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EC number: 947-718-9 | CAS number: -
- 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
![](https://chesar.echa.europa.eu/o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_ecotoxicological-information.png)
Toxicity to microorganisms
Administrative data
Link to relevant study record(s)
- Endpoint:
- toxicity to microorganisms, other
- Remarks:
- Inhibition of cell multiplication / Toxicity control from ready biodegradability study
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- Refer to the Analogue Approach Justification document provided in Section 13
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Duration:
- 16 h
- Dose descriptor:
- EC50
- Effect conc.:
- 8 062 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- WAF
- Basis for effect:
- other: inhibition of cell multiplication
- Remarks on result:
- other: Source: CAS 73296-86-3, monoester
- Duration:
- 16 h
- Dose descriptor:
- EC50
- Effect conc.:
- 9 411 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- WAF
- Basis for effect:
- other: inhibition of cell multiplication
- Remarks on result:
- other: Source: CAS 73296-86-3, diester
- Duration:
- 14 d
- Dose descriptor:
- other: % degradation (CO2 evolution)
- Effect conc.:
- 43.7 other: % degradation (CO2 evolution)
- Basis for effect:
- other: % degradation (CO2 evolution)
- Remarks on result:
- other: Source: Ready biodegradability study of CAS 73296-86-3, monoester
- Endpoint:
- toxicity to microorganisms, other
- Remarks:
- Toxicity control from biodegradation study
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 13 May - 11 June 1998
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- GLP guideline study without analytics
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- according to guideline
- Guideline:
- other: OECD 301B: Ready biodegradability - CO2 evolution
- Version / remarks:
- 17 July 1992
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- other: EU Method C.4-C (Determination of the "Ready" Biodegradability - Carbon Dioxide Evolution Test)
- Version / remarks:
- December 1992
- Deviations:
- no
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- TEST CONDITIONS
- the Toxicity control contained 34.4 mg of the test substance, 80.6 mg of the reference substance sodium acetate and inoculum in 2 L of test medium.
- Composition of medium:
A) 8.50 g KH2PO4, 21.75 g K2HPO4, 67.20 g Na2HPO4 x 12 H2O, 0.50 g NH4Cl, dissolved in 1L MilliQ water, pH 7.4 +/- 0.2
B) 22.50 g MgSO4 x 7 H2O dissolved in 1L MilliQ water
C) 36.40 g CaCl2 x 2 H2O dissolved in 1L MilliQ water
D) 0.25 FeCl3 x 6 H2O dissolved in 1L MilliQ water
1 litre mineral medium contained 10 mL of solution A) and 1 mL of solutions B) to D) and MilliQ water
- Test temperature: 20-22°C
- pH (range between test start and end): 7.5- 8.0
- Preparation of test solutions: mineral components, MilliQ water (ca. 80 % total volume) and inoculum (1% final volume) were added to each bottle. This mixture was aerated with CO2-free air overnight to purge the system of CO2.
SAMPLING
- Sampling frequency: every second or third day during the first 10 days, and thereafter at least every fifth day until the 28th day
- Sampling method: Titration with Phenolphthalein as indicator; the CO2 produced in each test bottle reacted with the Ba(OH)2 in the gas scrubbing bottle and precipitated out as barium carbonate. The amount of CO2 produced was determined by titrating the remaining Ba(OH)2 with 0.05 M standardised HCl.
- Test organisms (species):
- activated sludge of a predominantly domestic sewage
- Details on inoculum:
- - Source of inoculum/activated sludge: freshly obtained from a municipal sewage treatment plant, Waterschap de Maaskant, s'Hertogenbusch, Netherlands
- Storage conditions: sludge was kept under continous aeration until further treatment
- Preparation of inoculum for exposure: Before use, the sludge was allowed to settle for at least 30 minutes and the liquid decanted.
- Concentration of sludge: 3.6 g/L of suspended solids
- Initial cell/biomass concentration: concentration of sludge supernatant: 1.44 x 10E5 cells/mL; the test system contained 1.44 x 10E3 cells/mL - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 14 d
- Details on test conditions:
- TEST SYSTEM
- Culturing apparatus: 2 litre all-glass brown coloured bottles
- Number of culture flasks/concentration: 1 for toxicity control
- Method used to create aerobic conditions: The test was started by bubbling CO2-free air through the solution (rate ca. 30-100 mL/min).
