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EC number: 202-653-9 | CAS number: 98-29-3
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Endpoint summary
Administrative data
Description of key information
- Skin: corrosive (GHS corrosive category 1B)
- Eye: highly irritating (GHS category 1 of irreversible effects to the eye)
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From 16 February 1987 to 27 May 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to a recognised guideline and under GLP conditions. However, the purity of the test substance is not specified.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- other: Hybrid Albino New-Zealand
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Strain: Hybrid Albino New-Zealand
- Sex: males
- Sources: *Charles River: Saint Aubin Les Elbeuf - 76410 Cléon - France
*E.G.A.V: Saint Mars d'Egrenne - 61350 Passais La Conception - France
*E.S.D: Roman - 01400 Châtillon sur Chalaronne - France
- Age at study initiation: no data
- Weight at study initiation: 2.5 +/- 0.2 kg
- Housing: individual housing, in polystyrene cages, of internal dimensions 560x355x315 mm, with a perforated floor
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: one week
ENVIRONMENTAL CONDITIONS
- Temperature: 20 +/- 3°C
- Humidity: 30 to 70%
- Air changes: no data
- Photoperiod: 12 hrs dark / 12 hrs light
IN-LIFE DATES: From: 3 March 1987 To: 17 March 1987 - Type of coverage:
- semiocclusive
- Preparation of test site:
- other: clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- Concentration: 0.5 mL undiluted
- Duration of treatment / exposure:
- 4 hours
- Observation period:
- 14 days
- Number of animals:
- 6
- Details on study design:
- TEST SITE
- Area of exposure: a surface of about 6 cm2
- % coverage: no data
- Type of wrap: a Codex hydrophilic eight layer gauze pad
REMOVAL OF TEST SUBSTANCE
- Washing: the bandages were removed and if necessary excess test substance which had not penetrated was wiped away with a gauze pad moistened with distilled water
- Time after start of exposure: 4 hours
SCORING SYSTEM: based on erythema and oedema formation, according to directive OECD 404 - Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks on result:
- other: aspect of burn on all the zone of application
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- erythema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- erythema score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- erythema score
- Basis:
- animal #5
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- erythema score
- Basis:
- animal #6
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 3.34
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Remarks on result:
- other: see table of results
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 3.67
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 2.67
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Irritation parameter:
- edema score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 3.67
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Irritation parameter:
- edema score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 3.67
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Irritation parameter:
- edema score
- Basis:
- animal #5
- Time point:
- 24/48/72 h
- Score:
- 3
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Irritation parameter:
- edema score
- Basis:
- animal #6
- Time point:
- 24/48/72 h
- Score:
- 3.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 14 days
- Interpretation of results:
- Category 1B (corrosive) based on GHS criteria
- Conclusions:
- 4-tert-butylpyrocatechol 85% in water is classified as :
- Skin corrosive category 1B according to UN/EU GHS classification criteria - Executive summary:
In a dermal irritation study (Hazleton, 1987), hybrid albino New-Zealand White rabbits (6 males) were dermally exposed to 0.5 mL of 4 -tert-butylpyrocatechol 85% in water on a 6 cm2 body surface area. Test sites were covered with a semi-occlusive dressing for 4 hours. Animals were then observed for 14 days. Irritation was scored by the method of directive OECD 404.
After 1 hour of exposure, severe erythema and moderate (1/6 rabbits) or severe (5/6 rabbits) oedema were observed in all treated animals. Severe erythema was not reversible after 14 days and oedema was fully reversible within 14 days. In this study, 4 -tert-butylpyrocatechol 85% in water was corrosive to the skin based on the observed skin reactions.
Reference
Erythema:
animal |
mean 24/48/72 hours |
n°1 | 4.00 |
n°2 | 4.00 |
n°3 | 4.00 |
n°4 | 4.00 |
n°5 | 4.00 |
n°6 | 4.00 |
mean | 4.00 |
After 14 days: mean = 4.00 for all animals + presence of eschars on all the zone of application
Oedema:
animal |
mean 24/48/72 hours |
n°1 | 3.67 |
n°2 | 2.67 |
n°3 | 3.67 |
n°4 | 3.67 |
n°5 | 3.00 |
n°6 | 3.33 |
mean | 3.34 |
After 14 days: mean = 0.00 for all animals
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (corrosive)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From 16 February 1987 to 27 May 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to a recognised guideline and under GLP conditions. However, the purity of the test substance is not specified.
