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.:
201-186-8
CAS no.:
79-21-0
Index number:
607-094-00-8
Molecular formula:
C2H4O3
SMILES:
CC(=O)OO
InChI:
InChI=1S/C2H4O3/c1-2(3)5-4/h4H,1H3
Type of substance:
Mono constituent substance
Origin:
Organic
Registered compositions:
31
Of which contain:
8 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 (CLP00) approved by the European Union, this substance causes severe skin burns and eye damage, is very toxic to aquatic life, is a flammable liquid and vapour, is harmful if swallowed, is harmful in contact with skin, is harmful if inhaled and if heated may cause a fire.

Additionally, the classification provided by companies to ECHA in REACH registrations identifies that this substance is toxic if swallowed, is toxic if inhaled, is very toxic to aquatic life with long lasting effects, causes serious eye damage and may cause respiratory irritation.

Additionally, the classification provided by companies to ECHA in CLP notifications identifies that this substance may cause drowsiness or dizziness.

Breakdown of all 621 C&L notifications submitted to ECHA

Aquatic Acute 1 H400 Harmonised Classification
Flam. Liq. 3 H226 Harmonised Classification
Skin Corr. 1A H314 Harmonised Classification
Acute Tox. 4 H312 Harmonised Classification
Org. Perox. D H242 Harmonised Classification
Acute Tox. 4 H302 Harmonised Classification
Acute Tox. 4 H332 Harmonised Classification
Eye Dam. 1 H318
STOT SE 3 H335
Acute Tox. 3 H301
Aquatic Chronic 1 H410
Acute Tox. 3 H331
STOT SE 3 H336
Acute Tox. 2 H330
Org. Perox. F H242
https://www.echa.europa.eu/o/diss-blank-theme/images/cnl/graph/more.png 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

At least one notifier has indicated that an impurity or an additive present in the substance impacts the notified classification.

Properties of concern

  • ED
Under assessment as Endocrine Disrupting (ED list).

Regulatory context

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

Registration
Pre-registration:
Substance pre-registered under REACH.
Registration:
This substance has 21 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:
Industrial accident prevention and reporting requirements have been established for this substance.
Notified C&L:
Classification & Labelling has been notified by industry to ECHA for this substance.

Biocidal Products Regulation (BPR)

Active Substance:
This substance is approved for use as a Biocidal 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 ≥ 1 000 to < 10 000 tonnes per annum.

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

This substance is approved for use as a biocide in the EEA and/or Switzerland, for: human hygiene, disinfection, disinfection, veterinary hygiene, veterinary hygiene, food and animals feeds, food and animals feeds, drinking water, product preservation, preservation for liquid systems, controlling slimes.

This substance is being reviewed for use as a biocide in the EEA and/or Switzerland, for: disinfection, disinfection.

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

Other release to the environment of this substance is likely to occur from: indoor use as reactive substance.

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

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

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: health services and scientific research and development. 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 chemicals, closed processes with no likelihood of exposure, closed, continuous processes with occasional controlled exposure, laboratory work and non-industrial spraying.

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) and indoor use in close systems with minimal release (e.g. cooling liquids in refrigerators, oil-based electric heaters).

This substance is used in the following products: washing & cleaning products and textile treatment products and dyes.

This substance is used in the following activities or processes at workplace: transfer of chemicals, transfer of substance into small containers, mixing in open batch processes 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: washing & cleaning products, paper chemicals and dyes and textile treatment products and dyes.

This substance is used in the following areas: health services. This substance is used for the manufacture of: textile, leather or fur, chemicals, pulp, paper and paper products and food products.

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

Release to the environment of this substance can occur from industrial use: as processing aid and in processing aids at industrial sites.

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

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

ECHA has no data from registration dossiers on the precautionary measures for using this substance. Guidance on the safe use of the substance provided by manufacturers and importers of this substance.

