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Toxicological information

Repeated dose toxicity: inhalation

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Administrative data

sub-chronic toxicity: inhalation
other: A 13-week whole-body inhalation toxicity study in rats with neurotoxicity assessments and in vivo genotoxicity assessments
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
key study
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP compliant (except for test substance identity, stability and lot number), guideline study, available as unpublished report, no restrictions, fully adequate for assessment.

Data source

Reference Type:
study report
Report date:

Materials and methods

Test guidelineopen allclose all
according to guideline
OECD Guideline 413 (Subchronic Inhalation Toxicity: 90-Day Study)
The identity, strength, purity and composition or other characteristics to define the test substance along with storage stability was not determined in a GLP compliant laboratory.
according to guideline
EPA OPPTS 870.3465 (90-Day Inhalation Toxicity)
Principles of method if other than guideline:
A 13-week whole-body inhalation toxicity study in rats with neurotoxicity assessments and in vivo genotoxicity assessments
GLP compliance:
Limit test:

Test material

Constituent 1
Reference substance name:
Liquified Petroleum Gas
Liquified Petroleum Gas
Details on test material:
- Name of test material (as cited in study report): liquefied petroleum gas (LPG)
- Substance type: industrial gas
- Supplier: ChevronTexaco Energy Research & Technology Company, 100 Chevron Way, Richmond, CA 94802, USA
- Physical state: colourless gas or liquid in pressurized cylinders
- Analytical purity: 100% LPG
- Lot/batch No.: 120701-01
- Composition of test material, percentage of components (weight %): methane 0.012%, ethane 1.809%, propane & propylene 93.513%, n-butane 2.854%, n-pentane 0.064%, isobutane 1.246%, neopentane 0.003%, isopentane 0.404%, 2,3-dimethylbutane 0.006%, cyclopentane <0.001%, isobutene 0.038%, 1,3-butadiene <0.001%, t-2-butene 0.009%, c-2-butene 0.007%, 3-methyl-1-butene 0.004%, 1-pentene 0.014%, 2-methyl-1-butene 0.005%, t-2-pentene 0.003%, c-2-pentene 0.003%, 2-methyl-2-butene 0.005%, benzene <0.001%
- Expiration date of the lot/batch: 31 December 2007
- Storage condition of test material: Ambient conditions in an outside solvent shed except when in use in the inhalation laboratory.

Test animals

other: Sprague-Dawley CD
Details on test animals or test system and environmental conditions:
- Species: Albino rats (Outbred) VAF/Plus®, Sprague-Dawley derived (CD®), Crl:CD®(SD)IGS BR
- Source: Charles River Laboratories, Kingston, New York 12484, USA
- Age at study initiation: Approximately 8 weeks
- Weight at study initiation: Males mean 280 g (range 243-308 g); females mean 209.1 g (range 187-231 g)
- Fasting period before study: None
- Housing: Individually in stainless steel suspended cages with wire mesh floors and fronts.
- Diet: Certified Rodent diet No 5002 (PMI Nutrition International, St Louis, Missouri, USA) ad libitum
- Water: Municipal water ad libitum
- Acclimation period: Approximately 2 weeks

- Temperature: 17-25°C
- Humidity: 22-99%
- Air changes (per hr): Not reported
- Photoperiod: 12 hrs dark / 12 hrs light

IN-LIFE DATES: From: 20 April 2005 To: 27 July 2005

Administration / exposure

Route of administration:
inhalation: gas
Type of inhalation exposure:
whole body
other: air
Remarks on MMAD:
MMAD / GSD: MMAD 3.740, 2.785, 2.581, 2.166 µm; GSD 2.177, 2.242, 2.215, 2.070; total mass concentration 6.73E-3, 7.31E-3, 7.82E-3, 7.83E-3 mg/m3 for target concentrations of 0, 1000, 5000 and 10000 ppm respectively.
Details on inhalation exposure:
- Exposure apparatus: Stainless steel and glass whole body exposure chambers with a volume of approximately 1000 L
- Method of holding animals in test chamber: Individually housed in stainless steel, wire mesh cages within the exposure chamber, with the placement of animals in chambers rotated weekly to ensure uniform exposure.
- Generation: Pre-study trials had evaluated the optimal set of conditions and equipment that generated a stable and uniform atmosphere at the target exposure levels. Test substance flowed from cylinder into a copper tubing coil, maintained in a warm water bath. From the coil the test substance flowed through a metering valve to a mass flowmeter and then via tubing to the turret of the exposure chamber, where it was mixed with room air.
- Temperature, humidity in exposure chamber: 19-28°C, 22-61%
- Air flow rate: Operated at a minimum rate of 203 L/min. Final airflow set to provide at least one air change /5 mins (12/hour) and a T99 equilibrium time of at most 23 mins.
- Oxygen level: at least 19%
- Animal loading factor: below 5%
- Method of particle size determination: yes. Samples drawn for 20 secs at a flow rate of 5 L/min. MMAD, GSM and total mass concentration were calculated.
- Treatment of exhaust air: coarse filter, a HEPA filter and activated charcoal

