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EC number: 263-038-9 | CAS number: 61789-18-2
- 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
Short-term toxicity to fish
Administrative data
Link to relevant study record(s)
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From 08 August 1988 to 12 August 1988
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- no analytical monitoring
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- GLP compliance:
- yes (incl. QA statement)
- Analytical monitoring:
- no
- Details on sampling:
- A clear stock solution of 15 mg/mL was prepared by diluting 0.15 g of the test substance with distilled water in a 10 mL flask. The appropriate volume of stock solution was then added to 15 L of dilution water in each test aquaria and mixed by stirring.
- Vehicle:
- yes
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION
- Chemical name of vehicle: Water
- Concentration of vehicle in test medium (stock solution): Stock suspension of 15 mg/L was prepared by diluting 0.15 g of the test substance with distilled water in a 10 mL flask. - Test organisms (species):
- Oncorhynchus mykiss (previous name: Salmo gairdneri)
- Details on test organisms:
- TEST ORGANISM
- Species: Salmo gairdneri (new name: Oncorhynchus mykiss)
- Source: Commercial supplier in California
- Length at study initiation (length definition, mean, range and SD): Mean = 33 mm; range = 27-40 mm
- Weight at study initiation (mean and range, SD): Mean = 0.31 g; range = 0.12- 0.58 g
- Feeding during test: No
ACCLIMATION
- Acclimation period: 14 d
- Acclimation conditions (same as test or not): Yes
- Type and amount of food: Dry commercial pelleted food, ad libitum
- Feeding frequency: Daily, except during the 48 h prior to testing
- Health during acclimation (any mortality observed): Yes (i.e., 1.1%) - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 96 h
- Hardness:
- 34 mg/L as CaCO3
- Test temperature:
- 12-13 ⁰C
- pH:
- 7.5
- Dissolved oxygen:
- 67-72%
- Nominal and measured concentrations:
- Nominal: 0, 390, 670, 1,090, 1,820 and 3,030 µg/L (i.e., 0, 130, 223, 363, 607 and 1010 µg a.i./L)
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 18.9 L glass aquaria which contained 15 L of the test solution
- Aeration: No
- No. of organisms per vessel: Ten
- No. of vessels per concentration (replicates): No data
- No. of vessels per control (replicates): No data
- Biomass loading rate: 0.21 g/L
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: Deionized, reconstituted well water
- Alkalinity: 28 mg/L
- Conductivity: 150 µmhos/cm
- Culture medium different from test medium: No
- Intervals of water quality measurement: 24, 48, 72 and 96 h
OTHER TEST CONDITIONS
- Adjustment of pH: Not required
- Photoperiod: 16 h light and 8 h darkness
- Light intensity: 60 footcandles
EFFECT PARAMETERS MEASURED (with observation intervals if applicable): Mortalities were recorded at 0, 6, 24, 48, 72 and 96 h
TEST CONCENTRATIONS
- Spacing factor for test concentrations: <2
- Range finding study: Yes
- Test concentrations: 150 to 9,090 µg/L
- Results used to determine the conditions for the definitive study: After 96 h, 100% mortality at ≤1,520 µg/L. - Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- ca. 2 350 µg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: i.e., equivalent to 783 µg a.i./L
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC100
- Effect conc.:
- ca. 3 030 µg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: i.e., equivalent to 1010 µg a.i./L
- Key result
- Duration:
- 96 h
- Dose descriptor:
- NOEC
- Effect conc.:
- ca. 1 820 µg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- other: mortality, physical or behavioral abnormalities
- Remarks on result:
- other: i.e., equivalent to 607 µg a.i./L
- Details on results:
- After 96 h of exposure, 100% mortality was observed at the highest concentration (3,030 µg/L or 1010 µg a.i./L). No significant toxicant-related mortalities were observed at test concentrations ≤1820 µg/L or 607 µg a.i./L. The 96 h LC50 for rainbow trout exposed to the test substance was estimated by non-linear interpolation to be 2,350 µg/L, with a 95% confidence interval calculated by binomial probability of 1,820 - 3,030 µg/L. The NOAEC was established at 1,820 µg /L (or 607 µg a.i./L).
