0890 106 - WURTH ANTI-SQUEAK SPRAY
ChemWatch Material Safety Data Sheet
Issue Date: Mon 31-Jan-2005
CHEMWATCH 63497
0890 106 - WURTH ANTI-SQUEAK SPRAY
Manufacturer's Code 0890 106
AEROSOLS
Applied to break pad backing to prevent squealing. Application is by spray atomisation
from a hand held aerosol pack
Company: Wurth Australia Pty Ltd
Address:
4 Redwood Drive (abn 48 002 487 096)
Dingley
VIC, 3175
AUSTRALIA
Telephone: (+61 3) 9552 9552
Telephone: 1800 331 603
Emergency Tel: 1300 657 765
Fax: 03 9551 2994
HAZARDOUS SUBSTANCE. DANGEROUS GOODS.
According to the Criteria of NOHSC, and the ADG Code.
S5
Extremely flammable.
Irritating to eyes.
Risk of explosion if heated under confinement.
Harmful: danger of serious damage to health by prolonged exposure through
inhalation.
Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic
environment.
Possible risk of impaired fertility.
Vapours may cause drowsiness and dizziness.
Keep container in a well ventilated place.
Avoid exposure - obtain special instructions before use.
To clean the floor and all objects contaminated by this material, use water and
detergent.
Keep container tightly closed.
Keep away from food, drink and animal feeding stuffs.
Take off immediately all contaminated clothing.
In case of contact with eyes, rinse with plenty of water and contact Doctor or
Poisons Information Centre.
If swallowed, IMMEDIATELY contact Doctor or Poisons Information Centre. (show
this container or label).
If you feel unwell contact Doctor or Poisons Information Centre. (Show the label
if possible).
| NAME | CAS RN | % |
| acetone | 67-64-1 | 10-30 |
| naphtha petroleum, light, hydrotreated | 64742-49-0. | 10-30 |
| ethyl acetate | 141-78-6 | 1-30 |
| propane | 74-98-6 | 10-30 |
For advice, contact a Poisons Information Centre or a doctor.
· If swallowed do NOT induce vomiting.
· If vomiting occurs, lean patient forward or place on left side (head-down
position, if possible) to maintain open airway and prevent aspiration.
· Observe the patient carefully.
· Never give liquid to a person showing signs of being sleepy or with reduced
awareness; i.e. becoming unconsciousness
· Give water to rinse out mouth, then provide liquid slowly and as much as
casualty can comfortably drink.
· Seek medical advice.
If this product comes in contact with the eyes:
· Immediately hold eyelids apart and flush the eye continuously with running
water.
· Ensure complete irrigation of the eye by keeping eyelids apart and away from
eye and moving the eyelids by occasionally lifting the upper and lower lids.
· Continue flushing until advised to stop by the Poisons Information Centre or a
doctor, or for at least 15 minutes.
· Transport to hospital or doctor without delay.
· Removal of contact lenses after an eye injury should only be undertaken by
skilled personnel.
If solids or aerosol mists are deposited upon the skin:
· Flush skin and hair with running water (and soap if available).
· Remove any adhering solids with industrial skin cleansing cream.
· DO NOT use solvents.
· Seek medical attention in the event of irritation.
· If fumes or combustion products are inhaled remove from contaminated area.
· Lay patient down. Keep warm and rested.
· Prostheses such as false teeth, which may block airway, should be removed,
where possible, prior to initiating first aid procedures.
· Apply artificial respiration if not breathing, preferably with a demand valve
resuscitator, bag-valve mask device, or pocket mask as trained. Perform CPR if
necessary.
· Transport to hospital, or doctor.