- Details of trap for CO2 and volatile organics if used: 4 g Ba(OH)2 x 8 H2O per L MilliQ water was filtered through filter paper and stored in a sealed vessel to prevent absorption of CO2 from air. Three CO2 absorbers (bottles filled with 100 mL 0.0125 M Ba(OH)2 were connected in series to the exit air line of each test bottle. - Reference substance (positive control):
- yes
- Remarks:
- sodium acetate at a concentration of 40 mg/L, corresponding to TOC=12 mg/L
- Duration:
- 14 d
- Dose descriptor:
- other: % degradation
- Effect conc.:
- 43.7 other: % degradation
- Basis for effect:
- other: CO2 evolution
- Details on results:
- The toxicity control in the ready biodegradability study reached 43.7 % degradation (Pass level: 25%) within 14 days (based on ThCO2). Therefore, the test substance was assumed to be not inhibitory.
- Results with reference substance (positive control):
- The reference control containing sodium acetate reached the pass level of 60% biodegradation by day 14.
- Endpoint:
- toxicity to microorganisms, other
- Remarks:
- Inhibition of cell multiplication
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 16 April - 20 May 1998
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- GLP guideline study without analytical verification of the test item
- Qualifier:
- according to guideline
- Guideline:
- DIN 38412-8 (Pseudomonas Zellvermehrungshemmtest)
- Version / remarks:
- March 1991
- Qualifier:
- according to guideline
- Guideline:
- ISO 10712 (Water quality – Pseudomonas putida growth inhibition test (Pseudomonas cell multiplication inhibition test
- Version / remarks:
- January 1996
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Preparation of Water Accomodated Fractions (WAFs); Due to the highly hydrophobic character of the test substance, the substane remained floating at the surface. Therefore, WAFs were prepared from a stock solution of a nominal loading rate of 12.5 g/L. The stock solution was stirred for 48 hours and left stabilising for another 26 hours. The water phase in the middle of the separating funnel was used for this test and identified as the WAF.
- Controls: Blank control and positive control - Test organisms (species):
- Pseudomonas putida
- Details on inoculum:
- Details on Pseudomonas putida:
- Strain: P. putida MIGULA, Berlin 33/2 (DSM 50026)
- Source: BGA, Berlin, Germany
- Incubation temperature: 23 +/- 1 °C
- Incubation time: preliminary suspension cultures 6 +/- 1 hours, exposure 16 +/- 1 hours
- Age of bacteria stock culture at study initiation: max. 7 days
- Preliminary suspension cultures: a small amount of bacteria from the stock culture was inoculates in pre-culture medium (preparation see "Details on test conditions") in Erlenmeyer flasks. After incubation under continuous shaking in the darl, the final turbidity value of the bacterial suspension was adjusted up to FNU/436 nm = 50. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 16 h
- Nominal and measured concentrations:
- nominal: control, 310, 630, 1250, 2500, 5000 and 10000 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 mL Erlenmeyer flasks, covered with Aluminium caps
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 10
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: nutrient medium: 18 g of agar dissolved in water, plus 50 mL of solution I, 125 mL of solution III and 100 mL of solution IV, made up to one L with water. For preparation of individual solutions, please see below. The nutrient medium is allowed to gel in portions of 6-10 mL at a slant.
Preparation of pre-culture medium: 25 mL of stock solutions I and III plus 50 mL of solution IV, made up to 1 L with water
Preparation of individual solutions:
Stock solution I: 10.0 g NaNO3, 2.4 g K2HPO4, 1.2 g KH2PO4, 1.0 g yeast extract, dissolved in 500 mL MilliQ water
Stock solution II: 10.0 g NaNO3, 2.4 g K2HPO4, 1.2 g KH2PO4, dissolved in 500 mL MilliQ water
Stock solution III: 40.0 g D (+) glucose monohydrate, dissolved in 500 mL MilliQ water
Stock solution IV: 0.01 g Fe (III) citrate, 4.0 g MgSO4 x 7 H2O, dissolved in 1 L MilliQ water
for further details on test solution preparation, please see Table 1 in section "Any other information on material and methods"
OTHER TEST CONDITIONS
- Adjustment of pH: The pH of the test substance stock solution was 6.5.
