SAFETY DATA SHEET

BP Kerosine

Section 1. Identification
GHS product identifier BP Kerosine
Product code 0000003477
SDS no. 0000003477
Historic SDS no. YSTLM
Relevant identified uses of the substance or mixture and uses advised against
Use of the substance/ Fuel for domestic burners.
mixture Not suitable for flueless heaters and lamps.
For specific application advice see appropriate Technical Data Sheet or consult our
company representative.
Manufacturer
Supplier BP Australia Pty Ltd
Level 17, 717 Bourke Street
Docklands, Victoria 3008
ABN 53 004 085 616

www.bp.com.au

Technical Helpline Number: 1300 139 700

EMERGENCY TELEPHONE 1800 638 556
NUMBER

Section 2. Hazard(s) identification

Classification of the FLAMMABLE LIQUIDS - Category 3
substance or mixture SKIN CORROSION/IRRITATION - Category 2
CARCINOGENICITY - Category 2
SPECIFIC TARGET ORGAN TOXICITY - SINGLE EXPOSURE (Narcotic effects) -
Category 3
ASPIRATION HAZARD - Category 1

GHS label elements

Hazard pictograms

Signal word DANGER

Hazard statements H226 - Flammable liquid and vapour.
H304 - May be fatal if swallowed and enters airways.
H315 - Causes skin irritation.
H336 - May cause drowsiness or dizziness.
H351 - Suspected of causing cancer.
Precautionary statements
General P102 - Keep out of reach of children.
P101 - If medical advice is needed, have product container or label at hand.

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Section 2. Hazard(s) identification
Prevention P201 - Obtain special instructions before use.
P202 - Do not handle until all safety precautions have been read and understood.
P281 - Use personal protective equipment as required.
P280 - Wear protective gloves, protective clothing and eye or face protection.
P210 - Keep away from heat, hot surfaces, sparks, open flames and other ignition
sources. No smoking.
P241 - Use explosion-proof electrical, ventilating or lighting equipment.
P242 - Use non-sparking tools.
P243 - Take action to prevent static discharges.
P233 - Keep container tightly closed.
P271 - Use only outdoors or in a well-ventilated area.
P261 - Avoid breathing vapour.
P264 - Wash hands thoroughly after handling.
Response P308 + P313 - IF exposed or concerned: Get medical attention.
P304 + P340, P312 - IF INHALED: Remove person to fresh air and keep
comfortable for breathing. Call a POISON CENTER or doctor if you feel unwell.
P301 + P310, P331 - IF SWALLOWED: Immediately call a POISON CENTER or
physician. Do NOT induce vomiting.
P303 + P361 + P353 - IF ON SKIN (or hair): Take off immediately all contaminated
clothing. Rinse skin with water.
P362 - Take off contaminated clothing and wash before reuse.
P302 + P352 - IF ON SKIN: Wash with plenty of soap and water.
P332 + P313 - If skin irritation occurs: Get medical attention.
Storage P235 - Keep cool.
Disposal P501 - Dispose of contents and container in accordance with all local, regional,
national and international regulations.
Supplemental label Not applicable.
elements

Other hazards which do not Static accumulating flammable liquid can become electrostatically charged even in
result in classification bonded and grounded equipment. Sparks may ignite liquid and vapour may cause
flash fire or explosion.

Section 3. Composition and ingredient information

Substance/mixture Mixture
A complex mixture of hydrocarbons containing paraffins, naphthenes, olefins and aromatics with carbon numbers
predominantly between C9 and C16.
Ingredient name % (w/w) CAS number
Kerosine (petroleum) ≥90 8008-20-6
naphthalene <3 91-20-3
There are no additional ingredients present which, within the current knowledge of the supplier and in the
concentrations applicable, are classified as hazardous to health or the environment and hence require
reporting in this section.
Occupational exposure limits, if available, are listed in Section 8.

Section 4. First aid measures

Description of necessary first aid measures
Eye contact In case of contact, immediately flush eyes with plenty of water for at least 15
minutes. Eyelids should be held away from the eyeball to ensure thorough rinsing.
Check for and remove any contact lenses. Get medical attention.
Inhalation If inhaled, remove to fresh air. Get medical attention. If exposure to vapour, mists
or fumes causes drowsiness, headache, blurred vision or irritation of the eyes, nose
or throat, remove immediately to fresh air. Keep patient warm and at rest. If any
symptoms persist obtain medical advice.

