Tricyclodecanedimethanol

Repeated dose toxicity: inhalation

Administrative data

Endpoint:

repeated dose toxicity: inhalation

Remarks:

combined repeated dose and reproduction / developmental screening

Type of information:

migrated information: read-across based on grouping of substances (category approach)

Adequacy of study:

supporting study

Study period:

year of publication: 1990

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Acceptable, well-documented publication which meets basic scientific principles

Cross-reference

Reason / purpose for cross-reference:

reference to same study

Data source

Reference

Reference Type:

publication

Title:

Unnamed

Year:

1990

Report date:

1990

Materials and methods

Test guideline

Qualifier:

equivalent or similar to guideline

Guideline:

other: OECD TG 414

Principles of method if other than guideline:

Exposure to max. attainable vapor concentration of 1-octanol, 1-nonanol, and 1-decanol

GLP compliance:

not specified

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

Octan-1-ol

EC Number:

203-917-6

EC Name:

Octan-1-ol

Cas Number:

111-87-5

IUPAC Name:

octan-1-ol

Constituent 2

Reference substance name:

1-octanol

IUPAC Name:

1-octanol

Constituent 3

Reference substance name:

143-08-08

IUPAC Name:

143-08-08

Constituent 4

Reference substance name:

Nonan-1-ol

EC Number:

205-583-7

EC Name:

Nonan-1-ol

Cas Number:

143-08-8

Molecular formula:

C9H20O

IUPAC Name:

Nonan-1-ol

Constituent 5

Reference substance name:

Decan-1-ol

EC Number:

203-956-9

EC Name:

Decan-1-ol

Cas Number:

112-30-1

Molecular formula:

C10H22O

IUPAC Name:

decan-1-ol

Constituent 6

Reference substance name:

1-decanol

IUPAC Name:

1-decanol

Details on test material:

- Analytical purity: reagent-grade chemicals were purchased from commercial sources
- Lot/batch No.:
1-octanol and 1-decanol: both lot No. A15B; Eastman Kodak Co. Rochester, NY
1-nonanol: lot No. 7328 from EM Science, Cherry Hill, NJ:
- Other: samples of each chemical were analyzed for purity by gas chromatography using modifications of the NIOSH analytical methods 1401 and 1402

Specific details on test material used for the study:

CAS number IUPAC name
111-87-5 1-octanol
143-08-8 1-nonanol
112-30-1 1-decanol

Test animals

Species:

rat

Strain:

Sprague-Dawley

Sex:

female

Administration / exposure

Route of administration:

inhalation: vapour

Type of inhalation exposure:

whole body

Vehicle:

other: unchanged (no vehicle)

Details on inhalation exposure:

GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: 0.5 m³ Hinners-type chamber
- Method of holding animals in test chamber: animals were placed in stainless steel wire mesh cages
- Source and rate of air: compressed air
- Method of conditioning air: vapor generation equipment, housed in a sealed glove box
- System of generating particulates/aerosols: a constant flow of alcohol was mixed with a known volume of heated compressed air. Th eresulting vapor/air mixture was introduced into the chamber airflow system upstream from the orifice plate. The resulting turbulence downstream from the orifice plate produced a uniform mixing of the test chemcial throughout the exposure chamber.
- Temperature in air chamber: 70-80°F (21-27°C)
- Air flow rate: no data
- Air change rate: no data
- Method of particle size determination: no data
- Treatment of exhaust air: no data

TEST ATMOSPHERE
- Brief description of analytical method used:
(1) infrared analyzer (Miran 1A) continously recorded concentrations near the rats breathing zone
() charcoal tube samples were collected 2 days per week and analyzed using gas chromatography. Spiked samples were also used to evaluate the accuracy of the GC results.
- Samples taken from breathing zone: yes

VEHICLE : no

Analytical verification of doses or concentrations:

yes

Details on analytical verification of doses or concentrations:

(1) infrared analyzer (Miran 1A) continously recorded concentrations near the rats breathing zone
(2) charcoal tube samples were collected 2 days per week and analyzed using gas chromatography. Spiked samples were also used to evaluate the accuracy of the GC results.

Duration of treatment / exposure:

gestation days 1-19
6 h/day (1-decanol)
7 h/day (1-octanol and 1-nonanol)

Frequency of treatment:

7/week

Doses / concentrations

Remarks:

Doses / Concentrations:
400 (octanol), 150 (nonanol), 100 (decanol) mg/m³
Basis:
analytical conc.

No. of animals per sex per dose:

15

Control animals:

yes, sham-exposed

Details on study design:

- Dose selection rationale: maximum concentrations that could be generated as a vapor at an average chamber temperature of 70-80°F. Generation of higher exposure concentrations resulted in aerosol production inside the inhalation chamber.

- Rationale for animal assignment: random

Positive control:

Yes; in total 13 alcohols with carbon chain skeltons of C1- to C10 were tested.