For acute or short term repeated exposures to petroleum distillates or related hydrocarbons: · Primary threat to life, from pure petroleum distillate ingestion and/or inhalation, is respiratory failure. · Patients should be quickly evaluated for signs of respiratory distress (e.g. cyanosis, tachypnoea, intercostal retraction, obtundation) and given oxygen. Patients with inadequate tidal volumes or poor arterial blood gases (pO2 50 mm Hg) should be intubated. · Arrhythmias complicate some hydrocarbon ingestion and/or inhalation and electrocardiographic evidence of myocardial injury has been reported; intravenous lines and cardiac monitors should be established in obviously symptomatic patients. The lungs excrete inhaled solvents, so that hyperventilation improves clearance. · A chest x-ray should be taken immediately after stabilisation of breathing and circulation to document aspiration and detect the presence of pneumothorax. · Epinephrine (adrenalin) is not recommended for treatment of bronchospasm because of potential myocardial sensitisation to catecholamines. Inhaled cardioselective bronchodilators (e.g. Alupent, Salbutamol) are the preferred agents, with aminophylline a second choice. · Lavage is indicated in patients who require decontamination; ensure use of cuffed endotracheal tube in adult patients. [Ellenhorn and Barceloux: Medical Toxicology]
· Water spray or fog.
· Foam.
· Dry chemical powder.
· BCF (where regulations permit).
· Carbon dioxide.
· Alert Fire Brigade and tell them location and nature of hazard.
· May be violently or explosively reactive.
· Wear breathing apparatus plus protective gloves.
· Prevent, by any means available, spillage from entering drains or water
course.
· If safe, switch off electrical equipment until vapour fire hazard removed.
· Use water delivered as a fine spray to control fire and cool adjacent area.
· DO NOT approach containers suspected to be hot.
· Cool fire exposed containers with water spray from a protected location.
· If safe to do so, remove containers from path of fire.
· Equipment should be thoroughly decontaminated after use.
When any large container (including road and rail tankers) is involved in a fire,
consider evacuation by 100 metres in all directions.
· Liquid and vapour are highly flammable.
· Severe fire hazard when exposed to heat or flame.
· Vapour forms an explosive mixture with air.
· Severe explosion hazard, in the form of vapour, when exposed to flame or
spark.
· Vapour may travel a considerable distance to source of ignition.
· Heating may cause expansion or decomposition with violent container rupture.
· Aerosol cans may explode on exposure to naked flames.
· Rupturing containers may rocket and scatter burning materials.
· Hazards may not be restricted to pressure effects.
· May emit acrid, poisonous or corrosive fumes.
· On combustion, may emit toxic fumes of carbon monoxide (CO).
Other combustion products include carbon dioxide (CO2)
Avoid contamination with strong oxidising agents as ignition may result
2Y
PERSONAL PROTECTION EQUIPMENT
Breathing apparatus.
Gas tight chemical resistant suit.
Limit exposure duration to 1 BA set - 30 mins.
· Clean up all spills immediately.
· Avoid breathing vapours and contact with skin and eyes.
· Wear protective clothing, impervious gloves and safety glasses.
· Shut off all possible sources of ignition and increase ventilation.
· Wipe up.
· If safe, damaged cans should be placed in a container outdoors, away from all
ignition sources, until pressure has dissipated.
· Undamaged cans should be gathered and stowed safely.
· Clear area of personnel and move upwind.
· Alert Fire Brigade and tell them location and nature of hazard.
· May be violently or explosively reactive.
· Wear breathing apparatus plus protective gloves.
· Prevent, by any means available, spillage from entering drains or water
courses
· No smoking, naked lights or ignition sources.
· Increase ventilation.
· Stop leak if safe to do so.
· Water spray or fog may be used to disperse / absorb vapour.
· Absorb or cover spill with sand, earth, inert materials or vermiculite.
· If safe, damaged cans should be placed in a container outdoors, away from
ignition sources, until pressure has dissipated.
· Undamaged cans should be gathered and stowed safely.
· Collect residues and seal in labelled drums for disposal.
