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Please be aware that the REACH registration parts of this Brief Profile are no longer maintained; they remain frozen as of 19th May 2023.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 name:
  • IUPAC name: pentasodium 7-(2-{4-[(4-{[5-amino-4-sulfonato-2-(2-{4-[2-(sulfonatooxy)ethanesulfonyl]phenyl}diazen-1-yl)phenyl]amino}-6-chloro-1,3,5-triazin-2-yl)amino]-2-(carbamoylamino)phenyl}diazen-1-yl)naphthalene-1,3,6-trisulfonate
  • Substance names and other identifiers
EC / List no.:
422-930-1
CAS no.:
171599-84-1
Index number:
607-505-00-0
Molecular formula:
C34H24ClN12Na5O19S6
SMILES:
[Na+].[Na+].[Na+].[Na+].[Na+].NC(=O)NC1=CC(NC2=NC(NC3=CC(N)=C(C=C3N=NC3=CC=C(C=C3)S(=O)(=O)CCOS([O-])(=O)=O)S([O-])(=O)=O)=NC(Cl)=N2)=CC=C1N=NC1=CC2=C(C=C(C=C2C=C1S([O-])(=O)=O)S([O-])(=O)=O)S([O-])(=O)=O
InChI:
InChI=1S/C34H29ClN12O19S6.5Na/c35-31-41-33(43-34(42-31)40-25-14-22(36)29(70(57,58)59)15-26(25)46-44-17-1-4-19(5-2-17)67(49,50)8-7-66-72(63,64)65)38-18-3-6-23(24(11-18)39-32(37)48)45-47-27-13-21-16(10-30(27)71(60,61)62)9-20(68(51,52)53)12-28(21)69(54,55)56;;;;;/h1-6,9-15H,7-8,36H2,(H3,37,39,48)(H,51,52,53)(H,54,55,56)(H,57,58,59)(H,60,61,62)(H,63,64,65)(H2,38,40,41,42,43);;;;;/q;5*+1/p-5
Type of substance:
Multi constituent substance
Origin:
Organic
Registered compositions:
6
Of which contain:
0 impurities relevant for classification
0 additives relevant for classification
Substance Listed:
ELINCS (European LIst of Notified Chemical Substances) List

Hazard classification & labelling

According to the harmonised classification and labelling (CLP00) approved by the European Union, this substance is harmful to aquatic life with long lasting effects.

Breakdown of all 25 C&L notifications submitted to ECHA

Aquatic Chronic 3 H412 Harmonised Classification
0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%

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

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

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

Properties of concern

Regulatory context

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

Registration
Pre-registration:
Substance pre-registered under REACH.
Registration:
This substance has 5 active registrations under REACH, 1 Joint Submission(s) and 1 Individual Submission(s).
Please see Registrants/Suppliers details.
Evaluation
Dossier Evaluation:
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 ≥ 10 tonnes per annum.

This substance is used by consumers, in articles, by professional workers (widespread uses), in formulation or re-packing and at industrial sites.

This substance is used in the following products: textile treatment products and dyes and coating products.

Other release to the environment of this substance is likely to occur from: indoor use and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).

This substance is used in the following activities or processes at workplace: mixing in open batch processes.

Other release to the environment of this substance is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use in long-life materials with low release rate (e.g. flooring, furniture, toys, construction materials, curtains, foot-wear, leather products, paper and cardboard products, electronic equipment).

This substance can be found in products with material based on: fabrics, textiles and apparel (e.g. clothing, mattress, curtains or carpets, textile toys).

This substance is used in the following products: textile treatment products and dyes and coating products.

This substance is used in the following areas: printing and recorded media reproduction. This substance is used for the manufacture of: textile, leather or fur.

This substance is used in the following activities or processes at workplace: transfer of substance into small containers, transfer of chemicals, treatment of articles by dipping and pouring, calendering operations, non-industrial spraying, mixing in open batch processes, roller or brushing applications and the low energy manipulation of substances bound in materials or articles.