Registrants/suppliers

  • BIOXAL SA, Route des Varennes BP 30072 71103 CEDEX CHALON sur SAONE France
  • Brenntag GmbH, Messeallee 11 45131 Essen Germany
  • Cantel Medical (Italy) S.r.l., Via Laurentina 169 00071 Pomezia (RM) Italy
  • Christeyns NV, Afrikalaan 182 9000 Gent Belgium
  • Ecolab A.E., Fleming Street 15 GR-15123 Maroussi, Athens Greece
  • Ecolab Production France SAS, 94 Avenue Du General Patton Chalons-En-Champagne 51000 Chalons-En-Champagne France
  • Ecolab Production Italy s.r.l., Via Grandi 9/11 20089 Rozzano Italy
  • Evonik Peroxid GmbH, Industriestraße 1 9721 Weißenstein Carinthia Austria
  • Evonik Peroxide Spain s.l.u., Afueras s/n 50784 La Zaida Zaragoza Spain
  • ITW Novadan ApS, Platinvej 21 6000 Kolding Denmark
  • JSC "BS Chemical", Baltijos pr. 123-9 93224 Klaipeda Klaipeda Lithuania
  • Kemira Chemicals Oy, Harmajantie 3 P.O Box 7 FI-32741 SASTAMALA Finland
  • Kesla Pharma Wolfen GmbH, Keslastraße 1 06803 Bitterfeld-Wolfen Germany
  • MPD plus, s.r.o., Nabrezi Dr. Benese 2307 269 01 Rakovnik Czech Republic
  • Promox S.p.A., Via A. Diaz, 22/a - Peracetic Acid Plant Via A. Diaz, 21 - Organic Peroxide Plant 21038 Leggiuno - Varese Varese Italy
  • Rühl AG & Co. Chemische Fabrik KG, Hugenottenstraße 105 61381 Friedrichsdorf Germany
  • SaneChem sp.z o.o., Słodowiec 10/10 01-708 Warszawa Poland
  • Solimix, S.A., C/ Montseny 25, Polígono Industrial Sant Pere Molanta 08799 Olérdola Barcelona Spain
  • Solvay Chemie B.V., SCHEPERSWEG 1 6049 HERTEN Netherlands
  • SOPURA, rue de Trazegnies 199 6180 COURCELLES HAINAUT Belgium
  • Stockmeier Chemie Eilenburg GmbH & Co. KG, Gustav-Adolf-Ring 5 04838 Eilenburg Germany

