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EC number: 202-707-1 | CAS number: 98-85-1
- 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
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to microorganisms, other
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Remarks:
- for read across substance
- Justification for type of information:
- Data for the target chemical is summarized based on the structurally similar read across chemicals
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Qualifier:
- according to guideline
- Guideline:
- other: as mentioned below
- Principles of method if other than guideline:
- WoE report is based on two toxicity study of microorganism for the test chemical 1-phenylethan-1-ol :
1) To evaluate toxicity of test material on Staph. Aureus , E.coli , C.albicans
2)To evaluate antibacterial activity of test material on Activated sludge - Specific details on test material used for the study:
- IUPAC name: 1-phenylethan-1-ol
Mol. formula: C8H10O
Molecular Weight: 122.166 g/mol
Substance form: Colourless liquid
Substance type: organic
InChI: 1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3
Smiles :c1(ccccc1)C(C)O - Test organisms (species):
- other: 1) Staphylococcus aureus, Escherichia coli and Candida albicans 2) Activated sludge
- Details on inoculum:
- 1) - Laboratory culture: Staphylococcus
aureus, Escherichia coli and Candida albicans, obtained from Monmouth Medical Center, Long Branch, New Jersey
- Method of cultivation: Stock cultures were maintained on agar slants composed of tryptone , 0.3%; yeast extract, 0.3%; glucose, 09 K2HPO 4, 0.1%, and agar, 1% (referred to as TGY agar).
- Pretreatment: Test chemicals were tested initially at 0.1, 1.0 and 10
mg/l to determine the approximate range of activity. When no positive materials were found, these were repeated at 10, I00, and 1000 mg/l - Test type:
- static
- Water media type:
- other: 1. frreshwater 2. Growth media TGY broth
- Total exposure duration:
- 24 h
- Test temperature:
- 37°C
- Details on test conditions:
- 1) - Test vessel: 18 x 150 mm tubes; 10.0 ml/tube).
Fill volume : Test materials was added to the tubes as 10% (w/v) solutions.
-Tubes were inoculated with 50/ml of a 1 : 10 dilution in sterile 0.85% saline of a 24-hour shake culture (TGY broth). A minimum of 300,000 viable organisms were added to each tube. Tubes were mixed incubated at 37°C for 18 to 24 hr, sufficient time to obtain significant turbidity. on a Vortex mixer and incubated at 37°C for 18 to 24 hr, sufficient time to obtain significant turbidity - Duration:
- 24 h
- Dose descriptor:
- other: MIC
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- not specified
- Conc. based on:
- test mat.
- Basis for effect:
- growth inhibition
- Duration:
- 3 h
- Dose descriptor:
- EC50
- Effect conc.:
- > 1 000 mg/L
- Nominal / measured:
- not specified
- Conc. based on:
- test mat.
- Basis for effect:
- inhibition of respiration due to nitrification
- Validity criteria fulfilled:
- not specified
- Conclusions:
- The test chemical 1-phenylethan-1 ol is not likely to be toxic to microorganism atleast in the concentration range of 1000 mg/l
- Executive summary:
Data available for the structurally and functionally similar read across chemicals benzenemethanol and benzoic acid
has been reviewed to determine the short term toxicity of fish of the test chemical 1-phenylethan-1 ol (98 -85 -1).The studies are as mentioned below:1.The minimum inhibition concentration of test material benzenemethanol was evaluated for its toxicity on Staph. Aureus , E.coli , C.albicans .
Staphylococcus aureus, Escherichia coli and Candida albicans, obtained from Monmouth Medical Center, Long Branch, New Jersey. Stock cultures were maintained on agar slants composed of tryptone , 0.3%; yeast extract, 0.3%; glucose, 0.9 K2HPO 4, 0.1%, and agar, 1% (referred to as TGY agar). Test chemicals were tested initially at 0.1, 1.0 and 10 mg/l to determine the approximate range of activity. When no positive materials were found, these were repeated at 10, I00, and 1000 mg/l.18 x 150 mm tubes; 10.0 ml/tube was used as a test vessel .Test materials was added to the tubes as 10% (w/v) solutions. Tubes were inoculated with 50/ml of a 1 : 10 dilution in sterile 0.85% saline of a 24-hour shake culture (TGY broth). A minimum of 300,000 viable organisms were added to each tube. Tubes were mixed incubated at 37°C for 18 to 24 hr, sufficient time to obtain significant turbidity. on a Vortex mixer and incubated at 37°C for 18 to 24 hr, sufficient time to obtain significant turbidity.The minimum inhibition concentration of test chemical Benzenemethanol on Staph. Aureus , E.coli , C.albicans was observed to be >1000 mg/l
2.Test material benzoic acid was used as a test material to evaluate toxicity to microorganisms as per OECD guideline 209.Activated sludge was used as the test culture at pH 7.5 for 3 hr.The EC50 value on the basis of respiration inhibition test was observed to be >1000 mg/l.
