Not classified.
none
none
none
none
none
no data available
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. Give one or two glasses of water to drink. Refer for medical attention .
Symptoms unlikely from any form of exposure. (USCG, 1999)
Inhalation: remove to fresh air. Eyes: flush with water. Skin: flush with water, wash well with soap and water.
To fight fire, use water spray, mist, foam.
Special Hazards of Combustion Products: Irritating vapors of unburned chemical may form in fire. (USCG, 1999)
Use alcohol-resistant foam, powder, carbon dioxide.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Collect leaking and spilled liquid in sealable containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
Personal protection: particulate filter respirator adapted to the airborne concentration of the substance. Do NOT let this chemical enter the environment. Collect leaking and spilled liquid in sealable containers as far as possible. Absorb remaining liquid in sand or inert absorbent. Then store and dispose of according to local regulations.
Environmental considerations-land spill: Dig a pit, pond, lagoon, holding area to contain liquid or solid material. Dike surface flow using soil, sand bags, foamed polyurethane, or foamed concrete. Absorb bulk liquid with fly ash, cement powder, or commercial sorbents. SRP: If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner.
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.
Storage temp: ambient; venting: open.
TLV: 5 mg/m3, as TWA; A4 (not classifiable as a human carcinogen)
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 spectacles.
Protective gloves.
Use ventilation. Use local exhaust.
no data available
Liquid. Oily.
Colourless.
Practically odorless
-40.5 °C. Atm. press.:101.3 kPa.
295 °C. Atm. press.:101.3 kPa.
Class IIIB Combustible Liquid: Fl.P. at or above 200°F.; however, ignition is difficult.
Lower flammable limit: 0.7% by volume at 368 deg F (186 deg C)
162.7 °C. Atm. press.:101.3 kPa.
457 °C. Atm. press.:1 013 hPa.
no data available
no data available
31.3 centistokes at 0 deg C
less than 1 mg/mL at 66° F (NTP, 1992)
log Pow = 2.47. Remarks:No data on temp and pH.
0 mm Hg. Temperature:25 °C.
1.12 g/cm3. Temperature:25 °C.
7.66 (vs air)
no data available
Decomposes on heating and on burning. This produces toxic fumes and gases (phthalic anhydride - see ICSC 0315). Attacks some plastics.
Stable to light
CombustibleDIETHYL 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
May attack some forms of plastics.
When heated to decomp it emits acrid smoke and irritating fumes.
no data available
no data available
no data available
no data available
Cancer Classification: Group D Not Classifiable as to Human Carcinogenicity
no data available
no data available
no data available
A harmful contamination of the air will not or will only very slowly be reached on evaporation of this substance at 20°C.
AEROBIC: The aerobic half-life of diethyl phthalate in natural fresh water was estimated as 3 days(1). Diethyl phthalate was found to degrade to ethyl methyl phthalate, dimethyl phthalate, methyl phthalate and ethyl phthalate when co-contaminated with methanol(2). A shake flask experiment using microorganisms isolated from a municipal sludge resulted in complete aerobic degradation of 400 mg/L of diethyl phthalate in approximately 35 hours, 200 mg/L in 25 hours, 140 mg/L in 22 hours and 75 mg/L in 18 hours(3). Diethyl phthalate was completely degraded by Rhine River water at 20 deg C in a 3 day die-away test(4). Diethyl phthalate was 87-92% degraded in 10-50 days at 25 deg C from a concn of 100 mg/L using 30 mg/L activated sludge(5). Electrolytic respirometer studies have shown that diethyl phthalate is readily biodegradable under aerobic conditions(6-8). Diethyl phthalate had aerobic aquatic half-lives of 0.39 days in a river die-away test, 4.33 days in MITI test, and 0.71 days using microcosm periphlton, and an aerobic soil half-life of 1.83 days agitated in aqueous suspension(9).
Bluegill sunfish exposed to 9.42 ug/L of diethyl phthalate for 21 days had a measured BCF of 117(1). According to a classification scheme(2), this BCF value suggests that bioconcentration in aquatic organisms is high(SRC). An experimental log BCF of 2.07 was measured in clams(3).
A Koc value of diethyl phthalate of 1,726 was measured in podzol soil at pH 2.8 and 4.85% carbon, a value of 704 in alfisol soil at pH 6.7 and 1.25% carbon, a value of 320 in sediment at pH 7.1 and 1.58% carbon(1). An experimental log Koc of 1.99 was determined from unsaturated soil columns at pH 4.8(2). A Koc value of 69 was determined from measurements on soil samples from Broome County, NY(3). According to a classification scheme(4), these Koc values suggest that diethyl phthalate is expected to have low to high mobility in soil.
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