Brief Profile

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Please be aware that the REACH registration parts of this Brief Profile are no longer maintained; they remain frozen as of 19th May 2023. All other data parts (substance identity, C&L, key regulatory lists etc. are up to date).

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Brief Profile

The Brief Profile summarizes the non-confidential data on substances as it is held in the databases of the European Chemicals Agency (ECHA), including data provided by third parties. The Brief Profile is automatically generated; note that it does not currently distinguish between harmonised classification and minimum classification; information requirements under different legislative frameworks may therefore not be fully up to date or complete. For accuracy reasons, substance manufacturers and imports have the responsibility to consult official sources, e.g. the electronic edition of the Official Journal of the European Union.
This Brief Profile is covered by the ECHA Legal Notice.

Substance Description

Substance identity

EC / List no.:
292-604-8
CAS no.:
90640-82-7
Index number:
648-104-00-0
Molecular formula:
SMILES:
InChI:
Type of substance:
UVCB
Origin:
Organic
Registered compositions:
1
Of which contain:
0 impurities relevant for classification
0 additives relevant for classification
Substance Listed:
EINECS (European INventory of Existing Commercial chemical Substances) List

Hazard classification & labelling

Danger! According to the harmonised classification and labelling (ATP01) approved by the European Union, this substance may cause genetic defects and may cause cancer.

Additionally, the classification provided by companies to ECHA in REACH registrations identifies that this substance is toxic to aquatic life with long lasting effects, is suspected of causing genetic defects and is suspected of causing cancer.

Additionally, the classification provided by companies to ECHA in CLP notifications identifies that this substance is very toxic to aquatic life, is very toxic to aquatic life with long lasting effects, causes skin irritation and may cause an allergic skin reaction.

Breakdown of all 88 C&L notifications submitted to ECHA

Muta. 1B H340 Harmonised Classification
Carc. 1B H350 Harmonised Classification
Aquatic Acute 1 H400
Aquatic Chronic 1 H410
Skin Irrit. 2 H315
Skin Sens. 1 H317
Aquatic Chronic 2 H411
Muta. 2 H341
Carc. 2 H351
0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%

https://echa.europa.eu/o/diss-blank-theme/images/cnl/graph/tick.png Harmonised Classification

https://echa.europa.eu/o/diss-blank-theme/images/cnl/graph/Reach.png REACH registration dossiers notifications

https://echa.europa.eu/o/diss-blank-theme/images/cnl/graph/CLP.png CLP notifications

Properties of concern

  • C
Officially recognised in the EU as Carcinogenic (Harmonised C&L, Candidate list of SVHCs).
  • M
Officially recognised in the EU as Mutagenic (Harmonised C&L, Candidate list of SVHCs).
  • PBT
Officially recognised in the EU as Persistent, Bioaccumulative and Toxic (Candidate list of SVHCs).

Regulatory context

Registration, Evaluation, Authorisation & Restriction of Chemicals (REACH)

Registration
Pre-registration:
Substance pre-registered under REACH.
Registration:
This substance has 1 active registrations under REACH, 1 Joint Submission(s) and 0 Individual Submission(s).
Please see Registrants/Suppliers details.
Evaluation
Dossier Evaluation:
Substance Evaluation:
Authorisation
Candidate List:
Substance of very high concern (SVHC) and included in the candidate list for authorisation.
Annex XIV (Authorisation List):
Restriction
Annex XVII (Restriction List):

Persistent Organic Pollutants Regulation (POPs)

List of substances subject to the POPs Regulation:
List of substances proposed as POPs:

Classification Labelling & Packaging (CLP)

Harmonised C&L:
A European Union Harmonised Classification & Labelling has been assigned to this substance.
Seveso Annex I:
Notified C&L:
Classification & Labelling has been notified by industry to ECHA for this substance.

Biocidal Products Regulation (BPR)

Active Substance:
Biocidal Products:

Prior Informed Consent (PIC)

Annex I:
Annex V:

European Union Observatory for Nanomaterials (EUON)

EUON:

About this substance

This substance is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, for intermediate use only.

