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: A mixture of branched and linear C7-C9 alkyl 3-[3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]propionates
  • IUPAC name: Reaction mass of branched and linear C7-C9 alkyl 3-[3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]propionates
  • Other names
EC / List no.:
407-000-3
CAS no.:
127519-17-9
Index number:
607-281-00-4
Molecular formula:
C81H111N9O9
SMILES:
CCCCCCCOC(=O)CCC1=CC(N2N=C3C=CC=CC3=N2)=C(O)C(=C1)C(C)(C)C.CCCCCCCCOC(=O)CCC1=CC(N2N=C3C=CC=CC3=N2)=C(O)C(=C1)C(C)(C)C.CCCCCCCCCOC(=O)CCC1=CC(N2N=C3C=CC=CC3=N2)=C(O)C(=C1)C(C)(C)C
InChI:
InChI=1S/C28H39N3O3.C27H37N3O3.C26H35N3O3/c1-5-6-7-8-9-10-13-18-34-26(32)17-16-21-19-22(28(2,3)4)27(33)25(20-21)31-29-23-14-11-12-15-24(23)30-31;1-5-6-7-8-9-12-17-33-25(31)16-15-20-18-21(27(2,3)4)26(32)24(19-20)30-28-22-13-10-11-14-23(22)29-30;1-5-6-7-8-11-16-32-24(30)15-14-19-17-20(26(2,3)4)25(31)23(18-19)29-27-21-12-9-10-13-22(21)28-29/h11-12,14-15,19-20,33H,5-10,13,16-18H2,1-4H3;10-11,13-14,18-19,32H,5-9,12,15-17H2,1-4H3;9-10,12-13,17-18,31H,5-8,11,14-16H2,1-4H3 AuxInfo=1/0/N:84,17,18,19,83,82,81,80,79,78,1,2,77,4,3,21,22,76,13,11,12,14,5,6,10,23,15,16,9,7,8,25,20,24;99,67,68,69,98,97,96,95,94,51,52,93,54,53,71,72,92,63,61,62,64,55,56,60,73,65,66,59,57,58,75,70,74;91,42,43,44,90,89,88,87,26,27,86,29,28,46,47,85,38,36,37,39,30,31,35,48,40,41,34,32,33,50,45,49/E:(2,3,4)(11,12)(14,15)(23,24)(29,30);(2,3,4)(10,11)(13,14)(22,23)(28,29);(2,3,4)(9,10)(12,13)(21,22)(27,28)/rA:99CCCCCCNNNCCCCCCCCCCOCCCOOCCCCCCNNNCCCCCCCCCCOCCCOOCCCCCCNNNCCCCCCCCCCOCCCOOCCCCCCCCCCCCCCCCCCCCCCCC/rB:s1;d-2;d-1;s4;s3s5;d+6;s7;d+5s8;s8;s10;d-11;s12;d-13;d+10s14;s14;s16;s16;s16;s15;s12;s21;s22;s23;d23;;s26;d-27;d-26;s29;s28s30;d+31;s32;d+30s33;s33;s35;d-36;s37;d-38;d+35s39;s39;s41;s41;s41;s40;s37;s46;s47;s48;d48;;s51;d-52;d-51;s54;s53s55;d+56;s57;d+55s58;s58;s60;d-61;s62;d-63;d+60s64;s64;s66;s66;s66;s65;s62;s71;s72;s73;d73;s24;s76;s77;s78;s79;s80;s81;s82;s83;s49;s85;s86;s87;s88;s89;s90;s74;s92;s93;s94;s95;s96;s97;s98;/rC:-3.5961,-5.6321,0;-2.0562,-5.6321,0;-1.3027,-4.2888,0;-4.3823,-4.2888,0;-3.6289,-2.9456,0;-2.0889,-2.9456,0;-1.5976,-1.4715,0;-2.8425,-.554,0;-4.0874,-1.4715,0;-2.8425,.9856,0;-1.4992,1.7719,0;-1.4992,3.3117,0;-2.8425,4.0979,0;-4.1857,3.3446,0;-4.1857,1.8045,0;-5.4961,4.0653,0;-4.7099,5.3757,0;-6.8392,4.8187,0;-6.2822,2.7877,0;-5.4961,1.0185,0;-.1886,4.1308,0;1.1545,3.3446,0;2.4649,4.1308,0;3.8081,3.3446,0;2.4975,5.6049,0;16.6366,-6.0392,0;18.1762,-6.0392,0;18.9298,-4.6962,0;15.8501,-4.6962,0;16.6037,-3.3529,0;18.1435,-3.3529,0;18.6348,-1.8788,0;17.3899,-.9613,0;16.1451,-1.8788,0;17.4228,.6112,0;18.7659,1.3647,0;18.7659,2.8717,0;17.4228,3.6251,0;16.0793,2.8717,0;16.0793,1.3647,0;14.7363,3.5922,0;15.4897,4.9355,0;13.4261,4.3787,0;13.9829,2.3475,0;14.6708,.6767,0;20.0436,3.6579,0;21.3867,2.9044,0;22.7297,3.6579,0;24.0732,2.9044,0;22.7624,5.1649,0;-3.3337,-21.9471,0;-1.7938,-21.9471,0;-1.0405,-20.604,0;-4.1197,-20.604,0;-3.3663,-19.2608,0;-1.8267,-19.2608,0;-1.3352,-17.7867,0;-2.5801,-16.8694,0;-3.825,-17.7867,0;-2.5474,-15.2967,0;-1.2043,-14.5433,0;-1.2043,-13.0035,0;-2.5474,-12.2499,0;-3.8905,-13.0035,0;-3.8905,-14.5433,0;-5.2011,-12.2828,0;-4.4475,-10.9395,0;-6.5772,-11.4965,0;-6.02,-13.5278,0;-5.2666,-15.1983,0;.1061,-12.1517,0;1.4168,-12.9051,0;2.7599,-12.1517,0;4.103,-12.9051,0;2.7926,-10.6448,0;3.8736,1.7392,0;5.2167,.953,0;5.2167,-.5867,0;6.56,-1.3731,0;6.56,-2.9129,0;7.903,-3.6992,0;7.903,-5.239,0;9.2461,-6.0252,0;9.2461,-7.5648,0;24.1385,1.2666,0;25.4818,.513,0;25.4818,-1.0268,0;26.825,-1.7806,0;26.825,-3.3202,0;28.1681,-4.0738,0;28.1681,-5.6133,0;4.1685,-14.4778,0;5.5116,-15.2312,0;5.5116,-16.7712,0;6.8546,-17.5246,0;6.8546,-19.0642,0;8.1983,-19.8176,0;8.1983,-21.3576,0;9.5413,-22.111,0;
Type of substance:
UVCB
Origin:
Organic
Registered compositions:
9
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 toxic to aquatic life with long lasting effects.