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- other: Hybrid Albino New-Zealand
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Strain: Hybrid Albino New-Zealand
- Sex: males
- Sources: *Charles River: Saint Aubin Les Elbeuf - 76410 Cléon - France
*E.G.A.V: Saint Mars d'Egrenne - 61350 Passais La Conception - France
*E.S.D: Roman - 01400 Châtillon sur Chalaronne - France
- Age at study initiation: no data
- Weight at study initiation: 2.5 +/- 0.2 kg
- Housing: individual housing, in polystyrene cages, of internal dimensions 560x355x315 mm, with a perforated floor
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: one week
ENVIRONMENTAL CONDITIONS
- Temperature: 20 +/- 3°C
- Humidity: 30 to 70%
- Air changes: no data
- Photoperiod: 12 hrs dark / 12 hours light - Vehicle:
- other: no
- Controls:
- yes
- Amount / concentration applied:
- Amount applied: 0.1 ml
- Observation period (in vivo):
- 21 days
- Number of animals or in vitro replicates:
- 6
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
no washing
SCORING SYSTEM: based on changes in cornea, iris, conjunctivae and chemosis, according to guideline OECD 405
TOOL USED TO ASSESS SCORE: Heine's ophthalmoscope / fluorescein - Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 3.51
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks on result:
- other: see table of results
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 3.3
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 3.3
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 3.6
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #5
- Time point:
- 24/48/72 h
- Score:
- 3.6
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- chemosis score
- Basis:
- animal #6
- Time point:
- 24/48/72 h
- Score:
- 3.3
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 1.6
- Max. score:
- 3
- Reversibility:
- not reversible
- Remarks on result:
- other: see table of results
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1.6
- Max. score:
- 3
- Reversibility:
- not reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1.3
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- not reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 3
- Reversibility:
- not reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #5
- Time point:
- 24/48/72 h
- Score:
- 1.6
- Max. score:
- 3
- Reversibility:
- not reversible
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #6
- Time point:
- 24/48/72 h
- Score:
- 1.3
- Max. score:
- 3
- Reversibility:
- not reversible
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 2
- Reversibility:
- not reversible
- Remarks on result:
- other: see table of results
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 2
- Reversibility:
- not reversible
- Irritation parameter:
- iris score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 2
- Reversibility:
- not reversible
- Irritation parameter:
- iris score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 2
- Reversibility:
- not reversible
- Irritation parameter:
- iris score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 2
- Reversibility:
- not reversible
- Irritation parameter:
- iris score
- Basis:
- animal #5
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 2
- Reversibility:
- not reversible
- Irritation parameter:
- iris score
- Basis:
- animal #6
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 2
- Reversibility:
- not reversible
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Remarks on result:
- other: see table of results
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #3
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #4
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #5
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Irritation parameter:
- cornea opacity score
- Basis:
- animal #6
- Time point:
- 24/48/72 h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- not reversible
- Interpretation of results:
- Category 1 (irreversible effects on the eye) based on GHS criteria
- Conclusions:
- 4-tert-butylpyrocatechol 85% in water is classified as:
- Category 1 for irreversible effects on the eye according to UN/EU GHS classification - Executive summary:
In an eye irritation study (Hazleton, 1987), 0.1 mL 4 -tert-butylpyrocatechol 85% in water was instilled into the conjunctival sac of the right eye of hybrid Albino New-Zealand White rabbits (6 males) (no rinsing). Animals were then observed for 21 days. Ocular irritation was scored by the method of directive OECD 405.
After 1 hour of exposure, severe corneal opacity and iris lesions, moderate (4/6 rabbits) or severe (2/6 rabbits) chemosis and slight conjunctival redness were observed in all treated animals. These ocular irritation signs were not reversible after 21 days. In this study, 4 -tert-butylpyrocatechol 85% in water was highly irritating to the eye or causing irreversible effects on the eye based on the observed ocular reactions.
