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EC number: 237-695-7 | CAS number: 13927-71-4
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 3-14 April 2001
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 001
- Report date:
- 2001
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- Minors deviations were observed but not considered to have compromised the validity or integrity of the study.
- Principles of method if other than guideline:
- Minor deviations observed: relative humidity recorded in the animal room was sometimes outside of the target ranges specified in the protocol, the animal's breeder was CEGAV, the animals were given 110 pelleted diet (instead of 112).
- GLP compliance:
- yes
Test material
- Reference substance name:
- Bis(dibutyldithiocarbamato-S,S')copper
- EC Number:
- 237-695-7
- EC Name:
- Bis(dibutyldithiocarbamato-S,S')copper
- Cas Number:
- 13927-71-4
- Molecular formula:
- C18H36CuN2S4
- IUPAC Name:
- bis(dibutyldithiocarbamato-S,S')copper
- Test material form:
- solid
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
-sex: male
- Source: CEGAV, 61350 Saint Mars d'Egrenne, France
- Age at study initiation: no data
- Weight at study initiation: 3.2 ± 0.1 kg
- Housing: individually in polystyrene cages
- Diet (e.g. ad libitum): free access to 110 pelleted diet (UAR, Villemoisson, Epinay sur orge, France)
- Water (e.g. ad libitum): water filtered, ad libitum
- Acclimation period: at least 5 days before the beginning of the study
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18+/-3°C
- Humidity (%): 30-70%
- Air changes (per hr): 12
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- other: clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- undiluted
- Duration of treatment / exposure:
- 3 minutes and 4 hour(s)
- Observation period:
- 14 days
- Number of animals:
- 3
- Details on study design:
- ADMINISTRATION:
- Area of exposure: application for 4 hours on the right flank and for 3 minutes on the left flank
- Total quantity applied: 500 mg
- Administration frequency: once
- Removal of test substance: residual was wiped off by means of moistened cotton pad.
EXAMINATIONS:
- Scoring system: Draize's score
- Examination time points: 1h, 24 h, 48 h and 72 hours after the patch removal. When persistent irritation reactions were noted at 72 hours, the observation period was extended up daily to their complete reversibility (day 10).
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- fully reversible within: 10 days
- Remarks on result:
- other: not evaluated in the two other animals
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- 3 rabbits
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritant / corrosive response data:
- AFTER 3-MINUTE EXPOSURE: No cutaneous reaction was observed but a brown coloration of the skin which could have masked a possible very slight erythema between days 1 and 3.
AFTER 4-HOUR EXPOSURE:
- A brown coloration of the skin was noted in all animals. It could have masked a possible very slight or a well-defined erythema in 2 animals, up to day 3 (72h) or 5 but no cutaneous reaction was noted afterwards. In these two animals, no oedema was observed. However, it should be noted that in worst case, the mean irritation scores would have remained lower than 2, for these 2 animals.
- In the third rabbit, the brown coloration was resolved by the 24-hour scoring interval and a well-defined erythema was recorded: grade 2-erythema from day 2 up to day 5 and a grade 1 up to day 9. Moreover, a slight oedema (grade 2) was noted on day 3.
MEAN SCORES OVER 24, 48 AND 72h:
- For erythema: not calculable for 2 animals because of the skin coloration and 2.0 in the third animal.
- For oedema: 0.0, 0.0 and 0.7.