Additionally, the classification provided by companies to ECHA in REACH registrations identifies that this substance may cause damage to organs through prolonged or repeated exposure.

Breakdown of all 446 C&L notifications submitted to ECHA

Aquatic Chronic 2 H411 Harmonised Classification
STOT RE 2 H373
Not Classified
0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%

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

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

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

Properties of concern

Regulatory activities

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

Registration
Pre-registration:
Substance pre-registered under REACH.
Registration:
This substance has 12 active registrations under REACH, 1 Joint Submission(s) and 4 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):

Classification Labelling & Packaging (CLP)

Harmonised C&L:
A European Union Harmonised Classification & Labelling has been assigned to this substance.
Notification:
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 manufactured and/or imported in the European Economic Area in 100+ tonnes per year.

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: adhesives and sealants and coating products.

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

This substance is used in the following activities or processes at workplace: the low energy manipulation of substances bound in materials or articles and high energy work-up of substances bound in materials or articles (e.g. hot rolling/forming, grinding, mechanical cutting, drilling or sanding).

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 complex articles, with no release intended: vehicles. This substance can be found in products with material based on: wood (e.g. floors, furniture, toys).

This substance is used in the following products: adhesives and sealants, coating products and inks and toners.

This substance is used in the following areas: formulation of mixtures and/or re-packaging and building & construction work.

This substance is used in the following activities or processes at workplace: transfer of chemicals, mixing in open batch processes, roller or brushing applications, non-industrial spraying 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: outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives) and indoor use.

This substance is used in the following products: adhesives and sealants, coating products and inks and toners.

This substance is used in the following activities or processes at workplace: transfer of chemicals, mixing in open batch processes, transfer of substance into small containers and laboratory work.

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

This substance is used in the following products: adhesives and sealants, coating products and inks and toners.

