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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Carcinogenicity

Currently viewing:

Administrative data

Endpoint:
carcinogenicity: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Original reference not yet available

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Carcinogene alkylierende substanzen. I. Alkylhalogonide, -sulfate, -sulfonate und ringgespannte heterocyclen
Author:
Druckrey H, Kruse H, Preussman R, Ivankovic S, Landschutz Ch
Year:
1970
Bibliographic source:
Zeitschr Krebsforsch 74: 241-273. Cited in: EU RAR (2002).
Reference Type:
secondary source
Title:
EU Risk Assessment Report Dimethyl Sulphate
Author:
European Chemicals Bureau
Year:
2002
Bibliographic source:
EU RAR, Volume 12. Luxembourg 2002

Materials and methods

Principles of method if other than guideline:
evaluation of carcinogenicity of the test substance in rats after 19-week inhalative exposure
GLP compliance:
no

Test material

Constituent 1
Reference substance name:
Automatically generated during migration to IUCLID 6, no data available
IUPAC Name:
Automatically generated during migration to IUCLID 6, no data available
Details on test material:
- Name of test material (as cited in study report): Dimethyl sulphate
No further data

Test animals

Species:
rat
Strain:
other: BD II
Sex:
not specified
Details on test animals or test system and environmental conditions:
No further details

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure (if applicable):
not specified
Vehicle:
not specified
Details on exposure:
BD-rats (sex unspecified) were exposed to test substance in an inhalation chamber for 130 days (no further details)
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
130 days (19 weeks)
Frequency of treatment:
1 hour/day, 5 day/week, 19 weeks
Post exposure period:
experiments were terminated after 643 days
Doses / concentrationsopen allclose all
Remarks:
Doses / Concentrations:
approx. 17 and 55 mg/m3
Basis:
other: calculated
Remarks:
Doses / Concentrations:
3 and 10 ppm
Basis:
nominal conc.
in air
No. of animals per sex per dose:
20 in the 17 mg/m3 dose group and 27 in the 55 mg/m3 dose group
Control animals:
no
Details on study design:
no additional data
Positive control:
none

Examinations

Observations and examinations performed and frequency:
no data
Sacrifice and pathology:
no data
Other examinations:
no data
Statistics:
no data

Results and discussion

Results of examinations

Clinical signs:
effects observed, treatment-related
Mortality:
mortality observed, treatment-related
Body weight and weight changes:
not specified
Food consumption and compound intake (if feeding study):
not specified
Food efficiency:
not specified
Water consumption and compound intake (if drinking water study):
not specified
Ophthalmological findings:
not specified
Haematological findings:
not specified
Clinical biochemistry findings:
not specified
Urinalysis findings:
not specified
Behaviour (functional findings):
not specified
Organ weight findings including organ / body weight ratios:
not specified
Gross pathological findings:
effects observed, treatment-related
Histopathological findings: non-neoplastic:
effects observed, treatment-related
Histopathological findings: neoplastic:
effects observed, treatment-related
Details on results:
CLINICAL SIGNS, MORTALITY AND GROSS PATHOLOGY
Several deaths due to inflammation of the nasal cavity or pneumonia were reported.
HISTOPATHOLOGY: NEOPLASTIC (if applicable)
In the low dose group of 12 surviving animals 3 were found with malignant tumors (1 squamous cell carcinoma of the nasal epithelium, 2 nervous system tumors). In the high dose group 5/15 rats living more than 643 days developed malignant tumours: 3 squamous cell carcinomas of the nasal cavity, 1 tumor in the cerebellum, and 1 lymphosarcoma of the thorax with multiple lung metastases.

Effect levels

Dose descriptor:
LOAEL
Effect level:
17 mg/m³ air
Sex:
not specified
Basis for effect level:
other: The lowest dose evaluated was carcinogenic
Remarks on result:
other: Effect type: carcinogenicity (migrated information)

Any other information on results incl. tables

-

Applicant's summary and conclusion