- Brief description of analytical method used: Infrared spectrophotometer (IR) 4 times per chamber per day. Gas chromatography (GC) used to characterise at least 5 major components (comprising at least 90% by weight of test substance) once/week/chamber to show test substance stability and comparison between neat test substance and test atmospheres.
- Samples taken from breathing zone: yes
Analytical verification of doses or concentrations:
Details on analytical verification of doses or concentrations:
Exposure levels were determined using an infrared spectrophotometer 4 times/chamber/day. Particle size distribution measurements were also made once weekly using a TSI Aerodynamic Particle Sizer. The mean (± standard deviation) analytical exposure concentrations of LPG were
determined to be 0.0 ± 0.0, 1019 ± 58, 5009 ± 174 and 9996 ± 261 ppm for the air control and the exposure groups, respectively. Particle sizing results indicated that the atmospheres were essentially gas/vapor only, as expected, since there was no substantial difference in particle concentration between the test substance chambers and the air control chamber. Analysis of the major components in the neat test substance and the test atmospheres showed an acceptably close comparison between the neat test substance and the vaporized test substance. The data were consistent pretest and during the study indicating stability of the test substance and the atmosphere generation techniques.
Duration of treatment / exposure:
13 weeks
Frequency of treatment:
6 hours/day, 5 days/week for at least 65 exposures for the main study.
Doses / concentrationsopen allclose all
Doses / Concentrations:
0, 1000, 5000, 10000 ppm
other: target conc.
Doses / Concentrations:
0.0 ± 0.0, 1019 ± 58, 5009 ± 174, 9996 ± 261 ppm
analytical conc.
No. of animals per sex per dose:
10 males and females for th main study (plus 5 males and females for satellite analysis of neuropathology and genotoxicity (micronucleus).
Control animals:
yes, sham-exposed
Details on study design:
- Dose selection rationale: Based on results of a range-finding study (HLS Study number 03-6140) which showed no effects at 100, 1000 or 10000 ppm and no more than 50% of the lower explosion limit (LEL = 21000 ppm)


Observations and examinations performed and frequency:
- Time schedule: twice daily (mortality and severe toxic effects)

- Time schedule: During exposure, animals were observed at least once as a group for behavioural effects, signs of toxicity, and mortality. 10/sex/group were examined twice pretesting and weekly during the study period for clinical signs of toxicity

- Time schedule for examinations: On assignment to treatment group, on day of treatment began, and weekly thereafter

- Time schedule for examinations: weekly


- Time schedule for examinations: Pre-test and at study termination (all animals)

- Time schedule for collection of blood: at termination
- Anaesthetic used for blood collection: Yes (60% carbon dioxide/40% oxygen)
- Animals fasted: Yes (overnight)
- How many animals: 10 sex/group
- Parameters examined: haemoglobin concentration, haematocrit, erythrocyte count, platelet count, mean platelet volume, mean corpuscular volume, mean corpuscular haemoglobin, mean corpuscular haemoglobin concentration, red cell distribution width, total leucocyte count, reticulocyte count, differential leucocyte count, erythrocyte and platelet morphology, prothrombin time, activated partial thromboplastin time

- Time schedule for collection of blood: at termination
- Anaesthetic used for blood collection: Yes (60% carbon dioxide/40% oxygen)
- Animals fasted: Yes (overnight)
- How many animals: 10 sex/group
- Parameters examined: aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, lactate dehydrogenase, blood urea nitrogen, creatinine, glucose, creatinine kinase, choolesterol, total protein, albumin, total bilirubin, direct bilirubin, sodium, potassium, chloride, calcium, inorganic phosphorus, gamma-glutamyl transferase, triglycerides, globulin, albumin/globulin ratio, indirect bilirubin


- Time schedule for examinations: Pre-test and during 2nd, 4th, 8th and 13th week of exposure. Tested on a non-exposure day at least 16 hours after exposure.
- Dose groups that were examined: All
- Battery of functions tested: sensory observations, neuromuscular observations, physical observations and motor activity assessments
Sacrifice and pathology:
SACRIFICE: Fasted overnight prior to exsanguination following carbon dioxide inhalation.