This substance is used in the following areas: formulation of mixtures and/or re-packaging. This substance is used for the manufacture of: plastic products, fabricated metal products and machinery and vehicles.

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

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: do not breathe the dust, fume, gas, mist, vapours or spray; avoid release to the environment.

Response statements

In case of incident: Get medical advice/attention if you feel unwell. Collect spillage.

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

  • B.A. Special Chem & Color S.r.l., Via Alba , 20 21052 Busto Arsizio Italy
  • BASF Performance Products plc OR03, Charter Way SK10 2NX Macclesfield United Kingdom
  • BASF SE, Carl-Bosch-Str. 38 67056 Ludwigshafen am Rhein Rheinland-Pfalz Germany
  • Everlight Europe B.V., Rivium Boulevard 112b 2909LK Capelle a/d Ijssel Netherlands
  • REACH24H CONSULTING GROUP, Paramount Court, Corrig Road, Sandyford Dublin18 Dublin Ireland
  • REACH24H CONSULTING GROUP, Paramount Court, Corrig Road, Sandyford, Dublin 18, Ireland Dublin 18 Dublin Ireland
  • REACH24H CONSULTING GROUP (acts as the OR for Jiangsu FOPIA Chemicals Co., Ltd.), Paramount Court, Corrig Road, Sandyford Dublin18 Dublin Ireland
  • Rianlon GmbH, Charlottenstr. 75 40210 Duesseldorf Germany
  • Triconor Distribution B.V., Middelwijkstraat 23-25 3764CD Soest Netherlands

Other names

  • -
  • 3-(2H-Benzotriazolyl)-5-(1,1-di-methylethyl)-4-hydroxy-benzenepropanoic acid octyl esters
  • A mixture of branched and linear C7-C9 alkyl 3-[3-(2H-benzotriazol-2-yl)-5-(1,1-dimethyl-ethyl)-4-hydroxyphenyl]propionates
  • A mixture of branched and linear C7-C9 alkyl 3-[3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]propionates
  • Benzenepropanoic acid, 3-(2H-benzotriazol-2-yl)-5-(1,1- dimethylethyl)-4-hydroxy-, C7-9-branched and linear alkyl esters
  • Benzenepropanoic acid, 3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxy-, C7-9-branched and linear alkyl esters
  • branched and linear C7-C9 alkyl 3-[3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]propionates
  • C7-C9 Alkyl-3-2H benzotriazol-2-y-5-1,1 dimethylethyl-4-hydroxyphenylpropionaten
  • Chiguard® 5599
  • Chisorb 5582
  • Eversorb 82-2
  • heptyl 3-[3-(2H-1,2,3-benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate nonyl 3-[3-(2H-1,2,3-benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate octyl 3-[3-(2H-1,2,3-benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate
  • Mixture of branched and linear alkyl (C=7-9) ester of [3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]propionic acid
  • Mixture of branched and linear. C7-9 ester of [3-2h-benzotriazol-2-
  • Reaction mass of branched and linear C7-C9 alkyl 3-[3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]propionates
  • UVA 82
  • UV_BA 82
  • A mixture of branched and linear C7-C9 alkyl 3-[3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]propionates
  • reaction mass of branched and linear C7-C9 alkyl 3-[3-(2H-benzotriazol-2-yl)-5-(1,1-dimethylethyl)-4-hydroxyphenyl]propionates
  • CGL 384
  • Chiguard® 5599
  • Chisorb 5582
  • EVERSORB 82-2
  • THASORB UV 384
  • TINUVIN 384
  • UVA 82
  • UV_BA 82

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
  • 6 studies submitted
  • 4 studies processed
C Physical state at 20°C and 1013 hPa
Liquid (100%) [4]
C Form
Other (100%) [2]
C Substance type
Organic (100%) [1]

Type of Study provided
Studies with data
Key study 5
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
C Summaries
  • 4 summaries submitted
  • 4 summaries processed
Physical state at 20°C and 1013 hPa
Liquid (100%)

Melting/freezing point

Study results
  • 6 studies submitted
  • 5 studies processed
R Melting / freezing point
-29.4 °C [5]

Type of Study provided
Studies with data
Key study 6
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 4 summaries processed
Melting / freezing point at 101 325 Pa
-29.4 °C