From IERG (Canada/Australia) Isolation Distance - Downwind Protection Distance 8 metres IERG Number 49
FOOTNOTES 1 PROTECTIVE ACTION ZONE is defined as the area in which people are at risk of harmful exposure. This zone assumes that random changes in wind direction confines the vapour plume to an area within 30 degrees on either side of the predominant wind direction, resulting in a crosswind protective action distance equal to the downwind protective action distance. 2 PROTECTIVE ACTIONS should be initiated to the extent possible, beginning with those closest to the spill and working away from the site in the downwind direction. Within the protective action zone a level of vapour concentration may exist resulting in nearly all unprotected persons becoming incapacitated and unable to take protective action and/or incurring serious or irreversible health effects. 3 INITIAL ISOLATION ZONE is determined as an area, including upwind of the incident, within which a high probability of localised wind reversal may expose nearly all persons without appropriate protection to life-threatening concentrations of the material. 4 SMALL SPILLS involve a leaking package of 200 litres (55 US gallons) or less, such as a drum (jerrican or box with inner containers). Larger packages leaking less than 200 litres and compressed gas leaking from a small cylinder are also considered "small spills". LARGE SPILLS involve many small leaking packages or a leaking package of greater than 200 litres, such as a cargo tank, portable tank or a "one-tonne" compressed gas cylinder. 5 Guide 126 is taken from the US DOT emergency response guide book. 6 IERG information is derived from CANUTEC - Transport Canada.
Personal Protective Equipment advice is contained in Section 8 of the MSDS.
· Avoid all personal contact, including inhalation.
· Wear protective clothing when risk of exposure occurs.
· Use in a well-ventilated area.
· Prevent concentration in hollows and sumps.
· DO NOT enter confined spaces until atmosphere has been checked.
· Avoid smoking, naked lights or ignition sources.
· Avoid contact with incompatible materials.
· When handling, DO NOT eat, drink or smoke.
· DO NOT incinerate or puncture aerosol cans.
· DO NOT spray directly on humans, exposed food or food utensils.
· Avoid physical damage to containers.
· Always wash hands with soap and water after handling.
· Work clothes should be laundered separately.
· Use good occupational work practice.
· Observe manufacturer's storing and handling recommendations.
· Atmosphere should be regularly checked against established exposure standards
to ensure safe working conditions are maintained.
· Aerosol dispenser.
· Check that containers are clearly labelled.
Avoid storage with oxidisers
· Store in original containers in approved flame-proof area.
· DO NOT store in pits, depressions, basements or areas where vapours may be
trapped.
· No smoking, naked lights, heat or ignition sources.
· Keep containers securely sealed. Contents under pressure.
· Store away from incompatible materials.
· Store in a cool, dry, well ventilated area in an upright position.
· Avoid storage at temperatures higher than 40 deg C.
· Protect containers against physical damage and check regularly for leaks.
· Observe manufacturer's storing and handling recommendations.
No data available for acetone as (CAS: 67-64-1) / (CAS: 64742-49-0) / (CAS: 141-78-6) / (CAS: 74-98-6)
None assigned. Refer to individual constituents.
OSF=0.15 (naphtha petroleum, light, hydrotreated)
Exposed individuals are NOT reasonably expected to be warned, by smell, that the
Exposure Standard is being exceeded.
Odour Safety Factor (OSF) is determined to fall into either Class C, D or E.
The Odour Safety Factor (OSF) is defined as:
OSF= Exposure Standard (TWA) ppm/ Odour Threshold Value (OTV) ppm
Classification into classes follows:
Class OSF Description
A 550 Over 90% of exposed
individuals are aware by
smell that the Exposure
Standard (TLV-TWA for
example) is being
reached, even when
distracted by working
activities
B 26-550 As "A" for 50-90% of
persons being distracted
C 1-26 As "A" for less than 50%
of persons being
distracted
D 0.18-1 10-50% of persons aware
of being tested perceive
by smell that the
Exposure Standard is
being reached
E <0.18 As "D" for less than 10%
of persons aware of being
tested
"Worst Case" computer-aided prediction of vapour components/concentrations:
Composite Exposure Standard for Mixture (TWA) (mg/m³): 2820.6657 mg/m³
If the breathing zone concentration of ANY of the components listed below is
exceeded, "Worst Case" considerations deem the individual to be overexposed.