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) : After incubation for 16 hours, extinction values of the bacterial cell suspensions were measured and the cell multiplication inhibition for each test concentration was determined.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2 - Reference substance (positive control):
- yes
- Remarks:
- 3,5-dichlorophenol
- Duration:
- 16 h
- Dose descriptor:
- EC50
- Effect conc.:
- 8 062 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- WAF
- Basis for effect:
- other: inhibition of cell multiplication
- Duration:
- 16 h
- Dose descriptor:
- EC10
- Effect conc.:
- 2 582 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- WAF
- Basis for effect:
- other: inhibition of cell multiplication
- Details on results:
- For further details on inhibition values, please see Table 2 in section "Any other information on results"
- Results with reference substance (positive control):
- EC50 = 22 mg/L (accepted range 10-30 mg/L)
Multiplication factor of the bacteria was > 60. Therefore it was concluded, that the test was valid. - Endpoint:
- toxicity to microorganisms, other
- Remarks:
- Inhibition of cell multiplication
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 10 April - 20 May 1998
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Remarks:
- GLP guideline study without analytical verification of the test item
- Qualifier:
- according to guideline
- Guideline:
- DIN 38412-27 (Pseudomonas putida Zellvermehrungshemmtest)
- Version / remarks:
- March 1991
- Qualifier:
- according to guideline
- Guideline:
- ISO 10712 (Water quality – Pseudomonas putida growth inhibition test (Pseudomonas cell multiplication inhibition test
- Version / remarks:
- January 1996
- GLP compliance:
- yes
- Analytical monitoring:
- no
- Vehicle:
- no
- Details on test solutions:
- PREPARATION AND APPLICATION OF TEST SOLUTION (especially for difficult test substances)
- Method: Preparation of Water Accomodated Fractions (WAFs); Due to the highly hydrophobic character of the test substance, the substane remained floating at the surface. Therefore, WAFs were prepared from a stock solution of a nominal loading rate of 12.5 g/L. The stock solution was stirred for 48 hours and left stabilising for another 26 hours. The water phase in the middle of the separating funnel was used for this test and identified as the WAF.
- Controls: Blank control and positive control - Test organisms (species):
- Pseudomonas putida
- Details on inoculum:
- Details on Pseudomonas putida:
- Strain: P. putida MIGULA, Berlin 33/2 (DSM 50026)
- Source: BGA, Berlin, Germany
- Incubation temperature: 23 +/- 1 °C
- Incubation time: preliminary suspension cultures 6 +/- 1 hours, exposure 16 +/- 1 hours
- Age of bacteria stock culture at study initiation: max. 7 days
- Preliminary suspension cultures: a small amount of bacteria from the stock culture was inoculates in pre-culture medium (preparation see "Details on test conditions") in Erlenmeyer flasks. After incubation under continuous shaking in the darl, the final turbidity value of the bacterial suspension was adjusted up to FNU/436 nm = 50. - Test type:
- static
- Water media type:
- freshwater
- Limit test:
- no
- Total exposure duration:
- 16 h
- Nominal and measured concentrations:
- nominal: control, 310, 630, 1250, 2500, 5000 and 10000 mg/L
- Details on test conditions:
- TEST SYSTEM
- Test vessel: 100 mL Erlenmeyer flasks, covered with Aluminium caps
- No. of vessels per concentration (replicates): 3
- No. of vessels per control (replicates): 10
TEST MEDIUM / WATER PARAMETERS
- Source/preparation of dilution water: nutrient medium: 18 g of agar dissolved in water, plus 50 mL of solution I, 125 mL of solution III and 100 mL of solution IV, made up to one L with water. For preparation of individual solutions, please see below. The nutrient medium is allowed to gel in portions of 6-10 mL at a slant.