Boiling point

Study results
  • 6 studies submitted
  • 5 studies processed
R Boiling point
197.4 - 451 °C @ 11 - 101 300 Pa [6]

Type of Study provided
Studies with data
Key study 6
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 3 summaries processed
Boiling point at 101 325 Pa
451 °C

Density

Study results
  • 6 studies submitted
  • 5 studies processed
R Density
1.078 g/cm³ @ 20 °C [1]
R Relative density
1.07 - 1.08 @ 20 °C [6]

Type of Study provided
Studies with data
Key study 6
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 4 summaries processed
Relative density at 20°C
1.07 - 1.078

Vapour pressure

Study results
  • 6 studies submitted
  • 4 studies processed
R Vapour pressure
0 - 0.592 Pa @ 20 - 150 °C [13]

Type of Study provided
Studies with data
Key study 5
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 4 summaries processed
Vapour pressure
0 - 0 Pa @ 20 - 25 °C

Partition coefficient

Study results
  • 7 studies submitted
  • 5 studies processed
R Log Pow
9.2 @ 0 - 25 °C [7]

Type of Study provided
Studies with data
Key study 5 1
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 3 summaries processed
Log Kow (Log Pow)
9.2 @ 25 °C

Water solubility

Study results
  • 7 studies submitted
  • 4 studies processed
R Water solubility (mass/vol.)
18 - 300 µg/L @ 20 °C [4]

Type of Study provided
Studies with data
Key study 5
Supporting study 2
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 4 summaries processed
Water solubility
18 - 300 µg/L @ 20 °C

Solubility in organic solvents / fat solubility

Study results
  • 2 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
Data waiving
no waivers
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Surface tension

Study results
  • 6 studies submitted
  • 3 studies processed
R Surface tension
65 mN/m @ 300 µg/L and 20 °C [3]

Type of Study provided
Studies with data
Key study 6
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 3 summaries processed
Surface tension at 20 °C
65 mN/m @ 0.3 mg/L

Flash point

Study results
  • 7 studies submitted
  • 5 studies processed
R Flash point
148 °C @ 1.013 - 1 013 hPa [5]

Type of Study provided
Studies with data
Key study 6
Supporting study
Weight of evidence
Other 1
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 3 summaries processed
Flash point at 101 325 Pa
148 °C

Auto flammability

Study results
  • 5 studies submitted
  • 4 studies processed
R Autoflammability / self-ignition
415 °C @ 1.013 - 995 hPa [4]

Type of Study provided
Studies with data
Key study 5
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 3 summaries processed
Autoflammability / self-ignition at 101 325 Pa
415 °C

Flammability

Study results
  • 10 studies submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 4
Supporting study
Weight of evidence
Other 3
Data waiving
Not feasible
Sci. unjustified 3
Exposure cons.
Other
C Summaries
  • 4 summaries submitted
  • 3 summaries processed
Flammability
Non flammable (100%)

Explosiveness

Study results
  • 6 studies submitted
  • 3 studies processed
C Interpretation of results
Non-explosive (100%) [3]

Type of Study provided
Studies with data
Key study 6
Supporting study
Weight of evidence
Other
Data waiving
no waivers
C Summaries
  • 4 summaries submitted
  • 4 summaries processed
Explosiveness
Non-explosive (100%)

Oxidising

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 1
Data waiving
Not feasible
Sci. unjustified 3
Exposure cons.
Other 1
C Summaries
  • 3 summaries submitted
  • 3 summaries 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
9.2 [1]

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

No automatically processable data submitted

Viscosity

Study results
  • 2 studies submitted
  • 1 study processed
R dynamic viscosity (in mPa s)
1 290 - 16 900 [2]

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

No automatically processable data submitted

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

Study results
  • 2 studies submitted
  • 1 study processed
R Dissipation half life (DT50)
15.4 h [1]

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

No automatically processable data submitted

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
Supporting study
Weight of evidence
Other 1
Data waiving
Not feasible 1
Sci. unjustified
Exposure cons.
Other 1
R Summaries
  • 2 summaries submitted
  • 1 summary processed
Half-life for hydrolysis
3.918 months @ 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
  • 16 studies submitted
  • 5 studies processed
R COD
1.81 g O2/g test material [4]
C Interpretation of results
Under test conditions no biodegradation observed (100%) [1]