No significant toxicant-related mortalities were observed at test concentrations below 1010 µg a.i./l
No chemical analyses of testsubstance have been performed.
• TMAC is a quaternary ammonium compound which is not susceptible to hydrolyses or photodegradation.
• Stability of test solutions under test conditions has been shown in chronic daphnia tests with comparable quaternary compounds.
• There is no significant decrease observed over 3 days of testing.
• Quaternary ammonium compounds tend to adsorb to test organisms and glassware.
• Observed reduction of test concentration is maximal between 20 – 50 %
Conclusion:
The test substance was at least 50% available during the acute daphnia and fish tests.Further to the fish studies:
• The nominal effect data for fish are consistently about a factor 10 higher than for algae or daphnia.
• Repeating the acute fish tests will not improve the effect assessment for the aquatic compartment.
• Literature data on fish studies show comparable results
For ethical reasons we propose to calculate the effect data for fish assuming 50% availability as a worst-case.
Validity criteria were fulfilled, except for the concentration of the test substance during the test. See table 5
Test substance is moderately toxic according to EPA guidelines, but is very toxic according to European guidelines - Reported statistics and error estimates:
- Probit analysis
- Sublethal observations / clinical signs:
Deviation: The dissolved oxygen concentration were 75-77% of saturation (against 90% as per the protocol), however this deviation did not affect the results of the test.
Table 1: Mortality data
Test-Substance
Concentration
(nominal)[µg a.i./l]
Mortality
Percentage
0 h 24 h 48 h 72 h 96 h
0
0
0
0c
0d
130
0
0
0
0
223
0
0
0a
10
363
0a
0a
0b
0de
607
0
0a
0b
0de
1010
100
100
100
100
aOne of the surviving fish exhibited darkened pigmentation
bTwo of the surviving fish exhibited darkened pigmentation
cOne of the surviving fish exhibited darkened pigmentation and erratic swimming behavior
dOne of the surviving fish exhibited a complete loss of equilibrium
eSeveral of the surviving fish exhibited darkened pigmentation
Table 2: Oxygen concentrations
Test-Substance
Concentration
(nominal)[µg a.i./l]
concentration (mg/l) and percentage
0 h 24 h 48 h 72 h 96 h
0
8.1 (77)
9.2 (85)
8.1 (77)
8.2 (78)
6.4 (64)
130
8.0 (76)
8.8 (81)
7.8 (74)
8.0 (76)
7.2 (68)
223
7.9 (75)
8.8 (81)
7.8 (74)
7.8 (74)
6.8 (64)
363
7.9 (75)
8.4 (78)
7.4 (70)
7.7 (73)
6.8 (64)
607
7.9 (75)
8.2 (76)
7.4 (70)
7.3 (69)
6.8 (64)
1010
7.9 (75)
8.2 (76)
-
-
-
Table 3: pH values
Test-Substance
Concentration
(nominal)[µg a.i./l]
0 h 24 h 48 h 72 h 96 h
0
7.6
6.6
6.7
7.2
7.5
130
7.7
6.6
6.7
7.2
7.3
223
7.7
6.6
6.8
7.2
7.3
363
7.7
6.6
6.8
7.2
7.2
607
7.7
6.5
6.9
7.3
7.2
1010
7.7
6.6
-
-
-
Table 4: Effect data
48 h [µg a.i./l]1
95 % c.l.
96 h [µg a.i./l]1
95 % c.l.
