Reaction product of acid red 143 (free acid) or the respective sodium salt (e.g Lansyn red F-5B) (UVCB) with Tetrabutylammonium bromide (CAS nr.: 1643-19-2) resulting in a mixture of AR143-(TBN)2 (Main component), AR143-(TBN), AR143-(TBN)3, AR143-(TBN) without alkyl tail, AR143-(TBN)2 without alkyl tail.Chemical name main component AR143-(TBN)2:di-(tetra-n-butylammonium) salt of 1-benzoyl-4-[4'-(1'',1''-dimethylpropyl)-phenoxy]-6-phenylamino-2,7-dioxo-2,7-dihydro-3H-naphtho(1,2,3-de)quinolin, disulfonic acid

Skin irritation / corrosion

Administrative data

Endpoint:

skin irritation / corrosion, other

Remarks:

in vivo study after failed in vitro study due to the test item was not compatible with the test system

Type of information:

experimental study

Adequacy of study:

key study

Study period:

11/11/2016-03/03/2017

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2017

Report date:

2017

Materials and methods

Test guideline

Test guideline 1

Qualifier:

according to guideline

Guideline:

OECD Guideline 404 (Acute Dermal Irritation / Corrosion)

Version / remarks:

OECD Guidelines for Testing of Chemicals, No. 404, “Acute Dermal Irritation/Corrosion” adopted 28 July 2015

Test guideline 2

Qualifier:

according to guideline

Guideline:

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

Version / remarks:

Commission Regulation (EC) No 440/2008, L 142, Annex Part B, Method B.4, 30 May 2008

Test guideline 3

Qualifier:

according to guideline

Guideline:

EPA OPPTS 870.2500 (Acute Dermal Irritation)

Version / remarks:

EPA Health Effects Test Guidelines, OPPTS 870.2500 “Acute dermal irritation”, EPA 712-C-98-196,
(August 1998)

Test guideline 4

Qualifier:

according to guideline

Guideline:

other: Directive 2010/63/EU

Version / remarks:

Procedures and facilities comply with the requirements of Directive 2010/63/EU and the national legislation defined in the animal protection law concerning the protection of animals used for experimental and other scientific procedures

GLP compliance:

yes (incl. QA statement)

Test material

Test material information

1

Reference substance name:

Reaction product of acid red 143 (free acid) or the respective sodium salt (e.g Lansyn red F-5B) (UVCB) with Tetrabutylammonium bromide (CAS nr.: 1643-19-2) resulting in a mixture of AR143-(TBN)2 (Main component), AR143-(TBN), AR143-(TBN)3, AR143-(TBN) without alkyl tail, AR143-(TBN)2 without alkyl tail. Chemical name main component AR143-(TBN)2: di-(tetra-n-butylammonium) salt of 1-benzoyl-4-[4'-(1'',1''-dimethylpropyl)-phenoxy]-6-phenylamino-2,7-dioxo-2,7-dihydro-3H-naphtho(1,2,3-de)quinolin, disulfonic acid

EC Number:

944-248-6

Molecular formula:

Combinations of mono (C40H31N2O7S1) bi (C40H30N2O10S2) and trivalent (C40H29N2O13S3) AR143 with TBN (C16H36N+)

IUPAC Name:

Reaction product of acid red 143 (free acid) or the respective sodium salt (e.g Lansyn red F-5B) (UVCB) with Tetrabutylammonium bromide (CAS nr.: 1643-19-2) resulting in a mixture of AR143-(TBN)2 (Main component), AR143-(TBN), AR143-(TBN)3, AR143-(TBN) without alkyl tail, AR143-(TBN)2 without alkyl tail. Chemical name main component AR143-(TBN)2: di-(tetra-n-butylammonium) salt of 1-benzoyl-4-[4'-(1'',1''-dimethylpropyl)-phenoxy]-6-phenylamino-2,7-dioxo-2,7-dihydro-3H-naphtho(1,2,3-de)quinolin, disulfonic acid

Test material form:

solid

Details on test material:

- Stabilisation: stable
- Safety precautions: The routine hygienic procedures were sufficient to assure personnel health and safety
- Colour: brownish red
- Storage conditions: room temperature

Specific details on test material used for the study:

The test item was used as delivered by the sponsor.
In order to ensure good skin contact, it was moistened with aqua ad injectionem (AlleMan Pharma, lot no. 601101, expiry date: 12/2018)
The vehicle was chosen due to its non-irritating characteristics.

Test animals

Species:

rabbit

Strain:

New Zealand White

Details on test animals or test system and environmental conditions:

The animals were derived from a controlled full-barrier maintained breeding system (SPF). According to the German Act on Animal Welfare the animals were bred for experimental purposes.

Test system

Type of coverage:

semiocclusive

Preparation of test site:

clipped

Remarks:

Approximately 24 hours before the test, the fur was removed from the dorsal area of the trunk by using an electric clipper. Care was taken to avoid abrading the skin, and only animals with healthy intact skin were used.

Vehicle:

other: aqua ad injectionem

Amount / concentration applied:

A dose of 0.5 g of the test item was applied to each test site.

Duration of treatment / exposure:

The test item was not expected to produce corrosion, but might be irritating. Therefore, a single patch was applied to one animal for 4 hours.

Observation period:

The animals were observed for 72 hours after the patch removal.

Number of animals:

2

Details on study design:

The test item was applied at a single dose to a small area (approximately 6 cm2) of skin on one side of the dorsal area and covered with a gauze patch, which was held in place with a non-irritating tape. The untreated other side served as control. The test item was applied to the patch first and then applied to the skin. To ensure good skin contact, the test item was moistened with the vehicle. The patch was fixed with a semi-occlusive dressing. The limits of the application site were marked with an ink marker.

Results and discussion

In vivo

Results

Results 1

Irritation parameter:

edema score

Basis:

mean

Time point:

other: 1 h

Score:

>= 0 - <= 1

Max. score:

1

Remarks on result:

other: pink/purple staining of the skin by the test substance

Results 2

Irritation parameter:

erythema score

Basis:

mean

Time point:

24 h

Score:

<= 0

Max. score:

0

Remarks on result:

other: pink/purple staining of the skin by the test substance

Applicant's summary and conclusion

Interpretation of results:

GHS criteria not met

Conclusions:

Under the conditions of the present study, the single dermal application of the test item MKP1003 to two rabbits at a dose of 0.5 g showed neither irritant nor corrosive effects.
Neither mortalities nor significant clinical signs of toxicity were observed.
According to Annex I of Regulation (EC) 1272/2008, the test item MKP1003 does not have to be classified and has no obligatory labelling requirement for skin irritation.
According to GHS (Globally Harmonized Classification System), the test item MKP1003 has no obligatory labelling requirement for skin irritation.