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EC number: 203-430-9 | CAS number: 106-75-2
- 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:
- 1968
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Documentation insufficient for assessment. Due to different testing conditions (occlusive instead of semi aocclusive) different exposure times (1, 5, 15 min and 20 h instead of 4 h) the study is, hoever, not directly comparable to an OECD TG 405.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Report date:
- 1968
Materials and methods
- Principles of method if other than guideline:
- 2 rabbits were treated for 1, 5 and 15 minutes and 2 other animals for 20 hours using occlusive conditions. 0.5 ml test substance is applied onto the intact skin.
- GLP compliance:
- no
Test material
- Reference substance name:
- Oxydiethylene bis(chloroformate)
- EC Number:
- 203-430-9
- EC Name:
- Oxydiethylene bis(chloroformate)
- Cas Number:
- 106-75-2
- Molecular formula:
- C6H8Cl2O5
- IUPAC Name:
- oxydiethane-2,1-diyl dichlorocarbonate
- Details on test material:
- - Name of test material (as cited in study report): Diglycoldichlorkolensäureester
- Physical state: liquid
- Analytical purity: no data
- Other: pH 1; Melting point +4 °C; Boiling point 199 °C
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- Vienna White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Gaukler, Offenbach, Germany
- Weight at study initiation: 2.14 kg (male); 2,32 kg (male)
ENVIRONMENTAL CONDITIONS
no data
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 500 µl - Duration of treatment / exposure:
- 1, 5, and 15 minutes; 20 hours
- Observation period:
- 24 h and 8 days after treatment.
- Number of animals:
- 2
- Details on study design:
- TEST SITE
- Area of exposure: 2.5 * 2.5 cm application to the dorsal skin.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): 50 % Lutrol solution
- Time after start of exposure: 1, 5, 15 min post application, the 20 h exposure was not washed.
SCORING SYSTEM: descriptive scoring system comparable to draize score used in OECD TG 404
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 1.5
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks on result:
- other: 20 h occlusive
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 8 days
- Remarks on result:
- other: 20 h occlosive
- Irritant / corrosive response data:
- still moderate to strong eschar visible 8 days after application
Any other information on results incl. tables
The results indicate a strong potential for skin irritation
Exposition: |
20 h |
|||
Animal |
Reading |
Erythema |
Edema |
Comment |
1 |
24 h |
2 |
3 |
|
2 |
24 h |
2 |
0 |
|
1 |
48 h |
2 |
0 |
|
2 |
48 h |
2 |
0 |
|
1 |
8 d |
2 |
0 |
eschar formation; anemic, slight suprafacial necrosis |
2 |
8 d |
2 |
0 |
eschar formation |
mean |
24 - 48 h |
2.0 |
0 |
|
|
|
|
|
|
Exposition: |
15 min |
|||
Animal |
Reading |
Erythema |
Edema |
Comment |
1 |
24 h |
2 |
0 |
|
2 |
24 h |
1 |
0 |
|
1 |
48 h |
2 |
0 |
|
2 |
48 h |
2 |
0 |
|
1 |
8 d |
0 |
0 |
eschar formation |
2 |
8 d |
0 |
0 |
eschar formation |
mean |
24 - 48 h |
1.75 |
0 |
|
Exposition: |
5 min |
|||
Animal |
Reading |
Erythema |
Edema |
Comment |
1 |
24 h |
2 |
0 |
|
2 |
24 h |
1 |
0 |
|
1 |
48 h |
2 |
0 |
|
2 |
48 h |
1 |
0 |
|
1 |
8 d |
0 |
0 |
eschar formation |
2 |
8 d |
0 |
0 |
|
mean |
24 - 48 h |
1.50 |
0 |
|
|
|
|
|
|
Exposition: |
1 min |
|||
Animal |
Reading |
Erythema |
Edema |
Comment |
1 |
24 h |
2 |
0 |
|
2 |
24 h |
1 |
0 |
|
1 |
48 h |
2 |
0 |
|
2 |
48 h |
2 |
0 |
|
1 |
8 d |
0 |
0 |
eschar formation |
2 |
8 d |
0 |
0 |
eschar formation |
mean |
24 – 48 h |
1.75 |
0 |
|
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.