NOEC
-
-
607 (n)
-
LC50
783
607-1010
783
607-1010
1indicate if effect data are based on nominal (n) or measured (m) concentrations
Table 5: Validity criteria for acute fish test according to OECD Guideline 203
fulfilled
Not fullfilled
Mortality of control animals <10%
YES
Concentration of dissolved oxygen in all test vessels > 60% saturation
YES
Concentration of test substance³80% of initial concentration during test
*
*No analyses were performed, therefore it is not known if the test substance³80% of initial concentration during test
- Validity criteria fulfilled:
- yes
- Remarks:
- As per OECD guideline 203
- Conclusions:
- Based on the results, the 96 h LC50 and NOEC of the test substance were determined to be 2,350 and 1,820 µg a.i./L (i.e., equivalent to 783 and 607 µg a.i./L), respectively.
- Executive summary:
A study was conducted to determine the acute toxicity study of the test substance, Coco TMAC (33% active in water), to the rainbow trout (Oncorhynchus mykiss previous name: Salmo gairdneri) according to a method similar to OECD Guideline 203, in compliance with GLP. Ten Rainbow trouts per concentration were exposed to the test substance at 0, 390, 670, 1,090, 1,820 and 3,030 µg/L (i.e., equivalent to 0, 130, 223, 363, 607 and 1010 µg a.i./L) for 96 h under static conditions. Mortalities were determined after 0, 24, 48 72 and 96 h. No analytical determination of the test substance was performed. Throughout the test period no visible sign of undissolved material was observed in the exposure solutions. After 96 h of exposure, 100% mortality was observed at the highest concentration (3,030 µg/L or 1010 µg a.i./L). No significant toxicant-related mortalities were observed at test concentrations ≤1820 µg/L or 607 µg a.i./L. The 96 h LC50 for rainbow trout exposed to the test substance was estimated by non-linear interpolation to be 2,350 µg/L, with a 95% confidence interval calculated by binomial probability of 1,820 - 3,030 µg/L. The NOAEC was established at 1,820 µg /L (or 607 µg a.i./L). Under the conditions of the study, the 96-h LC50 and NOEC values of the test substance for acute toxicity to fish were determined at 783 and 607 µg a.i./L respectively (Surprenant, 1988).
- Endpoint:
- short-term toxicity to fish
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- From 22 June, 1987 to 08 August, 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 203 (Fish, Acute Toxicity Test)
- Version / remarks:
- OECD 203 adopted April 4, 1984
- Deviations:
- not specified
- GLP compliance:
- not specified
- Analytical monitoring:
- not specified
- Vehicle:
- yes
- Remarks:
- Reconstituted water
- Details on test solutions:
- Test substance was suspended in 2 L beaker, stirred up to 2 h with magnetic stirrer and then transferred to tank for each samples.
- Test organisms (species):
- Oncorhynchus mykiss (previous name: Salmo gairdneri)
- Details on test organisms:
- Rainbow trout Salmo gairdneri with a total length of 5±1 cm, was obtained from supplier (forellenhof fredesloh, Dr. O. Muller, 3413 Moringen 1).
About two weeks before the intended start of the investigation a collective of 900 fish was delivered to NATEC. According to the report of the supplier all these fish had passed a quality control and were inspected on health. On arrival at NATEC the fish were transferred to two circular maintenance vessels of 300 lit capacity each for adaptation to the environmental conditions during the test. During the first tine of the adaption phase (12 days) the mortality came to 7% of the fish population. Therefore the adaption phase was extended for 5 days. During this time the mortality only came to 0.5% of the fish population. Further, abnormalities or any other unequivocal symptoms of illness were not visible within the collective. The quality criteria which are demanded by the OECD guideline for the collective of fish for the time of adaptation were thus fulfilled. - Test type:
- static
- Water media type:
- freshwater
- Total exposure duration:
- 96 h
- Post exposure observation period:
- At 1, 24, 48, 72 and 96 h after the start of test, the fish of each test batch were inspected according test, to a fixed test protocol. Above all, these inspections comprised the registration of the number of dead fish. Dead fish must be removed from the tank and surviving fish are carefully observed for symptoms of illness or other abnormalities. These were for instance disorders of the swimming behavior, visible peculiarities of the respiratory functions, and changes of the outward appearance. Moreover at the time t=0 as well as at all inspections, water temperature and pH were determined by control measurements.