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Skin contact In case of contact, immediately flush skin with plenty of water for at least 15 minutes
while removing contaminated clothing and shoes. Drench contaminated clothing
with water before removing. This is necessary to avoid the risk of sparks from static
electricity that could ignite contaminated clothing. Contaminated clothing is a fire
hazard. Contaminated leather, particularly footwear, must be discarded. Clean
shoes thoroughly before reuse. Get medical attention.
Ingestion Do not induce vomiting. Never give anything by mouth to an unconscious person. If
unconscious, place in recovery position and get medical attention immediately.
Aspiration hazard if swallowed. Can enter lungs and cause damage. Get medical
attention immediately.

Most important symptoms/effects, acute and delayed

See Section 11 for more detailed information on health effects and symptoms.
Indication of immediate medical attention and special treatment needed, if necessary
Notes to physician Treatment should in general be symptomatic and directed to relieving any effects.
Product can be aspirated on swallowing or following regurgitation of stomach
contents, and can cause severe and potentially fatal chemical pneumonitis, which
will require urgent treatment. Because of the risk of aspiration, induction of vomiting
and gastric lavage should be avoided. Gastric lavage should be undertaken only
after endotracheal intubation. Monitor for cardiac dysrhythmias.
Specific treatments No specific treatment.
Protection of first-aiders No action shall be taken involving any personal risk or without suitable training. If it
is suspected that fumes are still present, the rescuer should wear an appropriate
mask or self-contained breathing apparatus. It may be dangerous to the person
providing aid to give mouth-to-mouth resuscitation.

Section 5. Firefighting measures

Extinguishing media
Suitable extinguishing In case of fire, use water fog, foam, dry chemical or carbon dioxide extinguisher or
media spray.
Unsuitable extinguishing Do not use water jet.
media

Specific hazards arising Flammable liquid and vapour. In a fire or if heated, a pressure increase will occur
from the chemical and the container may burst, with the risk of a subsequent explosion. Runoff to
sewer may create fire or explosion hazard. Vapours can form explosive mixtures
with air. Vapours are heavier than air and can spread along the ground or float on
water surfaces to remote ignition sources. Vapours may accumulate in low or
confined areas or travel a considerable distance to a source of ignition and flash
back. This product is a poor conductor of electricity and can become
electrostatically charged. If sufficient charge is accumulated, ignition of flammable
mixtures can occur. To reduce potential for static discharge, use proper bonding
and grounding procedures. This liquid may accumulate static electricity when filling
properly-grounded containers. Static accumulation may be significantly increased
by the presence of small quantities of water or other contaminants. Liquid will float
and may reignite on surface of water.
Hazardous thermal Combustion products may include the following:
decomposition products carbon oxides (CO, CO2) (carbon monoxide, carbon dioxide)

Special protective actions No action shall be taken involving any personal risk or without suitable training.
for fire-fighters Promptly isolate the scene by removing all persons from the vicinity of the incident if
there is a fire. Move containers from fire area if this can be done without risk. Use
water spray to keep fire-exposed containers cool.
Special protective Fire-fighters should wear positive pressure self-contained breathing apparatus
equipment for fire-fighters (SCBA) and full turnout gear.

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Section 5. Firefighting measures
Hazchem code 3Y

Section 6. Accidental release measures

Personal precautions, protective equipment and emergency procedures
For non-emergency Immediately contact emergency personnel. No action shall be taken involving any
personnel personal risk or without suitable training. Evacuate surrounding areas. Keep
unnecessary and unprotected personnel from entering. Do not touch or walk
through spilt material. No flares, smoking or flames in hazard area. Avoid breathing
vapour or mist. Provide adequate ventilation. Put on appropriate personal
protective equipment. Floors may be slippery; use care to avoid falling. Eliminate
all ignition sources.
For emergency responders Entry into a confined space or poorly ventilated area contaminated with vapour, mist
or fume is extremely hazardous without the correct respiratory protective equipment
and a safe system of work. Wear self-contained breathing apparatus. Wear a
suitable chemical protective suit. Chemical resistant boots. See also the
information in "For non-emergency personnel".