Other release to the environment of this substance is likely to occur from: indoor use (e.g. machine wash liquids/detergents, automotive care products, paints and coating or adhesives, fragrances and air fresheners).

This substance is used in the following products: textile treatment products and dyes, leather treatment products, paper chemicals and dyes, coating products, inks and toners and polymers.

This substance is used in the following activities or processes at workplace: transfer of chemicals, 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: textile treatment products and dyes, leather treatment products, paper chemicals and dyes, inks and toners and polymers.

This substance is used in the following areas: printing and recorded media reproduction. This substance is used for the manufacture of: textile, leather or fur, pulp, paper and paper products, wood and wood products and plastic products.

This substance is used in the following activities or processes at workplace: transfer of substance into small containers, transfer of chemicals, roller or brushing applications, treatment of articles by dipping and pouring, calendering operations, industrial spraying and mixing in open batch processes.

Release to the environment of this substance can occur from industrial use: in the production of articles.

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.

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.

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

  • Former NONS notifier unknown to ECHA - Contact the relevant French competent national authority., null
  • GAMMACOLOR SRL, via zeuner 5 20822 seveso Italy
  • Global Product Compliance (Europe) AB, IDEON, Beta 5, Scheelevägen 17 22363 Lund Sweden
  • Huntsman Textile Effects (Germany) GmbH, Rehlinger Str. 1 D-86462 Langweid a.Lech Germany
  • Only representative (No publishable name), null