Substance names and other identifiers

Acetic peroxide
Other
Acetyl hydroperoxide
Other
Acide peracetique
Other
Acide peroxyacetique
Other
Acido peroxiacetico
Other
Desoxon 1
Other
Estosteril
Other
Hydroperoxide, acetyl
Other
Kyselina peroxyoctova
Other
Monoperacetic acid
Other
Osbon AC
Other
PAA
Other
Peracetic acid
EC Inventory, REACH pre-registration, Other, Aerosols Directive - Flammable Contents - Labelling Requirements, EU Ecolabels - Restrictions for Hazardous Substances/Mixtures, Pressure Equipment Directive - Group 1 Fluids Hazardous Substances, Workplace Signs - minimum requirements & signs on containers and pipes
Peracetic acid
Biocidal active substances, REACH pre-registration, Other, Aerosols Directive - Flammable Contents - Labelling Requirements, EU Ecolabels - Restrictions for Hazardous Substances/Mixtures, Pressure Equipment Directive - Group 1 Fluids Hazardous Substances, Workplace Signs - minimum requirements & signs on containers and pipes
peracetic acid . . . %
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, End-of-Life Vehicles Directive - Hazardous Substances, Active Implantable Medical Devices Directive - Hazardous Substances, In Vitro Diagnostic Medical Devices Directive - Hazardous Substances, Marine Environmental Policy Framework Directive - Hazardous Substances, Medical Devices Directive - Hazardous Substances, General Product Safety Directive - Hazardous Substances, Safety and Health of Workers at Work Directive - Hazardous Substances, Waste Framework Directive, Annex III - Waste - Hazardous Properties, Physical, Biological and Chemical Agents & Processes and Work
peracetic acid . . . %
C&L Inventory
Peracetic acid generated by perhydrolysis of N-acetylcaprolactam by hydrogen peroxide in alkaline conditions
Biocidal active substances
Peracetic acid generated from 1,3-diacetyloxypropan-2-yl acetate and hydrogen peroxide
Biocidal active substances
Peracetic acid generated from tetra-acetylethylenediamine (TAED) and sodium percarbonate
Biocidal active substances
Peracetic acid generated from tetraacetylethylenediamine and hydrogen peroxide
Biocidal active substances
Peroxoacetic acid
Other
Peroxyacetic acid
Other
Proxitane 4002
Other
...% peroksiacto rūgštis (lt)
C&L Inventory
Acid peracetic (ro)
Biocidal active substances
Acid peracetic sintetizat din tetraacetiletilenediamină (TAED) și percarbonat de sodiu (ro)
Biocidal active substances
acid peracetic. . . % (ro)
C&L Inventory
acide peracétique à … % . . (fr)
C&L Inventory
Acide péracétique (fr)
Biocidal active substances
Acide péracétique produit à partir de tétracétyléthylènediamine (TAED) et de percarbonate de sodium (fr)
Biocidal active substances
Acido peracetico (it)
Biocidal active substances
acido peracetico . . . % (it)
C&L Inventory
Acido peracetico ottenuto da tetracetiletilendiamina (TAED) e percarbonato di sodio (it)
Biocidal active substances
Aċidu peraċetiku (mt)
Biocidal active substances
Aċidu peraċetiku ġġenerat minn tetra-aċetiletilenedijamina (TAED) u perkarbonat tas-sodju (mt)
Biocidal active substances
Kwas nadoctowy (pl)
Biocidal active substances
kwas nadoctowy ...% (pl)
C&L Inventory
Kwas nadoctowy uzyskany z tetraacetyloetylenodiaminy (TAED) i nadwęglanu sodu (pl)
Biocidal active substances
kyselina peroxyctová (sk)
Biocidal active substances
kyselina peroxyoctová (cs)
Biocidal active substances
kyselina peroxyoctová ... % (sk)
C&L Inventory
Kyselina peroxyoctová připravená z tetraacetyletylendiaminu (TAED) a peroxouhličitanu sodného (cs)
Biocidal active substances
No tetra-acetiletilēndiamīna (TAED) un nātrija perkarbonāta iegūta peroksietiķskābe (lv)
Biocidal active substances
Per-azijnzuur (nl)
Biocidal active substances
Peracetic acid (no)
Biocidal active substances
Peracetic acid generated from tetra-acetylethylenediamine (TAED) and sodium percarbonate (sk)
Biocidal active substances
perazijnzuur . . . % (nl)
C&L Inventory
Perazijnzuur, verkregen uit tetra-acetylethyleendiamine (TAED) en natriumpercarbonaat (nl)
Biocidal active substances
Perecetsav (hu)
Biocidal active substances
perecetsav …% (hu)
C&L Inventory
pereddikesyre (da)
Biocidal active substances
pereddikesyre . . . % (da)
C&L Inventory
Pereddikesyre genereret fra tetraacetylethylendiamin (TAED) og natriumpercarbonat (da)
Biocidal active substances
pereddiksyre ... % (no)
C&L Inventory
Pereddiksyre generert fra tetraacetylendiamin (TAED) og natriumperkarbonat (no)
Biocidal active substances
Peressigsäure (de)
Biocidal active substances
Peressigsäure . . . % (de)
C&L Inventory
