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EC number: - | 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
Endpoint summary
Administrative data
Description of key information
In accordance with Annex VIII, section 8.6.1, column 2 and Annex IX, section 8.6.1, column 1, no testing of oral or dermal repeated dose toxicity is required as inhalation is the most probable exposure pathway.
According to the results of the performed 90-day repeated dose toxicity inhalation study, „2-propanol and 2-butanol production, distn. residues“ does not need to be classified for specific target organ toxicity – repeated exposure.
None of the main components of the „2-propanol and 2-butanol production, distn. residues“ (DSBE, DIPE, SBA, TBA) meets the criteria for a classification as category 1 or 2 Specific Target Organ Toxicity - repeated exposure, as derived from literature values for oral / inhalation repeated dose toxicity, as far as values are known (see table below; all NOAEL (oral) > 100 mg/kg bw/day; all NOAEL (inhalation) > 250 ppmV/6h/day or 1 mg/litre/6h/day). This is in accordance with the results on the substance itself.
Table: Repeated-dose toxicity data for the main components of the reaction mass from the literature
|
Oral |
Inhalation |
DSBE (1) |
NOAEL: 1500 mg/kg/day (from analogue, SBA) (rat, 8-week) |
From analogue, SBA: NOAEL: 3500 ppm (maternal toxicity) (rat, 19-day) NOAEL: >7000 ppm (developmental toxicity) (rat, 19-day) From analogue, MEK (rat, 90-day): NOAEL 2500 ppm, LOAEL 5000 ppm |
DIPE (2) |
|
NOAEL: 480 ppm(rat, 90-day) NOAEC 13800 mg/m³, LOAEC: 7100 ppm (rat, subchronic, 13 weeks, exposure 6 h/day) |
SBA (3) |
|
NOAEL: 3500 ppm (maternal toxicity) (rat, 19-day) NOAEL: >7000 ppm (developmental toxicity) (rat, 19-day) From analogue, MEK (rat, 90-day): NOAEL 2500 ppm, LOAEL 5000 ppm |
TBA (4) |
Rat, 90-day: LOAEL = 490 mg/kg-bw/day NOAEL = 590 mg/kg-bw/day Mouse, 90-day: LOAEL = 3940 mg/kg-bw/day NOAEL = 1590 mg/kg-bw/day Rat, 2-year: LOAEL = 180 mg/kg-bw/day NOAEL = 90 mg/kg-bw Mouse, 2-year: LOAEL = 1030 mg/kg-bw/day NOAEL = 525 mg/kg-bw/day |
LOAEL = 3.27 mg/L (rat, mouse, 90-day) NOAEL = 1.63 mg/L (rat, mouse, 90-day) |
References:
(1) HIGH PRODUCTION VOLUME (HPV) CHEMICAL CHALLENGE PROGRAM TEST PLAN For sec-Butyl Ether CAS NO. 6863-58-7, Prepared by: ExxonMobil Chemical Company November 28, 2006
(2) ExxonMobil Chemical Company Shell Chemical LP For: American Chemistry Council, lsopropanol Panel, Diisopropyl Ether HPV Task Group December 12, 2005
(3) OECD SIDS Dossier for Butan-2-ol, CAS No.78-92-2, ExxonMobil Biomedical Sciences Inc., 09.01.2002
(4) Robust Summaries for t-Butanol, CAS Number 75-65-0 USEPA HPV Challenge Program Submission April 10, 2002
Justification for selection of repeated dose toxicity inhalation - systemic effects endpoint:
The NOAEC from the 90-day subchronic toxicity inhalation study was selected as a basis for DNEL derivation for systemic health effects.
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: inhalation - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- NOAEC
- 11 350 mg/m³
- Study duration:
- subchronic
- Species:
- rat
Repeated dose toxicity: inhalation - local effects
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Repeated dose toxicity: dermal - systemic effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Repeated dose toxicity: dermal - local effects
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Justification for classification or non-classification
According to the results of the performed 90-day repeated dose toxicity inhalation study, „2-propanol and 2-butanol production, distn. residues“ does not need to be classified for specific target organ toxicity – repeated exposure according to CLP (Regulation EC 1272/2008).
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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