Component Breathing Zone ppm Breathing Zone mg/m³ Mixture Conc: (%)
Component Breathing zone Breathing Zone Mixture Conc
(ppm) (mg/m³) (%)
ethyl acetate 940.2219 30.0
acetone 395.72 940.2219 30.0
propane 521.42 940.2219 30.0
ACETONE: TLV TWA: 500 ppm A4; BEI [ACGIH] TLV STEL: 750 ppm A4; BEI [ACGIH] PEL TWA: 1000 ppm, 2400 mg/m³ [OSHA Z1] TLV TWA: 500 ppm, 1188 mg/m³; STEL: 750 ppm, 1782 mg/m³ A4 NOTE: This substance has been classified by the ACGIH as A4 NOT classifiable as causing Cancer in humans ES TWA: 500 ppm, 1185 mg/m³; STEL: 1000 ppm, 2375 mg/m³ OES TWA: 750 ppm, 1810 mg/m³; STEL: 1500 ppm, 3620 mg/m³ NIOSH REL TWA: 250 ppm MAK Value: 500 ppm, 1200 mg/m³ IDLH Level: 2500 ppm (lower explosive limit) MAK Category I Peak Limitation: For local irritants Allows excursions of twice the MAK value for 5 minutes at a time, 8 times per shift. MAK Group IIc: Substances with MAK Values but no pregnancy risk group classification. These are substances which have been investigated but for which no information regarding possible damage to the foetus/embryo was found. Mention calls attention to the absence of adequate data. MAK values, and categories and groups are those recommended within the Federal Republic of Germany Odour Threshold Value: 3.6 ppm (detection), 699 ppm (recognition) Saturation vapour concentration: 237000 ppm @ 20 C NOTE: Detector tubes measuring in excess of 40 ppm, are available. Exposure at or below the recommended TLV-TWA is thought to protect the worker against mild irritation associated with brief exposures and the bioaccumulation, chronic irritation of the respiratory tract and headaches associated with long-term acetone exposures. The NIOSH REL-TWA is substantially lower and has taken into account slight irritation experienced by volunteer subjects at 300 ppm. Mild irritation to acclimatised workers begins at about 750 ppm - unacclimatised subjects will experience irritation at about 350-500 ppm but acclimatisation can occur rapidly. Disagreement between the peak bodies is based largely on the view by ACGIH that widespread use of acetone, without evidence of significant adverse health effects at higher concentrations, allows acceptance of a higher limit. Half-life of acetone in blood is 3 hours which means that no adjustment for shift-length has to be made with reference to the standard 8 hour/day, 40 hours per week because body clearance occurs within any shift with low potential for accumulation. A STEL has been established to prevent excursions of acetone vapours that could cause depression of the central nervous system. NAPHTHA PETROLEUM, LIGHT, HYDROTREATED: REL TWA: 100 ppm (total hydrocarbons) [Exxon] ETHYL ACETATE: TLV TWA: 400 ppm [ACGIH] PEL TWA: 400 ppm, 1400 mg/m³ (SKIN) [OSHA Z1] ES TWA: 200 ppm; STEL 400 ppm TLV TWA: 400 ppm, 1440 mg/m³ OES TWA: 400 ppm, 1460 mg/m³ MAK value: 400 ppm, 1500 mg/m³ MAK Category I Peak Limitation: For local irritants Allows excursions of twice the MAK value for 5 minutes at a time, 8 times per shift. MAK Group C: There is no reason to fear risk of damage to the developing embryo when MAK and BAT values are observed. MAK values, and categories and groups are those recommended within the Federal Republic of Germany IDLH Level: 2000 ppm (lower explosive limit) Odour Threshold Value: 6.4-50 ppm (detection), 13.3-75 ppm (recognition) The TLV-TWA provides a significant margin of safety from the standpoint of adverse health effects. Unacclimated subjects found the odour objectionably strong at 200 ppm. Mild nose, eye and throat irritation was experienced at 400 ppm. Workers exposed regularly at concentrations ranging from 375 ppm to 1500 ppm for several months showed no unusual signs or symptoms. PROPANE: TLV TWA: 2500 ppm [ACGIH] NOTICE OF INTENDED CHANGE TLV TWA: 1000 ppm [ACGIH] PEL TWA: 1000 ppm, 1800 mg/m³ [OSHA Z1] TLV TWA: 2500 ppm, 4508 mg/m³ NOTICE OF INTENDED CHANGE TLV TWA 1000 ppm ES TWA: simple asphyxiant IDLH Level: 2100 ppm (lower explosive limit)
· Safety glasses with side shields; or as required, · Chemical goggles. · Contact lenses pose a special hazard; soft lenses may absorb irritants and all lenses concentrate them.
