Phenol, para-alkylation products with C10-15 branched olefins (C12 rich) derived from propene oligomerization, reaction products with sulphur monochloride and dec-1-ene

Endpoint summary

Description of key information

Oral:
Based upon the results of this study, the apparent NOAEL (no observable adverse effect level) for subacute toxicity & neurotoxicity was considered to be 200 mg/kg/day. This was then adjusted for presence of oil to relate to the Registration material, and the value adopted was 100mg/kg. 
Dermal:
Repeated dermal applications of the test material caused no observable toxicity, with the exception of a slightly increased incidence and severity of skin irritation when compared to controls. The NOAEL for this study is considered to be >250 mg/kg b.wt./day males and female rats, highest dose tested. This is then adjusted to relate to the Registration material at 50% concentration, so the NOAEL value adopted is 125 mg/kg. 

Key value for chemical safety assessment

Repeated dose toxicity: via oral route - systemic effects

Link to relevant study records

Reference

Endpoint:

short-term repeated dose toxicity: oral

Type of information:

migrated information: read-across from supporting substance (structural analogue or surrogate)

Adequacy of study:

key study

Study period:

9th October 1991 to 7th December 1992

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: Guideline study following GLP. The reliability is reduced as the study is being used for read-across purposes.

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test)

Deviations:

no

Principles of method if other than guideline:

The potential subchronic toxicity (Phase A) & neurotoxicity (Phase B) related to the administration of the test material in the Sprague-Dawley Crl: CD®BR rat were evaluated in this combined repeated dose study.

GLP compliance:

yes

Limit test:

no

Species:

rat

Strain:

Sprague-Dawley

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: The Charles River Breeding Laboratories, Inc., Portage, Michigan 49081
- Age at study initiation: Young adult, 50 days old.
- Weight at study initiation: Males, 197g - 240g; Females, 145g - 179g
- Housing: Animals were housed individually in suspended, stainless steel wire-mesh cages.
- Diet/water (e.g. ad libitum): Purina® Certified Rodent Chow #5002 and municipal water were provided did libitum.
- Acclimation period: The animals were acclimated to laboratory conditions for 13 days prior to study initiation. The acclimation period included a one week pretest period for each phase. The animals were observed twice daily for mortality and moribundity.

ENVIRONMENTAL CONDITIONS
- Temperature : 68-76°F
- Humidity (%): 30-70%
occasional deviations from set temperature and humidity levels did not apparently effect the outcome of the study
- Air changes (per hr): approximately 10 fresh air changes per hour.
- Photoperiod (hrs dark / hrs light): 12 hours light/ 12 dark

Route of administration:

oral: gavage

Vehicle:

peanut oil

Details on oral exposure:

PREPARATION OF DOSING SOLUTIONS:
The required amount of test article for each group was drawn into a syringe. A specified amount of vehicle was placed in a storage container. The test article was added to the vehicle while mixing with a laboratory mixer until the test material had been incorporated. The preparation was then stirred (magnetic stir bar) throughout the sampling, dispensation and dosing procedures, and periods of non-use. Storage containers were wrapped in foil for additional light protection. Test article preparations were formulated weekly; the prepared suspensions for each dose group were stirred at least 30 minutes prior to sampling.

Analytical verification of doses or concentrations:

yes

Details on analytical verification of doses or concentrations:

Analytical Tests: Homogeneity, 8 and 14 day stability and test article concentration analyses were conducted on test material preparations.

Strata Sampled: The top, middle and bottom of the test material preparations were sampled for homogeneity and stability; the middle of a preparation was sampled for concentration.

Sample Volume: 10 ml

Samples were taken in duplicate. One set of samples was sent to the sponsor for analysis; the second set was retained at WIL Research Laboratories, Inc., at ambient temperature until issuance of the final report.

Samples were collected prior to study initiation (homogeneity and stability analyses) and from each dosing preparation on the first and last day of use (concentration analyses).

Duration of treatment / exposure:

28 days for all dose groups and 42 days for the control and high dose recovery groups

Frequency of treatment:

daily

Remarks:

Doses / Concentrations:
0, 50, 200 and 1000 mg/kg b.wt./day
Basis:
actual ingested

No. of animals per sex per dose:

There were 5 rats/sex/group for the 4-week exposure groups, and initially the same group size for the control and high dose 2-week recovery
groups. In addition there were control and high dose satellite groups of 10 males for neurotoxicity evaluations.

