Brief Profile

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.:
284-895-5
CAS no.:
84989-06-0
Index number:
648-122-00-9
Molecular formula:
SMILES:
InChI:
Type of substance:
UVCB
Origin:
Organic
Registered compositions:
3
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 if swallowed, is toxic in contact with skin, causes severe skin burns and eye damage, is toxic to aquatic life with long lasting effects, causes serious eye damage and may cause an allergic skin reaction.

Breakdown of all 6 C&L notifications submitted to ECHA

Acute Tox. 3 H301
Acute Tox. 3 H311
Skin Corr. 1B H314
Aquatic Chronic 2 H411
Muta. 1B H340 Harmonised Classification
Carc. 1B H350 Harmonised Classification
Eye Dam. 1 H318
Skin Sens. 1B H317
0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%

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

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

https://www.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).
  • C
There is no overall agreement among data submitters, but a minority indicate they consider this substance as Carcinogenic (16.67% of REACH registrations).
  • M
Officially recognised in the EU as Mutagenic (Harmonised C&L).
  • M
There is no overall agreement among data submitters, but a minority indicate they consider this substance as Mutagenic (16.67% of REACH registrations).
  • Ss
There is no overall agreement among data submitters, but a minority indicate they consider this substance as Skin sensitising (16.67% of REACH registrations).
  • PBT
Under assessment as Persistent, Bioaccumulative and Toxic (PBT list).

Regulatory context

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

Registration
Pre-registration:
Substance pre-registered under REACH.
Registration:
This substance has 2 active registrations under REACH, 1 Joint Submission(s) and 0 Individual Submission(s).
Please see Registrants/Suppliers details.
Evaluation
Dossier Evaluation:
Registration dossiers submitted to ECHA for this substance have been evaluated under REACH.
Substance Evaluation:
Authorisation
Candidate List:
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, at ≥ 100 to < 1 000 tonnes per annum.

This substance is used by professional workers (widespread uses), 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.

This substance is used in the following products: washing & cleaning products.

This substance is used in the following areas: agriculture, forestry and fishing and building & construction work. This substance is used for the manufacture of: machinery and vehicles, textile, leather or fur, wood and wood products and furniture.

This substance is used in the following activities or processes at workplace: transfer of chemicals and closed, continuous processes with occasional controlled exposure.

Other release to the environment of this substance is likely to occur from: indoor use as processing aid, outdoor use as processing aid, indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters) and outdoor use in close systems with minimal release (e.g. hydraulic liquids in automotive suspension, lubricants in motor oil and break fluids).

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

This substance is used in the following activities or processes at workplace: transfer of chemicals, closed batch processing in synthesis or formulation, batch processing in synthesis or formulation with opportunity for exposure, mixing in open batch processes and transfer of substance into small containers.

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

This substance is used in the following products: coating products and polymers.

This substance is used in the following areas: building & construction work. This substance is used for the manufacture of: chemicals, fabricated metal products, electrical, electronic and optical equipment, rubber products, plastic products, mineral products (e.g. plasters, cement), machinery and vehicles and furniture.

This substance is used in the following activities or processes at workplace: transfer of chemicals, closed batch processing in synthesis or formulation, closed, continuous processes with occasional controlled exposure and laboratory work.

Release to the environment of this substance can occur from industrial use: in the production of articles, in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and for thermoplastic manufacture.

This substance is used in the following activities or processes at workplace: transfer of chemicals at dedicated facilities, transfer of substance into small containers, closed processes with no likelihood of exposure, closed, continuous processes with occasional controlled exposure, closed batch processing in synthesis or formulation 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: avoid release to the environment; do not breathe the dust, fume, gas, mist, vapours or spray; do not eat, drink or smoke when using this product; wear protective gloves and/or clothing, and eye and/or face protection as specified by manufacturer/supplier.