Any other information on results incl. tables
Table 1: individual cutaneous examinations and mean values of the scores recorded at each reading (24, 48 and 72 hours) for the first animal (application for 3 minutes)
Rabbit number |
Dermal irritation |
scores |
Mean irritation score (1) |
|||
1h (D1) |
24h (D2) |
48h (D3) |
72h (D4) |
|||
994 |
Erythema |
C1 |
C1 |
C1 |
0 |
(2) |
Oedema |
0 |
0 |
0 |
0 |
0.0 |
|
Other |
* |
* |
* |
C |
|
(1) mean of scores on days 2, 3 and 4, (2): not calculated
* : none, D = day, h = hour
C = Brown coloration of the skin
C1 = brown coloration of the skin which could have masked a possible very slight erythema
Table 2: individual cutaneous examinations and mean values of the scores recorded at each reading (24, 48 and 72 hours) for each animal (application for 4 hours)
Rabbit number |
Dermal irritation |
scores |
Mean irritation score (1) |
|||
1h (D1) |
24h (D2) |
48h (D3) |
72h (D4) |
|||
994 |
Erythema |
C2 |
C2 |
C1 |
C1 |
(2) |
Oedema |
0 |
0 |
0 |
0 |
0.0 |
|
Other |
* |
* |
* |
* |
|
|
576 |
Erythema |
C2 |
C2 |
C1 |
0 |
(2) |
Oedema |
0 |
0 |
0 |
0 |
0.0 |
|
Other |
* |
* |
* |
C |
|
|
577 |
Erythema |
C2 |
2 |
2 |
2 |
2.0 |
Oedema |
0 |
0 |
2 |
0 |
0.7 |
|
Other |
* |
C |
C |
C |
|
Rabbit number |
Dermal irritation |
Scores |
|||||
D5 |
D6 |
D7 |
D8 |
D9 |
D10 |
||
994 |
Erythema |
C1 |
0 |
- |
- |
- |
- |
Oedema |
0 |
0 |
- |
- |
- |
- |
|
Other |
* |
C |
- |
- |
- |
- |
|
576 |
Erythema |
- |
- |
- |
- |
- |
- |
Oedema |
- |
- |
- |
- |
- |
- |
|
Other |
- |
- |
- |
- |
- |
- |
|
577 |
Erythema |
2 |
1 |
1 |
1 |
1 |
0 |
Oedema |
0 |
0 |
0 |
0 |
0 |
0 |
|
Other |
C |
C |
C |
C |
C |
C |
(1) mean of scores on days 2, 3 and 4, (2): not calculated
* : none, D = day, h = hour
C = Brown coloration of the skin
C1 = brown coloration of the skin which could have masked a possible very slight erythema
C2= brown coloration of the skin which could have masked a possible well-defined erythema
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Remarks:
- not skin irritating
- Conclusions:
- Under these experimental conditions, the test substance CDBC is slightly irritant when applied topically to rabbits.
- Executive summary:
The potential of the test substance CDBC to induce skin irritation was evaluated in rabbits according to OECD (404) and EC guidelines, and in compliance with the principles of GLP.
In the first instance, the test substance was applied for periods of 3 minutes and 4 hours to a single male rabbit. Since the test substance was not severely irritant on the first animal, it was than applied for 4 hours to two other animals. A single dose of 500 mg of CDBC in its original form was applied to the closely-clipped skin of one flank. Cutaneous reactions were observed approximately 1 hour, 24, 48 and 72 hours after removal of the dressing and then daily until reversibility of cutaneous reactions. The mean values of the scores for erythema and oedema were calculated for each animals.
After a 3-minute exposure (one animal): no cutaneous reactions were observed. A brown coloration of the skin was noted; it could have masked a possible very slight erythema between days 1 to 3.
After a 4 -hour exposure (three animals): A brown coloration of the skin was noted in all animals; it could have masked a possible very slight or well-defined erythema up to day 3 (one animal) or 5 (one animal). No cutaneous reactions were observed afterwards in these two animals. In the third animal, a well-defined erythema was noted from day 2 to day 5, then a very slight erythema was recorded up to day 9. A slight oedema was noted on day 3.
Mean scores over 24, 48 and 72 hours were not calculable for eryhtema because of the skin coloration for two animals. In the third animal, mean scores were 2.0 for erythema and 0.7 for oedema.
Under these experimental conditions, the test substance CDBC is slightly irritant when applied topically to rabbits.
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