This substance is used in formulation or re-packing, at industrial sites and in manufacturing.

ECHA has no public registered data indicating whether or in which chemical products the substance might be used.

ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

ECHA has no public registered data on the use of this substance in activities or processes at the workplace.

ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

ECHA has no public registered data indicating whether or into which articles the substance might have been processed.

ECHA has no public registered data indicating whether or in which chemical products the substance might be used.

ECHA has no public registered data on the types of manufacture using this substance.

ECHA has no public registered data on the use of this substance in activities or processes at the workplace.

ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

This substance has an industrial use resulting in manufacture of another substance (use of intermediates).

This substance is used in the following activities or processes at workplace: closed processes with no likelihood of exposure, closed, continuous processes with occasional controlled exposure, closed batch processing in synthesis or formulation, transfer of chemicals at dedicated facilities and laboratory work.

Release to the environment of this substance can occur from industrial use: formulation of mixtures.

This substance has an industrial use resulting in manufacture of another substance (use of intermediates).

This substance is used for the manufacture of: chemicals.

This substance is used in the following activities or processes at workplace: closed processes with no likelihood of exposure, closed, continuous processes with occasional controlled exposure, closed batch processing in synthesis or formulation, transfer of chemicals at dedicated facilities, transfer of substance into small containers and laboratory work.

Release to the environment of this substance can occur from industrial use: as an intermediate step in further manufacturing of another substance (use of intermediates).

This substance is used in the following activities or processes at workplace: closed processes with no likelihood of exposure, closed, continuous processes with occasional controlled exposure, closed batch processing in synthesis or formulation, transfer of chemicals at dedicated facilities, transfer of substance into small containers and laboratory work.

Release to the environment of this substance can occur from industrial use: manufacturing of the substance.

Precautions for using this substance have been recommended by its registrants under REACH, as follows:

Prevention statements

When handling this substance: obtain special instructions before use; avoid release to the environment; use personal protective equipment as required..

Guidance on the safe use of the substance provided by manufacturers and importers of this substance.

