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.
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Move the victim into fresh air. If breathing is difficult, give oxygen. If not breathing, give artificial respiration and consult a doctor immediately. Do not use mouth to mouth resuscitation if the victim ingested or inhaled the chemical.
Take off contaminated clothing immediately. Wash off with soap and plenty of water. Consult a doctor.
Rinse with pure water for at least 15 minutes. Consult a doctor.
Rinse mouth with water. Do not induce vomiting. Never give anything by mouth to an unconscious person. Call a doctor or Poison Control Center immediately.
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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 if necessary. Immediately flush contaminated eyes with gently flowing water. Do not induce vomiting. If vomiting occurs, lean patient forward or place on the 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. Poisons A and B
Do not use a direct water stream; it may spread the fire. Use water fog or fine spray, carbon-dioxide or dry-chemical extinguishers, or foam. Water fog applied gently may be used as a blanket to extinguish the fire.
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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.
Prevent further spillage or leakage if it is safe to do so. Do not let the chemical enter drains. Discharge into the environment must be avoided.
If a large spill does occur, contain spilled material if possible. Pump the contained material into suitable and properly labeled containers using appropriate safety equipment.
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.
Store PPh in carbon steel, stainless steel, or phenolic-lined steel drums. Do not store in aluminum, copper, galvanized iron, or galvanized steel.
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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.
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Liquid.
Clear, colourless.
Mild odor
11 °C.
241.2 °C. Atm. press.:1 013.25 hPa.
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Ca. 239 °F. Atm. press.:Ca. 760 mm Hg.
Ca. 480 °C. Atm. press.:Ca. 1 013 hPa.
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dynamic viscosity (in mPa s) = 22.7. Temperature:25.0°C.
In water, 15.1 g/L at 20 deg C
log Pow = 1.41. Temperature:24.1 °C.;log Pow = 1.48. Temperature:24.1 °C.;log Pow = 1.49. Temperature:24.1 °C.
0.01 hPa. Temperature:20 °C.
1.06. Temperature:20 °C.
5.27 (Air = 1)
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PPh is thermally stable at typical use temperatures...PPh can decompose at elevated temperatures.
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PPh is incompatible with strong acids, strong bases, and strong oxidizers and contact should be avoided.
Decomposition products depend upon the temperature, air supply, and the presence of other materials, but can include aldehydes, ketones, organic acids, and other compounds.
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AEROBIC: In aerobic soil biodegradation studies using two sandy loam soils and one sandy soil collected in Michigan, propylene glycol phenyl ether had an initial 50% removal rate of <1 day in the sandy loam soils and <5 days in the sandy soil at initial concentrations of 1.4-1.5 ppm(1); at initial concentrations of 107-108 ppm, 50% removal was <5 days in the sandy loam soils and <23 days in the sandy soil(1); maximum percentage of 14-CO2 evolved ranged from 31-66%(1); negligible removal occurred in sterile soil controls(1). Using the three Michigan soils, after 2 months under anaerobic conditions (at a nominal concentration of 10 ppm), a 16% reduction in propylene glycol phenyl ether was observed in sodium acetate supplemented microcosms whereas, in the sterile controls, a 7% reduction was observed(2). Using OECD Guideline 301F (Manometric Respirometry Test) with a sediment and activated sludge inoculum, propylene glycol phenyl ether had a 60% degradation in 9.8 days and 72% degradation in 28 days which met the criteria for being classified as readily biodegradable(2). 20-Day BODs of 42% and 50% have been reported for propylene glycol phenyl ether using a municipal seed and an industrial seed, respectively, but additional test conditions were unavailable(2). Using a mixture of phenoxypropanols (85% propylene glycol phenyl ether and 15% 2-phenoxy-1-propanol) at an initial concentration of 420-500 mg/L with the Zahns-Wellens test in accordance with OECD guidelines, approximately 88% of the mixture biodegraded in 18 days of incubation using non-adapted microorganisms from a sewage plant as inoculum(3); using adapted sewage plant microorganism, approximately 85% of the mixture biodegraded in 11 days(3); using microorganisms isolated from the Elbe River, approximately 90% of the mixture biodegraded in 21 days(3).
An estimated BCF of 2.5 was calculated in fish for propylene glycol phenyl ether(SRC), using a log Kow of 1.50(1) and a regression-derived equation(2). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).
Using a structure estimation method based on molecular connectivity indices(1), the Koc of propylene glycol phenyl ether can be estimated to be 23(SRC). According to a classification scheme(2), this estimated Koc value suggests that propylene glycol phenyl ether is expected to have very high mobility in soil.
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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