Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
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.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 701-290-8 | 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
Sensitisation data (human)
Administrative data
- Endpoint:
- sensitisation data (humans)
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 001
- Report date:
- 2001
Materials and methods
- Type of sensitisation studied:
- skin
- Study type:
- study with volunteers
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- human repeat insult patch test (HRIPT)
- GLP compliance:
- yes
Test material
- Reference substance name:
- Sucrose di(acetate) hexaisobutyrate
- EC Number:
- 204-771-6
- EC Name:
- Sucrose di(acetate) hexaisobutyrate
- Cas Number:
- 126-13-6
- IUPAC Name:
- Sucrose Acetate Isobutyrate
- Details on test material:
- Eastman SAIB-100, Industrial Grade
GMNP0119702
PM 01197-00
Lot#0023134
Glass bottle containing a transparent yellow gel
20% w/w in Acetone
Constituent 1
Method
- Type of population:
- general
- Ethical approval:
- confirmed, but no further information available
- Subjects:
- Two hundred fifty-five ( 49 males, 206 females) subjects were screened for the study. Two
hundred forty-one ( 44 males, 197 females) subjects, ages 18 and older, signed the
informed consent and were enrolled onto the study.
Thirty-eight subjects, who were enrolled, failed to complete the study. The subject number
and reason for non-completion are listed in Appendix IV.
Two hundred three subjects (40 males, 163 females) completed all phases of the study.
Study Initiated: April 9, 2001
Date Completed: June 29, 2001 - Details on study design:
- The objective of this study was to evaluate six individual test articles for the induction of contact sensitization by repetitive applications to the skin of human volunteers and to report any irritation observed with the test articles. Two hundred three subjects completed all phases of the study.
The test articles listed below were tested simultaneously in this study employing the referenced concentrations. The test articles were received by Hill Top Research on February 16, 2001.
A EAN 063039, PM 03758 "TOTM" Plasticizer of plastics
B EAN 002800, PM 01315 "TXIB" Plasticizer of plastics
C EAN 908266, PM 01197, SAIB-100, Industrial Grade
D EAN 975778, PM 23094 Fiber lubricant
E EAN 907040, PM 04595 "DOTP" plasticizer manufacturing of plastics
F EAN 900124, PM 00080 "DEP" plasticizer
Under the conditions of the study, HTR Code A (EAN 063039, PM 03758 "TOTM" Plasticizer), HTR Code B (EAN 002800, PM 01315 "TXIB" Plasticizer), HTR Code C (EAN 908266, PM 01197, SAIB-100, Industrial Grade), HTR CodeD (EAN 975778, PM 23094), HTR Code E (EAN 907040, PM 04595 "DOTP" plasticizer) and HTR Code F · (EAN 900124, PM 00080 "DEP" plasticizer) \Vere found to be non-irritating and did not elicit evidence of sensitization.
Results and discussion
- Results of examinations:
- There were nine adverse events which occurred during the course of this study. One of which was definitely related, one possibly related and the remainder unrelated to the test articles. These are listed in Appendix V. One of the reported adverse events was a severe adverse event (SAE). Subject No. 183 reported enlarged lymph nodes in the cervical area on April 13, 2001. The subject was discontinued from the study, went under a physician's
care and was initially diagnosed with breast cancer. Subsequent tests were inconclusive for cancer or any other diagnosis. The event was ongoing at the end of the study.
Under the conditions of the study, HTR Code A (EAN 063039, PM 03758 "TOTM" Plasticizer), HTR Code B (EAN 002800, PM 01315 "TXIB" Plasticizer), HTR Code C (EAN 908266, PM 01197, SAIB-100, Industrial Grade), HTR CodeD (EAN 975778, PM 23094), HTR Code E (EAN 907040, PM 04595 "DOTP" plasticizer) and HTR Code F · (EAN 900124, PM 00080 "DEP" plasticizer) \Vere found to be non-irritating and did not elicit evidence of sensitization.
Any other information on results incl. tables
HTR Code C (EAN 908266, PM 01197, SAIB-1 00, Industrial Grade): Responses during induction consisted of isolated instances of slight erythema and 2 occurrences of mild erythema. Responses during challenge consisted of 3 instances of slight erythema at 48 hours, all of which resolved by 96 hours, and a single instance of slight erythema first appearing at the 96-hour evaluation (Subject No. 1 02). Under the conditions of the study, EAN 908266, PM 01197, SAIB-100, Industrial Grade was found to be non-irritating and did not elicit evidence of sensitization.
Applicant's summary and conclusion
- Conclusions:
- Under the conditions of the study, SAIB was found to be non-irritating and did not elicit evidence of sensitization.
- Executive summary:
The objective of this study was to evaluate six individual test articles for the induction of contact sensitization by repetitive applications to the skin of human volunteers and to report any irritation observed with the test articles. One of the test articles was SAIB, which was applied to the skin of volunteers as a 20% solution in acetone. Data indicate that SAIB was found to be non-irritating and did not elicit evidence of sensitization.
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.