- Test temperature:
- 13-17ºC
- pH:
- 6.5-8.5
- Dissolved oxygen:
- Oxygen ≥ 60% of air saturation value
- Nominal and measured concentrations:
- 0, 2, 3, 4.5, 6.7, 10 mg/L nominal concentration
- Details on test conditions:
- There were 5 fishes per batch with 2 batches for one eahc concentration of test substance. Also there were two test batches for negative control. All testing conditions and parameters were made compliant to the OECD 203 guideline.
- Reference substance (positive control):
- no
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC0
- Effect conc.:
- ca. 2 000 µg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: i.e., equivalent to 700 µg a.i./L
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC50
- Effect conc.:
- ca. 3 200 µg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: i.e., equivalent to 1120 µg a.i./L
- Key result
- Duration:
- 96 h
- Dose descriptor:
- LC100
- Effect conc.:
- ca. 4 500 µg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Basis for effect:
- mortality (fish)
- Remarks on result:
- other: i.e., equivalent to 1580 µg a.i./L
- Sublethal observations / clinical signs:
The range finding test indicated a mortality for at least 10 mg/L. The regular inspections of the acute toxicity test 1, 24, 48, 72, 96 h after the test start rendered the following observations:
Table 1: Cumulative mortality at intervals during the test in (), cumulative percentage mortality in [%]:
Concentration [mg/L]
Time after test start [h]
0
1
24
48
72
96
10
0*)
(0)
0
(0)
10
(100)
10
(100)
10
(100)
10
(100)
6.7
0*)
(0)
0
(0)
10
(100)
10
(100)
10
(100)
10
(100)
4.5
0*)
(0)
0
(0)
10
(100)
10
(100)
10
(100)
10
(100)
3
0*)
(0)
0
(0)
1
(10)
1
(10)
2
(20)
2
(20)
2
0*)
(0)
0
(0)
0
(0)
0
(0)
0
(0)
0
(0)
Negative control
0*)
(0)
0
(0)
0
(0)
0
(0)
0
(0)
0
(0)
*) 10 fishes were taken at the beginning
Table 2: The conditions during the testing period were (mean vale), (): Span to smallest/greatest single value
No statement: Span = 0 or < 0.2:
Time after test start (t= h)
0 h
24 h
48 h
72 h
96 h
Oxygen concentration
10.3
10.1
(0.3)
10.1
10
10
Water temperature (ºC)
14
(0.7)
14.2
(1.1)
14.5
14.6
(0.3)
14.6
(0.3)
pH-Wert
8
(0.4)
8
8
8
8
Number of single values
17
15
9
9
9
- Validity criteria fulfilled:
- not specified
- Conclusions:
- Under study conditions, the LC0, LC50 and LC100 values at 96 h were found to be 2, 3.2 and 4.5 mg/L respectively (i.e., equivalent to 0.7, 1.12 and 1.58 mg a.i./L).
- Executive summary:
A study was conducted to determine the lethal effects of the test substance, Coco TMAC (35% active), to the rainbow trout (Oncorhynchus mykiss previous name: Salmo gairdneri) according to OECD 203 guideline. Rainbow trouts were exposed in separate batches to different concentrations of test substance in the test medium over period of 96 h (each tank 5 fishes, two tanks for one concentration) under static conditions. 10 more fishes were simultaneously kept in a two control batches (2 x 5) of the pure test medium water at otherwise identical conditions. Criteria for the inspections of test fish during the exposure period were above all , the mortality rates, but moreover abnormal symptoms in the swimming behavior, in visible physiological functions as well as in the outward appearance of the test fish were recorded. Fish were considered dead if touching of the caudal peduncle produced no reaction and if no breathing movements could be observed. Under study conditions, the LC0, LC50 and LC100 values at 96 h were found to be 2, 3.2 and 4.5 mg/L respectively (Dommrose 1987), which is equivalent to 0.7, 1.12 and 1.58 mg a.i./L.