Peressigsäure, hergestellt aus Tetraacetylethylendiamin (TAED) und Natriumpercarbonat (de)
Biocidal active substances
Peretikkahappo (fi)
Biocidal active substances
peretikkahappo . . . % (fi)
C&L Inventory
Perocetna kislina (sl)
Biocidal active substances
perocetna kislina, pridobljena iz tetraacetil etilendiamina (TAED) in natrijevega perkarbonata (sl)
Biocidal active substances
perocetna kislina...% (sl)
C&L Inventory
Peroctena kiselina (hr)
Biocidal active substances
peroctena kiselina . . . % (hr)
C&L Inventory
Peroctena kiselina dobivena iz tetraacetiletilendiamina (TAED) i natrijevog perkarbonata (hr)
Biocidal active substances
Peroksiacto rūgštis (lt)
Biocidal active substances
Peroksiacto rūgštis, gauta iš tetraacetiletilendiamino (TAED) ir natrio peroksokarbonato (lt)
Biocidal active substances
Peroksietiķskābe (lv)
Biocidal active substances
peroksyeddiksyre ... % (no)
C&L Inventory
peroxyoctová kyselina...% (cs)
C&L Inventory
Perättiksyra (sv)
Biocidal active substances
perättiksyra . . . % (sv)
C&L Inventory
Perättiksyra som framställs från tetraacetyletylendiamin (TAED) och natriumperkarbonat (sv)
Biocidal active substances
Peräädikhape (et)
Biocidal active substances
Peräädikhape … % (et)
C&L Inventory
peräädikhape, mis saadakse tetraatsetüületüleendiamiinist (TAED) ja naatriumperkarbonaadist (et)
Biocidal active substances
Tetra-asetyylietyleenidiamiinista (TAED) ja natriumperkarbonaatista tuotettu peretikkahappo (fi)
Biocidal active substances
Tetraacetil-etilén-diaminból (TAED) és nátrium-perkarbonátból előállított perecetsav (hu)
Biocidal active substances
Ácido peracético (es)
Biocidal active substances
Ácido peracético (pt)
Biocidal active substances
ácido peracético . . . % (es)
C&L Inventory
ácido peracético . . . % (pt)
C&L Inventory
Ácido peracético generado a partir de tetraacetiletilendiamina y percarbonato de sodio (es)
Biocidal active substances
Ácido peracético produzido a partir de tetra-acetiletilenodiamina (TAED) e percarbonato de sódio (pt)
Biocidal active substances
Υπεροξικό οξύ (el)
Biocidal active substances
υπεροξικό οξύ . . . % (el)
C&L Inventory
Υπεροξικό οξύ που παράγεται από τετρα-ακετυλοαιθυλενοδιαμίνη (TAED) και υπερανθρακικό νάτριο (el)
Biocidal active substances
Пероцетна киселина (bg)
Biocidal active substances
Пероцетна киселина, генерирана от тетраацетилетилендиамин (TAED) и натрив перкарбонат (bg)
Biocidal active substances
пероцетна киселина...% (bg)
C&L Inventory
…% paraetiķskābe (lv)
C&L Inventory
Ethaneperoxoic acid
Other
Ethaneperoxoic acid
C&L Inventory, Registration dossier, Other
PAA
Registration dossier
PERACETIC ACID
C&L Inventory, Registration dossier
Peracetic Acid
C&L Inventory, Registration dossier
peracetic acid . . . %
C&L Inventory
peracetic acid ...%
C&L Inventory
Peracetic acid anhydrous
Registration dossier
Peracetic acid generated by perhydrolysis of N-acetylcaprolactam by hydrogen peroxide in alkaline conditions
Biocidal active substances
Peracetic acid generated from 1,3-diacetyloxypropan-2-yl acetate and hydrogen peroxide
Biocidal active substances
Peracetic acid generated from tetra-acetylethylenediamine (TAED) and sodium percarbonate
Biocidal active substances
Peracetic acid generated from tetraacetylethylenediamine and hydrogen peroxide
Biocidal active substances
Peroxyacetic Acid
C&L Inventory
Peroxyacetic acid - Aqueous stabilised solution
Registration dossier
Peroxyethanoic Acid
Registration dossier
Reaction mass of 64-19-7 and 7722-84-1
C&L Inventory
Reaction mass of hydrogen peroxide and water
C&L Inventory
ASPERIX®
Registration dossier
Oxystrong
Registration dossier
PERACLEAN®
Registration dossier
Proxitane
Registration dossier
232259-02-8
CAS number
Other
232259-02-8
Deleted CAS number
Other
607-094-00-8
Index number
C&L Inventory
79-21-0
CAS number
EC Inventory, C&L Inventory, Biocidal active substances, Registration dossier, REACH pre-registration, Other, Aerosols Directive - Flammable Contents - Labelling Requirements, 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, Active Implantable Medical Devices Directive - Hazardous Substances, In Vitro Diagnostic Medical Devices Directive - Hazardous Substances, Marine Environmental Policy Framework Directive - Hazardous Substances, Medical Devices Directive - Hazardous Substances, Pressure Equipment Directive - Group 1 Fluids Hazardous Substances, 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, Physical, Biological and Chemical Agents & Processes and Work
89370-71-8
CAS number
Other
89370-71-8
Deleted CAS number
Other