Environmental precautions Avoid dispersal of spilt material and runoff and contact with soil, waterways, drains
and sewers. Inform the relevant authorities if the product has caused environmental
pollution (sewers, waterways, soil or air). In case of small spillages in closed waters
(i.e. ports), contain product with floating barriers or other equipment. Collect spilled
product by absorbing with specific floating absorbents. If possible, large spillages in
open waters should be contained with floating barriers or other mechanical means.
If this is not possible, control the spreading of the spillage, and collect the product by
skimming or other suitable mechanical means. The use of dispersants should be
advised by an expert, and, if required, approved by local authorities. Collect
recovered product and other contaminated materials in suitable tanks or containers
for recycle, recovery or safe disposal.

Methods and material for containment and cleaning up

Small spill Eliminate all ignition sources. Stop leak if without risk. Move containers from spill
area. Absorb with an inert material and place in an appropriate waste disposal
container. Use spark-proof tools and explosion-proof equipment. Dispose of via a
licensed waste disposal contractor. The method and equipment used must be in
conformance with appropriate regulations and industry practice on explosive
atmospheres.
Large spill Eliminate all ignition sources. Stop leak if without risk. Move containers from spill
area. Approach the release from upwind. Prevent entry into sewers, water courses,
basements or confined areas. Dike spill area and do not allow product to reach
sewage system and surface or ground water. Contain and collect spillage with non-
combustible, absorbent material e.g. sand, earth, vermiculite or diatomaceous earth
and place in container for disposal according to local regulations. Use spark-proof
tools and explosion-proof equipment. Contaminated absorbent material may pose
the same hazard as the spilt product. The method and equipment used must be in
conformance with appropriate regulations and industry practice on explosive
atmospheres. Dispose of via a licensed waste disposal contractor.

Section 7. Handling and storage

Precautions for safe handling
Protective measures Put on appropriate personal protective equipment (see Section 8). Avoid exposure -
obtain special instructions before use. Do not handle until all safety precautions
have been read and understood. Do not get in eyes or on skin or clothing. Do not
swallow. Aspiration hazard if swallowed. Can enter lungs and cause damage.
Never siphon by mouth. Avoid breathing vapour or mist. Use only with adequate
ventilation. Wear appropriate respirator when ventilation is inadequate. Keep in the
original container or an approved alternative made from a compatible material, kept
tightly closed when not in use. Store and use away from heat, sparks, open flame
or any other ignition source. Use explosion-proof electrical (ventilating, lighting and

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Section 7. Handling and storage
material handling) equipment. Use only non-sparking tools. Take precautionary
measures against electrostatic discharges. Empty containers retain product residue
and can be hazardous. Do not reuse container. Handling operations that can
promote accumulation of static charges include but are not limited to: mixing,
filtering, pumping at high flow rates, splash filling, creating mists or sprays, tank and
container filling, tank cleaning, sampling, gauging, switch loading, vacuum truck
operations. Restrict flow velocity according to API 2003 (2008), NFPA 77 (2007),
and Laurence Britton, “Avoiding Static Ignition Hazards in Chemical Operations”. To
reduce potential for static discharge, ensure that all equipment is properly grounded
and bonded and meets appropriate electrical classification requirements.
Advice on general Eating, drinking and smoking should be prohibited in areas where this material is
occupational hygiene handled, stored and processed. Wash thoroughly after handling. Remove
contaminated clothing and protective equipment before entering eating areas. See
also Section 8 for additional information on hygiene measures.

Conditions for safe storage, Store in accordance with local regulations. Store in a segregated and approved
including any area. Store in original container protected from direct sunlight in a dry, cool and well-
incompatibilities ventilated area, away from incompatible materials (see Section 10) and food and
drink. Store locked up. Eliminate all ignition sources. Separate from oxidising
materials. Keep container tightly closed and sealed until ready for use. Store and
use only in equipment/containers designed for use with this product. Containers
that have been opened must be carefully resealed and kept upright to prevent
leakage. Do not store in unlabelled containers. Use appropriate containment to
avoid environmental contamination.