Control animals:

yes, concurrent vehicle

Details on study design:

Dose concentrations were 0, 50, 200 and 1000 mg/kg b.wt./day administered in a dose volume of 5 mL/kg b.wt./day.

Positive control:

No data

Observations and examinations performed and frequency:

CAGE SIDE OBSERVATIONS: Yes
- Time schedule: all animals in all study phases were observed approximately one hour following dosing during the treatment period. Significant findings were noted.

DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: Detailed clinical observations were recorded daily for all animals, prior to dose administration.

BODY WEIGHT: Yes
- Time schedule for examinations: Individual body weights were recorded weekly, beginning one week prior to treatment.

HAEMATOLOGY: Yes
- Time schedule for collection of blood:
Clinical pathologic parameters were evaluated on all surviving rats (5/sex/group) selected for a scheduled necropsy following 28 days of test article administration. The same parameters were evaluated on all recovery animals in the control group (4 females; 5 males) and 1000 mg/kg/day group (5/sex/group) selected for necropsy on study day 42. Animals were fasted overnight before taking blood and urine samples. Blood was collected from the inferior vena cava at the time of necropsy. Urine was collected in metabolism cages; urine volume was determined from an overnight sample.
- Animals fasted: Yes
- Parameters examined:
Total Leukocyte Count (White Cell)
Erythrocyte Count (Red Cells)
Hemoglobin
Hematocrit
Mean Corpuscular Volume (MCV)
Mean Corpuscular Hemoglobin (MCH)
Mean Corpuscular Hemoglobin Concentration (MCHC)
Reticulocyte Count (Reticulocyte)
Platelet Count (Platelet)
RBC Morphology
Platelet Estimate
Differential WBC Count - Percent and Absolute
- Segmented Neutrophil (Segmented)
- Lymphocyte
- Monocyte
- Eosinophil
- Unsegmented Neutrophil (Unsegmented)
- Prothrombin Time (Pro Time)
Activated Partial Thromboplastin Time (APTT)


CLINICAL CHEMISTRY: Yes
- Time schedule for collection of blood:
Clinical pathologic parameters were evaluated on all surviving rats (5/sex/group) selected for a scheduled necropsy following 28 days of test article administration. The same parameters were evaluated on all recovery animals in the control group (4 females; 5 males) and 1000 mg/kg/day group (5/sex/group) selected for necropsy on study day 42. Animals were fasted overnight before taking blood and urine samples. Blood was collected from the inferior vena cava at the time of necropsy. Urine was collected in metabolism cages; urine volume was determined from an overnight sample.
- Animals fasted: Yes
- Parameters examined:
Glucose
Urea Nitrogen
Creatinine
Sodium
Potassium
Serum Aspartate Aminotransferasea (Aspartat Transfer)
Chloride
Calcium
Globulin
A/G Ratio
Lactate Dehydrogenase (Lactate 'Genase)
Triglycerides
Uric Acid
B/C Ratio
Serum Alanine Aminotransferaseb (Alanine Transfer)
Serum Alkaline Phosphatase (Alkaline Phos'tse)
Total Bilirubin (Total Bili)
Total Cholesterol (Cholesterol)
Total Protein
Phosphorus
Albumin
Creatine Kinase
Gamma Glutamyltransferase (Glutamyl Transfer)
Plasma Cholinesterase (Cholin Plasma)

URINALYSIS: Yes
- Time schedule for collection of urine:
Clinical pathologic parameters were evaluated on all surviving rats (5/sex/group) selected for a scheduled necropsy following 28 days of test article administration. The same parameters were evaluated on all recovery animals in the control group (4 females; 5 males) and 1000 mg/kg/day group (5/sex/group) selected for necropsy on study day 42. Animals were fasted overnight before taking blood and urine samples. Blood was collected from the inferior vena cava at the time of necropsy. Urine was collected in metabolism cages; urine volume was determined from an overnight sample.
- Metabolism cages used for collection of urine: Yes
- Animals fasted: Yes
- Parameters examined:
Volume
Color (CLOR)
Appearance (APP)
Specific gravity (SG)
pH
Protein (PRO)
Glucose (GLU)
Ketones (KET)
Bilirubin (BIL)
Occult blood (BLD)
Nitrites (NIT)
Leukocytes (WBC)
Microscopy of sediment (MICRO)

