Disodium 7-benzamido-4-hydroxy-3-[[4-[(4-sulphonatophenyl)azo]phenyl]azo]naphthalene-2-sulphonate

Endpoint summary

Description of key information

Skin Irritation: The primary irritation index as the measure of the acute irritation to the skin of rabbits was found to be 0 for both Erythema and Edema. The tested item is to be considered as non-irritant to the skin of rabbits.

Eye Irritation: The ocular reactions were scored by the method described in "Appraisal of the Safety of Chemicals in Food Drugs and Cosmetics" published by the Association of Food and Drug Officials of the U.S.A. .The tested substance is considered to be not irritant for the rabbits eyes.

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:

1975

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

study well documented, meets generally accepted scientific principles, acceptable for assessment

Principles of method if other than guideline:

The procedure adopted was the patch-test technique described in the "Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics" (1959) of the US Association of Food and Drug Officials (AFDO).

GLP compliance:

not specified

Species:

rabbit

Strain:

other: Russian breed

Details on test animals or test system and environmental conditions:

TEST ANIMALS- Body weight: from 1.5 to 2 kg- Housing: individually in metal cage - Diet: NAFAG, Gossau SG, rat food ad libitum- Water: tap water ad libitum ENVIRONMENTAL CONDITIONS- Temperature (°C): 18 ± 1- Humidity (%): 55 ± 5 %- Photoperiod (hrs dark / hrs light): 14 h light / 14 h dark

Type of coverage:

occlusive

Preparation of test site:

shaved

Vehicle:

not specified

Controls:

other: the untreated skin is used as a control.

Amount / concentration applied:

The tested substance was applied to each side, abraded and non abraded skin, in quantities of 0.5 g.

Duration of treatment / exposure:

24 h

Observation period:

up to 72 h

Number of animals:

six rabbits: 3 male and 3 female

Irritation parameter:

erythema score

Basis:

mean

Time point:

24/48/72 h

Score:

ca. 0

Max. score:

4

Reversibility:

other: not applicable

Irritation parameter:

edema score

Basis:

mean

Time point:

24/48/72 h

Score:

ca. 0

Max. score:

4

Reversibility:

other: not applicable

Irritant / corrosive response data:

The primary irritation index as the measure of the acute irritation to the skin of rabbits was found to be 0.

The results of the skin irritation test are summarized in Table 1.

Animal No. Sex	Skin Reaction	24 hrs after application		72 hrs after application
		intact skin	scarified skin	intact skin	scarified skin
1     m	Erythema	0	0	0	0
	Edema	0	0	0	0
2    m	Erythema	0	0	0	0
	Edema	0	0	0	0
3    m	Erythema	0	0	0	0
	Edema	0	0	0	0
4    f	Erythema	0	0	0	0
	Edema	0	0	0	0
5    f	Erythema	0	0	0	0
	Edema	0	0	0	0
6    f	Erythema	0	0	0	0
	Edema	0	0	0	0

The primary irritation index as the measure of the acute skin irritation provoked by the substance is defined as the average of all the ratings found after 24 and 72 hours on the intact and slightly scarified skin. Compounds producing combined averages (primary irritation indexes) of 2 or less are only mildly irritating; whereas those with indexes from 2 to 5 are moderate irritants, and those v/ith scores above 6 are considered severe irritants.

The primary irritation index of the tested item was 0.

Interpretation of results:

GHS criteria not met

Conclusions:

The primary irritation index as the measure of the acute irritation to the skin of rabbits was found to be 0.Therefore the tested item is to be considered as non-irritant to the skin of rabbits.

Executive summary:

The primary irritation effect was assessed following the "Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics" (1959) of the US Association of Food and Drug Officials (AFDO).

The result show no irritation on rabbit skin therefore the tested item is to be considered as non-irritant to skin under CLP classification.

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

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

study well documented, meets generally accepted scientific principles, acceptable for assessment

Principles of method if other than guideline:

The procedure adopted was the patch-test technique described in the "Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics" (1959) of the US Association of Food and Drug Officials (AFDO).

GLP compliance:

not specified

Species:

rabbit

Strain:

other: Russian breed

Details on test animals or tissues and environmental conditions:

TEST ANIMALS- Body weight: from 1.5 to 2 kg- Housing: individually in metal cage - Diet: NAFAG, Gossau SG, rat food ad libitum- Water: tap water ad libitum ENVIRONMENTAL CONDITIONS- Temperature (°C): 18 ± 1- Humidity (%): 55 ± 5 %- Photoperiod (hrs dark / hrs light): 14 h light / 14 h dark

Vehicle:

unchanged (no vehicle)

Controls:

other: The right eye was not treated and served as an untreated control.

Amount / concentration applied:

The test material in an amount of 0.1 g was inserted into the conjunctival sac of the left eye of the rabbits and the lids were gently closed for one second.