Light hydrocarbon vapours can build up in the headspace of tanks. These can
cause flammability/explosion hazards even at temperatures below the normal flash
point (note: flash point must not be regarded as a reliable indicator of the potential
flammability of vapour in tank headspaces). Tank headspaces should always be
regarded as potentially flammable and care should be taken to avoid static electrical
discharge and all ignition sources during filling, ullaging and sampling from storage
tanks. Do not enter storage tanks. If entry to vessels is necessary, follow permit to
work procedures. Entry into a confined space or poorly ventilated area
contaminated with vapour, mist or fume is extremely hazardous without the correct
respiratory protective equipment and a safe system of work. When the product is
pumped (e.g. during filling, discharge or ullaging) and when sampling, there is a risk
of static discharge. Ensure equipment used is properly earthed or bonded to the
tank structure. Electrical equipment should not be used unless it is intrinsically safe
(i.e. will not produce sparks). Explosive air/vapour mixtures may form at ambient
temperature. If product comes into contact with hot surfaces, or leaks occur from
pressurised fuel pipes, the vapour or mists generated will create a flammability or
explosion hazard. Product contaminated rags, paper or material used to absorb
spillages, represent a fire hazard, and should not be allowed to accumulate.
Dispose of safely immediately after use.
Not suitable Avoid all possible sources of ignition (spark or flame). Avoid excessive heat.

Section 8. Exposure controls and personal protection

Control parameters
Occupational exposure limits

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Section 8. Exposure controls and personal protection
Ingredient name Exposure limits
Kerosine (petroleum) ACGIH TLV (United States). Absorbed
through skin.
TWA: 200 mg/m³, (as total hydrocarbon
vapor) 8 hours. Issued/Revised: 1/2003
naphthalene Safe Work Australia (Australia).
STEL: 79 mg/m³ 15 minutes. Issued/
Revised: 5/1995
STEL: 15 ppm 15 minutes. Issued/Revised:
5/1995
TWA: 52 mg/m³ 8 hours. Issued/Revised:
5/1995
TWA: 10 ppm 8 hours. Issued/Revised:
5/1995

Appropriate engineering All activities involving chemicals should be assessed for their risks to health, to
controls ensure exposures are adequately controlled. Personal protective equipment should
only be considered after other forms of control measures (e.g. engineering controls)
have been suitably evaluated. Personal protective equipment should conform to
appropriate standards, be suitable for use, be kept in good condition and properly
maintained.
Your supplier of personal protective equipment should be consulted for advice on
selection and appropriate standards. For further information contact your national
organisation for standards.
Provide exhaust ventilation or other engineering controls to keep the relevant
airborne concentrations below their respective occupational exposure limits.
The final choice of protective equipment will depend upon a risk assessment. It is
important to ensure that all items of personal protective equipment are compatible.
Environmental exposure Emissions from ventilation or work process equipment should be checked to ensure
controls they comply with the requirements of environmental protection legislation. In some
cases, fume scrubbers, filters or engineering modifications to the process
equipment will be necessary to reduce emissions to acceptable levels.

Individual protection measures

Hygiene measures Wash hands, forearms and face thoroughly after handling chemical products, before
eating, smoking and using the lavatory and at the end of the working period.
Appropriate techniques should be used to remove potentially contaminated clothing.
Wash contaminated clothing before reusing. Ensure that eyewash stations and
safety showers are close to the workstation location.
Eye/face protection Chemical splash goggles.
Skin protection
Hand protection Wear chemical resistant gloves.

Do not re-use gloves. Protective gloves must give suitable protection against
mechanical risks (i.e. abrasion, blade cut and puncture). Protective gloves will
deteriorate over time due to physical and chemical damage. Inspect and replace
gloves on a regular basis. The frequency of replacement will depend upon the
circumstances of use.
Recommended: Nitrile gloves.
Skin protection Use of protective clothing is good industrial practice.
Personal protective equipment for the body should be selected based on the task
being performed and the risks involved and should be approved by a specialist
before handling this product.
Cotton or polyester/cotton overalls will only provide protection against light
superficial contamination that will not soak through to the skin. Overalls should be
laundered on a regular basis. When the risk of skin exposure is high (e.g. when
cleaning up spillages or if there is a risk of splashing) then chemical resistant aprons