Substance names and other identifiers

1,3,6-Naphthalenetrisulfonic acid, 7-(2-(2-((aminocarbonyl)amino)-4-((4-((5-amino-4-sulfo-2-(2-(4-((2-(sulfooxy)ethyl)sulfonyl)phenyl)diazenyl)phenyl)amino)-6-chloro-1,3,5-triazin-2-yl)amino)phenyl)diazenyl)-, sodium salt (1:?)
JAUNE TZ 4210
Other
Pentasodium 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-ethoxy)sulfonyl)phenylazo)phenylamino)-6-chloro-1,3,5-triazin-2-yl)amino-2-ureidophenylazo)naphtalene-1,3,6-trisulfonate
EC Inventory, C&L Inventory, REACH pre-registration, CAD - Chemical Agents Directive, Art. 2(b)(i) - Hazardous Agents, Construction Product Regulation - Art. 6(5) - SDS and Declaration, EU Ecolabels - Restrictions for Hazardous Substances/Mixtures, End-of-Life Vehicles Directive - Hazardous Substances, Marine Environmental Policy Framework Directive - Hazardous Substances, General Product Safety Directive - Hazardous Substances, Waste Framework Directive, Annex III - Waste - Hazardous Properties
pentasodium 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-ethoxy)sulfonyl)phenylazo)phenylamino)-6-chloro-1,3,5-triazin-2-yl)amino-2-ureidophenylazo)naphtalene-1,3,6-trisulfonate
JAUNE TZ 4210
C&L Inventory, REACH pre-registration, 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, Marine Environmental Policy Framework Directive - Hazardous Substances, General Product Safety Directive - Hazardous Substances, Waste Framework Directive, Annex III - Waste - Hazardous Properties
7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-etoxi)sulfonil)fenilazo)fenilamino)-6-cloro-1,3,5-triazin-2-il)amino-2-ureidofenilazo)naftaleno-1,3,6-trissulfonatoftaleno-1,3,6-trissulfonato de pentassódio (pt)
C&L Inventory
7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-etoxi)sulfonil)fenilazo)fenilamino)-6-cloro-1,3,5-triazin-2-il)amino-2-ureidofenilazo)naftaleno-1,3,6-trisulfonatoftaleno-1,3,6-trisulfonato de pentasodio (es)
C&L Inventory
7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-éthoxy)sulfonyl)phénylazo)phénylamino)-6-chloro-1,3,5-triazin-2-yl)amino-2-uréidophénylazo)naphtalène-1,3,6-trisulfonate de pentasodium (fr)
C&L Inventory
7-(4-(4-(5-ammino-4-solfonato-2-(4-((2-(solfonato-etossi)solfonil)fenilazo)fenilammino)-6-cloro-1,3,5-triazin-2-il)ammino-2-ureidofenilazo)naftalen-1,3,6-trisolfonato pentasodico (it)
C&L Inventory
7-(4-(4-(5-αμινo-4-σoυλφoνικo-2-(4-((2-(σoυλφoνικo-αιθoξυ)σoυλφoνυλo)φαινυλαζω)φαινυλαμινo)-6-χλωρo-1,3,5-τριαζιν-2-υλ)αμινo-2-oυρεϊδoφαινυλαζω)ναφθαλινo-1,3,6-τρισoυλφoνικό πεντανάτριo (el)
C&L Inventory
7-{4-[4-(5-amino-4-sulfoniano-2-{4-[(2-sulfonianoetoksy)sulfonylo]-fenyloazo}fenyloamino)-6-chloro-1,3,5-triazyn-2-ylo]amino-2-ureidofenyloazo}naftaleno-1,3,6-trisulfonian pentasodu (pl)
C&L Inventory
pentanaatrium-7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonatoetoksü)sulfonüül)fenüülaso)fenüülamino)-6-kloro-1,3,5-triasiin-2-üül)amino-2-ureidofenüülaso)naftaleen-1,3,6-trisulfonaat (et)
C&L Inventory
pentanatrijev 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-etoksi)sulfonil)fenilazo)fenilamino)-6-kloro-1,3,5-triazin-2-il)amino-2-ureidofenilazo)naftalen-1,3,6-trisulfonat (hr)
C&L Inventory
pentanatrijev 7-(4-{4-[5-amino-4-sulfonato-2-(4-{[2-(sulfonatoetoksi)sulfonil]fenilazo}fenilamino)-6-kloro-1,3,5-triazin-2-il]amino-2-ureidofenilazo}naftalen-1,3,6-trisulfonat (sl)
C&L Inventory
pentanatrio 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonatoetoksi)sulfonil)fenilazo)fenilamino)-6-chlor-1,3,5-triazin-2-il)amino-2-ureidofenilazo)naftalen-1,3,6-trisulfonatas (lt)
C&L Inventory
pentanatrium 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-ethoxy)sulfonyl)phenylazo)phenylamino)-6-chlor-1,3,5-triazin-2-yl)amino-2-ureidophenylazo)naphthalen-1,3,6-trisulfonat (da)
C&L Inventory
pentanatrium 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonatoethoxy)sulfonyl)fenylazo)fenylamino)-6-chloor-1,3,5-triazin-2-yl)amino-2-ureïdofenylazo)naftaleen-1,3,6-trisulfonaat (nl)
C&L Inventory
pentanatrium-7-(4-(4-(5-amino-4-sulfonaatto-2-(4-((2-(sulfonaattoetoksi)sulfonyyli)fenyyliatso)fenyyliamino)-6-kloori-1,3,5-triatsin-2-yyli)amino-2-ureidofenyyliatso)naftaleeni-1,3,6-trisulfonaatti (fi)
C&L Inventory