NEUROBEHAVIOURAL EXAMINATION: Yes
- Time schedule for examinations:
Observations on male rats in the control and 1000 mg/kg/day groups were made pre-study and then 14, 28 and 42 (recovery animals only) days after the first exposure to the test article. All observations were performed prior to test article administration. Testing was performed by the same technicians without knowledge of the animal group assignment. The FOB was performed in a sound-proofed room equipped with a white noise generator set to operate at 70 ± 10 db. with one exception; home cage observations were performed in the animal room.
- Battery of functions tested:
Hindlimb extensor strength
Grip strength-hind and forelimb
Hindlimb foot splay
Rotarod performance
Approach response
Touch response
Startle response
Tail pinch
Pupil response
Eye blink response
Forelimb extension
Hindlimb extension
Air righting reflex
Olfactory orientation

Sacrifice and pathology:

GROSS PATHOLOGY: Yes.
For the subchronic toxicity phase, 5 animals/sex/group were necropsied on study day 28 and the remaining animals in the control group (4 females; 5 males) and 1000 mg/kg/day group (5/sex/group) were necropsied on study day 42 (recovery).
The necropsy included an examination of the external surface, all orifices, and the cranial, thoracic, abdominal and pelvic cavities including the viscera.
The following organs were weighed for animals at the scheduled necropsy. Absolute weights, and organ to fmal body weight and brain weight were calculated.
Adrenals
Liver
Brain
Pituitary (Phase C only)
Kidneys
Ovaries or Testes

HISTOPATHOLOGY: Yes.
Microscopic examination of hematoxylin-eosin stained paraffin sections were conducted on the following tissues from control and 1000 mg/kg/day:
Adrenal Glands
All gross lesions
Brain
Ovaries
Epididymides
Pituitary Gland
Heart
Prostate
Kidneys
Seminal Vesicles
Liver
Spleen Testes

Other examinations:

A functional observation battery (home cage, handling, open field, sensory, neuromuscular and physiological observations) was conducted
pre-study and on days 14, 28 and 42 on 5 males of the control and high dose satellite groups.

Statistics:

Body weights, body weight changes, food consumption, and absolute and relative organ weights were analyzed by a one-way analysis of variance (ANOVA). If significant differences were indicated by the ANOVA, Dunnett's test was used to compare the control and treated groups.

Clinical signs:

effects observed, treatment-related

Mortality:

mortality observed, treatment-related

Body weight and weight changes:

effects observed, treatment-related

Food consumption and compound intake (if feeding study):

no effects observed

Food efficiency:

not examined

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

not examined

Ophthalmological findings:

not examined

Haematological findings:

no effects observed

Clinical biochemistry findings:

effects observed, treatment-related

Urinalysis findings:

no effects observed

Behaviour (functional findings):

no effects observed

Organ weight findings including organ / body weight ratios:

effects observed, treatment-related

Gross pathological findings:

no effects observed

Histopathological findings: non-neoplastic:

no effects observed

Histopathological findings: neoplastic:

not examined

Details on results:

CLINICAL SIGNS AND MORTALITY
No mortalities were observed in either sex at dose levels of 50, 200 or 1000 mg/kg/day.
The predominant clinical signs associated with test material administration occurred one hour following treatment at the 1000 mg/kg/day level in both males and females. These findings included salivation, clear material around the mouth and red or yellow staining around the mouth. These clinical signs were initially observed within the first two weeks of dosing and generally persisted until cessation of dose administration. Clear material around the mouth was observed as single incidents for two males and one female in the 200 mg/kg/day group.
Other clinical fmdings were observed during the study, but the frequency in the treated groups was similar to the control group or the findings were limited to a few animals. Therefore, these observations were considered to be incidental to test material administration.

BODY WEIGHT AND WEIGHT GAIN
Weekly group mean body weights in the 1000 mg/kg/day males were comparable to the control group values during the pretest week and for study weeks 0, 1 and 2. During study-weeks 3 and 4, however, group mean body weights at this high dose level were slightly lower (3-5 %) than the control group data. Correspondingly, cumulative group mean body weight changes (from study day 0) were slightly reduced during the intervals 0-3 and 0-4 weeks in the 1000 mg/kg/day males. Although these reductions were not statistically significant, they were considered to be treatment-related. A marginal improvement in cumulative mean body weight gains was noted during weeks 0-5 and 0-6, when the animals were not administered the test article.
Weekly group mean body weights and cumulative group mean body weight changes in the 50 and 200 mg/kg/day males and in the 50, 200 and 1000 mg/kg/day females were comparable to the control group values.