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Section 8. Exposure controls and personal protection
and/or impervious chemical suits and boots will be required.
Wear suitable protective clothing.
Footwear highly resistant to chemicals.
When there is a risk of ignition wear inherently fire resistant protective clothes and
gloves.
When there is a risk of ignition from static electricity, wear anti-static protective
clothing. For greatest effectiveness against static electricity, overalls, boots and
gloves should all be anti-static.
When the risk of skin exposure is high (from experience this could apply to the
following tasks: cleaning work, maintenance and service, filling and transfer, taking
samples and cleaning up spillages) then a chemical protective suit and boots will be
required.
Work clothing / overalls should be laundered on a regular basis. Laundering of
contaminated work clothing should only be done by professional cleaners who have
been told about the hazards of the contamination. Always keep contaminated work
clothing away from uncontaminated work clothing and uncontaminated personal
clothes.
Recommended: Avoid contact with skin and clothing. Wear suitable protective
clothing.
Other skin protection Appropriate footwear and any additional skin protection measures should be
selected based on the task being performed and the risks involved and should be
approved by a specialist before handling this product.
Respiratory protection Use with adequate ventilation.
If there is a requirement for the use of a respiratory protective device, but the use of
breathing apparatus (independent of ambient atmosphere) is not required, then a
suitable filtering device must be worn.
The filter class must be suitable for the maximum contaminant concentration (gas/
vapour/aerosol/particulates) that may arise when handling the product.
Recommended: Avoid breathing of vapours, mists or spray. Select and use
respirators in accordance with AS/NZS 1715/1716. When mists
or vapours exceed the exposure standards then the use of the
following is recommended: Approved respirator with organic
vapour and particulate (dust/mist) filters. Filter capacity and
respirator type depends on exposure level.
Refer to standards: Respiratory protection:AS/NZS 1715 and AS/NZS 1716
Gloves:AS/NZS 2161.1
Eye protection:AS/NZS 1336 and AS/NZS 1337

Section 9. Physical and chemical properties

Appearance
Physical state Liquid.
Colour Yellow. [Light]
Odour Hydrocarbon.
Odour threshold Not available.
pH Not available.
Melting point Not available.
Boiling point 90 to 300°C (194 to 572°F)
Flash point Closed cup: >23°C (>73.4°F) [Pensky-Martens.]
Evaporation rate Not available.
Flammability (solid, gas) Not applicable. Based on - Physical state
Lower and upper explosive Not available.
(flammable) limits
Vapour pressure 1 to 21 kPa (7.5 to 157.5 mm Hg) [37.8°C (100°F)]
Vapour density >1 [Air = 1]
Relative density Not available.

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Section 9. Physical and chemical properties
Density <820 kg/m³ (<0.82 g/cm³) at 15°C
Solubility Very slightly soluble in water.
Partition coefficient: n- Not available.
octanol/water
Auto-ignition temperature Not available.
Decomposition temperature Not available.
Viscosity Kinematic: 1 to 2.5 mm2/s (1 to 2.5 cSt) at 40°C

Section 10. Stability and reactivity

Reactivity No specific test data available for this product. Refer to Conditions to avoid and
Incompatible materials for additional information.
Chemical stability The product is stable.
Possibility of hazardous Under normal conditions of storage and use, hazardous reactions will not occur.
reactions Under normal conditions of storage and use, hazardous polymerisation will not
occur.
Conditions to avoid Avoid all possible sources of ignition (spark or flame). Avoid excessive heat.
Incompatible materials Reactive or incompatible with the following materials: oxidising materials.
Hazardous decomposition Under normal conditions of storage and use, hazardous decomposition products
products should not be produced.

Section 11. Toxicological information

Information on toxicological effects
Acute toxicity
Product/ingredient name Result Species Dose Exposure
Kerosine (petroleum) LC50 Inhalation Vapour Rat >5.28 mg/l 4 hours
Mortality and
Systemic Effects
LD50 Dermal Rabbit >2000 mg/kg -
Mortality and
Systemic Effects
LD50 Oral Rat >5000 mg/kg -
naphthalene LD50 Dermal Rabbit 20 g/kg -
LD50 Oral Rat 490 mg/kg -
Irritation/Corrosion
Product/ingredient name Result Species Score Exposure Observation
Kerosine (petroleum) Skin - Non-irritant to skin. Rabbit - 4 hours 100 -
%
Skin - Irritation Rabbit - 24 hours -
100%
Eyes - Non-irritating to the Rabbit - 100% -
eyes.
Skin Causes skin irritation.
Mutagenicity
Product/ingredient name Test Experiment Result
Kerosine (petroleum) Equivalent to OECD Experiment: In vitro Negative
476
Subject: Mammal - species
unspecified
Equivalent to OECD Experiment: In vitro Negative
476
Subject: Mammal - species
unspecified
Equivalent to OECD Experiment: In vitro Negative