Registrants/suppliers

  • DEZA a.s., Masarykova 753 75701 Valasske Mezirici Czech Republic

Substance names and other identifiers

Anthracene oil, anthracene-low
EC Inventory, Candidate list, Other, Cosmetic Products Regulation, Annex II - Prohibited Substances
Anthracene oil, anthracene-low
The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.
Candidate list, REACH pre-registration, Other, Cosmetic Products Regulation, Annex II - Prohibited Substances
Anthracene oil, anthracene-low; Anthracene Oil Fraction [he oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.]
The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.
Active Implantable Medical Devices Directive - Hazardous Substances, In Vitro Diagnostic Medical Devices Directive - Hazardous Substances, Medical Devices Directive - Hazardous Substances
Anthracene oil, anthracene-low; Anthracene Oil Fraction [The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.]
The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.
FCM Active and Intelligent Materials - CMRs not allowed for use, CAD - Chemical Agents Directive, Art. 2(b)(i) - Hazardous Agents, Construction Product Regulation - Annex I (3) - Hazardous Substances, Construction Product Regulation - Art. 6(5) - SDS and Declaration, EU Ecolabels - Restrictions for Hazardous Substances/Mixtures, End-of-Life Vehicles Directive - Hazardous Substances, In Vitro Diagnostic Medical Devices Regulation - Hazardous Substances, Marine Environmental Policy Framework Directive - Hazardous Substances, Medical Devices Regulation - Hazardous Substances, Protection of Pregnant and Breastfeeding Workers Directive, Annex I+II, General Product Safety Directive - Hazardous Substances, Workplace Signs - minimum requirements & signs on containers and pipes, Safety and Health of Workers at Work Directive - Hazardous Substances, Waste Framework Directive, Annex III - Waste - Hazardous Properties, Carc and Muta Directive, Annex I - Substances, Mixtures & Processes, Physical, Biological and Chemical Agents & Processes and Work
anthracenolie, med lavt indhold af anthracen Antracenoliefraktion Den tiloversblevne olie efter fjernelse, ved en krystallisationsproces, af et anthracenrigt fast stof (anthracenpasta) fra anthracenolie. Den er sammensat primært af bi, tri og tetracykliske aromatiske forbindelser. (da)
C&L Inventory
Anthracenový olej, s nízkým obsahem anthracenu Frakce anthracenového oleje [Olej zbývající po odstranění tuhé hmoty bohaté na anthracen (anthracenové pasty) krystalizačním procesem z anthracenového oleje. Je složen převážněz isomerů se dvěma, třemi a čtyřmi aromatickými jádry.] (cs)
C&L Inventory
Anthracenöl, anthracenarm Anthracenölfraktion [Öl, das nach einem Kristallisationsverfahren zum Entfernen eines anthracenreichen Feststoffes (Anthracenpaste) aus Anthracenöl zurückbleibt; besteht in erster Linie aus zwei-, drei- und viergliedrigen aromatischen Verbindungen] (de)
C&L Inventory
antraceenolie, antraceenarm Antraceenolie, fractie De olie die resteert na de verwijdering, door middel van een kristallisatieproces, van een antraceenrijke vaste stof (antraceenpasta) uit antraceenolie. Bestaat voornamelijk uit aromatische verbindingen met twee, drie of vier ringen. (nl)
C&L Inventory
Antraceno alyva, turi mažai antraceno Antraceno alyvos frakcija [Alyvos likutis, iš antraceno alyvos kristalizavimo būdu pašalinus daug antraceno turinčią kietą medžiagą (antraceno pastą). Jį sudaro daugiausia dvi-, tri- ir keturcikliai aromatiniai junginiai.] (lt)
C&L Inventory
Antracenolja, med lågt innehåll av antracen Antracenoljefraktion Oljeåterstoder efter avlägsnande, genom en kristallisationsprocess, av ett antracenrikt fast ämne (antracenpasta) från antracenolja. Består främst av två, tre eller fyra aromatiska ringar. (sv)
C&L Inventory
antracenolje, lavt antraceninnhold antracenoljefraksjon [Oljen som er igjen etter fjerning, ved en krystalliseringsprosess, av et antracenrikt fast stoff (antracenpasta) fra antracenolje. Består hovedsakelig av to-, tre- eller firerings aromatiske forbindelser.] (no)
C&L Inventory
antracensko olje, nizka vsebnost antracena frakcija antracenskega olja [Olje, ki ostane po odstranitvi z antracenom bogate trdne snovi (antracenske paste) iz antracenskega olja s procesom kristalizacije. Sestoji pretežno iz dva-, tri- in štiri-členskih aromatskih spojin.] (sl)
C&L Inventory
Antracensko ulje, nisko-antracensko Frakcija antracenskog ulja (Ulje preostalo nakon uklanjanja krute antracenom bogate tvari (antracenska pasta) iz antracenskog ulja postupkom kristalizacije. Sastavljeno je primarno od dvočlanih, tročlanih i četveročlanih aromatskih spojeva.) (hr)
C&L Inventory
Antracén olaj, antacénben szegény Antracén olaj frakció [Antracén olajból egy antracénben gazdag szilárd anyag (antracén paszta) kristályosítással történő eltávolítása után visszamaradó olaj. Elsősorban két-, három- és négytagú aromás vegyületekből áll.] (hu)
