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Diss Factsheets
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EC number: 616-436-5 | CAS number: 77098-07-8
- 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
Endpoint summary
Administrative data
Description of key information
Not a skin or eye irritant when tested in rabbits.
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Additional information
EYE IRRITATION
To assess the irritant and/or corrosive effects on the eyes of rabbits, TBPA Diol was instilled into the right eye of each of six rabbits. Observations were recorded at 1, 24, 48 and 72 hours after treatment. No positive ocular scores were recorded. The test article was not irritating to the eyes. This study was conducted according to Good Laboratory Practices. (Mallory et al. 1986. Primary Eye Irritation. PH 421-ET-009-86. Saytex RB-79 Diol. Lot # 19-1941-B. Pharmakon Research International, Inc. Waverly, PA. Sponsor: Ethyl Corporation, Baton Rouge, LA)
The right conjunctival sacs of the right eyes of three male and female New Zealand albino rabbits were instilled with 0.1 ml of TBPA Diol. Redness and chemosis of the conjunctiva were observed for 72 hours. Discharge was noted in one rabbit at 24 hours. TBPA Diol was not a primary eye irritant under the conditions of this test. (PHT 4-Diol Summaries of Toxicity Data. 1981. Great Lakes Chemical Corporation, West Lafayette, IN)
SKIN IRRITATION
The backs of three male and female New Zealand albino rabbits were clipped. The skin of three were abraded. A single application of TBPA Diol (0.5 ml) was made to the back of each rabbit under a gauze patch and wrapped with an airtight occlusive wrap. The skin was examined at 24, 48 and 72 hours post-dosing. No irritation was noted on the intact skin. Erythema and edema were observed on the abraded skin. The primary irritation index, according to the method of Draize, was 0.7. TBPA Diol was not a primary skin irritant under the conditions of this test. (PHT 4-Diol Summaries of Toxicity Data. 1981. Great Lakes Chemical Corporation, West Lafayette, IN)
Justification for classification or non-classification
The study results indicate the test article does not meet the criteria for classification and labeling under REACH.
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.
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