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EC number: 201-184-7 | CAS number: 79-19-6
- 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
Link to relevant study record(s)
- 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:
- guideline study
- Remarks:
- OECD 301 C
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 301 C (Ready Biodegradability: Modified MITI Test (I))
- Deviations:
- no
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material:Cold, dark place
- Stability under test conditions:Yes-Confirmation:Test solution Infrared absorption spectrum of test substance before start of culture and after completion of culture. As a result of measurement -Stable. - Oxygen conditions:
- aerobic
- Inoculum or test system:
- activated sludge (adaptation not specified)
- Details on inoculum:
- - Source of inoculum/activated sludge:
Collected from 10 sea breams:
Fucho River Treatment Plant (Sapporo City, Hokkaido)
Nakahama treatment plant (Osaka prefecture Osaka city
Kitakami River (Ishinomaki-shi, Miyagi)
Yoshino River (Tokushima City, Tokushima Prefecture)
Hiroshima Bay (Hiroshima-shi, Hiroshima)
Shiba processing plant (Kashima gun, Ibaraki prefecture>
Ochiai processing plant (Shinjuku-ku, Tokyo)
Shinano river (Niigata prefecture Nishikanbara gun)
Lake Biwa (Otsu City, Shiga Prefecture)
Dokai Bay (Kitakyushu City, Fukuoka Prefecture)
- Concentration of sludge: 30 mg/L - Duration of test (contact time):
- ca. 28 d
- Initial conc.:
- ca. 100 mg/L
- Based on:
- test mat.
- Parameter followed for biodegradation estimation:
- O2 consumption
- Parameter followed for biodegradation estimation:
- TOC removal
- Parameter followed for biodegradation estimation:
- test mat. analysis
- Details on study design:
- TEST CONDITIONS
- Composition of medium:21 Of JIS K OIO2 1985.
Three ml of each liquid: Liquid A, liquid B, liquid C and liquid D were mixed with purified water (Japan Pharmacopoeia, Takasugi Pharmaceutical Co., Ltd.) to make up 1 litre.
- Test temperature: 25+-2ºC
- pH: 7+-1
- pH adjusted: yes
TEST SYSTEM
- Number of culture flasks/concentration: 6 bottles (1 bottle - test substance in water, 3 bottles- test material in medium, 1 bottle- reference substance in medium and 1 bottle - medium)
- Method used to create aerobic conditions: Stirring, magnetic stirrer.
- Test solution volume: 300 ml
- Test performed in closed vessels due to significant volatility of test substance: Yes, (Coulometer made by Okura Electric Co., Ltd)
- Test performed in open system: No
CONTROL AND BLANK SYSTEM
- Inoculum blank: bottle with medium
- Abiotic sterile control: bottle - test substance with water
- Activity control: bottle with reference substance in medium - Reference substance:
- aniline
- Remarks:
- special grade reagent manufactured by Showa Chemical Industry Co., Ltd.)
- Key result
- Parameter:
- % degradation (O2 consumption)
- Value:
- ca. 0
- Sampling time:
- 28 d
- Key result
- Parameter:
- % degradation (TOC removal)
- Value:
- ca. 0
- Sampling time:
- 28 d
- Key result
- Parameter:
- % degradation (test mat. analysis)
- Value:
- ca. 0
- Sampling time:
- 28 d
- Validity criteria fulfilled:
- not specified
- Interpretation of results:
- under test conditions no biodegradation observed
- Conclusions:
- Under the test condition, test item is not biodegradable.
- Executive summary:
In accordance with GLP principles and OECD TG 301C (MITI - Ministry of International Trade and Industry, Japan) the test of aerobic biodegradability was determined. Mineral solution containing 100 mg/L of test item was inoculated with microorganisms and incubated under aerobic conditions (oxygen presence) for 28 days. The degradation was followed by the determination of oxygen uptake, TOC removal and Test material analysis. According to OECD criteria, the pass level for ready biodegradability is 60 %, test item attained 0 % of biodegradation and can be assumed as no readily biodegradable.
- Endpoint:
- biodegradation in water: ready biodegradability
- Type of information:
- (Q)SAR
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- results derived from a valid (Q)SAR model and falling into its applicability domain, with adequate and reliable documentation / justification
- Justification for type of information:
- Internationally accepted calculation method EPI-SUITE EPA(USA)
1. SOFTWARE
EPI-SUITE EPA (USA)
2. MODEL (incl. version number)
BIOWIN v 4.10
3. SMILES OR OTHER IDENTIFIERS USED AS INPUT FOR THE MODEL
SMILES : NC(=S)NN
4. SCIENTIFIC VALIDITY OF THE (Q)SAR MODEL
The QMRF is available in "Attached justification".
5. APPLICABILITY DOMAIN
The QPRF is available in “Attached justification”.
6. ADEQUACY OF THE RESULT
The QPRF is available in “Attached justification”. - Guideline:
- other: REACH Guidance on QSARs R.6
- Principles of method if other than guideline:
- Howard, P.H., Boethling, R.S., Stiteler, W.M., Meylan, W.M., Hueber, A.E., Beauman, J.A., Larosche, M.E. 1992. Predictive model for aerobic biodegradability developed from a file of evaluated biodegradation data. Environ. Toxicol. Chem. 11:593-603.
- GLP compliance:
- no
- Specific details on test material used for the study:
- SMILE:NC(=S)NN
- Key result
- Parameter:
- probability of ready biodegradability (QSAR/QSPR)
- Remarks on result:
- other: Not ready biodegradable-QSAR prediction
- Interpretation of results:
- not readily biodegradable
- Conclusions:
- The substance is predicted to be not readily biodegradable (EPISUITE, BIOWINN v4.10).
- Executive summary:
The substance is predicted to be not readily biodegradable (EPISUITE, BIOWINN v4.10).
Referenceopen allclose all
Biowin1 (Linear Model): 0.9143
Biowin2 (Non-Linear Model) : 0.9879
Biowin3 (Ultimate Survey Model): 2.9436 (weeks)
Biowin4 (Primary Survey Model) : 3.9217 (days )
Biowin5 (MITI Linear Model) : 0.1947
Biowin6 (MITI Non-Linear Model): 0.0000
Biowin7 (Anaerobic Linear Model): 0.2682
Ready Biodegradability Prediction: NO
Description of key information
Key study: According the National Institute of Technology and Evaluation (NITE) test item is not biodegradable under the test condition.
Supporting study: Internationally accepted calculation method EPI-SUITE EPA(USA). The substance is predicted to be not readily biodegradable (EPISUITE, BIOWIN v4.10).
Key value for chemical safety assessment
- Biodegradation in water:
- under test conditions no biodegradation observed
Additional information
Key study: According the National Institute of Technology and Evaluation (NITE) test item is not biodegradable.
Supporting study: Internationally accepted calculation method EPI-SUITE EPA(USA). The substance is predicted to be not readily biodegradable (EPISUITE, BIOWIN v4.10).
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.

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