No special equipment needed when handling small quantities. OTHERWISE: Wear general protective gloves, eg. light weight rubber gloves. Or as required: Wear chemical protective gloves, eg. PVC. Wear safety footwear.
No special equipment needed when handling small quantities. OTHERWISE: · Overalls. · Skin cleansing cream. · Eyewash unit. · Do not spray on hot surfaces.
Glove selection is based on a modified presentation of the: "Forsberg Clothing Performance Index". The effect(s) of the following substance(s) are taken into account in the computer-generated selection: Substance ________________________________________ acetone ethyl acetate PE/EVAL/PE A BUTYL/NEOPRENE B SARANEX-23 2-PLY B BUTYL B PVA B TEFLON B SARANEX-23 C CPE C HYPALON C NITRILE+PVC C PVC C NEOPRENE C NATURAL RUBBER C NATURAL+NEOPRENE C NITRILE C VITON/NEOPRENE C * CPI - Chemwatch Performance Index A: Best Selection B: Satisfactory; may degrade after 4 hours continuous immersion C: Poor to Dangerous Choice for other than short term immersion NOTE: As a series of factors will influence the actual performance of the glove, a final selection must be based on detailed observation. - * Where the glove is to be used on a short term, casual or infrequent basis, factors such as "feel" or convenience (e.g. disposability), may dictate a choice of gloves which might otherwise be unsuitable following long-term or frequent use. A qualified practitioner should be consulted.
Respiratory protection may be required when ANY "Worst Case" vapour-phase
concentration is exceeded (see Computer Prediction in "Exposure Standards").
Protection Factor Half-Face Respirator Full-Face Respirator
5 x ES Air-line* AX-2
- AX-PAPR-2
10 x ES - AX-3
10+ x ES - Air-line**
* - Continuous Flow; ** - Continuous-flow or positive pressure demand
^ - Full-face
The local concentration of material, quantity and conditions of use determine
the type of personal protective equipment required. For further information
consult site specific CHEMWATCH data (if available), or your Occupational
Health and Safety Advisor.
General exhaust is adequate under normal operating conditions. If risk of overexposure exists, wear SAA approved respirator. Correct fit is essential to obtain adequate protection. Provide adequate ventilation in warehouse or closed storage areas.
Red highly flammable liquid with a strong solvent odour; does not mix with
water.
Supplied as an aerosol pack. Contents under PRESSURE. Contains highly flammable
hydrocarbon propellant.
Liquid.
Does not mix with water.
Floats on water.
Molecular Weight: Not Applicable Boiling Range (ºC): Not Available Melting Range (ºC): Not Available Specific Gravity (water=1): 0.81 Solubility in water (g/L): Immiscible pH (as supplied): Not Applicable pH (1% solution): Not Applicable Vapour Pressure (kPa): 370 Volatile Component (%vol): Not Available Evaporation Rate: Not Available Relative Vapour Density (air=1): Not Available Flash Point (ºC): -60 Lower Explosive Limit (%): 2.1 Upper Explosive Limit (%): 9.3 Autoignition Temp (ºC): 490 Decomposition Temp (ºC): Not Available State: Liquid
· Elevated temperatures.
· Presence of open flame.
· Product is considered stable.
· Hazardous polymerisation will not occur.
Ingestion may result in nausea, pain, vomiting. Vomit entering the lungs by
aspiration may cause potentially lethal chemical pneumonitis.
Considered an unlikely route of entry in commercial/industrial environments
The material may produce severe irritation to the eye causing pronounced
inflammation. Repeated or prolonged exposure to irritants may produce
conjunctivitis.