Preparation of pre-culture medium: 25 mL of stock solutions I and III plus 50 mL of solution IV, made up to 1 L with water
Preparation of individual solutions:
Stock solution I: 10.0 g NaNO3, 2.4 g K2HPO4, 1.2 g KH2PO4, 1.0 g yeast extract, dissolved in 500 mL MilliQ water
Stock solution II: 10.0 g NaNO3, 2.4 g K2HPO4, 1.2 g KH2PO4, dissolved in 500 mL MilliQ water
Stock solution III: 40.0 g D (+) glucose monohydrate, dissolved in 500 mL MilliQ water
Stock solution IV: 0.01 g Fe (III) citrate, 4.0 g MgSO4 x 7 H2O, dissolved in 1 L MilliQ water
for further details on test solution preparation, please see Table 1 in section "Any other information on material and methods"
OTHER TEST CONDITIONS
- Adjustment of pH: The pH of the test substance stock solution was 7.5.
EFFECT PARAMETERS MEASURED (with observation intervals if applicable) :
After incubation for 16 hours, extinction values of the bacterial cell suspensions were measured and the cell multiplication inhibition for each test concentration was determined.
TEST CONCENTRATIONS
- Spacing factor for test concentrations: 2 - Reference substance (positive control):
- yes
- Remarks:
- 3,5-Dichlorophenol
- Duration:
- 16 h
- Dose descriptor:
- EC50
- Effect conc.:
- 9 411 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- WAF
- Basis for effect:
- other: inhibition of cell multiplication
- Duration:
- 16 h
- Dose descriptor:
- EC10
- Effect conc.:
- 4 792 mg/L
- Nominal / measured:
- nominal
- Conc. based on:
- test mat.
- Remarks:
- WAF
- Basis for effect:
- other: inhibition of cell multiplication
- Details on results:
- For further details on inhibition values, please see Table 2 in section "Any other information on results"
- Results with reference substance (positive control):
- EC50 = 22 mg/L (accepted range 10-30 mg/L)
Multiplication factor of the bacteria was > 60. Therefore it was concluded that the test was valid.
Referenceopen allclose all
Table 1: Degradation of the toxicity control
Day No. |
Degradation [%] |
2 |
0.0 |
5 |
12.0 |
7 |
20.5 |
9 |
30.6 |
14 |
43.7 |
19 |
59.4 |
23 |
66.3 |
27 |
69.5 |
29 |
77.3 |
Table 2: Validity criteria
Criterion from the guideline |
Outcome |
Validity criterion fulfilled |
Difference of extremes of replicate values of the removal of the test chemical at the plateau, at the end of the test or at the end of the 10-d window, as appropriate, is less than 20%. |
< 20% |
yes |
Percentage degradation of the reference compound has reached the pass levels by day 14 (>60%). |
64.6% |
yes |
The toxicity control should degrade to at least 35% (based on DOC) or at least 25% (based on ThOD or ThCO2) within 14 d. |
43.7% |
yes |
The total CO2 evolution in the inoculum blank at the end of the test should not normally exceed 40 mg/L medium. |
28.1 mg/L |
yes |
Table 2: Extinction values of bacterial cell suspensions.
Concentration of test item [mg/L] |
Mean extinction, corrected by turbidity control [FNU 436 nm] |
Inhibition [%] |
310 |
242 |
-13.1 |
630 |
233 |
-8.9 |
1,250 |
239 |
-11.4 |
2,500 |
193 |
9.9 |
5,000 |
157 |
26.9 |
10,000 |
77 |
64.4 |
Table 3: Validity criteria
Criterion from the guideline |
Outcome |
Validity criterion fulfilled |
The EC50 value of the reference substance 3,5 -dichlorophenol should be in the accepted range of 10 -30 mg/L. |
22 mg/L |
yes |
The inoculum used in the control batch should be multiplied by a factor of at least 60 within the test period. |
factor of 179 |
yes |
Table 2: Extinction values of bacterial cell suspensions.