Pentanatrium-7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-ethoxy)sulfonyl)phenylazo)phenylamino)-6-chlor-1,3,5-triazin-2-yl)amino-2-ureidophenylazo)naphthalin-1,3,6-trisulfonat (de)
C&L Inventory
pentanatrium-7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonatoetoksy)sulfonyl)fenylazo)fenylamino)-6-klor-1,3,5-triazin-2-yl)amino-2-ureidofenylazo)naftalen-1,3,6-trisulfonat (no)
C&L Inventory
pentanatrium-7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonatoetoxi)sulfonyl)fenylazo)fenylamino)-6-klor-1,3,5-triazin-2-yl)amino-2-ureidofenylazo)naftalen-1,3,6-trisulfonat (sv)
C&L Inventory
pentanatrium-7-({4-[(4-{5-amino-4-sulfonato-2-[(4-{[2-(sulfonatooxy)ethyl]sulfonyl}fenyl)azo]anilino}-6-chlor-1,3,5-triazin-2-yl)amino]-2-ureidofeny}lazo)naftalen-1,3,6-trisulfonát (cs)
C&L Inventory
pentanátrium-7-(4-(4-(5-amino-4-szulfonáto-2-(4-((2-(szulfonátoetoxi)szulfonil)fenilazo)fenilamino)-6-klór-1,3,5-triazin-2-il)amino-2-ureidofenilazo)naftalin-1,3,6-triszulfonát (hu)
C&L Inventory
pentanátrium-7-(4-{[4-(5-amino-4-sulfonáto-2-{4-[(2-sulfonátoetoxy)sulfonyl]fenyldiazenyl}fenylamino)-6-chlór-1,3,5-triazín-2-yl]amino}-2-ureidofenyldiazenyl)naftalén-1,3,6-trisulfonát (sk)
C&L Inventory
pentanātrija 7-(4-(4-(5-amino-4-sulfonāt-2-(4-((2-(sulfonātetoksi) sulfonil)fenilazo)fenilamino)-6-hlor-1,3,5-triazīn-2-il)amino-2-ureīdfenilazo)naftalēn-1,3,6-trisulfonāts (lv)
C&L Inventory
pentasodiu 7-(4-(4-(5-amino-4-sulfonat-2-(4-((2-(sulfonat-etoxi)sulfonil)fenilazo)fenilamino)-6-clor-1,3,5-triazin-2-il)amino-2-ureidofenilazo)naftalene-1,3,6-trisulfonat (ro)
C&L Inventory
пентанатриев 7-(4-(4-(5-амино-4-сулфонато-2-(4-((2-(сулфонатоетокси)сулфонил)фенилазо)фениламино)-6-хлоро-1,3,5-триaзин-2-ил)амино-2-уреидофенилaзо)нафталeн-1,3,6-трисулфонат (bg)
C&L Inventory
pentasodium 7-(2-{4-[(4-{[5-amino-4-sulfo-2-(2-{4-[2-(sulfooxy)ethanesulfonyl]phenyl}diazen-1-yl)phenyl]amino}-6-chloro-1,3,5-triazin-2-yl)amino]-2-(carbamoylamino)phenyl}diazen-1-yl)naphthalene-1,3,6-trisulfonate
Other
Pentasodium 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-ethoxy)sulfonyl)phenylazo)phenylamino)-6-chloro-1,3,5-triazin-2-yl)amino-2-ureidophenylazo)naphtalene-1,3,6-trisulfonate
C&L Inventory, Registration dossier
pentasodium 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-ethoxy)sulfonyl)phenylazo)phenylamino)-6-chloro-1,3,5-triazin-2-yl)amino-2-ureidophenylazo)naphtalene-1,3,6-trisulfonate
C&L Inventory, Registration dossier
pentasodium 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonatoethoxy)sulfonyl)phenylazo)phenylamino)-6-chloro-1,3,5-triazin-2-yl)amino-2-ureidophenylazo)naphtalene-1,3,6-trisulfonate
Registration dossier
Reaction mass of 1,3,6-Naphthalenetrisulfonic acid, 7-[2-[2-[(aminocarbonyl)amino]-4-[[4-[[5-amino-4-sulfo-2-[2-[4-[[2-(sulfooxy)ethyl]sulfonyl]phenyl]diazenyl]phenyl]amino]-6-chloro-1,3,5-triazin-2-yl]amino]phenyl]diazenyl]-, sodium salt and 1,3,6-Naphthalenetrisulfonic acid, 7-[2-[2-[(aminocarbonyl)amino]-4-[[4-[[5-amino-4-sulfo-2-[2-[4-(vinylsulfonyl)phenyl]diazenyl]phenyl]amino]-6-chloro-1,3,5-triazin-2-yl]amino]phenyl]diazenyl]-, sodium salt
Registration dossier
Reaction mass of Pentasodium 7-{[4-{[4-({5-amino-4-sulfonato-2-[(4-{[2-(sulfonatooxy)ethyl]sulfonyl}phenyl)diazenyl]phenyl}amino)-6-chloro-1,3,5-triazin-2-yl]amino}-2-(carbamoylamino)phenyl]diazenyl}naphthalene-1,3,6-trisulfonate andTetrasodium 7-{[4-({4-[(5-amino-2-{[4-(ethenylsulfonyl)phenyl]diazenyl}-4-sulfonatophenyl)amino]-6-chloro-1,3,5-triazin-2-yl}amino)-2-(carbamoylamino)phenyl] diazenyl}naphthalene-1,3,6-trisulfonate
Registration dossier
Reactive Yellow 9K
Registration dossier
sodium;7-[[4-[[4-[4-[[5-amino-4-sulfo-2-(2-sulfoethoxysulfonyl)phenyl]diazenyl]anilino]-6-chloro-1,3,5-triazin-2-yl]amino]-2-(carbamoylamino)phenyl]diazenyl]naphthalene-1,3,6-trisulfonic acid
Other
Reactive Yellow 9K
Registration dossier
171599-84-1
CAS number
C&L Inventory, Registration dossier, Other, 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, Marine Environmental Policy Framework Directive - Hazardous Substances, General Product Safety Directive - Hazardous Substances, Waste Framework Directive, Annex III - Waste - Hazardous Properties
607-505-00-0
Index number
C&L Inventory

