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EC number: 215-149-9 | CAS number: 1306-25-8
- 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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 012
- Report date:
- 2012
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- Cadmium telluride
- EC Number:
- 215-149-9
- EC Name:
- Cadmium telluride
- Cas Number:
- 1306-25-8
- Molecular formula:
- CdTe
- IUPAC Name:
- telluroxocadmium
- Details on test material:
- Name of test material: Cadmium telluride
Physical state: Black solid
Purity: > 99.99%
Batch number: 138683
Expiry date: 2 years from the first opening (24 May 2011) if kept under inert atmosphere (e.g. nitrogen)
Storage conditions: 20 ±5ºC under inert gas (e.g. nitrogen)
The pH of Test Item was measured as 5.0.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: S&K-LAP Kft. 2173 Kartal, Császár út 135, HUNGARY
- Age at study initiation: ~12 weeks old
- Weight at study initiation: 3075-3323 g
- Housing: Rabbits were individually housed in AAALAC approved metal wire rabbit cages (65x65 cm with height of 45 cm). Cages were of an open wire structure and cages were placed together to allow some social interaction with rabbit(s) in adjoining cages.
- Diet: Animals received PURINA Base – Lap gr. diet for rabbits produced by AGRIBRANDS Europe Hungary PLC, H-5300 Karcag, Madarasi út, Hungary, ad libitum
- Water: municipal tap water, as for human consumption, ad libitum, from an automatic system.
- Acclimation period: 12 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 17.1-19.0 °C
- Humidity (%): 24-60%
- Air changes (per hr): 15-20 air exchanges/hour
- Photoperiod (hrs dark / hrs light): 12 hours daily, from 6.00 a.m. to 6.00 p.m.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied: 0.5g - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 72h
- Number of animals:
- 3
- Details on study design:
- TEST SITE
- Area of exposure: approximately 6 cm² area of intact skin
REMOVAL OF TEST SUBSTANCE
- Washing: the remaining test item was removed with water at body temperature
- Time after start of exposure: After 4 hours
SCORING SYSTEM:
The dermal irritation scores were evaluated according to the scoring system by Draize (1959)
SCORING SYSTEM OF ERYTHEMA AND OEDEMA FORMATION
Erythema and eschar formation
No erythema 0
Very slight erythema (barely perceptible) 1
Well defined erythema 2
Moderate to severe erythema 3
Severe erythema (beet redness) to slight eschar
formation (injuries in depth) 4
Maximum possible erythema score: 4
Oedema formation
No oedema 0
Very slight oedema (barely perceptible) 1
Slight oedema (edges of it will be well defined
by definite raising) 2
Moderate oedema (raised appr. 1 mm) 3
Severe oedema (raised more than 1 mm and extending
beyond area of exp.) 4
Maximum possible oedema score: 4
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- animals #1, #2, #3
- Time point:
- other: 1h
- Score:
- 1.33
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- animals #1, #2, #3
- Time point:
- 24 h
- Score:
- 0.33
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- animals #1, #2, #3
- Time point:
- 48 h
- Score:
- 0
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- animals #1, #2, #3
- Time point:
- 72 h
- Score:
- 0
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Remarks:
- animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal)
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Remarks:
- animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal)
- Time point:
- 24/48/72 h
- Score:
- 0
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Remarks:
- animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal)
- Time point:
- 24/48/72 h
- Score:
- 0
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- animals #1, #2, #3
- Time point:
- other: 1h
- Score:
- 1
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- animals #1, #2, #3
- Time point:
- 24 h
- Score:
- 0
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- animals #1, #2, #3
- Time point:
- 48 h
- Score:
- 0
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- animals #1, #2, #3
- Time point:
- 72 h
- Score:
- 0
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Remarks:
- animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal)
- Time point:
- 24/48/72 h
- Score:
- 0
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Remarks:
- animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal)
- Time point:
- 24/48/72 h
- Score:
- 0
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Remarks:
- animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal)
- Time point:
- 24/48/72 h
- Score:
- 0
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0.11
- Other effects:
- MORTALITY : no mortality observed during the study.
BODY WEIGHTS: no effect of treatment on body weight.
CLINICAL OBSERVATION
General Daily Examination: no treatment-related clinical signs noted.
Examination of Skin-Irritancy:
At observation one hour after patch removal:
well defined erythema (score2) was noted in one animal, very slight erythema (score 1) was observed in two animals and very slight oedema (score 1) was noted in all animals. The test item was also staining on the hair and skin in all animals.