Type of Study provided
Studies with data
Key study 12
Supporting study 4
Weight of evidence
Other
Data waiving
no waivers
C Summaries
  • 4 summaries submitted
  • 3 summaries processed
Biodegradation in water
Inherently biodegradable (67%), Inherently biodegradable, not fulfilling specific criteria (33%)

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
  • 2 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 1
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Bioaccumulation: aquatic / sediment

Study results
  • 10 studies submitted
  • 0 studies processed

Study data not processed for brief profile

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

No automatically processable data submitted

Bioaccumulation: terrestrial

Data not provided by the registrant

Adsorption/desorption

Study results
  • 6 studies submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 2 1
Supporting study 3
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 1 summary processed
Koc at 20°C
939 700

Henrys law constant (H)

Study results
  • 2 studies submitted
  • 1 study processed
R H - (pressure) m³/mol
0 Pa m³/mol @ 25 °C [1]

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

No automatically processable data submitted

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
  • 3 summaries submitted
  • 3 summaries 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 42.5 - 100 µg/L (3)
Intermittent releases (freshwater) 32 - 1 000 µg/L (3)
Marine water 4.25 - 10 µg/L (3)
Intermittent releases (marine water) -
Sewage treatment plant (STP) 10 mg/L (3)
Sediment (freshwater) 2 950 - 7 280 mg/kg sediment dw (3)
Sediment (marine water) 295 - 728 mg/kg sediment dw (3)
Hazard for Air
Air -
Hazard for Terrestrial Organism
Soil 650 - 1 450 mg/kg soil dw (3)
Hazard for Predators
Secondary poisoning No potential to cause toxic effects if accumulated (in higher organisms) via the food chain (1)

Short–term toxicity to fish

Study results
  • 4 studies submitted
  • 3 studies processed
P/RResults
LC50 (4 days) 9.9 mg/L [3]
LC50 (72 h) 9.9 mg/L [2]
LC50 (48 h) 9.9 mg/L [1]
LC50 (24 h) 9.9 mg/L [2]
NOEC (4 days) 9.9 mg/L [3]

Type of Study provided
Studies with data
Key study 4
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 1 summary processed
LC50 for freshwater fish
9.9 mg/L
LC50 for marine water fish
9.9 mg/L

Long–term toxicity to fish

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
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Short–term toxicity to aquatic invertebrates

Study results
  • 8 studies submitted
  • 7 studies processed
P/RResults
EC50 (48 h) 3.2 mg/L [7]
EC50 (24 h) 16.4 mg/L [6]
EC100 (48 h) 21.2 mg/L [1]
NOEC (48 h) 500 µg/L [7]

Type of Study provided
Studies with data
Key study 8
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 3 summaries processed
EC50 / LC50 for freshwater invertebrates
3.2 mg/L
EC50 / LC50 for marine invertebrates
3.2 mg/L

Long–term toxicity to aquatic invertebrates

Study results
  • 2 studies submitted
  • 1 study processed
P/RResults
NOEC (21 days) 425 µg/L [1]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
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
  • 7 studies submitted
  • 4 studies processed
P/RResults
EC50 (72 h) 2 mg/L [4]
NOEC (72 h) 2 mg/L [4]

Type of Study provided
Studies with data
Key study 5
Supporting study 2
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 4 summaries submitted
  • 3 summaries processed
EC50 for freshwater algae
2 mg/L
EC50 for marine water algae
2 mg/L
EC10 or NOEC for freshwater algae
2 mg/L

Toxicity to aquatic plants other than algae

Data not provided by the registrant

Toxicity to microorganisms

Study results
  • 3 studies submitted
  • 1 study processed
P/RResults
IC50 (3 h) 100 mg/L [1]
NOEC (3 h) 100 mg/L [1]

Type of Study provided
Studies with data
Key study 3
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 1 summary processed
EC50 for microorganisms
100 mg/L
EC10 or NOEC for microorganisms
100 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 1
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Endocrine disrupter testing in aquatic vertebrates – in vivo

Data not provided by the registrant

Toxicity to terrestrial macroorganisms except arthropods

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
NOEC (56 days) 100 mg/kg soil dw [1]
NOEC (28 days) 1 g/kg soil dw [1]
LC50 (14 days) 1 g/kg soil dw [1]
LC0 (14 days) 1 g/kg soil dw [1]
LC100 (14 days) 1 g/kg soil dw [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 terrestrial arthropods

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
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Toxicity to terrestrial plants

