[No public or meaningful name is available]

Endpoint summary

Description of key information

Key study: OECD Guideline 404. GLP study. The test substance was determined to be non skin irritating/corrosive.
Key study: OECD Guideline 405. GLP study. The test subtance was determined to be non eye irritating/corrosive.

Key value for chemical safety assessment

Skin irritation / corrosion

Link to relevant study records

Reference

Endpoint:

skin irritation: in vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

From July 26, 2012 to August 21, 2012

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: Study was performed according to the OECD 404 and EU B4 Method with GLP.

Qualifier:

according to guideline

Guideline:

OECD Guideline 404 (Acute Dermal Irritation / Corrosion)

Deviations:

no

Qualifier:

according to guideline

Guideline:

EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)

Deviations:

no

Qualifier:

according to guideline

Guideline:

EPA OPPTS 870.2500 (Acute Dermal Irritation)

Deviations:

no

Qualifier:

according to guideline

Guideline:

other: JMAFF Guidelines (2000) including the most recent partial revisions.

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Species:

rabbit

Strain:

New Zealand White

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Charles River Deutschland, Kisslegg, Germany.
- Age at study initiation: at least 6 weeks old.
- Weight at study initiation: at least 1.0 kg.
- Housing: Animals were individually housed in labeled cages with perforated floors (Ebeco, Germany, dimensions 67 x 62 x 55 cm) and shelters (Ebeco, Germany, dimensions 40 x 32 x 23 cm).
- Diet (e.g. ad libitum): Pelleted diet for rabbits (Global Diet 2030 from Harlan Teklad®, Mucedola, Milanese, Italy) approximately 100 grams per day. Hay (TecniLab-BMI BV, Someren, The Netherlands) and wooden sticks (Swedish aspen wood, Bioservices, Uden, The Netherlands) were available during the study period.
- Water (e.g. ad libitum): Free access to tap water.
- Acclimation period: at least 5 days before start of treatment under laboratory conditions.

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21.0 ± 3.0ºC.
- Humidity (%): 40-70%.
- Air changes (per hr): approximately 15 air changes per hour.
- Photoperiod (hrs dark / hrs light): 12 hours artificial fluorescent light and 12 hours darkness per day.

IN-LIFE DATES: From: July 26, 2012 To: August 02, 2012.

Type of coverage:

semiocclusive

Preparation of test site:

other: clipped

Vehicle:

unchanged (no vehicle)

Controls:

other: Adjacent areas of the untreated skin of each animal served as controls.

Amount / concentration applied:

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 mL.

Duration of treatment / exposure:

4 hours

Observation period:

1, 24, 48 and 72 hours after the removal of the dressings and test substance.

Number of animals:

3 Males.

Details on study design:

TEST SITE
- Area of exposure: 2x3 cm.
- Type of wrap if used: Micropore tape.

REMOVAL OF TEST SUBSTANCE
- Washing (if done): the dressing was removed and the skin cleaned of residual test substance using tap water and watery ethanol (50% v/v) (water: Elix, Millipore S.A.S., Molsheim, France; ethanol: Merck, Darmstadt, Germany).
- Time after start of exposure: 4 hours

SCORING SYSTEM:

Erythema and eschar formation:
No erythema.........................................................0
Very slight erythema (barely perceptible).......1
Well-defined erythema.......................................2
Moderate to severe erythema...........................3
Severe erythema (beet redness) *....................4
*. Where signs of necrosis or corrosion (injuries in depth) prevent erythema scoring, the maximum grade for erythema (= 4) is given.

Oedema formation:
No oedema............................................................................................................................................................0
Very slight oedema (barely perceptible)..........................................................................................................1
Slight oedema (edges of area well-defined by definite raising)...................................................................2
Moderate oedema (raised approximately 1 millimeter).................................................................................3
Severe oedema (raised more than 1 millimeter and extending beyond the area of exposure)..............4

Irritation parameter:

erythema score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

erythema score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

erythema score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

edema score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

edema score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

edema score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritant / corrosive response data:

Irritation:
Four hours exposure to 0.5 mL of Condensation products of cyclopentanone and pentaldehyde, fractionation pitch resulted in very slight erythema and/or very slight oedema in the treated skin areas of the three rabbits. The skin irritation resolved within 24 hours after exposure in all animals.
Corrosion:
There was no evidence of a corrosive effect on the skin.

Other effects:

Coloration / Remnants:
Brown staining of the treated skin by the test substance was observed on Day 1, which did not hamper the scoring of the skin reactions.
Toxicity / Mortality:
No symptoms of systemic toxicity were observed in the animals during the test period and no mortality occurred.

Table1: Individual skin irritation scores.

Following exposure, Brown staining of the treated skin area was noted after removal of the test substance.