At observation 24 hours after patch removal:
very slight erythema (score 1) was observed in one animal and the test item was staining on the hair and skin in all animals.
At observation 48 and 72 hours after patch removal:
there were no observed clinical signs noted on the skin of the treated animals
As no clinical signs were observed the study was terminated after the 72 hours observation.
The animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal) for erythema were 0.33, 0.00 and 0.00 respectively.
The animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal) for oedema were 0.00, 0.00 and 0.00 respectively.
The Primary Irritation Index (considering readings at 24, 48 and 72 hours after patch removal) was calculated as 0.11.
Any other information on results incl. tables
SCORING OF ERYTHEMA FORMATION
TABLE 1
Animal No./ |
Body weight (g) |
1 h |
24 h |
48 h |
72 h |
|
at the beginning |
at the end |
|||||
00141/ M |
3323 |
3380 |
2 |
1 |
0 |
0 |
00123/M |
3120 |
3172 |
1 |
0 |
0 |
0 |
00149/M |
3075 |
3144 |
1 |
0 |
0 |
0 |
TOTAL |
- |
- |
4 |
1 |
0 |
0 |
MEAN |
- |
- |
1.33 |
0.33 |
0 |
0 |
SCORING OF OEDEMA FORMATION
TABLE 2
Animal No./ |
Body weight (g) |
1 h |
24 h |
48 h |
72 h |
|
at the beginning |
at the end |
|||||
00141/ M |
3323 |
3380 |
1 |
0 |
0 |
0 |
00123/M |
3120 |
3172 |
1 |
0 |
0 |
0 |
00149/M |
3075 |
3144 |
1 |
0 |
0 |
0 |
TOTAL |
- |
- |
3 |
0 |
0 |
0 |
MEAN |
- |
- |
1 |
0 |
0 |
0 |
M = male
d = day
h = hour
MEAN VALUES OF SKIN IRRITATION SCORES
(24, 48, 72 hours reading)
TABLE 3
Animal Number |
Sex |
Erythema |
Oedema |
00141 |
male |
0.33 |
0.00 |
00123 |
male |
0.00 |
0.00 |
00149 |
male |
0.00 |
0.00 |
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- According to the UN Globally Harmonised System of Classification and Labelling of Chemicals,Cadmium telluride does not require classification as a skin irritant.
- Executive summary:
An acute skin irritation study was performed with Cadmium telluride in New Zealand White rabbits. Parameters monitored during this study included mortality, body weight measurements and clinical observations. The irritancy of the test item was evaluated according to the Draize method (OECD No.: 404, 2002).
A weight of 0.5g granules test item was applied to the skin of the experimental animals as ground to a powder. The test item was applied as a single dose. Sufficient water to damp the material was used to ensure good contact with the skin and an adhesive clear plastic patch was applied. The trunk was wrapped in clear plastic with medical tubing used to hold the patch in place. The untreated skin of each animal served as control.
After 4 hours, the remaining test item was removed with water at body temperature.
To assess skin irritation, animals were examined at 1, 24, 48 and 72 hours after the patch removal. Additional general examinations were performed daily.
There was no mortality or systemic clinical changes related to Cadmium telluride administration.
There was no effect of treatment on body weight.
At observation one hour after patch removal,well defined erythema (score2) was noted in one animal, very slight erythema (score 1) was observed in two animals and very slight oedema (score 1) was noted in all animals.The test item was also staining on the hair and skin in all animals.
At observation 24 hours after patch removal,very slight erythema (score 1) was observed in one animal and the test item was staining on the hair and skin in all animals.
At observation 48 and 72 hours after patch removal,there were no observed clinical signs noted on the skin of the treated animals
As no clinical signs were observed the study was terminated after the 72 hours observation.
The animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal) for erythema were 0.33, 0.00 and 0.00 respectively.
The animals’ individual mean scores (considering readings at 24, 48 and 72 hours after patch removal) for oedema were 0.00, 0.00 and 0.00 respectively.
The Primary Irritation Index (considering readings at 24, 48 and 72 hours after patch removal) was calculated as 0.11.
According to Directive 2001/59/EC,Cadmium telluride does not require classification as a skin irritant.
According to the UN Globally Harmonised System of Classification and Labelling of Chemicals,Cadmium telluride does not require classification as a skin irritant.
According to the classification system based on the scheme devised by Draize (1959),Cadmium telluride is a "mild irritant".
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