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EC number: 931-740-0 | CAS number: -
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Toxicity to reproduction
Administrative data
- Endpoint:
- screening for reproductive / developmental toxicity
- Remarks:
- based on test type (migrated information)
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1992-03-05
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- Repeated-dose dermal toxicity, similar to that of OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test), studies performed with the only identified and quantified constituent of the registered substance, 2-ethylhexanol. Studies performed with pregnant Fischer F344 rats and they study the developmental toxicity of 2-ethylhexanol. In the absence of the studies conducted for registered substance these studies serve as a good surrogate studies.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 992
- Report date:
- 1992
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test)
- Deviations:
- yes
- Principles of method if other than guideline:
- Pregnant Fischer 344 rats were studied in two studies with an occluded dermal application:
1. Range-finding study
2. Main study - GLP compliance:
- yes
- Remarks:
- U.S EPA Health effects guidelines and Good Laboratory Practice regulations.
- Limit test:
- no
Test material
- Reference substance name:
- 2-ethylhexan-1-ol
- EC Number:
- 203-234-3
- EC Name:
- 2-ethylhexan-1-ol
- Cas Number:
- 104-76-7
- Molecular formula:
- C8H18O
- Details on test material:
- Surrogate material: 2-ethylhexanol.
Test substance - 2-ethylhexanol: 99,72% purity, gas chromatographic verification by the contract laboratory. (sample provided by the Shell developmental company, Houston, TX, USA).
Control substances: 2-methoxyethanol (dermal reference) and valproic acid (cavage reference) had purities of 99,9% and 98,0%, respectively.
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Virgin F344 rats (CDF(R) F344 Crl./Br.)
- Source: Charles River Breeding Laboratories (Kingston, NY)
- Age at study initiation: 70 days / 63 days
- Weight at study initiation: males 175-200g / females 130-150g
- Gestational day 0: appearance of copulatory plug
- Housing: singly
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 2-week quarantine period
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-24
- Humidity (%): 42-65
- Air changes (per hr): not disclosed
- Photoperiod (hrs dark / hrs light): 12 hour
Administration / exposure
- Route of administration:
- dermal
- Vehicle:
- unchanged (no vehicle)
- Details on exposure:
- TEST SITE
- Area of exposure: clipped and shaved dorsal skin of 9,7 cm2 (in the report ca. 1,5 cupic inches)
- Type of wrap if used:2 cupic inch gauze square, occluded with a Lycra-Spandex with Velcro closures. A 1.5x2.5 in. polyethylene patch was attached at the application site under the jacket.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): wiped gently with moist gauze and blotted dry.
- Time after start of exposure: 6-hours
TEST MATERIAL
- Amount(s) applied (volume or weight with unit):
1.Rangefinding study: 0.5, 1, 2, 3 (ml/kg/day) equivalent to 420, 840, 1680, 2520 (mg/kg/day). Positive control: 2-methoxyethanol: 0.5 and 1.5 (ml/kg/day) equivalent to 420 and 1260 (mg/kg/day). Oral cavage reference compound: Valproic acid 400 mg/kg bw/day.
2. Main study: 0.3, 1, 3 (ml/kg/day) equivalent to 252, 840, 2520 (mg/kg/day).Positive control: 2-methoxyethanol 1 (ml/kg/day) equivalent to 840 (mg/kg/day)
- Concentration (if solution): 100%
- Constant volume or concentration used: no
VEHICLE
- No vehicle - Details on mating procedure:
- - M/F ratio per cage: 1:1
- Length of cohabitation: not disclosed
- Proof of pregnancy:[vaginal plug referred to as day 0 of pregnancy: "Gestational day 0: appearance of copulatory plug" - Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- Gas chromatographic: at the beginning of the studies and in the end of the studies. Test material was verified to be stable over the treatment periods.
