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Diss Factsheets

Toxicological information

Acute Toxicity: dermal

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Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data
Justification for type of information:
Data is from Publication.

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
A toxicological assessment of aryl alkyl alcohol
Author:
Belsito et al.
Year:
2012
Bibliographic source:
Food and Chemical Toxicology
Reference Type:
publication
Title:
Fragrance material review
Author:
Scognamiglio et al.
Year:
2012
Bibliographic source:
Food and Chemical Toxicology
Reference Type:
other: Peer reviewed journal
Title:
Fragrance raw materials monographs
Author:
D. L. J. Opdyke
Year:
1974
Bibliographic source:
Food and Cosmetics Toxicology
Reference Type:
other: authoritative database
Title:
Acute Dermal toxicity - Test chemical
Author:
U.S. National Library of Medicine
Year:
2018
Bibliographic source:
ChemIDplus
Reference Type:
other: Authoritative database
Title:
Toxicity of test chemical
Author:
IFA GESTIS
Year:
2018
Bibliographic source:
GESTIS Substance Database

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: As mentioned below
Principles of method if other than guideline:
Acute dermal toxicity study of the given test chemical was performed in rabbit.
GLP compliance:
not specified
Test type:
other: not specified
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4-methoxybenzyl alcohol
EC Number:
203-273-6
EC Name:
4-methoxybenzyl alcohol
Cas Number:
105-13-5
Molecular formula:
C8-H10-O2
IUPAC Name:
(4-methoxyphenyl)methanol
Details on test material:
- IUPAC Name: 4-methoxybenzyl alcohol
- Common Name: Anisyl alcohol
- InChI: 1S/C8H10O2/c1-10-8-4-2-7(6-9)3-5-8/h2-5,9H,6H2,1H3
- Smiles: c1(ccc(OC)cc1)CO
- Molecular formula :C8H10O2
- Molecular weight :138.165 g/mole
- Substance type:organic
- Physical state:Liquid, colorless to yellowish fruity odour.

Test animals

Species:
rabbit
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
not specified

Administration / exposure

Type of coverage:
other: Dermal
Vehicle:
not specified
Details on dermal exposure:
not specified
Duration of exposure:
not specified
Doses:
1.25, 2.5, and 5.0 g/kg.
No. of animals per sex per dose:
Groups of four rabbits
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 6 days
- Frequency of observations and weighing: Animals were observed for mortality and clinical signs.
Statistics:
not specified

Results and discussion

Preliminary study:
not specified
Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
3 000 mg/kg bw
Based on:
test mat.
95% CL:
1 940 - 4 060
Mortality:
Mortalities included one rabbit from the 2.5 g/kg group on day 1, and all four rabbits from the 5.0 g/kg group by day 6.
Clinical signs:
other: Clinical signs of toxicity included loss of coordination and muscle tone in two animals at 5.0 g/kg and one animal at 2.5 g/kg. Slight to moderate erythema and edema was also observed in all animals.
Gross pathology:
not specified
Other findings:
not specified

Applicant's summary and conclusion

Interpretation of results:
other: Not classified
Conclusions:
Acute dermal toxicity dose (LD50) value was considered to be 3.0 g/kg, with 95% confidence limits of 1.94–4.06 g/kg, when Groups of four rabbits were treated with the given test chemical by dermal application.
Executive summary:

Acute dermal toxicity study was conducted by using the given test chemical in Groups of four rabbits at the dose concentration of 1.25, 2.5, and 5.0 g/kg. Animals were observed for mortality and clinical signs for 6 days.

Mortalities included one rabbit from the 2.5 g/kg group on day 1, and all four rabbits from the 5.0 g/kg group by day 6. Clinical signs of toxicity included loss of coordination and muscle tone in two animals at 5.0 g/kg and one animal at 2.5 g/kg. Slight to moderate erythema and edema was also observed in all animals.

Hence, the LD50 value was considered to be 3.0 g/kg, with 95% confidence limits of 1.94–4.06 g/kg, when Groups of four rabbits were treated with the given test chemical by dermal application.