Toxic effects may result from skin absorption.
The material may accentuate any pre-existing skin condition.
The material may cause skin irritation after prolonged or repeated exposure and
may produce a contact dermatitis (nonallergic). This form of dermatitis is often
characterised by skin redness (erythema) and swelling epidermis. Histologically
there may be intercellular oedema of the spongy layer (spongiosis) and
intracellular oedema of the epidermis.
Inhalation hazard is increased at higher temperatures.
Acute effects from inhalation of high concentrations of vapour are pulmonary
irritation, including coughing, with nausea; central nervous system depression -
characterised by headache and dizziness, increased reaction time, fatigue and
loss of co-ordination.
If exposure to highly concentrated solvent atmosphere is prolonged this may lead
to narcosis, unconsciousness, even coma and possible death.
WARNING:Intentional misuse by concentrating/inhaling contents may be lethal.
Principal routes of exposure are by skin contact/absorption and inhalation of
mist/vapours. Chronic solvent inhalation exposures may result in nervous system impairment
and liver and blood changes. [PATTYS]. Prolonged or continuous skin contact with the
liquid may cause defatting with drying, cracking, irritation and dermatitis following.
WARNING: Aerosol containers may present pressure related hazards.
Not available. Refer to individual constituents.
unless otherwise specified data extracted from RTECS - Register of Toxic Effects
of Chemical Substances
ACETONE:
IRRITATION TOXICITY
Eye (human): 500 ppm - irritant Oral (man) TDLo: 2857 mg/kg
Eye (rabbit): 3.95 mg - SEVERE Oral (rat) LD50: 5800 mg/kg
Eye (rabbit): 20mg/24hr -moderate Inhalation (human) TCLo: 500 ppm
Skin (rabbit):395mg (open) - mild Inhalation (man) TCLo: 12000 ppm/4 hr
Skin (rabbit): 500 mg/24hr - mild Inhalation (man) TCLo: 10 mg/m3/6 hr
Inhalation (rat) LC50: 50100 mg/m3/8 hr
Dermal (rabbit) LD50: 20000 mg/kg
NAPHTHA PETROLEUM, LIGHT, HYDROTREATED:
No significant acute toxicological data identified in literature search.
ETHYL ACETATE:
IRRITATION TOXICITY
Eye (human): 400 ppm Oral (rat) LD50: 5620 mg/kg
Inhalation (rat) LC50: 1600 ppm/8h
Inhalation (human) TCLo: 400 ppm
PROPANE:
No significant acute toxicological data identified in literature search.
Refer to data for ingredients, which follows: ACETONE: Hazardous Air Pollutant: No Fish LC50 (96hr.) (mg/l): 8300-40000 Daphnia magna EC50 (48hr.) (mg/l): 10 log Kow (Prager 1995): -0.24 log Kow (Sangster 1997): -0.24 log Pow (Verschueren 1983): -0.24 BOD5: 122% ThOD: 72 Half-life Soil - High (hours): 168 Half-life Soil - Low (hours): 24 Half-life Air - High (hours): 2790 Half-life Air - Low (hours): 279 Half-life Surface water - High (hours): 168 Half-life Surface water - Low (hours): 24 Half-life Ground water - High (hours): 336 Half-life Ground water - Low (hours): 48 Aqueous biodegradation - Aerobic - High (hours): 168 Aqueous biodegradation - Aerobic - Low (hours): 24 Aqueous biodegradation - Anaerobic - High (hours): 672 Aqueous biodegradation - Anaerobic - Low (hours): 96 Aqueous biodegradation - Removal secondary treatment - High (hours): 75% Aqueous biodegradation - Removal secondary treatment - Low (hours): 54% Aqueous photolysis half-life - High (hours): 270 Photooxidation half-life water - High (hours): 3.97E+06 Photooxidation half-life water - Low (hours): 9.92E+04 Photooxidation half-life air - High (hours): 2790 Photooxidation half-life air - Low (hours): 279 log Kow: -0.24 Half-life (hr) air: 312-1896 Half-life (hr) H2O surface water: 20 Henry's atm m3 /mol: 3.67E-05 BOD 5 if unstated: 0.31-1.76,46-55% COD: 1.12-2.07 ThOD: 2.2 BCF: 0.69 Toxicity Fish: LC50(96) 5540-13000mg/L Toxicity invertebrate: cell mult. inhib. 