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Section 11. Toxicological information
471
Subject: Non-mammalian species
Equivalent to OECD Experiment: In vivo Negative
475
Subject: Unspecified
Cell: Germ
Equivalent to OECD Experiment: In vivo Negative
478
Subject: Unspecified
Cell: Germ
Conclusion/Summary Based on available data, the classification criteria are not met.
Carcinogenicity
Product/ingredient name Result Species Dose Exposure
Kerosine (petroleum) Positive - Dermal - Mouse - 2 years
Unspecified
Negative - Dermal - Mouse - 2 years
Unspecified
Conclusion/Summary Suspected of causing cancer.
Reproductive toxicity
Product/ingredient name Maternal Fertility Developmental Species Dose Exposure
toxicity toxin
Kerosine (petroleum) - Negative - Rat Dermal 34 days
- Negative - Rat Oral 90 days
- - Negative Rat Oral 10 days
- - Negative Rat Inhalation 10 days
Specific target organ toxicity (single exposure)
Name Category Route of Target organs
exposure
Kerosine (petroleum) Category 3 - Narcotic effects
Aspiration hazard
Name Result
Kerosine (petroleum) ASPIRATION HAZARD - Category 1

Information on likely routes Routes of entry anticipated: Dermal, Inhalation.

of exposure
Potential acute health effects
Eye contact No known significant effects or critical hazards.
Inhalation Can cause central nervous system (CNS) depression. May cause drowsiness or
dizziness.
Skin contact Causes skin irritation.
Ingestion Irritating to mouth, throat and stomach. Aspiration hazard if swallowed -- harmful or
fatal if liquid is aspirated into lungs.

Symptoms related to the physical, chemical and toxicological characteristics

Eye contact Adverse symptoms may include the following:
pain or irritation
watering
redness

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Section 11. Toxicological information
Inhalation Adverse symptoms may include the following:
nausea or vomiting
headache
drowsiness/fatigue
dizziness/vertigo
unconsciousness
Skin contact Adverse symptoms may include the following:
irritation
redness
Ingestion Adverse symptoms may include the following:
nausea or vomiting

Delayed and immediate effects as well as chronic effects from short and long-term exposure
Eye contact Vapour, mist or fume may cause eye irritation. Exposure to vapour, mist or fume
may cause stinging, redness and watering of the eyes.
Inhalation Vapour, mist or fume may irritate the nose, mouth and respiratory tract.
Skin contact Prolonged or repeated contact can defat the skin and lead to irritation and/or
dermatitis.
Ingestion If swallowed, may irritate the mouth, throat and digestive system. If swallowed, may
cause abdominal pain, stomach cramps, nausea, vomiting, diarrhoea, dizziness and
drowsiness.
General No known significant effects or critical hazards.
Carcinogenicity Suspected of causing cancer. Risk of cancer depends on duration and level of
exposure.
Mutagenicity No known significant effects or critical hazards.
Teratogenicity No known significant effects or critical hazards.
Developmental effects No known significant effects or critical hazards.
Fertility effects No known significant effects or critical hazards.

Numerical measures of toxicity

Acute toxicity estimates
Route ATE value
Oral 16333.33 mg/kg

Other information Naphthalene has been reported to cause developmental toxicity in mice after oral
exposure to relatively high dose levels, but developmental toxicity was not observed
in NTP (National Toxicology Program) sponsored studies in rats and rabbits.
Ingestion or inhalation of naphthalene can result in hemolysis and other blood
abnormalities, and individuals (and infants) deficient in glucose-6-phosphate
dehydrogenase may be especially susceptible to these effects. Inhalation of
naphthalene may cause headache and nausea. Airborne exposure can result in eye
irritation. Naphthalene exposure has been associated with cataracts in animals and
humans.