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
Liquid (100%) [2]
C Form
Liquid (100%) [2]
C Odour
Other (100%) [2]
C Substance type
Organic (100%) [2]

Type of Study provided
Studies with data
Key study
Supporting study 1
Weight of evidence 2
Other
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Physical state at 20°C and 1013 hPa
Liquid (100%)
Form
Liquid (100%)
Colour
colourless (100%)

Melting/freezing point

Study results
  • 3 studies submitted
  • 2 studies processed
R Melting / freezing point
-73 - 18.8 °C @ 101.3 - 101.325 kPa [7]

Type of Study provided
Studies with data
Key study
Supporting study 1
Weight of evidence 2
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Melting / freezing point at 101 325 Pa
-43.9 °C

Boiling point

Study results
  • 4 studies submitted
  • 3 studies processed
R Boiling point
20 - 110 °C @ 13.332 - 1 013.25 hPa [9]

Type of Study provided
Studies with data
Key study
Supporting study 1
Weight of evidence 3
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Boiling point at 101 325 Pa
105 °C

Density

Study results
  • 4 studies submitted
  • 3 studies processed
R Relative density
1.13 - 1 278.076 @ -10 - 20 °C [5]

Type of Study provided
Studies with data
Key study
Supporting study 1
Weight of evidence 3
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Relative density at 20°C
1.135

Vapour pressure

Study results
  • 3 studies submitted
  • 3 studies processed
R Vapour pressure
14.1 - 26 hPa @ 20 °C [4]

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 1 2
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Vapour pressure
14.1 hPa @ 19.85 °C

Partition coefficient

Study results
  • 3 studies submitted
  • 3 studies processed
R Log Pow
-1.3 - -0.23 @ 25 °C and pH 5 - 9 [8]

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 1 2
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Log Kow (Log Pow)
-0.26 @ 20 °C

Water solubility

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Water solubility
100 g/L @ 20 °C

Solubility in organic solvents / fat solubility

Study results
  • 1 study submitted
  • 1 study processed
R Acetone
500 g/L @ 25 °C [1]
R Ethyl acetate
20 - 25 g/L @ 25 °C [1]
R Isopropanol
500 g/L @ 25 °C [1]

Type of Study provided
Studies with data
Key study 1
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
  • 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 2
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Surface tension at 20 °C
47.7 mN/m @ 150 mg/L

Flash point

Study results
  • 1 study submitted
  • 1 study processed
R Flash point
68 - 83 °C [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Flash point at 101 325 Pa
68 °C

Auto flammability

Study results
  • 2 studies submitted
  • 2 studies processed
R Autoflammability / self-ignition
280 - 435 °C @ 100.4 - 100.6 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

Flammability

Study results
  • 6 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 4
Sci. unjustified 2
Exposure cons.
Other
C Summaries
  • 1 summary submitted
  • 1 summary processed
Flammability
Flammable (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
Supporting study
Weight of evidence 3
Other
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Explosiveness
Non-explosive (100%)

Oxidising

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
Data waiving
Not feasible 3
Sci. unjustified
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

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers

No summary exists for this scientific endpoint

Dissociation constant

Study results
  • 3 studies submitted
  • 1 study processed
C Dissociating properties
Yes (100%) [1]
R Dissociation constant
8.24 @ 20 °C [1]

Type of Study provided
Studies with data
Key study 1
Supporting study 1 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
pKa at 20 °C
8.24

Viscosity

Study results
  • 3 studies submitted
  • 3 studies processed
R dynamic viscosity (in mPa s)
2.891 - 8.357 [3]
R kinematic viscosity (in mm²/s)
1.22 - 1.5 [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
Dynamic viscosity at 20 °C
2.89 mPa.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

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

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 1 1
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Half life in air
22 min
Degradation rate constant with OH radicals
4.022 cm³ molecule-1 s-1

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 2
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Half-life for hydrolysis
31.7 h @ 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
  • 4 studies submitted
  • 1 study processed
C Interpretation of results
Readily biodegradable (100%) [1]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other 2
Data waiving
no waivers
C Summaries
  • 1 summary submitted
  • 1 summary processed
Biodegradation in water
Readily biodegradable (100%)
Type of water
Freshwater (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
R Summaries
  • 1 summary submitted
  • 1 summary processed
Half-life in freshwater
5 min @ 20 °C

Biodegradation in soil

Study results
  • 4 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 3
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
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
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

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

No data available

Henrys law constant (H)

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

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Henry's law constant
0.217 Pa.m³.mol-1 @ 25 °C

Distribution modelling

Study results
  • 1 study submitted
  • 1 study processed
% Distribution in Media:
R Air 0.01 % [1]
R Water 99.95 % [1]
R Soil 0 % [1]
R Sediment 0.04 % [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers

No summary exists for this scientific endpoint

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 94 ng/L (1)
Intermittent releases (freshwater) 1.6 µg/L (1)
Marine water 4.9 ng/L (1)
Intermittent releases (marine water) -
Sewage treatment plant (STP) 51 µg/L (1)
Sediment (freshwater) 350 ng/kg sediment dw (1)
Sediment (marine water) 35 ng/kg sediment dw (1)
Hazard for Air
Air No hazard identified (1)
Hazard for Terrestrial Organism
Soil 320 µg/kg soil dw (1)
Hazard for Predators
Secondary poisoning No potential for bioaccumulation (1)