GROSS PATHOLOGY: Yes (all animals) - included external examinations as well as examination of the brain, spinal cord, organs and tissues of the cranial, thoracic, abdominal, and pelvic cavities and neck.

ORGAN WEIGHTS: Yes (all animals). Adrenal gland, brain, epididymes, heart, kidneys, liver, lungs (with mainstem bronchi), ovaries, pituitary, prostate, seminal vesicles, spleen, testes, thyroids (with parathyroids), Zymbals gland.

- tissues examined: (control and high dose only) adrenal glands, aorta (thoracic), bone (sternum/femur), brain (medulla/pons, cerebrum and cerebellum), epididymes, oesphagus, eye, heart, kidneys, large intestine (caecum, colon and rectum), lacrimal gland, larynx, liver, lungs (with mainstream bronchi), lymph node (mesenteric), lymph node (mediastinal), mammary glands, muscle (biceps femoris), nasopharngeal tissue, nerve (sciatic), optic nerve, ovaries, pancreas, prostate, salivary gland with submandibular lymph node, seminal vesicles, small intestine (duodenum, ileum and jejunum), spinal cord (cervical, thoracic and lumbar), spleen, stomach, testes, thymic region, thyroids with parathyroids, trachea, urinary bladder, uterus (body/horns with cervix), Zymbals glands, all macroscopic lesions and tissue masses.
Group mean values of parameters for all the exposure groups were compared to the control group mean values at each time interval, using appropriate statistical methods.

Results and discussion

Results of examinations

Clinical signs:
no effects observed
no mortality observed
Body weight and weight changes:
no effects observed
Food consumption and compound intake (if feeding study):
no effects observed
Ophthalmological findings:
no effects observed
Haematological findings:
no effects observed
Clinical biochemistry findings:
no effects observed
Behaviour (functional findings):
no effects observed
Organ weight findings including organ / body weight ratios:
no effects observed
Gross pathological findings:
no effects observed
Histopathological findings: non-neoplastic:
no effects observed
Details on results:
No treatment-related effect on survival, clinical observations, ophthalmology, terminal body weight, food consumption, functional observational battery, motor activity parameters, haematological parameters, clinical chemistry values, macroscopic or microscopic evaluations, or organ weights was observed at any exposure concentration.
One main study female was euthanised on test day 83 because of poor condition and weight loss. Histopathological examination suggested the loss of this animal was as a result of accidental trauma, and not related to exposure.

Effect levels

Dose descriptor:
systemic toxicity
Effect level:
10 000 ppm
Basis for effect level:
other: highest concentration tested

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion

No treatment-related effect on survival, clinical observations, ophthalmology, terminal body weight, food consumption, functional observational battery, motor activity parameters, haematological parameters, clinical chemistry values, macroscopic or microscopic evaluations, or organ weights was observed at any exposure concentration.

The no observed adverse effect concentration (NOAEC) for Liquified Petroleum Gas (LPG) was 10000 ppm in this study.
Executive summary:

This study was designed to assess the potential inhalation toxicity of liquified petroleum gas (LPG) when administered via whole-body exposures to rats for 13 weeks. The assessment included routine toxicology parameters as well as detailed evaluations of neurotoxicity and genotoxicity parameters.

Sprague-Dawley CD® rats (15/sex/group) were exposed for six hours per day to 0 (air control), 1000, 5000 or 10000 ppm of LPG for 5 days per week for 13 consecutive weeks (highest exposure concentration was selected for safety reasons and approximated 50% of the lower explosive limit).

At the end of the treatment period, all animals were euthanized and necropsied. The following parameters were evaluated: viability, clinical observations, body weights, feed consumption, functional observation battery and motor activity, estrus cycles, sperm assessments, micronucleus assessment, clinical pathology, organ weights, macroscopic and microscopic observations.

All animals (except one female animal exposed at the 10000 ppm level) survived to termination. There were no exposure-related differences in the test substance exposed animals compared to the air control animals. In conclusion,13 weeks of exposure of rats to liquified petroleum gas resulted in no adverse effects of exposure.

Therefore, the 10000 ppm exposure concentration was considered a NOAEC.