures with: air.

Avoid overheating. Avoid bunching of electrostatic charges. Avoid all sources of ignition. Ethyl Acetate: Avoid exposure to: light, sources of heat, naked flames. Ethanol: Avoid exposure to: sources of heat, naked flames. Dichloromethane: Avoid exposure to: naked flames, overheated surfaces. Methyl Methacrylate: Avoid exposure to: heat, UV rays. Avoid contact with: oxidising substances, reducing substances, acids, bases.

Methyl Methacrylate: oxidising substances, reducing substances, acids, bases.

In the event of thermal decomposition or fire, gases and vapours that are potentially dangerous to health may be released. DICHLOROMETHANE: May develop: dioxins, phosgenes, hydrochloric acid. METHYL METHACRYLATE: When heated to decomposition releases: harsh fumes, zinc alloys.

Disposal must be performed through an authorised waste management firm, in compliance with national and local regulations.

Reuse, when possible. Product residues should be considered special hazardous waste. The hazard level of waste containing this product should be evaluated according to applicable regulations.

HIN - Kemler: 30 Special provision: - EMS: F-E, S-D

HIN - Kemler: 30 Special provision: - EMS: F-E, S-D

HIN - Kemler: 30 Special provision: - EMS: F-E, S-D