Response statements

In case of incident: If swallowed: immediately call a poison center or doctor/physician. If on skin (or hair): take off immediately all contaminated clothing. Rinse skin with water or shower. If on skin (or hair): follow instructions specified by manufacturer/supplier. If swallowed: rinse mouth. Do not induce vomiting. If inhaled: remove victim to fresh air and keep at rest in a position comfortable for breathing. Immediately call a poison center or doctor/physician. Collect spillage. In case of fire: Use (measures specified by manufacturer/supplier) for extinction. If in eyes: rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do – continue rinsing.

Storage statements

Store this substance locked up; in a well-ventilated place and keeping container tightly closed.

Disposal statements

The substance must be disposed in accordance with local/regional/national/international regulation.

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
  • Rain Carbon Germany GmbH, Kekulestr. 30 44579 Castrop-Rauxel Germany

Substance names and other identifiers

Tar acids, xylenol fraction
EC Inventory, Other, Cosmetic Products Regulation, Annex II - Prohibited Substances
Tar acids, xylenol fraction Distillate Phenols [The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.]
The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.
C&L Inventory
Tar acids, xylenol fraction
The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.
REACH pre-registration, Other, Cosmetic Products Regulation, Annex II - Prohibited Substances
Tar acids, xylenol fraction; Distillate Phenols [he fraction of tar acids, rich in 2,4-and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.]
The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.
Active Implantable Medical Devices Directive - Hazardous Substances, In Vitro Diagnostic Medical Devices Directive - Hazardous Substances, Medical Devices Directive - Hazardous Substances
Tar acids, xylenol fraction; Distillate Phenols [The fraction of tar acids, rich in 2,4-and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.]
The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.
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
acidi di catrame, frazione xilenolo fenoli distillati Frazione di acidi di catrame, ricca di 2,4- e 2,5-dimetilfenolo, recuperata dalla distillazione di acidi di catrame grezzi di catrame di carbone a bassa temperatura. (it)
C&L Inventory
Acizi gudronici, fracţia xilenolului Distilate fenolice [Fracţia acizilor gudronici bogată în 2, 4-şi 2, 5-dimetil fenol, recuperată prin distilarea acizilor gudronici din gudronul de cărbune de temperatură scăzută.] (ro)
C&L Inventory
Acizi gudronici, fracţia xilenolului Distilate fenolice Fracţia acizilor gudronici bogată în 2, 4-şi 2, 5-dimetil fenol, recuperată prin distilarea acizilor gudronici din gudronul de cărbune de temperatură scăzută. (mt)
C&L Inventory
Darvas skābes, ksilenola frakcija Destilāta fenoli [2,4- un 2,5-dimetilfenolu bagātīgi saturoša darvas skābes frakcija, reģenerēta, zemā temperatūrā destilējot akmeņogļu darvas darvas skābes jēlfrakciju.] (lv)
C&L Inventory
dechtové kyseliny, dimetylfenolová (xylenolová) frakcia fenolové destiláty [Frakcia dechtových kyselín s vysokým obsahom 2,4- a 2,5-dimetylfenolu. Získava sa destiláciou surových dechtových kyselín z nízkoteplotného uhoľného dechtu.] (sk)
C&L Inventory
Deguto rūgštys, ksilenolių frakcija Fenolių distiliatai [Deguto rūgščių frakcija, turinti daug 2,4- ir 2,5-dimetilfenolių, gaunama distiliuojant žematemperatūrio akmens anglių deguto žalias deguto rūgštis.] (lt)
C&L Inventory
Fenolfrakciók, xilenol frakció Fenol párlatok [Kátrány sav frakció, 2,4- és 2,5-dimetilfenolban gazdag párlata, melyet az alacsony hőmérsékletű kőszénkátrányból származó nyers kátrány sav frakció desztillációjával nyernek vissza.] (hu)
C&L Inventory
Huiles de goudron acides, fraction xylénol; phénols produits par distillation;[fraction d'huiles acides de goudron riche en 2,4- et 2,5-méthylphénol, récupérée par distillation d'huiles acides brutes de goudron de houille à basse température.] phénols distillés Fraction des huiles de goudron acides riche en diméthyl-2,4 phénol et en diméthyl-2,5 phénol, récupérée par distillation des huiles acides brutes de goudron de houille à basse température. (fr)