28-7500mg/L Bioaccumulation: not sig Nitrif. inhib.: 75% decr. at 840mg/L Anaerobic effects: sig degrad Degradation Biological: sig processes Abiotic: Rxn OH*,photodissoc In air, acetone is lost by photolysis and reaction with photochemically produced hydroxyl radicals; the estimated half-life of these combined processes is about 22 days. The relatively long half-life allows acetone to be transported long distances from its emission source. Acetone is highly soluble and slightly persistent in water, with a half-life of about 20 hours; it is minimally toxic to aquatic life. Acetone released to soil volatilises although some may leach into the ground where it rapidly biodegrades. Acetone does not concentrate in the food chain. Drinking Water Standard: none available. Soil Guidelines: none available. Air Quality Standards: none available. NAPHTHA PETROLEUM, LIGHT, HYDROTREATED: No data for naphtha petroleum, light, hydrotreated. ETHYL ACETATE: Hazardous Air Pollutant: No log Pow (Verschueren 1983): 0.66/0.73 ThOD: 50.4 Hazardous Air Pollutant: No log Pow (Verschueren 1983): 0.66/0.73 BOD5: 15% COD: 1.54 (83%) ThOD: 1.82 Half-life Soil - High (hours): 168 Half-life Soil - Low (hours): 24 Half-life Air - High (hours): 353 Half-life Air - Low (hours): 35.3 Half-life Surface water - High (hours): 168 Half-life Surface water - Low (hours): 24 Half-life Ground water - High (hours): 336 Half-life Ground water - Low (hours): 48 Aqueous biodegradation - Aerobic - High (hours): 168 Aqueous biodegradation - Aerobic - Low (hours): 24 Aqueous biodegradation - Anaerobic - High (hours): 672 Aqueous biodegradation - Anaerobic - Low (hours): 96 Aqueous biodegradation - Removal secondary treatment - High (hours): 96% Aqueous biodegradation - Removal secondary treatment - Low (hours): 99.90% Photooxidation half-life water - High (hours): 9.60E+05 Photooxidation half-life water - Low (hours): 24090 Photooxidation half-life air - High (hours): 353 Photooxidation half-life air - Low (hours): 35.3 First order hydrolysis half-life (hours): 1.77E+04 Acid rate constant [M(H+)-HR]-1: 3.05E-08 Base rate constant [MOH)-HR]-1: 2.99E-05 log Kow : 0.66-0.73 Half-life (hr) air : 200 Half-life (hr) H2O surface water : 10 Henry's atm m3 /mol: 1.20E-04 BOD 5 if unstated: 0.1-1.24,16-36% COD : 1.54,83% ThOD : 1.82 PROPANE: Hazardous Air Pollutant: No log Kow (Sangster 1997): 2.36 log Kow : 2.36 Toxicity Fish: LC50(96)8.6-30mg/L Effects on algae and plankton: 50%decr grwth&O2 evol.0.1-2ppm Degradation Biological: slow processes Abiotic: hydrol
· Consult State Land Waste Management Authority for disposal.
· Discharge contents of damaged aerosol cans at an approved site.
· Allow small quantities to evaporate.
· DO NOT incinerate or puncture aerosol cans.
· Bury residues and emptied aerosol cans at an approved site.
Shipping Name:
AEROSOLS
Dangerous Goods Class: 2.1
UN/NA Number: 1950
ADR Number: None
Packing Group: None
Labels Required: flammable gas
Additional Shipping Information:
International Transport Regulations:
IMO: 2.1
2Y
S5
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CHEMWATCH. TEL (+61 3) 9572 4700.
Issue Date: Mon 31-Jan-2005
Print Date: Wed 9-Feb-2005