Referenceopen allclose all
Description of key information
Based on the available information and in accordance with the TMAC C biocides assessment report, the lower 96 h LC50 value of 0.14 mg a.i./L (or 140 µg a.i./L), has been considered further for hazard/risk assessment as a conservative approach.
Key value for chemical safety assessment
Fresh water fish
Fresh water fish
- Dose descriptor:
- LC50
- Effect concentration:
- 140 µg/L
Additional information
Study 1:A study was conducted to determine the acute toxicity study of the test substance, TMAC C (33% active in water), to the rainbow trout (Oncorhynchus mykissprevious name:Salmo gairdneri) according to a method similar to OECD Guideline 203, in compliance with GLP. Ten Rainbow trouts per concentration were exposed to the test substance at 0, 390, 670, 1,090, 1,820 and 3,030 µg/L (i.e., equivalent to 0, 130, 223, 363, 607 and 1010 µg a.i./L) for 96 h under static conditions. Mortalities were determined after 0, 24, 48 72 and 96 h. No analytical determination of the test substance was performed. Throughout the test period no visible sign of undissolved material was observed in the exposure solutions. After 96 h of exposure, 100% mortality was observed at the highest concentration (3,030 µg/L or 1010 µg a.i./L). No significant toxicant-related mortalities were observed at test concentrations ≤1820 µg/L or 607 µg a.i./L. The 96 h LC50 for rainbow trout exposed to the test substance was estimated by non-linear interpolation to be 2,350 µg/L, with a 95% confidence interval calculated by binomial probability of 1,820 - 3,030 µg/L. The NOAEC was established at 1,820 µg /L (or 607 µg a.i./L). Under the conditions of the study, the 96-h LC50 and NOEC values of the test substance for acute toxicity to fish were determined at 783 and 607 µg a.i./L respectively (Surprenant, 1988).
Study 2: A study was conducted to determine the lethal effects of the test substance, TMAC C (35% active), to the rainbow trout (Oncorhynchus mykissprevious name:Salmo gairdneri) according to OECD 203 guideline. Rainbow trouts were exposed in separate batches to different concentrations of test substance in the test medium over period of 96 h (each tank 5 fishes, two tanks for one concentration) under static conditions. 10 more fishes were simultaneously kept in a two control batches (2 x 5) of the pure test medium water at otherwise identical conditions. Criteria for the inspections of test fish during the exposure period were above all, the mortality rates, but moreover abnormal symptoms in the swimming behaviour, in visible physiological functions as well as in the outward appearance of the test fish were recorded. Fish were considered dead if touching of the caudal peduncle produced no reaction and if no breathing movements could be observed. Under study conditions, the LC0, LC50 and LC100 values at 96 h were found to be 2, 3.2 and 4.5 mg/L (or 2000, 3200, 4500 µg/L) respectively (Dommrose 1987), which is equivalent to 0.7, 1.12 and 1.58 mg a.i./L (or 700, 1120, 1580 µg a.i./L).
The biocide assessment report available from RMS Italy on TMAC C, considered the above study to be supportive because the endpoints were based on nominal concentrations, which could underestimate the toxicity. However, several available reliable read across studies with DDAC and BKC, also indicated toxicity in the same range. As final endpoint for TMAC C, the RMS considered the read across data to DDAC with the lowest 96h LC50 = 0.19 mg a.i./L (190 µg a.i./L) in Fathead minnow as the most sensitive species, which resulted in a 96h LC50 = 0.14 mg a.i./L (or 140 µg a.i./L) for TMAC C, by applying correction for MW (ECHA assessment report, 2016).
Therefore, based on the above information and in accordance with the TMAC C biocides assessment report, the lower 96 h LC50 value of 0.14 mg a.i./L (or 140 µg a.i./L), has been considered further for hazard/risk assessment as a conservative approach.
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