C&L Inventory
Katranske kiseline, fraksija ksilenola Destilat fenola (Frakcija katranskih kiselina bogata 2,4- i 2,5-dimetilfenolom, regenerirana destilacijom sirovih katranskih kiselina niskotemperaturnog ugljenog katrana.) (hr)
C&L Inventory
katranske kisline, ksilenolska frakcija fenolni destilati [Frakcija katranskih kislin bogatih s 2,4- in 2,5-dimetilfenolom pridobljena z destilacijo surovih kislin nizkotemperaturnega premogovega katrana.] (sl)
C&L Inventory
Kwasy smołowe, frakcja ksylenolu Destylaty fenolowe Frakcja fenoli smołowych bogata w 2,4- i 2,5-dimetylofenol, odzyskiwana przez destylację surowych fenoli z niskotemperaturowej smoły węglowej. (pl)
C&L Inventory
Kyselé složky dehtu, xylenolová frakce Destilované fenoly [Frakce kyselých složek dehtu bohatá na 2,4- a 2,5-dimethylfenol, získaná destilací nízkoteplotních surových kyselých složek dehtu.] (cs)
C&L Inventory
Oοξέα πίσσας, κλάσμα ξυλενόλης Απόσταγμα φαινόλης [To κλάσμα των οξέων πίσσας, πλούσιο σε 2,4- και 2,5-διμεθυλοφαινόλη, που ανακτάται με απόσταξη ακατέργαστων οξέων λιθανθρακόπισσας χαμηλής θερμοκρασίας.] (el)
C&L Inventory
Teersäuren, Xylenolfraktion Destillat-Phenole [die an 2,4- und 2,5-Dimethylphenol reiche Teersäuren-Fraktion, gewonnen durch Destillation der rohen Teersäuren von Niedertemperaturkohlenteer] (de)
C&L Inventory
Teerzuren, xylenolfractie Gedestilleerde fenolen De teerzuurfractie, rijk aan 2,4- en 2,5-dimethylfenol, die wordt verkregen door destillatie van ongezuiverde teerzuren uit lage-temperatuur-koolteer. (nl)
C&L Inventory
Tervahapot, ksylenolifraktio Tislefenolit Tervahappofraktio, joka sisältää runsaasti 2,4- ja 2,5-dimetyylifenolia, kerätty tislaamalla matalalämpötilaisia kivihiilitervan raakoja tervahappoja. (fi)
C&L Inventory
Tjärsyror, xylenolfraktion Destillerade fenoler Tjärsyrefraktion, rik på 2,4- och 2,5-dimetylfenol, erhållen genom destillation av råtjärsyra från lågtemperaturstenkolstjära. (sv)
C&L Inventory
tjæresyrer, xylenolfraksjon destillat fenoler [Fraksjon av tjæresyrer, rik på 2,4- og 2,5-dimetylfenol, gjenvunnet ved destillasjon av råtjæresyrer fra lavtemperaturstenkulltjære.] (no)
C&L Inventory
tjæresyrer, xylenolfraktion Fenoldestillater Fraktionen af tjæresyrer, rig på 2,4- og 2,5-dimethylphenol, genvundet ved destillation af rå tjæresyrer fra lavtemperatursstenkulstjære. (da)
C&L Inventory
Tõrva happed, ksülenooli fraktsioon Destillaatfenoolid (2,4- ja 2,5-dimetüülfenoolirikas tõrvahapete fraktsioon, mis saadakse madalatemperatuurse kivisöetõrva toortõrvahapete destillatsioonil.) (et)
C&L Inventory
ácidos de alquitrán, fracción de xilenol fenoles destilados fracción de ácidos de alquitrán, rica en 2,4- y 2,5-dimetilfenol, recuperada por destilación de ácidos de alquitrán de hulla a baja temperatura crudo (es)
C&L Inventory
Ácidos do alcatrão, fracção dos xilenóis Fenóis destilados Fracção dos ácidos do alcatrão, rica em 2,4- e 2,5-dimetilfenóis, obtida por destilação dos ácidos brutos do alcatrão de carvão de baixa temperatura. (pt)
C&L Inventory
Катранени киселини, фракция на ксилен Фенолни дестилати [Фракция на катранени киселини, богата на 2,4- и 2,5- диметилфенол, получена при дестилация на сурови катранени киселини от нискотемпературни каменовъглени катрани.] (bg)
C&L Inventory
2,3-dimethylphenol; 2,4-dimethylphenol; 2,5-dimethylphenol; 2,6-dimethylphenol; 3,4-dimethylphenol; 3,5-dimethylphenol
Other
Tar acids, 2,4-/2,5-xylenol fraction
Registration dossier
Tar acids, xylenol fraction
C&L Inventory, Registration dossier
Dimethyl-phenols
Registration dossier
lehky xylenol
Registration dossier
light xylenol
Registration dossier
xylenol fraction
Registration dossier
xylenol mixture
Registration dossier
Xylenols
Registration dossier
648-122-00-9
Index number
C&L Inventory
84989-06-0
CAS number
EC Inventory, C&L Inventory, 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
  • 3 studies submitted
  • 3 studies processed
C Physical state at 20°C and 1013 hPa
Liquid (67%), Solid (33%) [3]
C Form
Liquid (50%), Crystalline (50%) [2]
C Odour
Characteristic of aromatic compounds (50%), Other (50%) [2]
C Substance type
Organic (100%) [3]

