Orthoboric acid, compound with 2,2',2''-nitrilotriethanol

Skin irritation / corrosion

Administrative data

Endpoint:

skin irritation: in vivo

Type of information:

migrated information: read-across from supporting substance (structural analogue or surrogate)

Adequacy of study:

key study

Study period:

72 hours

Reliability:

1 (reliable without restriction)

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1993

Report date:

1993

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

other: commision directive: 84/449/EEC 1984

Deviations:

no

GLP compliance:

yes (incl. QA statement)

Test material

Test material information

Constituent 1

Reference substance name:

Orthoboric acid, compound with 2-aminoethanol

EC Number:

247-421-8

EC Name:

Orthoboric acid, compound with 2-aminoethanol

Cas Number:

26038-87-9

Molecular formula:

C2H7NO.xBH3O3

IUPAC Name:

orthoboric acid, compound with 2-aminoethanol

Details on test material:

- Name of test material (as cited in study report):Monoethanolamine polyborate
- Molecular formula (if other than submission substance):
- Molecular weight (if other than submission substance):
- Smiles notation (if other than submission substance):
- InChl (if other than submission substance):
- Structural formula attached as image file (if other than submission substance): see Fig.
- Substance type:
- Physical state:yellow viscous liquid
- Analytical purity:
- Impurities (identity and concentrations):
- Composition of test material, percentage of components:
- Isomers composition:
- Purity test date:
- Lot/batch No.:PM672
- Expiration date of the lot/batch:
- Radiochemical purity (if radiolabelling):
- Specific activity (if radiolabelling):
- Locations of the label (if radiolabelling):
- Expiration date of radiochemical substance (if radiolabelling):
- Stability under test conditions:
- Storage condition of test material:
- Other:

Test animals

Species:

rabbit

Strain:

New Zealand White

Details on test animals or test system and environmental conditions:

Healthy female New Zealand White rabbits were obtainedfrom Froxfield Farms (UK) Ltd, Froxfield, Hampshire, and on arrival animals were identified with metal ear tags. Animals were allowed an acclimitisation period of at least five days.
The rabbits were individually housed in grid bottomed metal cages. An antibiotic-free rabbit diet (SQC Standard rabbit pellets produced by Special Diets Services, With am, Essex) and mains drinking water via an automatic watering system were freely available. Certificates of analysis for both diet and drinking water are held on file at Toxicol laboratories.

The rabbit holding room was air conditioned with temperature in the range 17-20 deg. C and relative humidity in the range 37-51% during the acclimitisation and study periods.

Test system

Type of coverage:

semiocclusive

Preparation of test site:

other: clipped

Vehicle:

unchanged (no vehicle)

Controls:

not required

Amount / concentration applied:

TEST MATERIAL
- Amount(s) applied (volume or weight with unit):0.5g
- Concentration (if solution):

VEHICLE
- Amount(s) applied (volume or weight with unit):
- Concentration (if solution):
- Lot/batch no. (if required):
- Purity:

Duration of treatment / exposure:

4 hours

Observation period:

72 hours

Number of animals:

3 female

Details on study design:

One hour after the removal of the patches and test article, the treated sites were assessed for signs of reaction to treatment. Similar examinations were made 24, 48 and 72 hours after patch removal.

Results and discussion

In vivo

Results

Results 1

Irritation parameter:

erythema score

Basis:

mean

Time point:

24/48/72 h

Score:

<= 0

Max. score:

0.3

Reversibility:

no data

Results 2

Irritation parameter:

edema score

Basis:

mean

Time point:

24/48/72 h

Score:

<= 0

Max. score:

0

Reversibility:

no data

Irritant / corrosive response data:

1 hour observation
Rabbit number Erythema Oedema Comments
660 0 0 None
677 0 0 None
678 1 0 None
24 hour observation
Rabbit number Erythema Oedema Comments
660 0 0 None
677 0 0 None
678 1 0 None
48 hour observation
Rabbit number Erythema Oedema Comments
660 0 0 None
677 0 0 None
678 0 0 None
72 hour observation
Rabbit number Erythema Oedema Comments
660 0 0 None
677 0 0 None
678 0 0 None

Other effects:

none

Any other information on results incl. tables

Mean scores for erythema and oedema (calculated from the values recorded at the 24,48 and 72 hour readings) were used.

Applicant's summary and conclusion

Interpretation of results:

not irritating

Remarks:

Migrated information Criteria used for interpretation of results: EU

Conclusions:

According to the criteria described in EEC Commision Directive 91/325/EEC of 1st March 1991, the test article would not require labelling with either of the risk phrases "R34 Causes burns" or "R38 Irritating to skin" under the conditions of this study.

Executive summary:

The purpose of this study was to assess the degree of irrititaion produced by the test article when applied to the skin of the albino rabbit. The procedures e used were in accordance with EEC Annex V guidlines.

A 0.5 aliquot of the test article was applied over a previouslly clipped area of about 6 sq cm of the dorsal skin of each of 3 albino rabbits. The test article was held in contact with the skin, under a semi-occlusive patch assembly, for a 4 hour period. The patches were then removed and skin reaction assessed after one, 24, 48 and 72 hours.

The treated site on 2 of the 3 rabbits remained free from apparent irritation throughout the 72 hour observation period. A barely perceptable erythema was noted at the treated site on the third animal one and 24 hours after patch removal but was no longer apparent at the 48 and 72 hour examinations.

The test article did not produce significant irritation in any animal.

According to the criteria described in EEC Commision Directive 91/325/EEC of 1st March 1991, the test article would not require labelling with either of the risk phrases "R34 Causes burns" or "R38 Irritating to skin" under the conditions of this study.

NOTE: Any of data in this dataset are disseminated by the European Union on a right-to-know basis and this is not a publication in the same sense as a book or an article in a journal. The right of ownership in any part of this information is reserved by the data owner(s). The use of this information for any other, e.g. commercial purpose is strictly reserved to the data owners and those persons or legal entities having paid the respective access fee for the intended purpose.