C&L Inventory
antracénový olej, s nízkym obsahom antracénu frakcia antracénového oleja [Olej, ktorý zostáva po oddelení tuhej látky bohatej na antracén (antracénovej pasty) z antracénového oleja kryštalizáciou. Pozostáva predovšetkým z dvoj-, troj- a štvorjadrových aromatických zlúčenín.] (sk)
C&L Inventory
Antracēna eļļa, antracēna saturs neliels Antracēna eļļas frakcija [Eļļa, kas atlikusi pēc tam, kad no antracēna eļļas kristalizācijas procesā aizvākta antracēnu bagātīgi saturoša cietviela (antracēna pasta). Galvenokārt sastāv no divu, triju un četru ciklu aromātiskiem ogļūdeņražiem.] (lv)
C&L Inventory
Huile anthracénique, à faible teneur en anthracène; fraction d'huile anthracénique;[Huile résultant de l'extraction, par cristallisation, d'un solide riche en anthracène (pâte anthracénique) à partir d'huile anthracénique. Se compose principalement de composés aromatiques à deux, trois ou quatre cycles.] fraction d'huile anthracénique Huile restant après l'élimination de l'huile anthracénique, par cristallisation, de la pâte anthracénique (solide riche en anthracène). Se compose principalement de composés aromatiques comportant 2, 3 ou 4 cycles. (fr)
C&L Inventory
olio di antracene, a basso contenuto di antracene Frazione di olio di antracene olio che rimane dopo la rimozione da olio di antracene, per mezzo di un processo di cristallizzazione, di un solido ricco di antracene (pasta di antracene) . Costituito prevalentemente da composti aromatici a due, tre e quattro anelli. (it)
C&L Inventory
Óleo de antraceno, baixo teor de antraceno Fracção do óleo de antraceno Óleo que fica depois da remoção, do óleo de antraceno, por um processo de cristalização, de um sólido rico em antraceno (pasta de antraceno). É constituído principalmente por compostos aromáticos com dois, três e quatro anéis. (pt)
C&L Inventory
Ţiţei antracenic, având un conţinut scăzut de antracen Fracţia ţiţeiului antracenic [Uleiul rămas după îndepărtarea prin cristalizare a solidului bogat în antracen (pastă de antracen) din ţiţeiul antracenic. Este compus cu precădere din doi, trei şi patru compuşi aromatici.] (ro)
C&L Inventory
Ţiţei antracenic, având un conţinut scăzut de antracen Fracţia ţiţeiului antracenic Uleiul rămas după îndepărtarea prin cristalizare a solidului bogat în antracen (pastă de antracen) din ţiţeiul antracenic. Este compus cu precădere din doi, trei şi patru compuşi aromatici. (mt)
C&L Inventory
έΈλαιο ανθρακενίου, χαμηλής περιεκτικότητας σε ανθρακένιο Κλάσμα ελαίου ανθρακενίου [To έλαιο που παραμένει μετά την απομάκρυνση, με κρυστάλλωση, στερεού πλούσιου σε ανθρακένιο (πάστα ανθρακενίου) από έλαιο ανθρακενίου. Aποτελείται κυρίως από αρωματικές ενώσεις με δύο, τρεις και τέσσερις δακτυλίους.] (el)
C&L Inventory
Антраценова фракция, с ниско съдържание на антрацен Антраценова фракция [Фракция, оставаща след отделяне, посредством процес на кристализация, на богатото на антрацен твърдо вещество (антраценова паста), от антраценовата фракция. Състои се основно от ди-, три- и тетра-циклени ароматни съединения.] (bg)
C&L Inventory
Anthracene oil, anthracene-low
C&L Inventory, Registration dossier
Anthracene oil, anthracene-low
Registration dossier
Fenanthrenový zbytek
Registration dossier
FZ
Registration dossier
648-104-00-0
Index number
C&L Inventory
90640-82-7
CAS number
EC Inventory, C&L Inventory, Candidate list, Registration dossier, REACH pre-registration, Other, FCM Active and Intelligent Materials - CMRs not allowed for use, CAD - Chemical Agents Directive, Art. 2(b)(i) - Hazardous Agents, Construction Product Regulation - Annex I (3) - Hazardous Substances, Construction Product Regulation - Art. 6(5) - SDS and Declaration, Cosmetic Products Regulation, Annex II - Prohibited Substances, EU Ecolabels - Restrictions for Hazardous Substances/Mixtures, End-of-Life Vehicles Directive - Hazardous Substances, Active Implantable Medical Devices Directive - Hazardous Substances, In Vitro Diagnostic Medical Devices Directive - Hazardous Substances, In Vitro Diagnostic Medical Devices Regulation - Hazardous Substances, Marine Environmental Policy Framework Directive - Hazardous Substances, Medical Devices Directive - Hazardous Substances, Medical Devices Regulation - Hazardous Substances, Protection of Pregnant and Breastfeeding Workers Directive, Annex I+II, General Product Safety Directive - Hazardous Substances, Workplace Signs - minimum requirements & signs on containers and pipes, Safety and Health of Workers at Work Directive - Hazardous Substances, Waste Framework Directive, Annex III - Waste - Hazardous Properties, Carc and Muta Directive, Annex I - Substances, Mixtures & Processes, Physical, Biological and Chemical Agents & Processes and Work