- Duration of treatment / exposure:
- 6-hours per day
- Frequency of treatment:
- daily
Doses / concentrationsopen allclose all
- Remarks:
- Doses / Concentrations:
252 mg/kg bw/day
Basis:
other: analytical per unit bodyweight
- Remarks:
- Doses / Concentrations:
420 mg/kg bw/day
Basis:
other: analytical per unit bodyweight
- Remarks:
- Doses / Concentrations:
840 mg/kg bw/day
Basis:
other: analytical per unit bodyweight
- Remarks:
- Doses / Concentrations:
1680 mg/kg bw/day
Basis:
other: analytical per unit bodyweight
- Remarks:
- Doses / Concentrations:
2520 mg/kg bw/day
Basis:
other: analytical per unit bodyweight
- No. of animals per sex per dose:
- Range-finding study: 8 animals per study group
Main study: 25 animals per study group - Control animals:
- yes, sham-exposed
- other: Positive control: 2-methoxyethanol... (see attached file)
- Details on study design:
- - Dose selection rationale: range-finding study performed
- Rationale for animal assignment (if not random): random - Positive control:
- Dermal route, positive control: 2-methoxyethanol, oral reference (cavage): Valproic acid
Examinations
- Parental animals: Observations and examinations:
- CAGE SIDE OBSERVATIONS: Yes
- Time schedule: daily, before and after treatment. Draize-score represented.
CLINICAL SIGNS
- Time schedule: daily and skin irritation (scored based on FHSA, 1985).
BODY WEIGHT: Yes
- Time schedule for examinations: Body weights on gestational days 0, 6,9, 12, 15 and 21.
FOOD CONSUMPTION AND COMPOUND INTAKE (if feeding study):
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes, 3-day intervals, through destational days 0-21.
WATER CONSUMPTION AND COMPOUND INTAKE (if drinking water study): No data - Oestrous cyclicity (parental animals):
- Not disclosed, animals were deemed suitable after fecal sampling, histological testing of selected organs, and serum viral antibody testing examination. After a 2-week quarantine period animals were mated 1:1.
- Sperm parameters (parental animals):
- Not disclosed.
- Litter observations:
- All live fetuses were sexed, weighed, and examined for external malformations and for variations.
- Postmortem examinations (parental animals):
- Pregnant females were sacrificed on gestational day 21 by euthanization with CO2 asphyxiation. Maternal body cavities were opened by midline thoracolaporotomy. Maternal uterine weights and liver weights (both studies) and spleen, adrenals, kidneys, and thymus weighs (main study) were recorded. Corpora lutea and uterine implantation sites were counted, and ovaries cervices, vaginas, and abdominal and thoracic cavities were examined grossly. Uteri were examined externally, removed, and dissected longitudinally to expose the contents. All live and dead fetuses and resorption sites were noted,; uteri from nongravid females were tested for early resorptions with ammonium sulfide solution.
- Postmortem examinations (offspring):
- After external examination approximately 50% of the live fetuses per litter from the main study were examined for visceral (thoracic and abdominal) and craniofacial abnormalities. The remainder were examined for skeletal malformations and variations after evisceration, fixation in ethanol, and staining with alizarin red S.
- Statistics:
- The units of comparison were pregnant rat or the litter. Quantitative continuous variables such as maternal body and organ weights were compared to 2-ethylhexanol and sham control groups, between dermal reference (2-methoxyethanol) and sham control groups, and between cavage reference and naive control group. Levene's test for equal variances, ANOVA, and t-tests with Bonferroni probabilities for pairwise comparisons were used. The pooled t-test was used when Levene's test indicated homogeneous variances, all groups were compared by an ANOVA for unequal variances followed when necessary by the separate variance t-test.
Results and discussion
Results: P0 (first parental generation)
General toxicity (P0)
- Clinical signs:
- effects observed, treatment-related
- Description (incidence and severity):
- skin irritation >252 mg/kg bw/day
- Body weight and weight changes:
- effects observed, treatment-related
- Description (incidence and severity):
- body weight reduction >840 mg/kg bw/day
- Food consumption and compound intake (if feeding study):
- effects observed, treatment-related
- Description (incidence and severity):
- body weight reduction >840 mg/kg bw/day
- Organ weight findings including organ / body weight ratios:
- no effects observed
- Histopathological findings: non-neoplastic:
- no effects observed
- Other effects:
- no effects observed
Reproductive function / performance (P0)
- Reproductive function: oestrous cycle:
- not examined
- Reproductive function: sperm measures:
- not examined
- Reproductive performance:
- not examined
Details on results (P0)
Treatment -related effects attributable to 2-ethylhexanol at the application site were exfoliation, encrustation and erythema. There was no edema. Exfoliation and encrustation occurred in both range-finding and main studies at all treatment levels of 2-ethylhexanol. There was no erythema or edema in sham controls. Erythema occurred during treatment with 2-ethylhexanol at levels of 830 mg/kg bw/day and above. Draize scores revealed that irritation was essentially mild. Maximum mean treatment scores occurred on gd10 at 1680 mg/kg bw/day (draize-score 0.4, range-finding study), on gd 11 at 2520 mg/kg bw/day (draize-score 1.1, range-finding study), and on gd 14 at 1680 mg/kg bw/day (draize-score 0.3, main study).
There was no exacerbation by continuent treatment. Erythema subsided immediately after cessation of treatment. There was no exfoliation, encrustation, erythema or edema at the application of positive control, 2-methoxyethanol.
Nasal encrustation and ocula encrustation and discharge were seen mostly in the main study with 2-ethylhexanol and 2-methoxyethanol and in sham controls. Since these effects occurred in controls and mostly disappeared after treatment ceased they are attributed to handling stress.
NOAEL was set at 252 mg/kg bw/day based on skin irritation property, described by draize score on parental animals.
CLINICAL SIGNS
Reduced body weight with 1680 mg/kg bw/day (range-finding study) and 2520 mg/kg bw/day (main study), NOAEL was determined to be 840 mg/kg bw/day. Other effects were not found: gravid uterine weight, early deliveries, pregnancies, fetus viability , early resorptions, and late resorptions.
Effect levels (P0)
- Dose descriptor:
- NOAEL
- Effect level:
- >= 252 mg/kg bw/day (actual dose received)
- Based on:
- test mat.
- Sex:
- female
- Basis for effect level:
- other: see 'Remark'
- Remarks on result:
- not determinable
- Remarks:
- no NOAEL identified
Results: F1 generation
General toxicity (F1)
- Clinical signs:
- no effects observed
- Mortality / viability:
- no mortality observed
- Body weight and weight changes:
- no effects observed
- Sexual maturation:
- not examined
- Organ weight findings including organ / body weight ratios:
- not examined
- Gross pathological findings:
- no effects observed
- Histopathological findings:
- not examined
Details on results (F1)
Effect levels (F1)
- Dose descriptor:
- NOAEL
- Generation:
- F1
- Effect level:
- > 2 520 mg/kg bw/day (actual dose received)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: see 'Remark'
- Remarks on result:
- not determinable
- Remarks:
- no NOAEL identified
Overall reproductive toxicity
- Reproductive effects observed:
- not specified
Applicant's summary and conclusion
- Conclusions:
- Developmental and teratogenic toxicity was determined in this dermal screening test with 2-ethylhexanol, besides reduction of body weight in highest doses and mild skin irritation in all doses, 2-ethylhexanol did not exhibit toxicity to fetuses and risk to pregnancy. Both effects (reduction of body weight, skin irritation) occurred during treatment and were transient or ameliorated after treatment ceased. This study includes approriate sham controls and reference compound via oral cavage. There were no effects on gestational parameters and no significant differences from controls in the incidence of fetal malformations and soft tissue or skeletal variations.
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