Eye irritation, Category 2
H319 Causes serious eye irritation
P264 Wash ... thoroughly after handling.
P280 Wear protective gloves/protective clothing/eye protection/face protection/hearing protection/...
P305+P351+P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
none
none
no data available
Fresh air, rest.
Remove contaminated clothes. Rinse and then wash skin with water and soap.
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 one or two glasses of water to drink. Refer for medical attention .
Vapor is irritating to the mucous membrane of the eye and respiratory tract. Inhalation can cause dizziness, nausea, some anesthesia. Very high concentrations have a narcotic effect. The liquid is not highly irritating to the skin but can cause dermatitis. (USCG, 1999)
Absorption ... occurs readily from the lung.
Alcohol foam, foam, carbon dioxide, dry chemical .
Excerpt from ERG Guide 129 [Flammable Liquids (Water-Miscible / Noxious)]: HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Those substances designated with a (P) may polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. (ERG, 2016)
Use water spray, alcohol-resistant foam, dry powder, carbon dioxide. In case of fire: keep drums, etc., cool by spraying with water.
Remove all ignition sources. Personal protection: filter respirator for organic gases and vapours adapted to the airborne concentration of the substance. Cover the spilled material with inert absorbent. Carefully collect remainder.
Remove all ignition sources. Personal protection: filter respirator for organic gases and vapours adapted to the airborne concentration of the substance. Cover the spilled material with inert absorbent. Carefully collect remainder.
Collect and arrange disposal. Keep the chemical in suitable and closed containers for disposal. Remove all sources of ignition. Use spark-proof tools and explosion-proof equipment. Adhered or collected material should be promptly disposed of, in accordance with appropriate laws and regulations.
NO open flames, NO sparks and NO smoking. Above 58°C use a closed system, ventilation and explosion-proof electrical equipment. Use non-sparking handtools. 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.
Fireproof. Separated from acids, bases, amines and oxidants.... MATERIALS WHICH ARE TOXIC AS STORED OR WHICH CAN DECOMPOSE INTO TOXIC COMPONENTS ... SHOULD BE STORED IN A COOL WELL-VENTILATED PLACE, OUT OF THE DIRECT RAYS OF THE SUN, AWAY FROM AREAS OF HIGH FIRE HAZARD, AND SHOULD BE PERIODICALLY INSPECTED ... INCOMPATIBLE MATERIALS SHOULD BE ISOLATED .
TLV: 50 ppm as TWA.MAK: 96 mg/m3, 20 ppm; peak limitation category: I(2); skin absorption (H); pregnancy risk group: D
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.
Protective gloves. Protective clothing.
Use ventilation, local exhaust or breathing protection.
no data available
Liquid.
COLORLESS LIQUID
FAINT PLEASANT ODOR
-44 °C.
167.9 °C. Atm. press.:760 Torr.
Class II Combustible Liquid: Fl.P. at or above 100°F and below 140°F.
1.8% LOWER & 6.9% UPPER
63.5 °C. Atm. press.:101.3 kPa.;62.5 °C. Atm. press.:101.3 kPa.;61 °C. Atm. press.:101.3 kPa.
643 °C. Atm. press.:1.013 atm. Remarks:Atmospheric pressure is not reported. An atm pressure is only added for TCC reasons.
no data available
no data available
dynamic viscosity (in mPa s) = 28.7. Temperature:-25.0°C.;dynamic viscosity (in mPa s) = 6.621. Temperature:0.0°C.;dynamic viscosity (in mPa s) = 2.798. Temperature:25.0°C.
Miscible with water
log Pow = 1.9. Remarks:Temperature was not reported.
1 mm Hg. Temperature:68 °F. Remarks:Reported as 1 mm Hg at 68oF.;1.35 hPa. Temperature:20 °C. Remarks:Converted from the value in mmHg and °F.
0.9 a relative density doesn't have unit. Temperature:20 °C.
4 (vs air)
no data available
1800 ppm [Based on 10% of the lower explosive limit for safety considerations even though the relevant toxicological data indicated that irreversible health effects or impairment of escape existed only at higher concentrations.]