Scientific properties

Physical and chemical properties

This section provides physicochemical information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. The quality and correctness of the information remains the responsibility of the data submitter. The Agency thus cannot guarantee the correctness of the information displayed.

Appearance/physical state / colour

Study results
  • 1 study submitted
  • 1 study processed
C Physical state at 20°C and 1013 hPa
Solid (100%) [1]
C Form
Compact (100%) [1]
C Odour
Faint (100%) [1]
C Substance type
Organic (100%) [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Melting/freezing point

Study results
  • 1 study submitted
  • 1 study processed
R Melting / freezing point
38.2 °C @ 101.3 kPa [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Boiling point

Study results
  • 1 study submitted
  • 1 study processed
R Boiling point
290 - 347 °C @ 101.3 kPa [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Density

Study results
  • 1 study submitted
  • 1 study processed
R Density
1.124 g/cm³ @ 20 °C [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Vapour pressure

Study results
  • 1 study submitted
  • 1 study processed
R Vapour pressure
8.8 - 930 Pa @ 20 - 114 °C [2]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Partition coefficient

Study results
  • 1 study submitted
  • 1 study processed
R Log Pow
3.9 - 5.2 @ 25 °C and pH 7 - 7.5 [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Water solubility

Study results
  • 3 studies submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study 2
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Solubility in organic solvents / fat solubility

Data not provided by the registrant

Surface tension

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Flash point

Study results
  • 1 study submitted
  • 1 study processed
R Flash point
165 °C @ 101.325 kPa [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Auto flammability

Study results
  • 1 study submitted
  • 1 study processed
R Autoflammability / self-ignition
525 °C @ 101.3 kPa [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Flammability

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Flammability
Non flammable (100%)

Explosiveness

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Oxidising

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Oxidation reduction potential

Data not provided by the registrant

pH

Data not provided by the registrant

Dissociation constant

Data not provided by the registrant

Viscosity

Study results
  • 1 study submitted
  • 1 study processed
R kinematic viscosity (in mm²/s)
3 [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Environmental fate and pathways

This section provides environmental fate and pathways information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. The quality and correctness of the information remains the responsibility of the data submitter. The Agency thus cannot guarantee the correctness of the information displayed.

Phototransformation in air

Data not provided by the registrant

Hydrolysis

Data not provided by the registrant

Phototransformation in water

Data not provided by the registrant

Phototransformation in soil

Data not provided by the registrant

Biodegradation in water - screening tests

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Biodegradation in water & sediment - simulation tests

Data not provided by the registrant

Biodegradation in soil

Data not provided by the registrant

Bioaccumulation: aquatic / sediment

Data not provided by the registrant

Bioaccumulation: terrestrial

Data not provided by the registrant

Adsorption/desorption

Data not provided by the registrant

Henrys law constant (H)

Data not provided by the registrant

Distribution modelling

Data not provided by the registrant

Ecotoxicological information

This section provides ecotoxicological information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. The quality and correctness of the information remains the responsibility of the data submitter. The Agency thus cannot guarantee the correctness of the information displayed.

Predicted No-Effect Concentration (PNEC)

R Summaries
  • 1 summary submitted
  • 1 summary processed

The Predicted No-Effect Concentration (PNEC) value is the concentration of a substance below which adverse effects in the environment are not expected to occur. Please note that when more than one summary is provided, PNEC values may refer to constituents of the substance and not to the substance as a whole. More detailed information is available in the dossiers.