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

No automatically processable data submitted

Melting/freezing point

Study results
  • 2 studies submitted
  • 2 studies processed
R Melting / freezing point
-20 - 30 °C @ 101.325 kPa [2]

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

No automatically processable data submitted

Boiling point

Study results
  • 4 studies submitted
  • 4 studies processed
R Boiling point
198 - 220 °C @ 101.3 - 101.325 kPa [4]

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

No automatically processable data submitted

Density

Study results
  • 3 studies submitted
  • 3 studies processed
R Density
1.021 - 1.024 g/cm³ @ 20 °C [2]
R Relative density
1 - 1.021 @ 15.5 - 20 °C [2]

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 3
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Relative density at 20°C
1

Vapour pressure

Study results
  • 2 studies submitted
  • 1 study processed
R Vapour pressure
1.331 hPa @ 20 °C [1]

Type of Study provided
Studies with data
Key study 1
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Vapour pressure
1.331 hPa @ 20 °C

Partition coefficient

Study results
  • 2 studies submitted
  • 2 studies processed
R Log Pow
2.21 - 2.5 @ 25 °C and pH 6.4 - 7 [2]

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

No automatically processable data submitted

Water solubility

Study results
  • 2 studies submitted
  • 2 studies processed
R Water solubility (mass/vol.)
4.7 - 11 g/L @ 20 °C and pH 6 - 7 [2]

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

No automatically processable data submitted

Solubility in organic solvents / fat solubility

Data not provided by the registrant

Surface tension

Study results
  • 2 studies submitted
  • 0 studies processed

No automatically processable data submitted

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

No automatically processable data submitted

Flash point

Study results
  • 3 studies submitted
  • 3 studies processed
R Flash point
94 - 95 °C @ 101.3 - 101.325 kPa [3]

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

No automatically processable data submitted

Auto flammability

Study results
  • 3 studies submitted
  • 2 studies processed
R Autoflammability / self-ignition
470 - 515 °C @ 101.3 - 101.325 kPa [2]

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 2
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
R Summaries
  • 1 summary submitted
  • 1 summary processed
Autoflammability / self-ignition at 101 325 Pa
470 °C