Duration of treatment / exposure:

30 sec

Observation period (in vivo):

up to 7 days

Number of animals or in vitro replicates:

six rabbits (3 male and 3 female)

Irritation parameter:

cornea opacity score

Basis:

mean

Time point:

24/48/72 h

Score:

0

Max. score:

80

Reversibility:

fully reversible

Irritation parameter:

cornea opacity score

Basis:

mean

Time point:

other: 4 days

Score:

0

Max. score:

80

Reversibility:

fully reversible

Irritation parameter:

cornea opacity score

Basis:

mean

Time point:

7 d

Score:

0

Max. score:

80

Reversibility:

fully reversible

Irritation parameter:

iris score

Basis:

mean

Time point:

24/48/72 h

Score:

0

Max. score:

10

Reversibility:

fully reversible

Irritation parameter:

iris score

Basis:

mean

Time point:

other: 4 days

Score:

0

Max. score:

10

Reversibility:

fully reversible

Irritation parameter:

iris score

Basis:

mean

Time point:

7 d

Score:

0

Max. score:

10

Reversibility:

fully reversible

Irritation parameter:

chemosis score

Basis:

mean

Time point:

24 h

Score:

8

Max. score:

20

Reversibility:

fully reversible

Irritation parameter:

chemosis score

Basis:

mean

Time point:

48 h

Score:

6

Max. score:

20

Reversibility:

fully reversible

Irritation parameter:

chemosis score

Basis:

mean

Time point:

72 h

Score:

2

Max. score:

20

Reversibility:

fully reversible

Irritation parameter:

chemosis score

Basis:

mean

Time point:

other: 4 days

Score:

0

Max. score:

20

Reversibility:

fully reversible

Irritation parameter:

chemosis score

Basis:

mean

Time point:

7 d

Score:

0

Max. score:

20

Reversibility:

fully reversible

Irritation parameter:

conjunctivae score

Basis:

mean

Time point:

24/48/72 h

Remarks on result:

no indication of irritation

Irritant / corrosive response data:

The primary irritation index as the measure of the acute irritation to the eye of rabbits was found to be 0.

Interpretation of results:

GHS criteria not met

Conclusions:

Not eye irritant

Executive summary:

The primary irritation effect was assested following the "Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics" (1959) of the US Association of Food and Drug Officials (AFDO).

The result does not show irritation on rabbit eye following the indicated guideline and the tested item is to be considered as non-irritant to eye based on CLP criteria, table 3.2.2.7.1.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed (not irritating)

Respiratory irritation

Endpoint conclusion

Endpoint conclusion:

no study available

Justification for classification or non-classification

SKIN IRRITATION/CORROSION

A corrosive substance is a substance that produces destruction of skin tissue, namely, visible necrosis through the epidermis and into the dermis, in at least 1 tested animal after exposure up to 4 hour duration.

Three subcategories are provided within theCorrosive category 1:

Subcategory 1Awhere responses are noted following up to 3 minutes exposure and up to 1 hour observation;

Subcategory 1Bwhere responses are described following exposure between 3 minutes and 1 hour and observations up to 14 days;

Subcategory 1C where responses occur after exposures between 1 hour and 4 hours and observations up to 14 days

To classify a substance as irritant, the major criterion is that at least 2 of 3 tested animals have a mean score of ≥ 2,3 - ≤ 4,0.

Category 2:

- Mean value of ≥ 2,3 - ≤ 4,0 for erythema/ eschar or for oedema in at least 2 of 3 tested animals from gradings at 24, 48 and 72 hours after patch removal or, if reactions are delayed, from grades on 3 consecutive days after the onset of skin reactions; or

- Inflammation that persists to the end of the observation period normally 14 days in at least 2 animals, particularly taking into account alopecia (limited area), hyperkeratosis, hyperplasia, and scaling; or

- In some cases where there is pronounced variability of response among animals, with very definite positive effects related to chemical eposure in a single animal but less than the criteria above.

The substance is not classified as skin irritant because in the performed studies, the tested similar substances don't meet the classification criteria of the CLP regulation n. 1272/2008.

EYE IRRITATION

Serious eye damage means the production of tissue damage in the eye, or serious physical decay of vision, following application of a test substance to the anterior surface of the eye, which is not fully reversible within 21 days of application.

Eye irritation means the production of changes in the eye following the application of test substance to the anterior surface of the eye, which are fully reversible within 21 days of application.

Irreversible effects on the eye (Category 1):

If, when applied to the eye of an animal, a substance produces:

- at least in one animal effects on the cornea, iris or conjunctiva that are not expected to reverse or have not fully reversed within an observation period of normally 21 days; and/ or

- at least in 2 of 3 tested animals, a positive response of corneal opacity ≥ 3 and/or iritis > 1,5 calculated as the mean scores following grading at 24, 48 and 72 hours after installation of the test material.

These observations include animals with grade 4 cornea lesions and other severe reactions (e.g., destruction of cornea) observed at any time during the test, as well as persistent corneal opacity, discoloration of the cornea by a dye substance, adhesion, pannus, and interference with the function of the iris or other effects that impair sight. In this context, persistent lesions are considered those which are not fully reversible within an observation period of normally 21 days. Substances are also classified in Category 1 if they fulfil the criteria of corneal opacity ≥ 3 or iritis > 1,5 detected in a Draize eye test with rabbits, recognising that such severe lesions usually do not reverse within a 21-day observation period.

The substance does not meet the requirements to be classified in Category 1.

Irritating to eyes (Category 2)

when applied to the eye of an animal, a substance produces:

- at least in 2 of 3 tested animals, a positive response of: corneal opacity ≥ 1 and/or iritis ≥ 1, and/or conjunctival redness ≥ 2 and/or conjunctival oedema (chemosis) ≥ 2

calculated as the mean scores following grading at 24, 48 and 72 hours after installation of the test material, and which fully reverses within an observation period of 21 days.

The substance is not classified as eye irritant because in the performed studies, the tested similar substances don't meet the classification criteria of the CLP regulation n. 1272/2008.