Study results
  • 2 studies submitted
  • 1 study processed
P/RResults
EC50 (14 days) 100 mg/kg soil dw [3]
LC50 (72 h) 100 mg/kg soil dw [1]
LC50 (48 h) 100 mg/kg soil dw [1]
LC50 (24 h) 100 mg/kg soil dw [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

Toxicity to soil microorganisms

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
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

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 1
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

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
  • 3 summaries submitted
  • 3 summaries 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) 350 µg/m³ repeated dose toxicity
Acute /short term: Hazard unknown (no further information necessary)
Local Effects
Long-term: Hazard unknown (no further information necessary)
Acute /short term: Hazard unknown (no further information necessary)
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 165 µg/kg bw/day repeated dose toxicity
Acute /short term: No hazard identified
Local Effects
Long-term: Hazard unknown (no further information necessary)
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) 5.7 µg/m³ repeated dose toxicity
Acute /short term: Hazard unknown (no further information necessary)
Local Effects
Long-term: Hazard unknown (no further information necessary)
Acute /short term: Hazard unknown (no further information necessary)
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 3.33 µg/kg bw/day repeated dose toxicity
Acute /short term: No hazard identified
Local Effects
Long-term: Hazard unknown (no further information necessary)
Acute /short term: Hazard unknown (no further information necessary)
ORAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 3.3 µg/kg bw/day repeated dose toxicity
Acute /short term: Hazard unknown (no further information necessary)
EYE Exposure
No hazard identified

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
  • 2 summaries submitted
  • 2 summaries processed
Bioaccumulation potential:
Low bioaccumulation potential
Absorption values
Oral: 50 %
Dermal: 50 %
Inhalation: 100 %

Acute toxicity

Study results
oral
  • 9 studies submitted
  • 6 studies processed
P/RResults
LD50 2 000 mg/kg bw (rat) [1]
M/CInterpretations of results
Practically nontoxic [1]

Type of Study provided
oral
Studies with data
Key study 7
Supporting study 1
Weight of evidence
Other 1
Data waiving
no waivers
inhalation
  • 4 studies submitted
  • 1 study processed
P/RResults
LC50 (4 h) 5.8 mg/L air (rat) [1]
M/CInterpretations of results
Practically nontoxic [1]

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

dermal
Studies with data
Key study 3
Supporting study 1
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
M/C Summaries
  • 4 summaries submitted
  • 4 summaries processed
Oral route:
No adverse effect observed LD50 2 000 mg/kg bw
Inhalation route:
No adverse effect observed Discriminating conc. 5.8 mg/m³
Dermal route:
No adverse effect observed LD50 2 000 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 7
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
Study data: eye
  • 9 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: eye
Studies with data
Key study 7
Supporting study 1
Weight of evidence
Other 1
Data waiving
no waivers
M/C Summaries
  • 4 summaries submitted
  • 4 summaries 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
  • 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 7
Supporting study 1
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
M/C Summaries
  • 4 summaries submitted
  • 4 summaries processed
Skin sensitisation
No adverse effect observed (not sensitising)
Respiratory sensitisation
No study available

Repeated dose toxicity

Study results
Study data: oral
  • 9 studies submitted
  • 3 studies processed
P/RResults
NOAEL (rat): 2 - 10 mg/kg bw/day [2]
LOAEL (rat): 50 - 500 mg/kg bw/day [3]
NOEL (rat): 2 mg/kg bw/day [1]

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

No data available

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

No data available

Study data: dermal
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 2 summaries submitted
  • 2 summaries processed
Oral route - systemic effects:
Adverse effect observed NOAEL 2 mg/kg bw/day (subchronic, rat)

Genetic toxicity

Study results
Study data: in vitro
  • 13 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 10 2
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
Study data: in vivo
  • 8 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: in vivo
Studies with data
Key study 6 1
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 4 summaries submitted
  • 1 summary processed
Toxicity - InVitro
No adverse effect observed (negative)

Carcinogenicity

Data not provided by the registrant

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 1 1
Supporting study 1
Weight of evidence
Other 2
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 2
Study data: developmental
  • 6 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: developmental
Studies with data
Key study 3
Supporting study 2
Weight of evidence
Other 1
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
  • 2 summaries submitted
  • 1 summary processed
Effect on developmental toxicity
Oral route:
Adverse effect observed NOAEL 30 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