 

Animal		300^1				299				301
Time after exposure		Erythema (0-4)	Oedema (0-4)	comments		Erythema (0-4)	Oedema (0-4)	comments		Erythema (0-4)	Oedema (0-4)	comments
1 hour		1	0	a		1	1	a		1	1	a
24 hours		0	0	-		0	0	-		0	0	-
48 hours		0	0	-		0	0	-		0	0	-
72 hours		0	0	-		0	0	-		0	0	-

¹Sentinel.

Comments:

a.     Brown staining of the skin by the test substance.

 

Table2: Mean value irritation scores.

Animal		Mean 24, 48 and 72 hrs
		Erythema		Oedema
300		0.0		0.0
299		0.0		0.0
301		0.0		0.0

 

Table3: Animal specifications.

Animal		Sex		Age at start		Body weights (grams)
				(weeks)		prior to application	at termination
300		♂		10-12		2451	2521
299		♂		11-13		2329	2406
301		♂		11-13		2239	2360

 

Interpretation of results:

GHS criteria not met

Conclusions:

The substance does not have to be classified.

Executive summary:

The primary skin irritation/corrosion of the substance was determinated according to OECD 404 guideline with GLP. Slight irritation was observed in all three animals (both score: oedema and erythema) in the treated skin areas after four hours with the score 1, this result was fully reversible within 24 hours after exposure in all animals.

There was no evidence of a corrosive effect on the skin.

 

Brown staining of the treated skin by the test substance was observed on Day 1, which did not hamper the scoring of the skin reactions.

 

No symptoms of systemic toxicity were observed in the animals during the test period and no mortality occurred.

  

Based on these results Condensation products of cyclopentanone and pentaldehyde, fractionation pitch does not have to be classified and has no obligatory labelling requirement for skin irritation according to the:

- Globally Harmonized System of Classification and Labelling of Chemicals (GHS) of the United Nations (2011),

- Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed (not irritating)

Eye irritation

Link to relevant study records

Reference

Endpoint:

eye irritation: in vivo

Type of information:

experimental study

Adequacy of study:

key study

Study period:

From July 30, 2012 to August 09, 2012

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: Study was performed according to the 405 OECD Guideline, with GLP.

Reason / purpose for cross-reference:

reference to other study

Qualifier:

according to guideline

Guideline:

OECD Guideline 405 (Acute Eye Irritation / Corrosion)

Deviations:

no

Qualifier:

according to guideline

Guideline:

EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)

Deviations:

no

Qualifier:

according to guideline

Guideline:

EPA OPPTS 870.2400 (Acute Eye Irritation)

Deviations:

no

Qualifier:

according to guideline

Guideline:

other: Japanese Ministry of Agriculture, Forestry and Fisheries (JMAFF), 12 Nohsan, Notification No. 8147, April 2011

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Species:

rabbit

Strain:

New Zealand White

Details on test animals or tissues and environmental conditions:

TEST ANIMALS
- Source: Charles River Deutschland, Kisslegg, Germany.
- Age at study initiation: at least 6 weeks old.
- Weight at study initiation: at least 1.0 kg.
- Housing: animals were individually housed in labeled cages with perforated floors (Ebeco, Germany, dimensions 67 x 62 x 55 cm) and shelters (Ebeco, Germany, dimensions 40 x 32 x 23 cm)
- Diet (e.g. ad libitum): Pelleted diet for rabbits (Global Diet 2030 from Harlan Teklad®, Mucedola, Milanese, Italy) approximately 100 grams per day. Hay (TecniLab-BMI BV, Someren, The Netherlands) and wooden sticks (Swedish aspen wood, Bioservices, Uden, The Netherlands) were available during the study period.
- Water (e.g. ad libitum): Free access to tap water.
- Acclimation period: Acclimatization period was at least 5 days before start of treatment under laboratory conditions.

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21.0 ± 3.0ºC
- Humidity (%): 40-70%
- Air changes (per hr): approximately 15 air changes per hour.
- Photoperiod (hrs dark / hrs light): 12 hours artificial fluorescent light and 12 hours darkness per day.

IN-LIFE DATES: From July 30, 2012 to August 09, 2012

Vehicle:

unchanged (no vehicle)

Controls:

other: other: Each animal was treated by instillation of the test substance, in one of the eyes. The other eye remained untreated and served as the reference control.

Amount / concentration applied:

TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 mL

Observation period (in vivo):

Approximately 1, 24, 48 and 72 hours after instillation of the test substance.

Number of animals or in vitro replicates:

3 males.

Details on study design:

STUDY DESIGN:
The study was performed in a stepwise manner and was started by treatment of a single rabbit (sentinel). The two other animals were treated in a similar manner one week later, after considering the degree of eye irritation observed in the first animal.