Short–term toxicity to fish

Study results
  • 10 studies submitted
  • 3 studies processed
P/RResults
LC50 (4 days) 78 - 11 000 µg/L [4]
NOEC (4 days) 24 - 6 700 µg/L [3]

Type of Study provided
Studies with data
Key study 3
Supporting study 6
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

Study results
  • 1 study submitted
  • 1 study processed
P/RResults
NOEC (33 days) 2.2 µg/L [1]
NOEC (9 days) 22.4 µg/L [1]
NOEC (8 days) 22.4 - 22 400 ng/L [2]
LOEC (33 days) 7.5 µg/L [1]
LOEC (9 days) 22.4 µg/L [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
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
  • 12 studies submitted
  • 2 studies processed
P/RResults
EC50 (48 h) 270 - 730 µg/L [2]
EC100 (48 h) 1.4 - 1.6 mg/L [2]
NOEC (48 h) 130 - 560 µg/L [2]

Type of Study provided
Studies with data
Key study 2
Supporting study 8
Weight of evidence
Other 2
Data waiving
no waivers
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Long–term toxicity to aquatic invertebrates

Study results
  • 1 study submitted
  • 1 study processed
P/RResults
NOEC (21 days) 12.1 µg/L [1]

Type of Study provided
Studies with data
Key study 1
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
  • 6 studies submitted
  • 1 study processed
P/RResults
EC50 (72 h) 160 µg/L [1]
NOEC (72 h) 61 µg/L [1]

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

Toxicity to aquatic plants other than algae

Data not provided by the registrant

Toxicity to microorganisms

Study results
  • 2 studies submitted
  • 2 studies processed
P/RResults
EC50 (3 h) 5.1 - 38.6 mg/L [2]
EC50 (30 min) 5.3 mg/L [1]
NOEC (3 h) 16.7 mg/L [1]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 for microorganisms
5.1 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
Exposure cons.
Other 1
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
  • 2 studies submitted
  • 1 study processed
P/RResults
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 1
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
R Summaries
  • 1 summary submitted
  • 1 summary processed
Short-term EC50 / LC50
1 g/kg soil dw

Toxicity to terrestrial arthropods

Data not provided by the registrant

Toxicity to terrestrial plants

Study results
  • 2 studies submitted
  • 1 study processed
P/RResults
NOEC (21 days) 180 mg/kg soil dw [3]
EC50 (21 days) 320 - 413 mg/kg soil dw [3]
EC25 (21 days) 278 - 363 mg/kg soil dw [3]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
R Summaries
  • 1 summary submitted
  • 1 summary processed
Short-term EC50 / LC50
320 mg/kg soil dw

Toxicity to soil microorganisms

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
NOEC (28 days) 295.2 mg/kg soil dw [1]
NOEC (28 h) 933.6 mg/kg soil dw [1]
EC25 (28 days) 813 mg/kg soil dw [1]
EC25 (28 h) 933.6 mg/kg soil dw [1]
EC50 (28 days) 933.3 mg/kg soil dw [1]

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
R Summaries
  • 1 summary submitted
  • 1 summary processed
Short-term EC50
933.3 mg/kg soil dw

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
Exposure cons.
Other 1
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) 560 µg/m³ irritation (respiratory tract)
Acute /short term: (DNEL) 560 µg/m³ irritation (respiratory tract)
Local Effects
Long-term: (DNEL) 560 µg/m³ sensitisation (respiratory tract)
Acute /short term: (DNEL) 560 µg/m³ irritation (respiratory tract)
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (High hazard (no threshold derived)) -
Acute /short term: High hazard (no threshold derived)
Local Effects
Long-term: (High hazard (no threshold derived)) -
Acute /short term: (High hazard (no threshold derived)) -
EYE Exposure
High hazard (no threshold derived)
Data for the GENERAL POPULATION
INHALATION Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 280 µg/m³ irritation (respiratory tract)
Acute /short term: (DNEL) 280 µg/m³ irritation (respiratory tract)
Local Effects
Long-term: (DNEL) 280 µg/m³ irritation (respiratory tract)
Acute /short term: (DNEL) 280 µg/m³ irritation (respiratory tract)
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (High hazard (no threshold derived)) -
Acute /short term: (High hazard (no threshold derived)) -
Local Effects
Long-term: (High hazard (no threshold derived)) -
Acute /short term: (High hazard (no threshold derived)) -
ORAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DNEL) 1.25 mg/kg bw/day developmental toxicity / teratogenicity
Acute /short term: (DNEL) 1.25 mg/kg bw/day developmental toxicity / teratogenicity
EYE Exposure
High hazard (no threshold derived)

