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EC number: 204-327-1 | CAS number: 119-47-1
- 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
Developmental toxicity / teratogenicity
Administrative data
- Endpoint:
- developmental toxicity
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: GLP and OECD Guideline study (TG 421), acceptable documented (abstract and result tables in English, publication in Japanese)
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 999
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: OECD Guideline 421 (Reproduction/Developmental Toxicity Screening Test)
- Deviations:
- no
- GLP compliance:
- yes
- Limit test:
- no
Test material
- Reference substance name:
- 6,6'-di-tert-butyl-2,2'-methylenedi-p-cresol
- EC Number:
- 204-327-1
- EC Name:
- 6,6'-di-tert-butyl-2,2'-methylenedi-p-cresol
- Cas Number:
- 119-47-1
- Molecular formula:
- C23H32O2
- IUPAC Name:
- 2-tert-butyl-6-[(3-tert-butyl-2-hydroxy-5-methylphenyl)methyl]-4-methylphenol
- Details on test material:
- purity: 98.2%, produced by Sumitomo Chemical, Lot No: 710140
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Crj: CD(SD)
- Details on test animals or test system and environmental conditions:
- Weight at study initiation: (P) Males: 332-383 g; Females: 206-238 g
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- other: in 5% gum arabic
- Details on mating procedure:
- Male/female per cage: 171, length of cohabitation: at the most 14 d, until proof of pregnancy (formation of vaginal closing or sperm detection in vagina)
- Duration of treatment / exposure:
- male: 50-52 d, female: 40-48 d (from 14 days before mating to the day 3 of lactation)
- Frequency of treatment:
- daily
- Duration of test:
- male: 50-52 d, female: 40-48 d (from 14 days before mating to the day 3 of lactation)
- No. of animals per sex per dose:
- 12/per dose group/sex
- Control animals:
- yes, concurrent vehicle
- Details on study design:
- clinical observations: general appearance twice a day, organ weights: testis, epididymis, cauda epididymis, ovary, microscopic evalauations:( control and all teatment groups): testis, caput epididymis, (control and 800 mg/kg group): seminal vesicle, ovary
Examinations
- Maternal examinations:
- BODY WEIGHT: Yes,
DETAILED CLINICAL OBSERVATIONS: Yes
FOOD CONSUMPTION: Yes
POST-MORTEM EXAMINATIONS: Yes
- Ovaries and uterine content:
- lengh of gestation, corporal lutea, implantation scars, implantation index, gestation index, pups born, delivery index, live pups born, sex ratio at birth. birth index,
- Fetal examinations:
- Dead pups on day 0 of lactation, live birth index, live pups on day 4 of lactation, viability index, external anomalies, body weights of pups
- Statistics:
- Dunnett's or Scheffe's test for continuous data and Chi square test for quantal data
- Indices:
- live birth index, viability index, implantation index, gestation index, delivery index
Results and discussion
Results: maternal animals
Maternal developmental toxicity
- Details on maternal toxic effects:
- Maternal toxic effects:yes
Details on maternal toxic effects:
decrease in body weight gain,
Effect levels (maternal animals)
open allclose all
- Dose descriptor:
- NOAEL
- Effect level:
- 50 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Basis for effect level:
- other: maternal toxicity
- Dose descriptor:
- LOAEL
- Effect level:
- 200 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Basis for effect level:
- other: maternal toxicity
- Dose descriptor:
- NOAEL
- Effect level:
- 50 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Basis for effect level:
- other: developmental toxicity
- Dose descriptor:
- LOAEL
- Effect level:
- 200 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Basis for effect level:
- other: developmental toxicity
Results (fetuses)
Effect levels (fetuses)
- Dose descriptor:
- NOAEL
- Effect level:
- 50 mg/kg bw/day
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: Pups (200 mg/kg bw): Pup numbers on day 0 and 4 of lactation were decreased
- Remarks on result:
- other: Pups (200 mg/kg bw): Pup numbers on day 0 and 4 of lactation were decreased
Fetal abnormalities
- Abnormalities:
- not specified
Overall developmental toxicity
- Developmental effects observed:
- not specified
Any other information on results incl. tables
Dams:
Females (200 mg/kg bw):Suppression of body weight gain during the lactation period, lower food consumption was evident during the pre-mating, pregnancy and lactation periods, decrease in the number of corpora lutea, decrease in number of implantation scars and number of pups born
Females (800 mg/kg bw):Supression of body weight gain was noted during the pregnancy and lactation periods, lower food consumption was noted during the pre-mating, pregnancy and lactation periods; decrease in the number of corpora lutea, decrease in number of implantation scars and number of pups born, 1 dam was unable to deliver pups, and 1 dam lost all their pups during the lactation period
Offspring:
Pups (200 mg/kg bw): Pup numbers on day 0 and 4 of lactation were decreased
Pups (800 mg/kg bw): the number of pups on day 0 and 4 of lactation, live birth index, and body weights of both sexes on day 4 of lactation were decreased, and the number of stillbirths was increased
Organ weight of female rats
Dose (mg/kg) | 0 | 12.5 | 50 | 200 | 800 |
number of dams | 12 | 12 | 12 | 12 | 12 |
Body weight (g) | 310.4 ± 12.3 | 312.2 ± 18.9 | 310.7 ± 17.2 | 287. 4± 13.3** | 281.9 ± 22.9** |
Ovaries (mg) | 94.50 ± 12.06 | 91.43 ± 10.00 | 89.88 ± 8.77 | 89.69 ± 16.74 | 88.78 ± 14.65 |
significantly different from control (**p<0.01)
Number of estrous cases and reproductive performance
Dose (mg/kg) | 0 | 12.5 | 50 | 200 | 800 |
Number of females | 12 | 12 | 12 | 12 | 12 |
Number of estrous cases before mating (14 days) | 3.3 ± 0.5 | 3.5 ± 0.5 | 3.5 ± 0.5 | 3.7 ± 0.5 | 3.2 ± 0.6 |
Fertility index (%) | 100.0 | 100.0 | 100.0 | 91.7 | 100.0 |
number of pregnant females with live pups | 12 | 12 | 12 | 11 | 10 |
Observation of pups
Dose (mg/kg) | 0 | 12.5 | 50 | 200 | 800 |
Number of dams | 12 | 12 | 12 | 12 | 12 |
Lengh of gestation (days) | 22.08 ± 0.29 | 22.00 ± 0.00 | 22.33 ± 0.49 | 22.45 ± 0.52 | 22.27 ± 0.65 |
Corpa lutea | 16.4 ± 3.0 | 16.4 ± 2.6 | 16.3 ± 1.5 | 15.1 ± 1.4 | 14.1 ± 1.6* |
Implantation scars | 14.3 ± 3.0 | 14.7 ± 1.1 | 15.2 ± 1.3 | 13.5 ± 1.4 | 13.1 ± 1.5* |
Implantation index | 86.9 ± 14.7 | 91.0 ± 12.8 | 93.6 ± 7.4 | 90.1 ± 8.5 | 93.1 ± 7.2 |
Gestation index (%) | 100 | 100 | 100 | 100 | 83.3 |
Pups born | 13.5 ± 3.3 | 13.5 ± 1.0 | 14.8 ± 1.3 | 11.7 ± 1.4** | 12.2 ± 1.8* |
Live pups born | 13.1 ± 3.2 | 13.3 ± 0.8 | 14.3 ± 1.3 | 11.5 ± 1.0** | 11.3 ± 4.1 |
Birth index (%) | 90.7 ± 9.4 | 91.2 ± 4.8 | 94.7 ± 4.4 | 86.0 ± 9.6 | 83.8 ± 28.8 |
Dead pups on day 0 of lactation | 0.4 ± 0.7 | 0.2 ± 0.4 | 0.4 ± 0.5 | 0.2 ± 0.6 | 0.9 ± 2.7 |
Live birth index (%) | 97.1 ± 4.6 | 98.9 ± 2.5 | 97.2 ± 3.5 | 98.8 ± 3.9 | 89.9 ± 30.0 |
Live pups on day 4 of lactation | 13.1 ± 3.2 | 13.3 ± 0.8 | 14.3± 1.4 | 11.4 ± 1.0** | 12.4 ± 1.8 |
Viability index (%) | 100.0 ± 0.0 | 100.0 ± 0.0 | 99.4 ± 2.0 | 98.5 ± 3.4 | 100.0 ± 0.0 |
External anomalies (%) | 0.0 ± 0.0 | 0.0 ± 0.0 | 0.0 ± 0.0 | 0.0 ± 0.0 | 0.0 ± 0.0 |
Body weight of pups | |||||
Male Day 0 | 6.78 ± 0.40 | 6.81 ± 0.23 | 6.90 ± 0.50 | 7.60 ± 0.52** | 6.97 ± 0.71 |
Male Day 4 | 11.02 ± 0.83 | 11.05 ± 0.77 | 10.58 ± 1.11 | 11.29 ± 1.14 | 9.68 ± 1.72* |
Female Day 0 | 6.43 ± 0.37 | 6.40 ± 0.17 | 6.53 ± 0.44 | 7.25 ± 0.49** | 6.61 ± 0.66 |
Female Day 4 | 10.33 ± 0.81 | 10.36 ± 0.67 | 10.20 ± 1.15 | 10.77 ± 1.04 | 9.30 ± 1.64 |
Significantly different from control (*p<0.05, **p<0.01)
Applicant's summary and conclusion
- Executive summary:
In a reproduction/developmental toxicity screening test (OECD Guideline 421) with rats toxic effects of the test substance Vulcanox BKF were seen. In dams suppression of the body weight gain was noted in the 200 mg/kg bw/day treatment group during the lactation period. In the highest dose group (800 mg/kg bw/day) a suppression of body weight gain was seen during the pregnancy and lactation periods. Lower food consumption was noted in the 200 and 800 mg/kg bw/day groups during pre-mating, pregnancy, and lactating periods. Decreases in the number of corpora lutea, number of implantation scars, and number of pups born were noted at 200 and 800 mg/kg bw/day. In addition, 1 dam was unable to deliver pups, and 1 dam lost all their pups during the lactation period at 800 mg/kg bw/day. No external anomalies were found in any of the pups evaluated
The maternal NOAEL for developmental toxicity was assessed to be 50 mg/kg bw/ day and the NOAEL for pup development is considered to be 50 mg/kg bw/day (MHWJ 1999).
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