TREATMENT:
Each animal was treated by instillation of 0.1 mL of the test substance, in the conjunctival sac of one of the eyes after gently pulling the lower lid away from the eyeball. The lids were then gently held together for about one second to prevent loss of the test substance. The other eye remained untreated and served as the reference control.
Immediately after the 24-hour observation, a solution of 2% fluorescein (Merck, Darmstadt, Germany) in water (adjusted to pH 7.0) was instilled into both eyes of each animal to quantitatively determine corneal epithelial damage. Any bright green stained area, indicating epithelial damage, was estimated as a percentage of the total corneal area.
After the final observation, the animals were sacrificed by intra-venous injection of Euthasol® 20% (AST Farma BV, Oudewater, The Netherlands).


SCORING SYSTEM:
CORNEAL IRRITATION
Opacity: degree of density (area most dense taken for reading)
No ulceration or opacity (may include slight dulling of normal luster) 0
Scattered or diffuse areas of opacity, details of iris clearly visible 1
Easily discernible translucent area, details of iris slightly obscured 2
Nacreous area, no details of iris visible, size of pupil barely discernible 3
Opaque cornea, iris not discernible through the opacity 4

Area of cornea involved:
No ulceration or opacity 0
One quarter or less but not zero 1
Greater than one quarter, but less than half 2
Greater than half, but less than three quarters 3
Greater than three quarters, up to whole area 4

IRIS
Normal 0
Markedly deepened rugae, congestion, swelling, moderate circumcorneal hyperaemia, or injection, any of these or combination thereof, iris still reacting to light(sluggish reaction is positive) 1
No reaction to light, hemorrhage, gross destruction (any or all of these) 2

CONJUNCTIVAL IRRITATION
Redness (refers to palpebrae and sclera, excluding cornea and iris):
Blood vessels normal 0
Some blood vessels definitely hyperaemic (injected) 1
Diffuse, crimson color, individual vessels not easily discernible 2
Diffuse beefy red 3

Chemosis (refers to lids and/or nictitating membranes):
No swelling ………………………………………… 0
Any swelling above normal (includes nictitating membranes) 1
Obvious swelling with partial eversion of lids 2
Swelling with lids about half closed 3
Swelling with lids more than half closed 4

Discharge:
No discharge (may include small amounts observed in inner canthus of normal animals) 0
Any amount different from normal and/or lacrimation 1
Discharge with moistening of the lids and hairs just adjacent to lids 2
Discharge with moistening of the lids and hairs (considerable area around the eye) 3


TOOL USED TO ASSESS SCORE: Immediately after the 24-hour observation, a solution of 2% fluorescein (Merck, Darmstadt, Germany) in water (adjusted to pH 7.0) was instilled into both eyes of each animal to quantitatively determine corneal epithelial damage. Any bright green stained area, indicating epithelial damage, was estimated as a percentage of the total corneal area.

Irritation parameter:

cornea opacity score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

cornea opacity score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

cornea opacity score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

iris score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

2

Irritation parameter:

iris score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

2

Irritation parameter:

iris score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

2

Irritation parameter:

conjunctivae score

Remarks:

(Redness)

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

3

Irritation parameter:

conjunctivae score

Remarks:

(Redness)

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

3

Irritation parameter:

conjunctivae score

Remarks:

(Redness)

Basis:

animal #3

Time point:

24/48/72 h

Score:

0.33

Max. score:

3

Irritation parameter:

chemosis score

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

chemosis score

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

chemosis score

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

4

Irritation parameter:

conjunctivae score

Remarks:

(Discharge)

Basis:

animal #1

Time point:

24/48/72 h

Score:

0

Max. score:

3

Irritation parameter:

conjunctivae score

Remarks:

(Discharge)

Basis:

animal #2

Time point:

24/48/72 h

Score:

0

Max. score:

3

Irritation parameter:

conjunctivae score

Remarks:

(Discharge)

Basis:

animal #3

Time point:

24/48/72 h

Score:

0

Max. score:

3

Irritant / corrosive response data:

IRRITATION:
Instillation of approximately 0.1 mL of Condensation products of cyclopentanone and pentaldehyde, fractionation pitch into one eye of each of three rabbits resulted in irritation of the conjunctivae, which consisted of redness, chemosis and/or discharge. The irritation had completely resolved within 24 hours in two animals and within 48 hours in the other animal.
No iridial irritation or corneal opacity was observed, and treatment of the eyes with 2% fluorescein 24 hours after test substance instillation revealed no corneal epithelial damage.

CORROSION:
There was no evidence of ocular corrosion.

Other effects:

COLORATION/REMNANTS:
No staining of (peri) ocular tissues by the test substance was observed and no test substance remnants were seen.
Brown staining of the fur on the head and paws, caused by the test substance, was noted during the observation period.