Hazard for Aquatic Organisms
Freshwater 1.1 µg/L (1)
Intermittent releases (freshwater) -
Marine water 1.1 µg/L (1)
Intermittent releases (marine water) -
Sewage treatment plant (STP) -
Sediment (freshwater) -
Sediment (marine water) -
Hazard for Air
Air -
Hazard for Terrestrial Organism
Soil -
Hazard for Predators
Secondary poisoning -

Short–term toxicity to fish

Data not provided by the registrant

Long–term toxicity to fish

Data not provided by the registrant

Short–term toxicity to aquatic invertebrates

Study results
  • 6 studies submitted
  • 4 studies processed
P/RResults
EC50 (24 h) 1.2 - 29.3 µg/L [3]
LC50 (4 days) 68.9 - 13 300 µg/L [2]
LC50 (48 h) 3.6 - 4 260 µg/L [4]
EC0 (24 h) 30 µg/L [1]
EL50 (48 h) 22.4 mg/L [1]

Type of Study provided
Studies with data
Key study 4
Supporting study 1 1
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Long–term toxicity to aquatic invertebrates

Data not provided by the registrant

Toxicity to aquatic algae and cyanobacteria

Study results
  • 6 studies submitted
  • 4 studies processed
P/RResults
EC50 (24 h) 3.3 - 24 µg/L [1]
EC50 (22 h) 3.9 - 37.4 µg/L [1]
NOEC (40 h) 19.4 µg/L [1]
NOEC (22 h) 1.5 - 1.7 µg/L [1]
EC10 (72 h) 8.6 - 33.1 µg/L [2]

Type of Study provided
Studies with data
Key study 1 3
Supporting study 2
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Toxicity to aquatic plants other than algae

Data not provided by the registrant

Toxicity to microorganisms

Data not provided by the registrant

Sediment toxicity

Data not provided by the registrant

Endocrine disrupter testing in aquatic vertebrates – in vivo

Data not provided by the registrant

Toxicity to terrestrial macroorganisms except arthropods

Data not provided by the registrant

Toxicity to terrestrial arthropods

Data not provided by the registrant

Toxicity to terrestrial plants

Data not provided by the registrant

Toxicity to soil microorganisms

Data not provided by the registrant

Toxicity to birds

Data not provided by the registrant

Toxicity to mammals

Data not provided by the registrant

Toxicological information

This section provides toxicological information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. The quality and correctness of the information remains the responsibility of the data submitter. The Agency thus cannot guarantee the correctness of the information displayed.

Derived No- or Minimal Effect Level (DN(M)EL)

Data not provided by the registrant

Toxicokinetics, metabolism, and distribution

Data not provided by the registrant

Acute toxicity

Study results
oral
  • 1 study submitted
  • 1 study processed
P/RResults
LD50 4 030 mg/kg bw (rat) [1]

Type of Study provided
oral
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
inhalation
  • 0 studies submitted
  • 0 studies processed

No data available

inhalation
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
dermal
  • 0 studies submitted
  • 0 studies processed

No data available

dermal
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
other routes
  • 0 studies submitted
  • 0 studies processed

No data available

other routes
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Irritation / corrosion

Study results
Study data: skin
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: skin
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Study data: eye
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: eye
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Sensitisation

Study results
Study data: skin
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: skin
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Study data: respiratory
  • 0 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: respiratory
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Repeated dose toxicity

Data not provided by the registrant

Genetic toxicity

Study results
Study data: in vitro
  • 3 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: in vitro
Studies with data
Key study 1 2
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Study data: in vivo
  • 0 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: in vivo
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Carcinogenicity

Data not provided by the registrant

Toxicity to reproduction

Data not provided by the registrant

Neurotoxicity

Data not provided by the registrant

Immunotoxicity

Data not provided by the registrant

Endocrine disrupter mammalian screening - in vivo

Data not provided by the registrant