Flammability

Study results
  • 5 studies 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 5
Exposure cons.
Other
C Summaries
  • 1 summary submitted
  • 1 summary processed
Flammability
Not classified (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 1
Exposure cons.
Other
C Summaries
  • 1 summary submitted
  • 1 summary processed
Explosiveness
Non-explosive (100%)

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 1
Exposure cons.
Other
C Summaries
  • 1 summary submitted
  • 1 summary processed
Oxidising
Non oxidising (100%)

Oxidation reduction potential

Data not provided by the registrant

pH

Data not provided by the registrant

Dissociation constant

Study results
  • 3 studies submitted
  • 3 studies processed
C Dissociating properties
Yes (100%) [3]
R Dissociation constant
10.19 - 10.6 @ 25 °C [4]

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

No automatically processable data submitted

Viscosity

Study results
  • 3 studies submitted
  • 3 studies processed
R dynamic viscosity (in mPa s)
3.5 - 10.4 [2]
R kinematic viscosity (in mm²/s)
17.44 [1]

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 2 1
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Static viscosity at 20 °C
17.44 mm²/s

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

Study results
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

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
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

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
  • 26 studies submitted
  • 25 studies processed
R BOD5
1.76 mg O2/g test material [1]
C Interpretation of results
Inherently biodegradable (52%), Readily biodegradable (32%), Under test conditions no biodegradation observed (16%) [25]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence 25
Other
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Biodegradation in water
Inherently biodegradable (100%)

Biodegradation in water & sediment - simulation tests

Study results
  • 0 studies submitted
  • 0 studies processed

Study data not processed for brief profile

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

No automatically processable data submitted

Biodegradation in soil

Study results
  • 3 studies submitted
  • 0 studies processed

Study data not processed for brief profile

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

No automatically processable data submitted

Bioaccumulation: aquatic / sediment

Study results
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

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
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Bioaccumulation: terrestrial

Data not provided by the registrant

Adsorption/desorption

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
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

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 100 µg/L (1)
Intermittent releases (freshwater) 24 µg/L (1)
Marine water 10 µg/L (1)
Intermittent releases (marine water) 15 µg/L (1)
Sewage treatment plant (STP) 1.14 mg/L (1)
Sediment (freshwater) 1.84 mg/kg sediment dw (1)
Sediment (marine water) 184 µg/kg sediment dw (1)
Hazard for Air
Air No hazard identified (1)
Hazard for Terrestrial Organism
Soil 96 µg/kg soil dw (1)
Hazard for Predators
Secondary poisoning No potential for bioaccumulation (1)

Short–term toxicity to fish

Study results
  • 41 studies submitted
  • 38 studies processed
P/RResults
LC50 (4 days) 4.4 - 57.5 mg/L [44]
LC50 (69 h) 66.8 mg/L [1]
LC50 (48 h) 4.4 - 41 mg/L [16]
LC50 (24 h) 4.4 - 10.4 mg/L [9]
LC50 (6 h) 4.7 - 14.9 mg/L [8]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence 36 3
Other
Data waiving
no waivers
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Long–term toxicity to fish

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
NOEC (32 days) 1.35 mg/L [1]
NOEC (30 days) 1.5 - 3.2 mg/L [2]
LOEC (32 days) 2.57 mg/L [1]

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

No automatically processable data submitted

Short–term toxicity to aquatic invertebrates

Study results
  • 40 studies submitted
  • 38 studies processed
P/RResults
EC50 (4 days) 1.5 - 30 mg/L [9]
EC50 (48 h) 2.37 - 94 mg/L [10]
EC50 (24 h) 4.9 - 11 mg/L [3]
IC50 (24 h) 11.36 - 28.32 mg/L [12]
LC50 (48 h) 9.6 - 208 mg/L [20]

Type of Study provided
Studies with data
Key study 1
Supporting study 1
Weight of evidence 37 1
Other
Data waiving
no waivers
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Long–term toxicity to aquatic invertebrates