TOXICITY/MORTALITY:
No symptoms of systemic toxicity were observed in the animals during the test period and no mortality occurred.

Table 1. Individual eye irritation scores.

Animal	Time after dosing	Cornea			Iris	Conjunctivae			Comments
		Opacity (0-4)	Area (0-4)	Fluor area (%)^2	(0-2)	Redness (0-3)	Chemosis (0-4)	Discharge (0-3)
309^1	1 hour	0	0	-	0	1	0	0	e
	24 hours	0	0	0	0	0	0	0	e
	48 hours	0	0	-	0	0	0	0	e
	72 hours	0	0	-	0	0	0	0	-
303	1 hour	0	0	-	0	1	0	1	e
	24 hours	0	0	0	0	0	0	0	e
	48 hours	0	0	-	0	0	0	0	e
	72 hours	0	0	-	0	0	0	0	-
306	1 hour	0	0	-	0	1	1	1	e
	24 hours	0	0	0	0	1	0	0	e
	48 hours	0	0	-	0	0	0	0	e
	72 hours	0	0	-	0	0	0	0	-

¹Sentinel,

²Green staining after fluorescein treatment (percentage of total corneal area).

Comments:

e     Brown staining of the head and paws by the test substance.

Table 2. Mean value eye irritation scores.

Animal	Mean 24, 48 and 72 hours
	Corneal opacity	Iris	Conjunctivae
			Redness	Chemosis
309	0.0	0.0	0.0	0.0
303	0.0	0.0	0.0	0.0
306	0.0	0.0	0.3	0.0

 

 Table 3. Animal specifications.

Animal	Sex	Age at start (weeks)	Body weighs (grams)
			prior to application	at termination
309	male	11-13	2659	2721
303	male	12-14	2637	2689
306	male	12-14	2591	2711

 

Interpretation of results:

GHS criteria not met

Conclusions:

The test substance does not have to be classified for eye irritation.

Executive summary:

The assessment of acute eye irritation/corrosion study with Condensation products of cyclopentanone and pentaldehyde, fractionation pitch in the rabbit was determined according to the OECD 405 and the EU B5 Guidelines, with GLP.

Single samples of 0.1 mL of test substance were instilled into one eye of each of three rabbits. Observations were made 1, 24, 48 and 72 hours after instillation. Instillation of the test substance resulted in irritation of the conjunctivae, which consisted of redness, chemosis and/or discharge. The irritation had completely resolved within 24 hours in two animals and within 48 hours in the other animal.

Brown staining of the fur on the head and paws, caused by the test substance, was noted during the observation period.

Based on these results, Condensation products of cyclopentanone and pentaldehyde, fractionation pitch does not have to be classified and has no obligatory labelling requirement for eye irritation according to the:

- Globally Harmonized System of Classification and Labelling of Chemicals (GHS) of the United Nations (2011),

- Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures

 

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed (not irritating)

Respiratory irritation

Endpoint conclusion

Endpoint conclusion:

no study available

Additional information

Key study: Experimental result on test item Condensation products of cyclopentanone and pentaldehyde, fractionation pitch.

Eye irritation/corrosion:

The possible eye corrosive and irritative potential of the test substance was carried out according to the 405 OECD Guideline (GLP study). 0.1 mL of test substance were into one eye of each of three rabbits.

Irritation: The test substance caused irritation of the conjunctivae, which consisted of redness, chemosis and/or discharge. The irritation had completely resolved within 24 hours in two animals and within 48 hours in the other animal.

No iridial irritation or corneal opacity was observed, and treatment of the eyes with 2% fluorescein 24 hours after test substance instillation revealed no corneal epithelial damage.

Corrosion: There was no evidence of ocular corrosion.

Skin irritation/corrosion:

The possible skin corrosive and irritative potential of the test substance was carried out according to the 404 OECD Guideline (GLP study). 0.5 mL of test substance was applicated onto clipped skin for 4 hours using a semi-occlusive dressing.

Irritation: The test substance caused a very slight erythema and/or very slight oedema in the treated skin areas of the three rabbits.

The skin irritation resolved within 24 hours after exposure in all animals.

Corrosion: There was no evidence of a corrosive effect on the skin.

 

Justification for selection of skin irritation / corrosion endpoint:
Only one study available. GLP compliant and of high quality (Klimisch 1).

Justification for selection of eye irritation endpoint:
Only one study available. GLP compliant and of high quality (Klimisch 1).

Justification for classification or non-classification

Based on these results, Condensation products of cyclopentanone and pentaldehyde, fractionation pitch does not have to be classified and has no obligatory labelling requirement for eye and skin irritation according to the:

- Globally Harmonized System of Classification and Labelling of Chemicals (GHS) of the United Nations (2011),

- Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures.