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EC number: 684-206-1 | CAS number: 258864-54-9
- 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
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- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
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- Endpoint summary
- Stability
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- 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
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- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
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- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
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- Specific investigations
- Exposure related observations in humans
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- Additional toxicological data

Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2015-03-27 - 2015-05-29
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 015
- Report date:
- 2015
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
- Deviations:
- no
- GLP compliance:
- yes
- Test type:
- acute toxic class method
- Limit test:
- no
Test material
- Reference substance name:
- trihexyl(tetradecyl)phosphanium chloride
- Cas Number:
- 258864-54-9
- Molecular formula:
- C32H68ClP
- IUPAC Name:
- trihexyl(tetradecyl)phosphanium chloride
- Test material form:
- liquid
- Remarks:
- Homogenous Liquid
Constituent 1
- Specific details on test material used for the study:
- Trade name: CYPHOS IL 101 Phosphonium Salt
Physical state: liquid
Composition of test material, percentage of components: Trihexyl(tetradecyl)phosphonium chloride (258864-54-9), > 95%
Lot/batch No.: WEC031280
Expiration date of the lot/batch: >1 year (March 2016) when stored at room temperature and protected from direct contact with water (hydrophobic)
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Charles River Stone Ridge NY, USA
- Females nulliparous and non-pregnant: yes
- Age at study initiation: Approx. 9 weeks old
- Weight at study initiation: 201 - 302 g for males and 197 - 220 for females; the weight variation did not exceed 20%
- Fasting period before study: Animals were deprived of food for 16-20 hours prior to dosing.
- Housing: housed in suspended wire cages; 5/sex/cage prior to dosing and 3/sex/cage following dosing; containing absorbent paper as bedding material.
- Diet: Fresh PMI Rat Chow (Diet #5012); ad libitum except just prior to dosing
- Water; ad libitum; tap water
- Acclimation period: At least 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): controlled temperature
- Photoperiod (hrs dark / hrs light): 12/12
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- unchanged (no vehicle)
- Details on oral exposure:
- The test article was used as received.
MAXIMUM DOSE VOLUME APPLIED: 2000 ml/kg - Doses:
- Females: 300 and 2000 mg/kg bw
Males: 300 mg/kg bw - No. of animals per sex per dose:
- - 300 mg/kg bw: 3 females and 3 males
- 2000 mg/kg bw: 3 females - Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Mortality/Viability was observed twice daily. The time of death was recorded as precisely as possible. Body weights were measured on Days 1 (pre-administration), 8, at death and on Day 15 in the survivors. Clinical signs were observed at periodic intervals on the day of dosing (Day 1) and once daily thereafter, until Day 15.
- Necropsy of survivors performed: yes
The animals surviving to the end of the observation period were sacrificed by oxygen/carbon dioxide procedure. All animals assigned to the study were subjected to necropsy and descriptions of all internal macroscopic abnormalities recorded. - Statistics:
- No statistical analysis was performed.
Results and discussion
Effect levels
- Sex:
- female
- Dose descriptor:
- LD50
- Effect level:
- > 300 - < 2 000 mg/kg bw
- Based on:
- test mat.
- Mortality:
- All animals survived following a single 300 mg/kg bw oral dose.
All three females died on Day 1 or Day 5 following a single 2000 mg/kg bw oral dose. - Clinical signs:
- other: 300 mg/kg bw: Abnormal physical signs including chromorhinorrhea, yellow staining, localized hair loss, soiling, and wetness of the anogenital area, few feces, chromodacryorrhea, unkempt appaerence, and piloerection were observed. 2000 mg/kg bw: Prior to
- Gross pathology:
- 300 mg/kg bw (females/males): Hair loss on the anogenital area was found at macroscopic post mortem examination of two females that survived until termination. No abnormalities were found at macroscopic post mortem examination of one female and all three males that survived until termination.
2000 mg/kg bw (females): The gross necropsy revealed localized hair loss, yellow and brown staining, soilin, and wetness of the anogenital area, chromodacryorrhea, chromorhinorrhea, brown staining of the nose/mouth area, and abnormalities of the gastrointestinal tract.
Applicant's summary and conclusion
- Interpretation of results:
- Category 4 based on GHS criteria
- Conclusions:
- The oral LD50 value of Trihexyltetradecylphosphonium chloride in Sprague Dawley rats was established to be greater than 300 mg/kg but less than 2000 mg/kg body weight.
- Executive summary:
A GLP-compliant acute toxicity study according to OECD Guideline 423 was conducted. A group of 3 female Sprague Dawley rats was given a single oral dose of Trihexyltetradecylphosphonium chloride at 300 mg/kg bw. An additional three healthy males were dosed as a confirmatory group at 300 mg/kg bw. Three additional healthy females were dosed at 2000 mg/kg. The rats were observed for 14 days.
300 mg/kg: All three females and males survived following a single 300 mg/kg oral dose. Abnormal physical signs were observed and all six animals gained body weights by study termination; one animal lost weight from Day 0 to Day 7. The gross necropsy revealed hair loss on the anogenital area.
2000 mg/kg: All three females died, on Day 1 or Day 5, following a single 2000 mg/kg oral dose. Prior to death, abnormal physical signs were observed. Terminal body weight loss was observed among all three animals. The gross necropsy revealed hair loss, yellow and brown staining, soiling, and wetness of the anogenital area, chromodacryorrhea, chromiorhinorrhea, brown stainig of the nose/mouth area, and abnormalities of the gastrointestinal tract.
In conclusion, the oral LD50 value of Trihexyltetradecylphosphonium chloride in Sprague Dawley rats was established to be greater than 300 mg/kg but less than 2000 mg/kg body weight.
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