Concentration of test item [mg/L] |
Mean extinction, corrected by turbidity control [FNU 436 nm] |
Inhibition [%] |
310 |
207 |
3.7 |
630 |
251 |
-17.0 |
1,250 |
284 |
-32.8 |
2,500 |
251 |
-17.0 |
5,000 |
189 |
11.8 |
10,000 |
97 |
55.1 |
Table 3: Validity criteria
Criterion from the guideline |
Outcome |
Validity criterion fulfilled |
The EC50 value of the reference substance 3,5 -dichlorophenol should be in the accepted range of 10 -30 mg/L. |
22 mg/L |
yes |
The inoculum used in the control batch should be multiplied by a factor of at least 60 within the test period. |
factor of 179 |
yes |
Description of key information
Key value for chemical safety assessment
Additional information
Since no studies investigating the toxicity of Isooctadecanoic acid, mixed esters with oxybis[propanediol] to microorganisms are available, in accordance with Regulation (EC) No 1907/2006 Annex XI, 1.5, a read-across to the structurally related source substance Isooctadecanoic acid, ester with oxybis[propanediol] (CAS 73296-86-3) was conducted. The source substance is representative to evaluate the toxicity of the target substance to microorganisms.
The target substance Isooctadecanoic acid, mixed esters with oxybis[propanediol] exists as two different grades. Grade One is characterized by mainly triesters of C18 iso fatty acids of the alcohol component diglycerol. Grade Two is characterized by mainly tetraesters of C18 iso fatty acids of the alcohol component diglycerol.
The source substance Isooctadecanoic acid, ester with oxybis[propanediol] (CAS 73296-86-3) is characterized as a UVCB substance containing polyglycerol as alcohol component. Polyglycerol components are esterified to give mainly monoesters of C18 iso fatty acids.
Two studies are available for the source substance Isooctadecanoic acid, ester with oxybis[propanediol] (CAS 73296-86-3). Both studies investigated the effect of the test material on the inhibition of cell multiplication of Pseudomonas putida. Both were conducted in identical test systems. The studies were conducted according to ISO 10712 and DIN38412-8. The cells were exposed to nominal loading rates of 310, 630, 1250, 2500, 5000 and 10000 mg/ in a static freshwater system. After incubation for 16 hours, extinction values of the bacterial cell suspensions were measured and the cell multiplication inhibition for each test concentration was determined. An EC50 (16 h) of 8062 mg/L was calculated for the first study and an EC50 (16h) of 9411 mg/L for the second study.
In addition, for Isooctadecanoic acid, ester with oxybis[propanediol] (CAS 73296-86-3), a toxicity control from a ready biodegradability study is also available. This study supports the results from the cell multiplication-tests with Pseudomonas putida. If a compound degrades well in a ready biodegradability test, or does not inhibit the degradation of a positive control at a certain concentration, this concentration can be used as a NOEC value. This approach is in accordance with the Guidance on information requirements and chemical safety assessment (Chapter R.7b: Endpoint specific guidance, ECHA 2017).
A substance can be assumed to be not inhibitory to aquatic microorganisms, if in the toxicity control of a ready biodegradation test, more than 25% degradation based on oxygen demand (BOD/ThOD) occurred within 14 days (OECD guideline 301). The study for Isooctadecanoic acid, ester with oxybis[propanediol] (CAS 73296-86-3) was conducted according to OECD 301 B and EU Method C.4-C. Non-adapted, domestic activated sludge was exposed to 17.2 mg/L of the test material and 40.3 mg/L of the reference substance sodium acetate. The toxicity control attained 43.7 % degradation after 14 days of incubation. Hence, the substance is not toxic to aquatic microorganisms in the toxicity control and the test item concentration of 17.3 mg/L can be used as NOEC.
Based on the results for the structurally related read-across substance Isooctadecanoic acid, ester with oxybis[propanediol] (CAS 73296-86-3) (in accordance with Regulation (EC) No 1907/2006 Annex XI, 1.5) which is characterized by a similar ecotoxicological profile and comparable structure, it can be concluded that no toxicity of the target substance Isooctadecanoic acid, mixed esters with oxybis[propanediol] to microorganisms is expected.
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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