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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Acute Toxicity: inhalation

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP, non-guideline study, available as unpublished report, restrictions in design and/or reporting but otherwise adequate for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1977
Report date:
1977

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
2 rats/sex exposed (whole body) for 4 hours to atmospheres of Shellsol A and observed for the following 14 days
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Reference substance name:
Solvent naphtha (petroleum), light arom.
EC Number:
265-199-0
EC Name:
Solvent naphtha (petroleum), light arom.
Cas Number:
64742-95-6
IUPAC Name:
64742-95-6
Constituent 2
Reference substance name:
Shellsol A
IUPAC Name:
Shellsol A
Details on test material:
- Name of test material (as cited in study report): Shellsol A
- Substance type: hydrocarbon solvent (essentially C9 isomers, particularly trimethylbenzenes)
- Physical state: liquid
- Source: Shell Nederland Raffinarderij B.V. refinery, Pernis, Rotterdam, The Netherlands

Test animals

Species:
rat
Strain:
other: CD (COBS)
Sex:
male/female
Details on test animals or test system and environmental conditions:
- Source: Charles River (UK) Ltd., Manston, Kent, UK
- Age at study initiation: 7-8 weeks
- Weight at study initiation: no data
- Housing: no data
- Diet: ad libitum (except during exposure)
- Water: ad libitum (except during exposure)
- Acclimation period: no data

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure:
whole body
Vehicle:
other: air
Details on inhalation exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: tubular glass chamber (2 rats/sex/chamber)
- Exposure chamber volume: no data
- System of generating atmosphere: Atmospheres generated dynamically by the near saturation of air supplied to the test chamber

TEST ATMOSPHERE
- Brief description of analytical method used: monitored continuously by means of a high temperature total hydrocarbon analyser (calibrated using a gravimetric procedure)
Analytical verification of test atmosphere concentrations:
yes
Duration of exposure:
4 h
Concentrations:
10.2 mg/L
No. of animals per sex per dose:
2
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: no data
- Necropsy of survivors performed: no
Statistics:
not applicable

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
10 200 mg/m³ air
Exp. duration:
4 h
Remarks on result:
other: no mortalities at highest dose tested
Mortality:
no mortalities
Clinical signs:
other: lethargic behaviour

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The acute (4 hour) inhalation LC50 of Shellsol A to male and female rats was greater than 10,200 mg/m3 (10.2 mg/L)
Executive summary:
Rats were exposed for 4 hours to a near saturated atmosphere of Shellsol A (a mixture of trimethylbenzenes) at 10.2 mg/L. There were no deaths and no adverse signs other than lethargic behaviour; The acute LC50 was greater than 10,200 mg/m3.