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Diss Factsheets
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EC number: 609-530-2 | CAS number: 38172-91-7
- 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- 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:
- 1 987
- Report date:
- 1987
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- GLP compliance:
- no
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Golpanol PAP
- IUPAC Name:
- Golpanol PAP
- Details on test material:
- - Name of test material (as cited in study report): Golpanol PAP / 2-Propyn-1-ol, compd. with methyloxirane
- Physical state: liquid
- Analytical purity: approx. 50%
- Impurities (identity and concentrations): < 1% Propargylalcohol, approx. 35% water, approx. 7% Propylenglycol, aprox. 7% higher alcoxylated products
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Dr. K. Thomae GmbH, Biberach, Germany
- Weight at study initiation: male (mean): 186g, female (mean): 184g
- Fasting period before study: 16 hours
- Housing: 5 animals per cage (grouped according to doses)
- Diet (e.g. ad libitum): ad libitum
- Water (e.g. ad libitum): ad libitum
- Acclimation period: 1 week
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 - 24°C
- Humidity (%): 30 - 70%
- Air changes (per hr): fully airconditioned
- Photoperiod (hrs dark / hrs light): 12 hours / 12 hours
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- water
- Doses:
- 215, 464, 2150, 5000 mg/kg
- No. of animals per sex per dose:
- 5
- Control animals:
- not specified
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: at least once per day (observation), after 7 and 13 days (weighing)
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight
Results and discussion
Effect levelsopen allclose all
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 464 - < 2 150 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: all male and female animals dosed with 2150mg/Kg died after 1 day, 2/5 males dosed with 464mg/Kg died after 7 days, 0/5 females dosed with 464mg/Kg died until the end of the study
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 464 - < 2 150 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: all female animals dosed with 2150mg/Kg died after 1 day; all female animals dosed with 464mg/Kg survived until the end of the study
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- ca. 464 mg/kg bw
- Based on:
- test mat.
- Remarks on result:
- other: 2/5 male animals dosed with 464mg/Kg died 7 days after treatment
- Mortality:
- male/female:
5000mg/Kg: 5/5 animals after 1 day
2150mg/Kg: 5/5 animals after 1 day
male:
464mg/Kg: 2/5 animals after 7 days
No mortality was observed after administration of 215 mg/kg in males and females as well as after treatment of females with 464 mg/kg.
female:
5000mg/Kg: 5/5 animals after 1 day
2150mg/Kg: 5/5 animals after 1 day
- Clinical signs:
- other: 5000mg/Kg, males and females: dyspnea, apathy, abnormal position, atonia, paresis, poor general state after <15min - 4h staggering: <15min - 1h exsiccosis: 4h piloerection: 1h - 4h 2150mg/Kg, males and females: dyspnea, apathy, staggering, paresis, poor
- Gross pathology:
- male and female animals that died spontaneously on day 1 or 7:
general congestion, liver: lobular perphery yellow brown, stomach: bloody ulceration in the glandular stomach
sacrified animals (male, female): no pathological findings
Any other information on results incl. tables
LD50 male animals: ca. 464 mg/kg; LD50 female animals > 464 < 2150 mg/kg
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.