Section 12. Ecological information

Toxicity
Product/ingredient name Result Species Exposure

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Section 12. Ecological information
Kerosine (petroleum) EL50 1 to 3 mg/l Nominal Fresh water Algae 72 hours
LL50 677.9 mg/l Nominal Fresh water Micro-organism 72 hours
LOEL 1 mg/l Nominal Fresh water Algae 72 hours
NOEL 1 mg/l Nominal Fresh water Algae 24 hours
NOEL 1 mg/l Nominal Fresh water Algae 48 hours
NOEL 1.641 mg/l Nominal Fresh water Micro-organism 72 hours
Acute EL50 1.4 mg/l Nominal Fresh Daphnia 48 hours
water
Acute LL50 2 to 5 mg/l Fresh water Fish 96 hours
Acute NOEL 0.3 mg/l Nominal Fresh Daphnia 48 hours
water
Acute NOEL 2 mg/l Fresh water Fish 96 hours
Chronic EL50 0.89 mg/l Fresh water Daphnia 21 days
Chronic EL50 0.81 mg/l Fresh water Daphnia 21 days
Chronic LOEL 1.2 mg/l Fresh water Daphnia 21 days
Chronic LOEL 0.48 mg/l Fresh water Daphnia 21 days
Chronic NOEL 0.48 mg/l Fresh water Daphnia 21 days
Chronic NOEL 1.2 mg/l Fresh water Daphnia 21 days
Chronic NOEL 0.098 mg/l Nominal Fish 28 days
Fresh water
naphthalene EC50 0.4 mg/l Algae 96 hours
EC50 2.16 mg/l Crustaceans 48 hours
Conclusion/Summary Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic
environment.

Persistence and degradability

Expected to be biodegradable.

Bioaccumulative potential
This product is not expected to bioaccumulate through food chains in the environment.
Product/ingredient name LogPow BCF Potential
naphthalene 3.4 - low

Mobility in soil
Soil/water partition Not available.
coefficient (KOC)
Mobility Spillages may penetrate the soil causing ground water contamination.

Other ecological information Spills may form a film on water surfaces causing physical damage to organisms.
Oxygen transfer could also be impaired.

Section 13. Disposal considerations

Disposal methods The generation of waste should be avoided or minimised wherever possible.
Significant quantities of waste product residues should not be disposed of via the
foul sewer but processed in a suitable effluent treatment plant. Dispose of surplus
and non-recyclable products via a licensed waste disposal contractor. Disposal of
this product, solutions and any by-products should at all times comply with the
requirements of environmental protection and waste disposal legislation and any
regional local authority requirements. Waste packaging should be recycled.
Incineration or landfill should only be considered when recycling is not feasible. This
material and its container must be disposed of in a safe way. Care should be taken
when handling emptied containers that have not been cleaned or rinsed out. Empty
containers or liners may retain some product residues. Vapour from product
residues may create a highly flammable or explosive atmosphere inside the
container. Do not cut, weld or grind used containers unless they have been cleaned
thoroughly internally. Avoid dispersal of spilt material and runoff and contact with

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Section 13. Disposal considerations
soil, waterways, drains and sewers.
Special Precautions for No additional special precautions identified.
Landfill or Incineration

Section 14. Transport information

ADG IMDG IATA
UN number UN1223 UN1223 UN1223

UN proper KEROSENE KEROSENE. Marine pollutant KEROSENE

shipping name
Transport hazard 3 3 3
class(es)

Packing group III III III

Environmental Yes. The environmentally Yes. Yes. The environmentally
hazards hazardous substance mark is hazardous substance mark is
not required. not required.
Additional Hazchem code 3Y The marine pollutant mark is The environmentally
information Initial emergency response not required when transported hazardous substance mark
guide 15 in sizes of ≤5 L or ≤5 kg. may appear if required by
Emergency schedules other transportation
F-E, S-E regulations.

Special precautions for user Not available.

Transport in bulk according Proper shipping name MARPOL Annex 1 rules apply for bulk shipments
to IMO instruments by sea.
Category: Kerosene

Section 15. Regulatory information

Standard for the Uniform Scheduling of Medicines and Poisons
Not scheduled - When packed in containers having capacity of greater than 20 litres.
S5 - When packed in containers having capacity of less than 20 litres.

Consumer products - This product is exempt per Appendix A of the SUSMP.