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
  • 2 studies processed
C Physical state at 20°C and 1013 hPa
Solid (100%) [2]
C Form
Solid: particulate/powder (50%), Powder (50%) [2]
C Odour
Odourless (100%) [1]
C Substance type
Organic (100%) [2]

Type of Study provided
Studies with data
Key study 1 1
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Physical state at 20°C and 1013 hPa
Solid (100%)
Form
Solid: particulate/powder (100%)
Colour
brown (50%), red (50%)
Colour Intensity
dark (100%)

Melting/freezing point

Study results
  • 3 studies submitted
  • 2 studies processed
R Melting / freezing point
400 °C @ 101.325 kPa [2]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Melting / freezing point at 101 325 Pa
400 °C

Boiling point

Study results
  • 3 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 2
Exposure cons.
Other
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Density

Study results
  • 3 studies submitted
  • 2 studies processed
R Relative density
1.76 @ 20 °C [2]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Relative density at 20°C
1.76

Vapour pressure

Study results
  • 3 studies submitted
  • 1 study processed
R Vapour pressure
0 Pa @ 25 °C [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other 1
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
R Summaries
  • 1 summary submitted
  • 1 summary processed
Vapour pressure
0 Pa @ 25 °C

Partition coefficient

Study results
  • 3 studies submitted
  • 2 studies processed
R Log Pow
-2 @ 20 °C and pH 7 [2]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Log Kow (Log Pow)
-2 @ 20 °C

Water solubility

Study results
  • 3 studies submitted
  • 2 studies processed
R Water solubility (mass/vol.)
385 g/L @ 21 °C [2]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Water solubility
385 g/L @ 21 °C

Solubility in organic solvents / fat solubility

Data not provided by the registrant

Surface tension

Study results
  • 3 studies submitted
  • 2 studies processed
R Surface tension
51.9 mN/m @ 1.1 g/L and 20 °C [2]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Surface tension at 20 °C
51.9 mN/m @ 1 100 mg/L