Examinations

Observations and examinations performed and frequency:

CAGE SIDE OBSERVATIONS: Yes
- Time schedule: daily

DETAILED CLINICAL OBSERVATIONS: No data

BODY WEIGHT: Yes
- Time schedule for examinations: weekly

FOOD CONSUMPTION:
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: group means reported

FOOD EFFICIENCY:
- Body weight gain in kg/food consumption in kg per unit time X 100 calculated as time-weighted averages from the consumption and body weight gain data: No

WATER CONSUMPTION: Yes
- Time schedule for examinations: weekly

OPHTHALMOSCOPIC EXAMINATION: No data

HAEMATOLOGY: No data

CLINICAL CHEMISTRY: No data

URINALYSIS: No data

NEUROBEHAVIOURAL EXAMINATION: no

Sacrifice and pathology:

For developmental toxicology evaluations dams were sacrificed on day 20 of gestation. Fetuses were removed, weighted, sexed and examined for external malformations. The frequency of visceral malformations and variations was determined in one half of the fetuses and the frequency of visceral malformations and variations in the other half.

Statistics:

One-way multivariate analysis of variance/ analysis of variance (MANOVA/ANOVA): number of corpora lutea, resorptions, male and female pups, mean male and female pup weight.
ANOVA: maternal weights, feed and water intake data,
ANOVA: fetal incidence data; also Variance Test for homogeneity of the binominal distribution; Kuskal-Wallis test was used if nonparametric analysis was more appropriate.

Results and discussion

Results of examinations

Clinical signs:

no effects observed

Mortality:

no mortality observed

Body weight and weight changes:

no effects observed

Food consumption and compound intake (if feeding study):

no effects observed

Food efficiency:

not specified

Water consumption and compound intake (if drinking water study):

no effects observed

Ophthalmological findings:

not specified

Haematological findings:

not specified

Clinical biochemistry findings:

not specified

Urinalysis findings:

not specified

Behaviour (functional findings):

no effects observed

Organ weight findings including organ / body weight ratios:

not specified

Gross pathological findings:

no effects observed

Histopathological findings: non-neoplastic:

not examined

Histopathological findings: neoplastic:

not examined

Target system / organ toxicity

Critical effects observed:

not specified

Applicant's summary and conclusion

Conclusions:

Maximum attainable vapor concentrations of aliphatic alcohols decrease rapidly withincreasing chain length. Max. inhalation concentration of 1-nonanol was 150 mg/m³. No maternal toxicity nor toxicity to reproduction was noted in dams exposed during gestation days 1-19 (7h/day). No developmental toxicity or teratogenicy was seen in the progeny.
In total 13 alcohols were tested, with carbon chain lengths ranging from C1 to C10. Maternal toxicity was only seen with C1 to C4 alcohols at ≥5000 ppm, but not with higher alcohols, probably due to the rapid decline of the vapor pressure with increasing chanin length. This implicates for isononanol (and other long chain alcohols):
(1) acute inhalation toxicity testing may scientifically be unjustified, due to low attainable vapor concentrations
(2) repeated inhalation toxicity testing: as above
(3) isononanol: repeated inhalation toxicity testing scientifically unjustified

Executive summary:

The effects of repeated inhalation exposure to 1-octanol, 1-nonanol, and 1-decanol was tested in female rats (15 per group) at the maximum attainable vapor concentrations of 400, 150, and 100 mg/m³, respectively. The rats were exposed during days 1 -19 of gestation for 6h (decanol) or 7 h/day (octanol and nonanol). Dams were sacrificed on gestation day 20, and dams and pups were examined for signs of maternal toxicity, toxicity to reproduction, and developmental toxicity.

(1) maximum attainable vapour concentrations at inhalation chamber temperatures between 21 -27°C were 400, 150, and 100 mg/m³ for octanol, nonanol, and decanol, respectively. Concentrations are bases on analytical data.

(2) No treatment related effects were seen

(2.1) dams:

- maternal toxicity: no signs of toxicity, no mortality, maternal body weight, mean food and mean water consumption unchanged compared to sham-treated controls

- toxicity to reproduction: mean numbers of corpora lutea/litter, resorptions/litter, male or female pups/litter all unchanged compared to sham-treated controls

(2.2) pups

- developmental toxicity: male and female pup weights unchanged compared to controls

- teratogenicity: frequency of skeletal or visceral malformations unchanged

(Nelson et al., Tox Ind Health 6:373 -387, 1990; Nelson et al., J Am Coll Tox 9:93 -97, 1990 (T04167 and T04176)

Overall

The vapour pressure of long chain aliphatic alcohols (carbon chain length C5 and more) is insufficient to reach toxic atmosphere concentrations. This is also valid for octahydro-4,7-methano-1H-indenedimethanol (TCD-Alcohol DM), a dialcohol with a carbon structure of C12. The vapour pressure is determined to be < 1 hPa (extrapolated from experimental result, see Sect. 4.6)