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EC number: 947-912-3 | 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
Dermal absorption
Administrative data
- Endpoint:
- dermal absorption in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study report with acceptable restrictions (no data on analytical purity of unlabelled test substance, non-GLP, limited documentation of methods and results)
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 985
- Report date:
- 1985
Materials and methods
- Principles of method if other than guideline:
- An in vivo percutaneous absorption study was carried out with the substance using both control rats and rats treated topically with 2000 mg/kg bw/day for thirteen weeks. The percutaneous absorption of the substance in rats was measured over 4 days following a single topical administration of 14C-labelled test substance (2000 mg/kg bw).
- GLP compliance:
- no
Test material
- Reference substance name:
- Bis(tridecyl) adipate
- EC Number:
- 241-029-0
- EC Name:
- Bis(tridecyl) adipate
- Cas Number:
- 16958-92-2
- Molecular formula:
- C32H62O4
- IUPAC Name:
- ditridecyl adipate
Constituent 1
- Radiolabelling:
- yes
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Details on the strain: Rat/crl COBS CD[SD] BR/Charles River, Lakeview, New Jersey
- Source: Charles River, Lakeview, New Jersey
- Age at study initiation: 49 days
- Weight at study initiation: males: 161.9 - 166.8 g; females: 149.2 - 150.5 g
- Housing: individually, in suspended, stainless steel cages, with wire mesh bottoms and fronts
- Diet: Purina Certified Lab Chow #5002 in pellet form, ad libitum
- Water: tap water, delivered by an automatic watering system, ad libitum
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21
- Humidity (%): 50
- Photoperiod (hrs dark / hrs light): 12/12
Administration / exposure
- Type of coverage:
- occlusive
- Vehicle:
- unchanged (no vehicle)
- Duration of exposure:
- 1. Pretreated rats: 13 weeks topical exposure (unlabelled test substance)
Treatment: 4 days (14C-labelled test substance)
2. Untreated rats: control rats from 13-week dermal study
Treatment: 4 days (14C-labelled test substance) - Doses:
- 2000 mg/kg bw
- No. of animals per group:
- 5 animals/sex/dose
- Control animals:
- no
- Details on study design:
- APPLICATION OF DOSE:
A plastic ring with an inside area of 1.2 cm2 was attached securely to the back of each rat with adhesives. A single dose of the test substance was applied to completely cover the skin inside the ring (58 µL). The amount of test substance used was equivalent to the high dose used in the thirteen week study (on a µg/cm2 skin surface basis).
SITE PROTECTION / USE OF RESTRAINERS FOR PREVENTING INGESTION: yes
To prevent the rats from removing the test substance, a wire mesh cover was attached to the ring. Each rat was fitted with a carboard "Elizabethan" collar and placed in a separate metabolism cage for once-daily collection of urine and feces.
SAMPLE COLLECTION
- Collection of urine and faeces: once daily
- Terminal procedure: blood, tissues and organs were removed from the rats after sacrifice for determination of levels of radioactivity, as measured by liquid scintillation counting.
- Analysis of organs: liver, kidney. stomach, bladder, small intestine, and large intestine
Results and discussion
Percutaneous absorptionopen allclose all
- Key result
- Dose:
- 2000 mg/kg bw
- Parameter:
- percentage
- Absorption:
- 10.6 - 11.6 %
- Remarks on result:
- other: 4 days
- Remarks:
- rats previously untreated
- Key result
- Dose:
- 2000 mg/kg bw
- Parameter:
- percentage
- Absorption:
- 9.1 - 10.8 %
- Remarks on result:
- other: 4 days
- Remarks:
- rats pre-treated for 13 weeks at 2000 mg/kg bw/day with the test substance
Any other information on results incl. tables
Table 1: Percentage of the applied 14C-labelled test substance recovered in the body
|
Male |
Female |
Control rats |
11.6% (SD = 3.2) |
10.6% (SD = 5.3) |
Pre-treated rats |
10.8% (SD = 1.6) |
9.1% (SD = 0.6) |
No significant differences were observed in comparing the percutaneous absorption of the test substance in male and female rats. Furthermore, no significant differences were observed in comparing the percutaneous absorption of the substance in control and pretreated rats. Thus, it appears that repeated treatment of the skin with the test substance at 2000 mg/kg bw/day for thirteen weeks had no effect on the percutaneous absorption of the substance in male and female rats.
The absorbed substance was observed to eliminate very slowly from the animals following diffusion through the stratum corneum. After four days, 52-63% of the substance absorbed by control rats and 81-87% absorbed by treated rats was still retained in the body. These results suggest that thirteen weeks of dermal treatment with the substance had an effect on the elimination of absorbed test substance from the animals.
Table 2: In vivo percutaneous absorption of 14C-labelled test substance (2000 mg/kg bw) in control rats
|
|
Summed & applied dose recovered (mean & SD of 4 rats) |
|||
Sex |
Days |
Urine |
Faeces |
Tissues |
Total |
Male |
1 |
0.19 (0.21) |
0.02 (0.01) |
- |
0.21 (0.22) |
2 |
0.87 (0.75) |
0.08 (0.12) |
- |
0.95 (0.82) |
|
3 |
2.68 (1.65) |
0.36 (0.31) |
- |
3.04 (1.88) |
|
4 |
3.52 (1.76) |
0.70 (0.25) |
7.35 (1.50) |
11.57 (3.18) |
|
Female |
1 |
0.04 (0.07) |
0.04 (0.04) |
- |
0.08 (0.12) |
2 |
0.31 (0.47) |
0.08 (0.08) |
- |
0.39 (0.55) |
|
3 |
3.75 (4.21) |
0.25 (0.24) |
- |
4.00 (4.14) |
|
4 |
4.73 (4.61) |
0.42 (0.23) |
5.49 (1.00) |
10.64 (5.33) |
Table 3: In vivo percutaneous absorption of 14C-labelled test substance (2000 mg/kg bw) in pre-treated rats
|
|
Summed & applied dose recovered (mean & SD of 4 rats) |
|||
Sex |
Days |
Urine |
Faeces |
Tissues |
Total |
Male |
1 |
0.05 (0.07) |
0.06 (0.03) |
- |
0.11 (0.08) |
2 |
0.27 (0.22) |
0.14 (0.07) |
- |
0.41 (0.25) |
|
3 |
0.56 (0.40) |
0.37 (0.16) |
- |
0.92 (0.42) |
|
4 |
0.73 (0.43) |
0.64 (0.27) |
9.42 (1.64) |
10.79 (1.56) |
|
Female |
1 |
0.13 (0.13) |
0.06 (0.03) |
- |
0.18 (0.13) |
2 |
0.70 (0.68) |
0.14 (0.07) |
- |
0.85 (0.73) |
|
3 |
1.02 (0.86) |
0.26 (0.13) |
- |
1.28 (0.98) |
|
4 |
1.34 (0.90) |
0.35 (0.15) |
7.43 (1.29) |
9.13 (0.55) |
Applicant's summary and conclusion
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.