Flash point

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
Data waiving
Not feasible 1
Sci. unjustified 1
Exposure cons.
Other
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Auto flammability

Study results
  • 3 studies submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Autoflammability / self-ignition at 101 325 Pa
435 °C

Flammability

Study results
  • 3 studies submitted
  • 2 studies processed
C Interpretation of results
GHS criteria not met (100%) [2]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Flammability
Not classified (100%)

Explosiveness

Study results
  • 3 studies submitted
  • 2 studies processed
C Interpretation of results
GHS criteria not met (100%) [2]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Explosiveness
Non-explosive (100%)

Oxidising

Study results
  • 3 studies submitted
  • 2 studies processed
C Interpretation of results
GHS criteria not met (100%) [2]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Oxidising
No (100%)

Oxidation reduction potential

Data not provided by the registrant

pH

Data not provided by the registrant

Dissociation constant

Study results
  • 2 studies submitted
  • 1 study processed
C Dissociating properties
Yes (100%) [1]
R Dissociation constant
-6 - 16.8 [7]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
pKa at 20 °C
16.8

Viscosity

Data not provided by the registrant

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
  • 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
Other 2
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Half-life for hydrolysis
1 years @ 25 °C

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
  • 6 studies submitted
  • 3 studies processed
R COD
759 mg O2/g test material [1]
C Interpretation of results
Not inherently biodegradable (33%), Not readily biodegradable (33%), Under test conditions no biodegradation observed (33%) [3]

Type of Study provided
Studies with data
Key study 3
Supporting study 1
Weight of evidence
Other 2
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Biodegradation in water
Under test conditions no biodegradation observed (100%)
Type of water
Freshwater (100%)

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

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 16 µg/L (1)
Intermittent releases (freshwater) 1 mg/L (1)
Marine water 1.6 µg/L (1)
Intermittent releases (marine water) -
Sewage treatment plant (STP) 10 mg/L (1)
Sediment (freshwater) 59 µg/kg sediment dw (1)
Sediment (marine water) 5.9 µg/kg sediment dw (1)
Hazard for Air
Air No hazard identified (1)
Hazard for Terrestrial Organism
Soil 2.19 µg/kg soil dw (1)
Hazard for Predators
Secondary poisoning No potential for bioaccumulation (1)

Short–term toxicity to fish

Study results
  • 2 studies submitted
  • 1 study processed
P/RResults
LC50 (4 days) 100 mg/L [1]

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

No automatically processable data submitted

Long–term toxicity to fish

Data not provided by the registrant

Short–term toxicity to aquatic invertebrates

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
EC50 (48 h) 100 mg/L [2]
EC50 (24 h) 100 mg/L [1]
EC100 (48 h) 100 mg/L [1]
NOEC (48 h) 100 mg/L [1]

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

No automatically processable data submitted

Long–term toxicity to aquatic invertebrates

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
NOEC (21 days) 490 - 800 µg/L [2]
LOEC (21 days) 1.55 - 4.9 mg/L [2]
EC10 (21 days) 800 µg/L [1]
EC50 (21 days) 8.6 mg/L [1]

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

No automatically processable data submitted

Toxicity to aquatic algae and cyanobacteria

Study results
  • 6 studies submitted
  • 3 studies processed
P/RResults
EC50 (72 h) 10.9 - 89.9 mg/L [4]
NOEC (72 h) 900 - 100 000 µg/L [3]
EC10 (72 h) 600 - 2 800 µg/L [2]

Type of Study provided
Studies with data
Key study 3
Supporting study 1
Weight of evidence
Other 2
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 for freshwater algae
89.9 mg/L
EC10 or NOEC for freshwater algae
2.8 mg/L

Toxicity to aquatic plants other than algae

Data not provided by the registrant

Toxicity to microorganisms

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
EC50 (30 min) 100 mg/L [1]
IC50 (30 min) 100 mg/L [1]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 for microorganisms
100 mg/L
EC10 or NOEC for microorganisms
100 mg/L