FOOD CONSUMPTION AND COMPOUND INTAKE (if feeding study)
No adverse effects were apparent on food consumption (evaluated as g/animal/day and g/kg/day) for males or females at dose levels of 50, 200 or 1000 mg/kg/day.

HAEMATOLOGY
Hematology parameters in the treated groups were similar to those values observed for the control group. Hemoglobin and hematocrit week 6 (recovery) values in the 1000 mg/kg/day males were significantly lower (p < 0.05) than the concurrent control group values. These reductions were not considered to be treatment-related because:
1) the week 6 values were comparable to the week 4 values;
2) the values were within the observed ranges of the WIL historical control data for hemoglobin (10.76-22.24 g/dL) and hematocrit (35.66-65.34%);
3) a decrease in these parameters at week 4, not week 6, could have indicated a treatment-related effect.

CLINICAL CHEMISTRY
No test article related changes were apparent in serum chemistry parameters at any dose level tested. Glucose levels were lower in the 1000 mg/kg/day males (21 %) and in the 50 (37 %), 200 (41 %) and 1000 mg/kg/day females (27%) than the concurrent control group values at the week 4 evaluation. The reductions in the treated female groups were statistically significant (p < 0.05 or p < 0.01) but the response was not dose-related. The values were, however, within the observed ranges of the WIL historical control data for glucose in males (1.2 - 270.8 mg/dL) and females (16.2 - 215.8 mg/dL). (All clinical pathology historical control "ranges" consist of the mean value ± 2 standard deviations.) Cholesterol values for males and females at the 1000 mg/kg/day dose level were significantly reduced (p < 0.05) below concurrent control group values at the week 4 evaluation. These values were within the observed ranges of the WIL historical control data for males (22.0 - 88.0 mg/dL) and females (26.6 - 101.4 mg/dL). The toxicological significance of these reductions was uncertain.

URINALYSIS
No test article related differences were apparent in the urinalysis parameters between the control and treated groups.

NEUROBEHAVIOUR
No remarkable differences were apparent between the control group and the treated group when sensorimotor responses were evaluated for weeks -1 (pretest), 2, 4 and 6 (recovery).

ORGAN WEIGHTS
Slight increases in group mean absolute adrenal gland weights at the 1000 mg/kg/day dose level were noted at the week 4 necropsy in males (12%) and females (6%), and at the week 6 (recovery) necropsy in males (14%) and females (19%). When evaluated relative to the final body weight and brain weight, increases in the group mean adrenal gland weight were apparent; the weight relative to the fmal body weight for the 1000 mg/kg/day recovery females was statistically significant (p <0.01). These adrenal weight increases were interpreted to be a potential effect of test material administration. No apparent effects on group mean adrenal gland weights were noted in the males and females at the 50 and 200 mg/kg/day dose levels.
Group mean kidney, liver, testes and ovaries weights were apparently unaffected by test material administration. At week 4, statistically significant elevations in group mean kidney weight in the 1000 mg/kg/day males (p < 0.05) and group mean liver weight in the 1000 mg/kg/day females (p < 0.01) were noted when organ weights were evaluated-relative to the final body weight. However, concurrent increases in the organ weights on an absolute and relative to brain weight basis were not observed.

GROSS PATHOLOGY
No treatment-related internal findings were observed in animals at the scheduled week 4 or week 6 (recovery) necropsies. Macroscopic tissue changes were noted similarly in the control and treated animals or were generally single fmdings.

HISTOPATHOLOGY: NON-NEOPLASTIC
Microscopic examination of the gross lesions observed at the week 4 and week 6 necropsies did not reveal any effects of test material administration. Findings were noted in a limited number of animals in the treated groups or in control and treated groups at a similar incidence.

Key result

Dose descriptor:

NOAEL

Effect level:

200 mg/kg bw/day (actual dose received)

Based on:

test mat.

Sex:

male

Basis for effect level:

organ weights and organ / body weight ratios

Critical effects observed:

not specified

Conclusions:

Based upon the results of this study, the apparent NOAEL (no observable adverse effect level) for subchronic toxicity & neurotoxicity was considered to be 200 mg/kg/day.

