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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

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:
study well documented, meets generally accepted scientific principles, acceptable for assessment
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1955
Report date:
1955

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Not specified
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
(chloromethyl)vinylbenzene
EC Number:
250-005-9
EC Name:
(chloromethyl)vinylbenzene
Cas Number:
30030-25-2
Molecular formula:
C9H9Cl
IUPAC Name:
1-(chloromethyl)-3-ethenylbenzene; 1-(chloromethyl)-4-ethenylbenzene
Test material form:
liquid

Test animals

Species:
rabbit
Strain:
not specified
Sex:
not specified

Administration / exposure

Control animals:
not specified

Results and discussion

Effect levelsopen allclose all
Key result
Sex:
not specified
Dose descriptor:
LD100
Effect level:
1 000 mg/kg bw
Based on:
test mat.
Sex:
not specified
Dose descriptor:
LD0
Effect level:
500 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

Material Condition of skin No. of Application Site Response - Remarks
100% Intact 1 Ear Slight reddening of the skin, a trace of edema, and slight necrosis developing to scab and scar formation.
100% Intact 1 Belly Moderate reddening of the skin, trace of edema, moderate necrosis developing to scab and scar formation.
100% Abraded 1 Belly Moderate reddening of the skin, trace of edema, moderate necrosis developing to heavy scab and scar formation.
10 % in Dowanol 50 B Intact 10 Ear No response developing to a slight reddening of the skin and slight necrosis after 6 or 7 applications.
11 % in Dowanol 50 B Intact 4 Belly Essentially no response developing to moderate reddening of the skin and slight necrosis after 4 applications.
12 % in Dowanol 50 B Abrades 3 Belly Essentially no response developing to marked edema and necrosis after 3 applications with development of heavy scab and scar formation 

Skin contact - Absorption (24 hours Exposure)

Animal Preparation used Dose (g/kg) No. died / No. Treated Response - Remarks
Rabbit 10 % in propylene glycol 0.5 0/2 No apparent effect other than extensive scab and scar formation
Rabbit 10 % in propylene glycol 1.0 2/2 Death occurred in 1 day

Applicant's summary and conclusion

Interpretation of results:
other: Category 3 based on EU GHS
Conclusions:
The undiluted test material vinylbenzyl chloride has a severe effect on intact and abraded skin. Repeated, prolonged contact, over a period of 1 to 2 days is capable of causing marked to severe damage.
This material is markedly irritating and damaging to skin on prolonged or repeated contact. It has a moderate acute toxicity by skin absorption.
Executive summary:

The undiluted test material vinylbenzyl chloride has a severe effect on intact and abraded skin. Repeated, prolonged contact, over a period of 1 to 2 days is capable of causing marked to severe damage.

This material was found to be markedly irritating and damaging to skin on prolonged or repeated contact. It had a moderate acute toxicity by skin absorption. After 24 hours skin contact / absorption at a dose of 0.5 g/kg bw (10% solution in propylene glycol), no death and no apparent effect other than extensive scab and scar formation was noted in 2 out of 2 exposed animals. At a dose level of 1 g/kg bw 2 test animals died within 1 day. Based on these these observations, vinylbenzyl chloride was classified in Cat. 3 of acute dermal toxicity.