Decomposes on heating or on burning or on contact with acids, bases and amines. This produces acetone and mesityl alcohol. Reacts violently with oxidants. This produces flammable/explosive gas (hydrogen - see ICSC 0001).
Decomposed by prolonged exposure to alkalis & by distillation at atmospheric pressure
MODERATE WHEN EXPOSED TO HEAT OR FLAME ...Acetyl bromide reacts violently with alcohols or water, [Merck 11th ed., 1989]. Mixtures of alcohols with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. Example: An explosion will occur if dimethylbenzylcarbinol is added to 90% hydrogen peroxide then acidified with concentrated sulfuric acid. Mixtures of ethyl alcohol with concentrated hydrogen peroxide form powerful explosives. Mixtures of hydrogen peroxide and 1-phenyl-2-methyl propyl alcohol tend to explode if acidified with 70% sulfuric acid, [Chem. Eng. News 45(43):73(1967); J, Org. Chem. 28:1893(1963)]. Alkyl hypochlorites are violently explosive. They are readily obtained by reacting hypochlorous acid and alcohols either in aqueous solution or mixed aqueous-carbon tetrachloride solutions. Chlorine plus alcohols would similarly yield alkyl hypochlorites. They decompose in the cold and explode on exposure to sunlight or heat. Tertiary hypochlorites are less unstable than secondary or primary hypochlorites, [NFPA 491 M, 1991]. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)].
no data available
Strong oxidizers, strong alkalis.
When heated to decomp it emits acrid smoke and fumes.
no data available
no data available
no data available
no data available
no data available
no data available
The substance is irritating to the eyes, skin and respiratory tract. If this liquid is swallowed, aspiration into the lungs may result in chemical pneumonitis. Exposure far above the OEL could cause lowering of consciousness.
The substance defats the skin, which may cause dryness or cracking.
A harmful contamination of the air will not or will only very slowly be reached on evaporation of this substance at 20°C.
Two sets of tests using acclimated mixed microbial cultures as inoculum gave percent theoretical BOD of 47%(1) and 46%(2) after 5 days for 4-hydroxy-4-methyl-2-pentanone under aerobic conditions(1,2). A percent theoretical BOD of 3% was observed after 5 days in screening tests using the standard dilution technique under aerobic conditions and effluent sewage from a biological sanitary waste treatment plant as inoculum; 31% theoretical BOD was observed after 5 days using adapted effluent sewage(3). No information regarding biodegradation in natural media was found(SRC).
An estimated BCF of 0.50 can be calculated(SRC) from an estimated log Kow of -0.098(2) using a recommended regression equation(1). Based upon the estimated BCF and the reported infinite solubility of the compound in water(3), 4-hydroxy-4-methyl-2-pentanone will not be expected to significantly bioconcentrate in aquatic organisms(SRC).
An estimated Koc of 21 can be calculated(SRC) from an estimated log Kow of -0.098(2) using a recommended regression equation(1). Based upon the estimated Koc and the reported infinite solubility of the compound in water(3), 4-hydroxy-4-methyl-2-pentanone will not be expected to strongly adsorb to sediment or suspended particulate matter(4,SRC). It will be expected to exhibit very high mobility in soil(4), and therefore, 4-hydroxy-4-methyl-2-pentanone may leach through soil to groundwater if it does not volatilize or biodegrade first(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: UN1148 (For reference only, please check.)
IMDG: UN1148 (For reference only, please check.)
IATA: UN1148 (For reference only, please check.)
ADR/RID: DIACETONE ALCOHOL (For reference only, please check.)
IMDG: DIACETONE ALCOHOL (For reference only, please check.)
IATA: DIACETONE ALCOHOL (For reference only, please check.)
ADR/RID: 3 (For reference only, please check.)
IMDG: 3 (For reference only, please check.)
IATA: 3 (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
This card is only valid for the pure substance.The technical product may contain up to 5% acetone (see ICSC 0087), resulting in high flammability.Other UN Classification for technical product: UN hazard class 3, UN pack group II.