Executive summary:

The potential subchronic toxicity, neurotoxicity and reproductive toxicity related to the administration of the test material in the Sprague-Dawley Crl: CD®BR rat were evaluated in this combined repeated dose study conducted in line with OECD guideline 422 with slightly expanded scope. The test article was administered by the oral route (gavage) daily for 28 consecutive days to animals in the subchronic toxicity (5/sex/group) and neurotoxicity phases (5 males/group), followed by a 14 day recovery period in the control and high dose groups.

Dose levels were 50, 200 and 1000 mg/kg/day. A concurrent control group received the vehicle, peanut oil, on a comparable regimen. A dose volume of 5 ml/kg was used for all groups. Parameters common to all study phases included viability, clinical signs, body weights, food consumption and necropsy evaluations. Clinical pathology and organ weight data were collected in the subchronic toxicity phase. Neuropathology and functional observational battery data were collected in the neurotoxicity phase.

The adverse effects observed in this study are summarized below:

* Salivation, clear material around the mouth, red or yellow staining around the mouth and/or red material around the nose were treatment-related clinical signs noted one-hour following dosing in males and females receiving 1000 mg/kg/day.

* Weekly group mean body weights and body weight gains in males were decreased at a dose level of 1000 mg/kg/day. This occurred during weeks 3-4 in the subchronic toxicity phase & weeks 2-4 in the neurotoxicity phase. A possible recovery was noted by the 1000 mg/kg/day males during weeks 5 and 6 in the subchronic toxicity and neurotoxicity phases.

* Increased group mean adrenal gland and pituitary gland weights (absolute and relative to brain weights) were observed in males receiving 1000 mg/kg/day during the reproduction phase. A potential effect on adrenal gland weight was apparent also for females at the 1000 mg/kg/day level, noted during the subchronic toxicity phase. No other organ weights (brain, liver, kidneys, testes or ovaries) were adversely affected.

Based upon the results of this study, the apparent NOAEL (no observable adverse effect level) for subchronic toxicity & neurotoxicity was considered to be 200 mg/kg/day.

The study is being used as read across to a structurally similar substance.

Endpoint conclusion

Endpoint conclusion:

adverse effect observed

Dose descriptor:

NOAEL

100 mg/kg bw/day

Study duration:

subacute

Species:

rat

Quality of whole database:

Database is adequate for characterisation for test material; good quality 422 and also 407. The original NOAEL in the study is 200mg/kg bw/day. The presence of oil in the test samples is then accounted for and ultimate NOAEL adopted for Registration material is 50% of the above value (100mg/kg bw/day).

Repeated dose toxicity: inhalation - systemic effects

Endpoint conclusion

Endpoint conclusion:

no study available

Repeated dose toxicity: inhalation - local effects

Endpoint conclusion

Endpoint conclusion:

no study available

Repeated dose toxicity: dermal - systemic effects

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed

Dose descriptor:

NOAEL

125 mg/kg bw/day

Study duration:

subacute

Species:

rat

Quality of whole database:

Database is adequate for characterisation for test material. The original NOAEL is 250mg/kg bw/day. The presence of oil in the test samples is then accounted for and ultimate NOAEL adopted for Registration material is 50% of the above value (125 mg/kg)

Repeated dose toxicity: dermal - local effects

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed

Study duration:

subacute

Species:

rabbit

Quality of whole database:

Adequate: 3 studies on similar materials.

Additional information

There are no available data for this endpoint for CAS: 96152-43-1, therefore studies from supporting, structurally similar substances have been used as for read-across purposes to address the endpoints. The NOAELs derived have been adjusted for the Registration material to account for the presence of oil.

Oral

- In the key study for repeat dose toxicity, oral exposure (Lamb, 1993, report number: WIL-187001), the study was conducted to the OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test) and GLP. This study was used as the key study to adress this endpoint as the substance was tested at the lowest dose levels and therefore is considered to give the worst case scenario for assessment purposes. The reliability rating for this study is 1, however this is being used as read across to a supporting substance as there was no available data to fulfil this endpoint for the test material and so the reliability rating will be reduced to 2, according to the criteria of Klimisch, 1997. This study is being used as read across from Phenol, tetrapropenyl-, sulfurized, carbonates, calcium salts, overbased CAS No. 122384-87-6/68784-26-9.

The following supporting study is also available:

- In the Schroeder, 1998 study (Huntingdon Life Sciences report number: 96-4084) the study was conducted according to OECD Guideline 407 (Repeated Dose 28-Day Oral Toxicity in Rodents). The study was conducted in line with GLP.

