Registration Dossier
Registration Dossier
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The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
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EC number: 930-993-4 | CAS number: -
Sensitisation data (human)
Administrative data
- Endpoint:
- sensitisation data (humans)
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- other information
- Study period:
- 19 Feb 1990 - 23 Feb 1990
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Comparable to guideline study with acceptable restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 990
- Report date:
- 1990
Materials and methods
- Type of sensitisation studied:
- skin
- Study type:
- study with volunteers
- Principles of method if other than guideline:
- An approprite quantity of each concentration (0.33 and 0.66 g/mL) of the test material was applied to a Johnson & Johnson 1.8 cm x 1.8 cm band aid clinical occlusive patch. A patch containing deionized distilled water was used as a control. The patches were applied to the designated test sites on the back of each subject (55 persons; age: 18 - 60 years). After the fourty-eight hour occlusive period, the patches were removed. The test sites were graded shortly after removal of the patches once the skin had equilibrated. Twenty-four hours after the patches were removed, each site was graded again. Because some reactions may appear even later, resuls were read again 48 hours after removal of the patch.
- GLP compliance:
- no
Test material
- Reference substance name:
- Zeolite, cuboidal, crystalline, synthetic, non-fibrous
- IUPAC Name:
- Zeolite, cuboidal, crystalline, synthetic, non-fibrous
- Details on test material:
- - Name of test material (as cited in study report): Abscents 55
- Related CAS number: 1318-02-1
- Lot/batch No.: Sample number 53-35; Lot 13979-29
- Storage condition of test material: at room temperature
Constituent 1
Method
- Type of population:
- general
- Controls:
- internal controls (patch with deionized distilled water)
- Route of administration:
- dermal
Results and discussion
- Results of examinations:
- 54 persons completed the entire study. There were no adverse reactions seen or reported during the study. Under the conditions of this study, no reactions were reported for the test material.
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.