Reference
Irritant/corrosive response data for each animal at each observation time
Score at time point / Reversibility |
Cornea |
Iris |
Conjunctivae |
Chemosis |
Max. score: 4 |
Max. score: 2 |
Max. score: 3 |
Max. score: 4 |
|
60 min |
4/4/4/4/4/4 |
2/2/2/2/2/2 |
1/1/1/1/1/1 |
3/4/3/3/4/3 |
24 h |
4/4/4/4/4/4 |
2/2/2/2/2/2 |
1/1/2/2/2/1 |
3/3/3/4/4/3 |
48 h |
4/4/4/4/4/4 |
2/2/2/2/2/2 |
2/1/2/2/1/1 |
3/3/4/4/3/3 |
72 h |
4/4/4/4/4/4 |
2/2/a/2/2/2 |
2/2/2/2/2/2 |
4/4/4/4/4/4 |
Average 24h, 48h, 72h |
4/4/4/4/4/4 |
2/2/2/2/2/2 |
1.6/1.3/2/2/1.6/1.3 |
3.3/3.3/3.6/4/3.6/3.3 |
Reversibility*) |
n. |
n. |
n. |
n. |
Average time (unit) for reversion |
> 21 days |
> 21 days |
> 21 days |
> 21 days |
*) Reversibility: c. = completely reversible;n.c.= not completely reversible; n. = not reversible
a: the degree and the surface of the corneal opacification returned the impossible interpretation.
NB: a total necrosis of the eye was observed in 2 out of the 6 rabbits examined on day 14, on day 21, a necrosis area located on a quarter of the corneal surface was noted in the 3 surviving rabbits and the absence of direct photomotor reflex was still noted in 2 of them (the 2 rabbits showing a necrosis on day 14 were sacrified after the reading and another animal was found dead on day 20).
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irreversible damage)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
4-tert-butylpyrocatechol, as a 85% solution in water, was tested for its skin and eye irritation properties in New Zealand White rabbits following dermal application or ocular conjunctival instillation during the same study (Hazleton study No. 705411).
4 -tert-butylpyrocatechol was also tested for its skin irritation properties in New Zealand White rabbits following dermal application (HRC study No. 91607D/DIC 207/SE).
Both studies were considered of reliability 2 according to Klimisch cotation criteria.
For skin irritation, of the two studies available, the first one (Hazleton, 1987) was selected as a key study, based on the higher number of animals used (6 rabbits), the longer exposure time (up to 4 hours) and the larger body surface (6 cm²) used for dermal application. The other study (HRC, 1991), using a 3 -minute application in 3 rabbits, was used as a supporting study. For eye irritation, the available study was used as a key study, of reliability 2 (Hazleton, 1987). Another data for in vivo eye irritation (reliability 2) was available from a reference handbook (1996).
All in vivo results were consistent with a risk of serious skin or eye damage:
- After three minutes of dermal exposure, necrosis with very slight oedema was evident at all treatment sites. These reactions persisted and were still visible at several sites of application on day 14. Following one hour of dermal exposure of a 85% aqueous solution, severe skin erythema and moderate to severe edema were observed (score 4). Skin erythema and edema were not reversible after 14 days of observation. Edema was fully reversible within 14 days.
- After one hour of ocular exposure to a 85% aqueous solution, severe corneal opacity and iritis, moderate to severe chemosis and slight conjunctival redness were observed. None of these findings was reversible after 21 days of observation.
The test substance was therefore classified as corrosive to the skin (or corrosive category 1B) and highly irritating to the eye (or category 1 of irreversible effects to the eye).
Justification for selection of skin irritation / corrosion
endpoint:
The study was conducted according to a recognised guideline and
under GLP conditions.
Justification for selection of eye irritation endpoint:
The study was conducted according to a recognised guideline and
under GLP conditions.
Effects on skin irritation/corrosion: corrosive
Effects on eye irritation: highly irritating
Justification for classification or non-classification
Based on the severity (necrotic findings) and absence of recovery of the changes observed in both skin and eye tissues (for up to 21 days of observation), 4-tert-butylpyrocatechol was classified as following: corrosive category 1B, H314: causes severe skin burns and eye damage and Eye damage category 1, H318: causes serious eye damage based on the criteria of UN/EU GHS.
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