Study results
  • 4 studies submitted
  • 3 studies processed
P/RResults
NOEC (21 days) 1 mg/L [1]
NOEC (48 h) 2 mg/L [1]
EC10 (80 days) 2 mg/L [1]

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

No automatically processable data submitted

Toxicity to aquatic algae and cyanobacteria

Study results
  • 14 studies submitted
  • 11 studies processed
P/RResults
EC50 (4 days) 100 mg/L [1]
EC50 (72 h) 14 - 27.9 mg/L [5]
EC50 (48 h) 7.8 - 75 mg/L [3]
NOEC (4 days) 65 mg/L [1]
NOEC (72 h) 1.7 - 50 mg/L [9]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence 13
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 for freshwater algae
7.8 mg/L
EC10 or NOEC for freshwater algae
1.7 mg/L

Toxicity to aquatic plants other than algae

Data not provided by the registrant

Toxicity to microorganisms

Study results
  • 26 studies submitted
  • 14 studies processed
P/RResults
EC50 (48 h) 157 mg/L [1]
EC50 (24 h) 160 mg/L [1]
EC50 (60 min) 225 - 500 mg/L [3]
IC50 (4 days) 91 - 890 mg/L [2]
IC50 (60 h) 52.05 - 203.39 mg/L [6]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence 25
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 for microorganisms
11.4 mg/L
EC10 or NOEC for microorganisms
17 mg/L

Sediment toxicity

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
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Endocrine disrupter testing in aquatic vertebrates – in vivo

Data not provided by the registrant

Toxicity to terrestrial macroorganisms except arthropods

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
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Toxicity to terrestrial arthropods

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
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Toxicity to terrestrial plants

Study results
  • 6 studies submitted
  • 2 studies processed
P/RResults
EC50 (14 days) 96 - 100 mg/kg soil dw [2]
EC50 (7 days) 67 - 69 mg/kg soil dw [2]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence 5
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Short-term EC50 / LC50
96 mg/kg soil dw

Toxicity to soil microorganisms

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
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Toxicity to birds

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
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

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)

M/C Summaries
  • 1 summary submitted
  • 1 summary processed

The derived no- or minimum effect level (DN(M)EL) is the level of exposure above which a human should not be exposed to a substance. Please note that when more than one summary is provided, DN(M)EL values may refer to constituents of the substance and not to the substance as a whole. More detailed information is available in the dossiers.

Data for WORKERS
INHALATION Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 4.9 mg/m³ repeated dose toxicity
Acute /short term: (Medium hazard (no threshold derived)) -
Local Effects
Long-term: (Medium hazard (no threshold derived)) -
Acute /short term: (Medium hazard (no threshold derived)) -
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (Medium hazard (no threshold derived)) -
Acute /short term: (Medium hazard (no threshold derived)) -
Local Effects
Long-term: (Medium hazard (no threshold derived)) -
Acute /short term: (Medium hazard (no threshold derived)) -
EYE Exposure
Medium hazard (no threshold derived)
Data for the GENERAL POPULATION
INHALATION Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 870 µg/m³ repeated dose toxicity
Acute /short term: (Medium hazard (no threshold derived)) -
Local Effects
Long-term: (Medium hazard (no threshold derived)) -
Acute /short term: (Medium hazard (no threshold derived)) -
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (Medium hazard (no threshold derived)) -
Acute /short term: (Medium hazard (no threshold derived)) -
Local Effects
Long-term: (Medium hazard (no threshold derived)) -
Acute /short term: (Medium hazard (no threshold derived)) -
ORAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 250 µg/kg bw/day repeated dose toxicity
Acute /short term: (DNEL) 17.5 mg/kg bw/day acute toxicity
EYE Exposure
Medium hazard (no threshold derived)

Toxicokinetics, metabolism, and distribution

Study results
Study data: basic toxicokinetics
  • 0 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: basic toxicokinetics
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Study data: dermal absorption
  • 0 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: dermal absorption
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Bioaccumulation potential:
No bioaccumulation potential