Toxicokinetics, metabolism, and distribution

Study results
Study data: basic toxicokinetics
  • 4 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 3
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
Study data: dermal absorption
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: dermal absorption
Studies with data
Key study 1
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
  • 21 studies submitted
  • 13 studies processed
P/RResults
LD50 5.8 - 5 000 mg/kg bw (rat) [54]
M/CInterpretations of results
Category 3 based on GHS criteria [1]

Type of Study provided
oral
Studies with data
Key study 13
Supporting study 3 2
Weight of evidence
Other 2 1
Data waiving
no waivers
inhalation
  • 14 studies submitted
  • 1 study processed
P/RResults
LC50 (4 h) 186 - 4 080 mg/m³ air (rat) [4]
M/CInterpretations of results
Category 4 based on GHS criteria [1]

inhalation
Studies with data
Key study 2
Supporting study 10 1
Weight of evidence
Other 1
Data waiving
no waivers
dermal
  • 10 studies submitted
  • 3 studies processed
P/RResults
LD50 17.8 - 2 000 mg/kg bw (rat) [2]
LD50 50.9 - 1 990 mg/kg bw (rabbit) [12]
M/CInterpretations of results
Category 4 based on GHS criteria [2]

dermal
Studies with data
Key study 3
Supporting study 4
Weight of evidence
Other 3
Data waiving
no waivers
other routes
  • 1 study submitted
  • 1 study processed
P/RResults
LD50 212 mg/kg bw (mouse) [1]

other routes
Studies with data
Key study
Supporting study
Weight of evidence 1
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route:
Adverse effect observed LD50 50 mg/kg bw
Inhalation route:
Adverse effect observed LC50 204 mg/m³
Dermal route:
Adverse effect observed LD50 1 147 mg/kg bw

Irritation / corrosion

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

Study data not processed for brief profile

Type of Study provided
Study data: skin
Studies with data
Key study 4
Supporting study 9
Weight of evidence
Other 2
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 2
Supporting study 3
Weight of evidence
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 (irritating)
Respiratory
Adverse effect observed (irritating)

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 3
Weight of evidence
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
No adverse effect observed (not sensitising)
Respiratory sensitisation
No study available

Repeated dose toxicity

Study results
Study data: oral
  • 5 studies submitted
  • 2 studies processed
P/RResults
NOAEL (rat): 1.17 - 38 mg/kg bw/day [4]
NOAEL (rat): 200 mg/L drinking water [1]
LOAEL (rat): 3.37 - 67.4 mg/kg bw/day [2]
NOEL (rat): 0.37 - 7.4 mg/kg bw/day [2]

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

No automatically processable data submitted

Study data: inhalation
Studies with data
Key study
Supporting study
Weight of evidence 7
Other 1
Data waiving
no waivers
Study data: dermal
  • 3 studies submitted
  • 0 studies processed

No automatically processable data submitted

Study data: dermal
Studies with data
Key study
Supporting study
Weight of evidence
Other 3
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route - systemic effects:
Adverse effect observed NOAEL 23.4 mg/kg bw/day (subchronic, rat)

Genetic toxicity

Study results
Study data: in vitro
  • 29 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 6
Supporting study
Weight of evidence 1
Other 22
Data waiving
no waivers
Study data: in vivo
  • 7 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 3
Data waiving
no waivers
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Carcinogenicity

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

No automatically processable data submitted

Toxicity to reproduction

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

Study data not processed for brief profile

Type of Study provided
Study data: reproduction
Studies with data
Key study
Supporting study
Weight of evidence 2
Other 1
Data waiving
no waivers
Study data: developmental
  • 3 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
Other 1 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
  • 1 summary submitted
  • 1 summary processed
Effect on developmental toxicity
Oral route:
No adverse effect observed NOAEL 12.5 mg/kg bw/day (subchronic, 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

Categories Display