Industrial Products - Labelling requirements for SUSMP do not apply to a poison that is packed and sold solely for
industrial, laboratory or manufacturing use. However, this product is labelled in accordance with NOSHC National
Code of Practice for labelling of workplace substances.
Model Work Health and Safety Regulations - Scheduled Substances
No listed substance

Montreal Protocol
Ingredient name List name Status
Not listed.

Stockholm Convention on Persistent Organic Pollutants

Ingredient name List name Status
Not listed.

Rotterdam Convention on Prior Informed Consent (PIC)

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Section 15. Regulatory information
Ingredient name List name Status
Not listed.

International lists
National inventory
REACH Status For the REACH status of this product please consult your company contact, as
identified in Section 1.
Australia inventory (AICS) Contact local supplier or distributor.
Canada inventory Not determined.
China inventory (IECSC) Not determined.
Japan inventory (ENCS) Not determined.
Korea inventory (KECI) Not determined.
Philippines inventory Not determined.
(PICCS)
Taiwan Chemical Not determined.
Substances Inventory
(TCSI)
United States inventory Not determined.
(TSCA 8b)

Section 16. Any other relevant information

History
Date of printing 4/9/2021
Date of issue/Date of 4/9/2021
revision
Date of previous issue 2/1/2016
Version 2
Prepared by Product Stewardship
Key to abbreviations ADG = Australian Dangerous Goods
ATE = Acute Toxicity Estimate
BCF = Bioconcentration Factor
GHS = Globally Harmonized System of Classification and Labelling of Chemicals
IATA = International Air Transport Association
IBC = Intermediate Bulk Container
IMDG = International Maritime Dangerous Goods
LogPow = logarithm of the octanol/water partition coefficient
MARPOL = International Convention for the Prevention of Pollution From Ships,
1973 as modified by the Protocol of 1978. ("Marpol" = marine pollution)
NOHSC = National Occupational Health and Safety Commission
REACH = Registration, Evaluation, Authorisation and Restriction of Chemicals
Regulation [Regulation (EC) No. 1907/2006]
STEL = Short term exposure limit
SUSMP = Standard Uniform Schedule of Medicine and Poisons
UN = United Nations
TWA = Time weighted average
VOC = Volatile Organic Compound
SADT = Self-Accelerating Decomposition Temperature
Varies = may contain one or more of the following 64741-88-4, 64741-89-5,
64741-95-3, 64741-96-4, 64742-01-4, 64742-44-5, 64742-45-6, 64742-52-5,
64742-53-6, 64742-54-7, 64742-55-8, 64742-56-9, 64742-57-0, 64742-58-1,
64742-62-7, 64742-63-8, 64742-65-0, 64742-70-7, 72623-85-9, 72623-86-0,
72623-87-1
Procedure used to derive the classification

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Section 16. Any other relevant information
Classification Justification
FLAMMABLE LIQUIDS - Category 3 On basis of test data
SKIN CORROSION/IRRITATION - Category 2 Calculation method
CARCINOGENICITY - Category 2 Calculation method
SPECIFIC TARGET ORGAN TOXICITY - SINGLE Calculation method
EXPOSURE (Narcotic effects) - Category 3
ASPIRATION HAZARD - Category 1 Calculation method
Indicates information that has changed from previously issued version.
Notice to reader
All reasonably practicable steps have been taken to ensure this data sheet and the health, safety and environmental
information contained in it is accurate as of the date specified below. No warranty or representation, express or implied
is made as to the accuracy or completeness of the data and information in this data sheet.

The data and advice given apply when the product is sold for the stated application or applications. You should not use
the product other than for the stated application or applications without seeking advice from BP Group.

It is the user’s obligation to evaluate and use this product safely and to comply with all applicable laws and regulations.
The BP Group shall not be responsible for any damage or injury resulting from use, other than the stated product use
of the material, from any failure to adhere to recommendations, or from any hazards inherent in the nature of the
material. Purchasers of the product for supply to a third party for use at work, have a duty to take all necessary steps to
ensure that any person handling or using the product is provided with the information in this sheet. Employers have a
duty to tell employees and others who may be affected of any hazards described in this sheet and of any precautions
that should be taken. You can contact the BP Group to ensure that this document is the most current available.
Alteration of this document is strictly prohibited.

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