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)

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) 47 mg/m³ repeated dose toxicity
Acute /short term: (DNEL) 47 mg/m³ -
Local Effects
Long-term: No hazard identified
Acute /short term: No hazard identified
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 6.67 mg/kg bw/day repeated dose toxicity
Acute /short term: No hazard identified
Local Effects
Long-term: No hazard identified
Acute /short term: No hazard identified
EYE Exposure
No hazard identified
Data for the GENERAL POPULATION
INHALATION Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 11.6 mg/m³ repeated dose toxicity
Acute /short term: (DNEL) 11.6 mg/m³ -
Local Effects
Long-term: No hazard identified
Acute /short term: No hazard identified
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 3.33 mg/kg bw/day repeated dose toxicity
Acute /short term: No hazard identified
Local Effects
Long-term: No hazard identified
Acute /short term: No hazard identified
ORAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 1.67 mg/kg bw/day repeated dose toxicity
Acute /short term: (DNEL) 1.67 mg/kg bw/day repeated dose toxicity
EYE Exposure
No hazard identified

Toxicokinetics, metabolism, and distribution

Study results
Study data: basic toxicokinetics
  • 1 study 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
Not feasible
Sci. unjustified
Exposure cons.
Other 1
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:
Low bioaccumulation potential
Absorption values
Oral: 20 %
Dermal: 10 %
Inhalation: 10 %

Acute toxicity

Study results
oral
  • 4 studies submitted
  • 2 studies processed
P/RResults
LD50 2 000 mg/kg bw (rat) [2]
M/CInterpretations of results
GHS criteria not met [2]

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

No automatically processable data submitted

inhalation
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons. 1
Other
dermal
  • 3 studies submitted
  • 2 studies processed
P/RResults
LD50 2 000 mg/kg bw (rat) [2]
M/CInterpretations of results
GHS criteria not met [2]

dermal
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
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
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route:
No adverse effect observed LD50 2 000 mg/kg bw
Dermal route:
No adverse effect observed LD50 2 000 mg/kg bw

Irritation / corrosion

Study results
Study data: skin
  • 5 studies submitted
  • 0 studies processed

Study data not processed for brief profile

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

Study data not processed for brief profile

Study data: eye
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
Not feasible
Sci. unjustified 2
Exposure cons.
Other
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Skin
No adverse effect observed (not irritating)
Eye
No adverse effect observed (not irritating)
Respiratory
No study available

Sensitisation

Study results
Study data: skin
  • 5 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: skin
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 1
Data waiving
Not feasible
Sci. unjustified 2
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
No adverse effect observed (not sensitising)
Respiratory sensitisation
No study available

Repeated dose toxicity

Study results
Study data: oral
  • 2 studies submitted
  • 1 study processed
P/RResults
NOAEL (rat): 1 000 mg/kg bw/day [1]
NOEL (rat): 200 mg/kg bw/day [1]

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

No automatically processable data submitted

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

No automatically processable data submitted

Study data: dermal
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons. 1
Other
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route - systemic effects:
No adverse effect observed NOAEL 1 000 mg/kg bw/day (subacute, rat)

Genetic toxicity

Study results
Study data: in vitro
  • 7 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 1
Weight of evidence
Other 2
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
Study data: in vivo
  • 6 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: in vivo
Studies with data
Key study 4
Supporting study
Weight of evidence
Other 2
Data waiving
no waivers
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Carcinogenicity

Data not provided by the registrant

Toxicity to reproduction

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

Study data not processed for brief profile

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

Study data not processed for brief profile

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

Study data not processed for brief profile

Study data: other studies
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Effect on fertility
Oral route:
No adverse effect observed NOAEL 1 000 mg/kg bw/day (subacute, rat)
Effect on developmental toxicity
Oral route:
No adverse effect observed NOAEL 1 000 mg/kg bw/day (subacute, rat)

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