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EC number: 202-709-2 | CAS number: 98-87-3
- 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
Biodegradation in water: screening tests
Administrative data
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- The authors tested the biodegradability of benzyl chloride according to the OECD guideline 301C. GLP standards are not specified and validity criteria are partially met. Thus the study should be considered a Klimisch 2c study as it is comparable to a guideline study with acceptable restrictions.
Data source
Reference
- Reference Type:
- publication
- Title:
- Biodegradation and bioaccumulation. Data of existing chemicals based on the CSCL Japan.
- Author:
- Ministry of International Trade and Industry
- Year:
- 1 992
- Bibliographic source:
- Japan Chemical INdustry Ecology-Toxicology & Information Center
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 C (Ready Biodegradability: Modified MITI Test (I))
- Deviations:
- no
- GLP compliance:
- not specified
Test material
- Reference substance name:
- α,α-dichlorotoluene
- EC Number:
- 202-709-2
- EC Name:
- α,α-dichlorotoluene
- Cas Number:
- 98-87-3
- Molecular formula:
- C7H6Cl2
- IUPAC Name:
- (dichloromethyl)benzene
- Reference substance name:
- Dichloromethylbenzene
- EC Number:
- 249-854-8
- EC Name:
- Dichloromethylbenzene
- Cas Number:
- 29797-40-8
- IUPAC Name:
- (dichloromethyl)benzene
- Details on test material:
- - Name of test material (as cited in study report): Dichloromethylbenzene
No more data available
Constituent 1
Constituent 2
- Specific details on test material used for the study:
- Details on properties of test surrogate or analogue material (migrated information):
No data available
Study design
- Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge (adaptation not specified)
- Details on inoculum:
- - Source of inoculum/activated sludge (e.g. location, sampling depth, contamination history, procedure):
Locations:
sludge samples were taken at 10 places in Japan
Fukogawa city sewage plant (Sapporo-shi Hokkaido)
Fukashiba industry sewage plant (Kashima-gun Ibaragi)
Nakahama city sewage plant (Osaka-shi Osaka)
Ochiai city sewage plant (Shinjuku-ku Tokyo)
Kitakami river (Ishinomaki-shi Miyagi)
Shinano river (Nishikanbara-gun Niigata)
Yoshino river (Tokushima-shi Tokushima)
Lake Biwa (Otsu-shi Shiga)
Hiroshima bay (Hiroshima-shi Hiroshima)
Dookai bay (Kitakyushu-shi Fukuoka)
Sampling time:
March, June, September and December in every year
Sampling method:
Returned sludge of sewage was collected
For rivers, lake and sea the surface water and surface soil which were in contact with the atmosphere were collected
Mixing of fresh and old activated sludge:
5 L of the filtrate of the supernatant of an activated sludge in use was mixed with 500 mL of the filtrate of the supernatant of a newly collected sludge. The mixture was cultured at pH 7.0 +/- 1.0 under sufficient aeration (i.e. prefiltered open air was used)
- Laboratory culture:
About 30 minutes after ceasing the aeration to the sludge mixture, supernatant corresponding to about 1/3 of the whole volume was removed. Then an equal volume of dechlorination water was added to the remaining portion and aerated again. Afterwards synthetic sewage (i.e. glucose, peptone and monopotassium phosphate dissolved in dechlorination water, each with a 5% (W/V) concentration and adjustment of pH with sodium hydroxide to 7.0 +/- 1.0) was added so that the ratio was 0.1% (W/V). This procedure was repeated every day and the culturing was carried out at 25°C +/- 2°C.
- Preparation of inoculum for exposure:
The methodology for measuring the concentration of suspended solid was in accordance with Japanese Industrial Standards (JIS) K 0102-1986-14.1
Preparation of basal culture medium; each 3 mL of solution A, solution B, solution C and solution D (i.e. described in JIS K 0102-1986-21) were made up to 1000 mL with purified water after which the pH of the solution was adjusted to 7.0 pH.
- Concentration of sludge: 30 mg/L
No more data available - Duration of test (contact time):
- 28 d
Initial test substance concentration
- Initial conc.:
- 100 mg/L
- Based on:
- test mat.
Parameter followed for biodegradation estimation
- Parameter followed for biodegradation estimation:
- O2 consumption
- Details on study design:
- TEST CONDITIONS
- Test temperature: 25 +/- 1 °C
- Other:
Control of cultivation:
During cultivation, appearance of the supernatant, precipitability, formation of flock, pH and dissolved oxygen concentration in the solution as well as temperature were checked. When necessary adjustements were made. Microflora in the activated sludge was microscopically observed ans sludge with no normal symptom was used for the test.
TEST SYSTEM
- Culturing apparatus: Closed system oxygen consumption measuring apparatus (Coulometer: Ohkura Electric Co., Ltd.)
- Number of culture flasks/concentration: each test vessel contained 300 mL of basal culture medium containing a concentration of suspended solid of 30 mg/L or 100 mg/L into which 30 mg or 9 mg of the test substance was added
- Method used to create aerobic conditions: The absorbent for carbon dioxide was Soda lime n°1 (extra pure reagent, Wako Pure Chemical Industries, Ltd.)
CONTROL AND BLANK SYSTEM
- Inoculum blank: one inoculum blank was performed, the test vessel contained 300 mL of basal culture medium and the concentration of suspended solid reached to 30 mg/L or 100 mg/L
- Procedure control: a test vessel containing 300 mL of basal culture medium into which 30 mg of aniline (reference substabce) was added and the concentration of suspended solid reached to 30 mg/L or 100 mg/L
- Other: A test vessel containing 300 mL of purified water into which 30 or 9 mg of the tet substance was added.
No more data available
Reference substance
- Reference substance:
- aniline
Results and discussion
- Preliminary study:
- No data available
- Test performance:
- No data available
% Degradation
- Parameter:
- % degradation (O2 consumption)
- Value:
- 89 - 92
- Sampling time:
- 2 wk
- Details on results:
- Since the biodegradation of the substance had reached a plateau at day 14, the study was terminated before the intitially planned 28 days.
BOD5 / COD results
- Results with reference substance:
- The percentage of biodegradation of the reference substance was more than 40% and 60% at day 7 and 14 respectively.
Applicant's summary and conclusion
- Validity criteria fulfilled:
- not specified
- Interpretation of results:
- readily biodegradable
- Conclusions:
- Under the test conditions, 89-92% of benzal chloride (CAS n° 98-87-3) was degradated after 2 weeks incubation in an activated sludge in an OECD guidline 301C test.
- Executive summary:
The authors tested the biodegradability of benzal chloride (CAS n° 98 -87 -3) according to the OECD guideline 301C. In the test condition, at 100 mg/L, 89 - 92% of the test substance was biodegradated after 14 days following the biological oxigen demand.
No data was available on the GLP status of the study. The validity criteria for the percentage of biodegradation of the reference substance was met. The other validity criteria could not be checked since not all data were available. However considering that the authors followed the OECD guideline 301C and the test was documented with sufficient details, the study should be considered as reliable with restrictions, as this study is comparable to a guideline study with acceptable restrictions.
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