Acute toxicity

Study results
oral
  • 6 studies submitted
  • 5 studies processed
P/RResults
LD50 121 - 980.62 mg/kg bw (rat) [5]
M/CInterpretations of results
Other [5]

Type of Study provided
oral
Studies with data
Key study 1
Supporting study
Weight of evidence 5
Other
Data waiving
no waivers
inhalation
  • 7 studies submitted
  • 0 studies processed

No automatically processable data submitted

inhalation
Studies with data
Key study 1
Supporting study
Weight of evidence 5
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
dermal
  • 6 studies submitted
  • 4 studies processed
P/RResults
LD50 2 400 mg/kg bw (rat) [1]
LD0 2 400 mg/kg bw (rat) [1]
LD50 301 - 2 050 mg/kg bw (rabbit) [3]
M/CInterpretations of results
Other [4]

dermal
Studies with data
Key study 1
Supporting study
Weight of evidence 4
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
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
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route:
Adverse effect observed LD50 121 mg/kg bw
Dermal route:
Adverse effect observed LD50 301 mg/kg bw

Irritation / corrosion

Study results
Study data: skin
  • 8 studies 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 6
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
Study data: eye
  • 6 studies 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 4
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Skin
Adverse effect observed (corrosive)
Eye
Adverse effect observed (irreversible damage)
Respiratory
No study available

Sensitisation

Study results
Study data: skin
  • 6 studies 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 3
Other 1
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
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
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Skin sensitisation
Adverse effect observed (sensitising)
Respiratory sensitisation
No study available

Repeated dose toxicity

Study results
Study data: oral
  • 11 studies submitted
  • 8 studies processed
P/RResults
NOAEL (rat): 50 - 150 mg/kg bw/day [7]
NOAEL (rat): 3 750 ppm [1]
NOAEL (mouse): 1 250 ppm [1]
NOEL (rat): 300 mg/kg bw/day [1]

Type of Study provided
Study data: oral
Studies with data
Key study 2
Supporting study
Weight of evidence 8
Other 1
Data waiving
no waivers
Study data: inhalation
  • 3 studies submitted
  • 0 studies processed

No automatically processable data submitted

Study data: inhalation
Studies with data
Key study 1
Supporting study
Weight of evidence 1
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
Study data: dermal
  • 3 studies submitted
  • 0 studies processed

No automatically processable data submitted

Study data: dermal
Studies with data
Key study 1
Supporting study
Weight of evidence 1
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route - systemic effects:
Adverse effect observed NOAEL 50 mg/kg bw/day (subchronic, rat)

Genetic toxicity

Study results
Study data: in vitro
  • 20 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 3
Supporting study
Weight of evidence 17
Other
Data waiving
no waivers
Study data: in vivo
  • 11 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: in vivo
Studies with data
Key study 3
Supporting study
Weight of evidence 8
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Toxicity - InVitro
Adverse effect observed (positive)
Toxicity - InVivo
No adverse effect observed (negative)

Carcinogenicity

Study results
  • 3 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence 2
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route:
Adverse effect observed NOAEL 230 mg/kg bw/day (chronic, rat)

Toxicity to reproduction

Study results
Study data: reproduction
  • 7 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: reproduction
Studies with data
Key study 2
Supporting study
Weight of evidence 5
Other
Data waiving
no waivers
Study data: developmental
  • 7 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: developmental
Studies with data
Key study 1
Supporting study
Weight of evidence 6
Other
Data waiving
no waivers
Study data: other studies
  • 3 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: other studies
Studies with data
Key study 1
Supporting study
Weight of evidence 2
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Effect on fertility
Oral route:
No adverse effect observed NOAEL 450 mg/kg bw/day (chronic, rat)
Effect on developmental toxicity
Oral route:
Adverse effect observed NOAEL 100 mg/kg bw/day (subacute, rabbit)

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