no data available
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Fresh air, rest.
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. Rest.
No symptoms reported for any rate of exposure. (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. Esters and related compounds
Extinguish with dry chemical, foam or carbon dioxide. Water may be ineffective on fire.
This chemical is combustible. (NTP, 1992)
Wear self-contained breathing apparatus for firefighting if necessary.
Avoid dust formation. Avoid breathing mist, gas or vapours.Avoid contacting with skin and eye. Use personal protective equipment.Wear chemical impermeable gloves. Ensure adequate ventilation.Remove all sources of ignition. Evacuate personnel to safe areas.Keep people away from and upwind of spill/leak.
Collect leaking and spilled liquid in sealable plastic or metal containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
ACCIDENTAL RELEASE MEASURES Personal precautions, protective equipment and emergency procedures Use personal protective equipment. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. For personal protection see section Environmental precautions Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Methods and materials for containment and cleaning up Keep in suitable, closed containers for disposal.
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.
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.
no data available
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Ensure adequate ventilation. Handle in accordance with good industrial hygiene and safety practice. Set up emergency exits and the risk-elimination area.
Wear tightly fitting safety goggles with side-shields conforming to EN 166(EU) or NIOSH (US).
Wear fire/flame resistant and impervious clothing. Handle with gloves. Gloves must be inspected prior to use. Wash and dry hands. The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and the standard EN 374 derived from it.
If the exposure limits are exceeded, irritation or other symptoms are experienced, use a full-face respirator.
no data available
Clear liquid
Mild odor
-50°C
425.8°C at 760 mmHg
Combustible.
Lower flammable limit: 0.3% by volume at 508 deg F
227.6°C
755° F (USCG, 1999)
no data available
no data available
108 cP at 20 deg C
Insoluble (NTP, 1992)
log Kow = 10.36 (est)
5.28X10-7 mm Hg at 25 deg C
0.964g/cm3
15.4 (NTP, 1992) (Relative to Air)
no data available
Attacks some forms of plastic.
Stable under recommended storage conditions.
CombustibleDIISODECYL PHTHALATE is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Can generate electrostatic charges. [Handling Chemicals Safely 1980. p. 250].
no data available
Strong oxidizing agents
When heated to decomposition it emits acrid smoke and irritating vapors.
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AEROBIC: In a semi-continuous activated sludge test (Soap and Detergent Association biodegradation test method), the mean degradation for diisodecyl phthalate was 68% in 24 hr(1). In a die-away phase of the testing, it took 9 days to achieve 90% degradation(1). Diisodecyl phthalate is confirmed to be degradable in the screening procedure of the Japanese Ministry of Trade and Industry (MITI) which uses a mixed inoculum derived from soil, fresh water and sewage(2). In an acclimated shake flask CO2 evolution test, loss of parent compound (primary degradation) as well as CO2 evolution (ultimate degradation) was measured using an inoculum prepared from soil and sewage, >99% of diisodecyl phthalate was lost and 56% of theoretical CO2 was evolved after 28 days(3). The biodegradation half-life was 9.6 days with a 4.9 day lag(3). Diisodecyl phthalate, present at 100 mg/L, reached 2% of its theoretical BOD in 2 weeks using an activated sludge inoculum at 30 mg/L in the Japanese MITI test(4). Diisodecyl phthalate, present at a concentration of 100 ppm, was degraded 14 and 30% after three days cultivation in water from the Mino River and Akashi Beach, Japan, respectively(5). Diisodecyl biodegraded 67% from an initial concentration of 48 ppm and 100 ppm in 28 days in activated sludge at 22 and 25 deg C, respectively(6). Diisodecyl phthalate degraded 42% in 21 days at 25 deg C from a starting concentration of 100 ppm(6). An aerobic aquatic half-life of 23 days was given for diisodecyl phthalate(7).
BCFs of <3.6 and <14.4 were measured for diisodecyl phthalate at chemical concentrations of 1 and 0.1 mg/L, respectively, using carp (Cyprinus carpio) which were exposed over an 8-week period(1). According to a classification scheme(2), these BCFs suggest that bioconcentration in aquatic organisms is low(SRC). The mean log BCF of diisodecyl phthalate in Daphnia magna as determined in a 21 day test using ring-labeled chemical was 2.06(3), corresponding to a BCF of 115(SRC). The mean log BCF in mussels (Mytilus edulis) was 3.54 between 14 and 28 days also using ring-labeled ester(4), corresponding to a BCF of 3467(SRC). However depuration was rapid in mussels, the half-life being 3.5 days(4).
Using a structure estimation method based on molecular connectivity indices(1), the log Koc of diisodecyl phthalate can be estimated to be 6.04(SRC). Other estimated log Koc values reported were 5.46 and 5.78(2). According to a classification scheme(3), these estimated log Koc values suggest that diisodecyl phthalate is expected to be immobile in soil. The average Koc of (14)C-diisodecyl phthalate using three standard USEPA sediments (supplied and characterized by the EPA) was measured at 2.86X10+5(4).
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: no data available
IMDG: no data available
IATA: no data available
ADR/RID: no data available
IMDG: no data available
IATA: no data available
ADR/RID: no data available
IMDG: no data available
IATA: no data available
ADR/RID: no data available
IMDG: no data available
IATA: no data available
ADR/RID: No
IMDG: No
IATA: No
no data available
no data available
The information in this MSDS is only applicable to the specified product, unless otherwise specified, it is not applicable to the mixture of this product and other substances. This MSDS only provides information on the safety of the product for those who have received the appropriate professional training for the user of the product. Users of this MSDS must make independent judgments on the applicability of this SDS. The authors of this MSDS will not be held responsible for any harm caused by the use of this MSDS.