The reliability rating for this study is 1, however this is being used as read across to a supporting substance as there was no available data to fulfil this endpoint for the test material and so the reliability rating will be reduced to 2, according to the criteria of Klimisch, 1997. The study is being used as read across to a structurally similar substance (Phenol, tetrapropenyl-, sulfurized, calcium salts; CAS No. 122384-85-4/68855-45-8). NOAEL = 300 mg/kg b.wt./day for males and females based on increased adrenal weights and increased food consumption without commensurate body weight gain.

A further repeat dose study (28 and 90d, Haas 2010) exists on a related material from 2010, however the study information does not add key information to that above, despite the longer duration, and the NOAELs are higher than those derived above.

Dermal

- In the key study for repeated dose toxicity, dermal exposure (Korenaga et al, 1986, report number: SOCAL 2319), the study was conducted to the OECD Guideline 410 (Repeated Dose Dermal Toxicity: 21/28-Day Study) and GLP. The reliability rating for this study would be 1, however this is being used as read across to a supporting substance as there was no available data to fulfil this endpoint for the test material and so the reliability rating will be reduced to 2, according to the criteria of Klimisch, 1997.

Other supporting studies available however are not considered to be as reliable and so the results are not used in a hazard conclusion.

- The Biodynamics study, 1981 was not considered the key study as it was conducted less recently than the above key study, there was no GLP data and no guideline was specified although it seems similar to OECD 410 with deviations. Deviations are as follows: Only 2 dose groups were used, dressing was only a paper towel, not gauze as specified in the OECD guideline and the test site was wiped with a paper towel, no solvent used to remove test material. A reliability rating of 2 was assigned according to the criteria of Klimisch, 1997. Treatment-related effects were evident in the low- and high-dose males treated with the test material as indicated by marked, statistically significant, dose-related decreases in the absolute and relative (organ/body weight ratios) weights of the testes (absolute weight decreases of approximately 70% and 80%) and epididymides (absolute weight decreases of approximately 40% and 50%) at the end of the treatment period. The results of the microscopic examinations indicated that the topical administration of 25% and 100% (w/v) of the test material, for the period used in this study, causes topical irritating skin lesions in both male and female rabbits. Male rabbits, receiving 25% and 100% (w/v) of the test material, had an increased incidence of aspermatogenesis, reduced numbers of spermatids and a diffuse tubular hypoplasia when compared to control males. These changes had not completely resolved themselves in the four week recovery rabbits receiving 25% and 100% (w/v) of the test material.

- The Biodynamics study, 1983 was not considered the key study as it was conducted less recently than the above key study and no guideline was specified although it seems similar to OECD 410 with deviations. Deviations are as follows: Only 2 dose groups were used there was no data on dressing or removal of test material at the test site and only males were used in this study, OECD specifies 5 males/females per dose. A reliability rating of 2 was assigned according to the criteria of Klimisch, 1997. Increased incidence of desquamation, red raised pustules and red raised areas of eschar noted in the high dose group animals when compared to the control group animals. At necropsy, 2 animals in each of the treated groups were noted to have scabs, sores or necrotic areas on the dorsal cervical skin. The Group 2 animals showed an increase in mean epididymal weights while the group 3 animals showed a decrease in mean epididymal weights when compared to control group animals. These findings are statistically significant.

Total bilirubin and total protein levels were decreased in group 2 animals when compared to the control group values. Total bilirubin and glucose levels and the albumin/globulin ratio were decreased in Group 3 animals when compared to the control group animals.

Inhalation

In accordance with column 2 of REACH Annex XI, section 8.6, it is considered justifiable to omit the inhalation study. The substance only exists in liquid form and it will not be aerosolized in its normal use pattern and is not anticipated to form small particles or droplets. As such testing via the inhalation route is not considered appropriate for this substance.

Justification for selection of repeated dose toxicity via oral route - systemic effects endpoint:
Systemic parental toxicity: increased pituitary weight. Also some neonatal toxicity at this level.

Justification for selection of repeated dose toxicity dermal - local effects endpoint:
Repeated dermal applications of the test material caused no observable toxicity in the highest quality study, with the exception of a slightly increased incidence and severity of skin irritation when compared to controls.

Repeated dose toxicity: via oral route - systemic effects (target organ) neurologic: pituitary

Justification for classification or non-classification

The key toxicity values for repeated dose toxicity were above those requiring classification in accordance to Directive 67/548/EEC or the CLP Regulation (EC) No 1272/2008. Therefore classification was not considered to be necessary.