Reference
Description of key information
Toxicity to microorganism:
Data available for the structurally and functionally similar read across chemicals has been reviewed to determine the short term toxicity of fish of the test chemical 1-phenylethan-1 ol (98 -85 -1).The studies are as mentioned below:
1.The minimum inhibition concentration of test material was evaluated for its toxicity on Staph. Aureus , E.coli , C.albicans .
Staphylococcus aureus, Escherichia coli and Candida albicans, obtained from Monmouth Medical Center, Long Branch, New Jersey. Stock cultures were maintained on agar slants composed of tryptone , 0.3%; yeast extract, 0.3%; glucose, 0.9 K2HPO 4, 0.1%, and agar, 1% (referred to as TGY agar). Test chemicals were tested initially at 0.1, 1.0 and 10 mg/l to determine the approximate range of activity. When no positive materials were found, these were repeated at 10, I00, and 1000 mg/l.18 x 150 mm tubes; 10.0 ml/tube was used as a test vessel .Test materials was added to the tubes as 10% (w/v) solutions. Tubes were inoculated with 50/ml of a 1 : 10 dilution in sterile 0.85% saline of a 24-hour shake culture (TGY broth). A minimum of 300,000 viable organisms were added to each tube. Tubes were mixed incubated at 37°C for 18 to 24 hr, sufficient time to obtain significant turbidity. on a Vortex mixer and incubated at 37°C for 18 to 24 hr, sufficient time to obtain significant turbidity.The minimum inhibition concentration of test chemical on Staph. Aureus , E.coli , C.albicans was observed to be >1000 mg/l.
2. Test material was used as a test material to evaluate toxicity to microorganisms as per OECD guideline 209.Activated sludge was used as the test culture at pH 7.5 for 3 hr.The EC50 value on the basis of respiration inhibition test was observed to be >1000 mg/l.
Based on the above effect concentration it can be concluded that test substance 1-phenylethan-1 ol has no adverse effect on microorganism
Key value for chemical safety assessment
- EC50 for microorganisms:
- 1 000 mg/L
Additional information
Toxicity to microorganism:
Data available for the structurally and functionally similar read across chemicals has been reviewed to determine the short term toxicity of fish of the test chemical 1-phenylethan-1 ol (98 -85 -1).The studies are as mentioned below:
1.
The minimum inhibition concentration of test material Benzenemethanol was evaluated for its toxicity on Staph. Aureus , E.coli , C.albicans .
Staphylococcus aureus, Escherichia coli and Candida albicans, obtained from Monmouth Medical Center, Long Branch, New Jersey. Stock cultures were maintained on agar slants composed of tryptone , 0.3%; yeast extract, 0.3%; glucose, 0.9 K2HPO 4, 0.1%, and agar, 1% (referred to as TGY agar). Test chemicals were tested initially at 0.1, 1.0 and 10 mg/l to determine the approximate range of activity. When no positive materials were found, these were repeated at 10, I00, and 1000 mg/l.18 x 150 mm tubes; 10.0 ml/tube was used as a test vessel .Test materials was added to the tubes as 10% (w/v) solutions. Tubes were inoculated with 50/ml of a 1 : 10 dilution in sterile 0.85% saline of a 24-hour shake culture (TGY broth). A minimum of 300,000 viable organisms were added to each tube. Tubes were mixed incubated at 37°C for 18 to 24 hr, sufficient time to obtain significant turbidity. on a Vortex mixer and incubated at 37°C for 18 to 24 hr, sufficient time to obtain significant turbidity.The minimum inhibition concentration of test chemical Benzenemethanol on Staph. Aureus , E.coli , C.albicans was observed to be >1000 mg/l
2. Test material was used as a test material to evaluate toxicity to microorganisms as per OECD guideline 209.Activated sludge was used as the test culture at pH 7.5 for 3 hr.The EC50 value on the basis of respiration inhibition test was observed to be >1000 mg/l.
Based on the above effect concentration it can be concluded that test substance 1-phenylethan-1 ol has no adverse effect on microorganism
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