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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Repeated dose toxicity: dermal

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Administrative data

Endpoint:
short-term repeated dose toxicity: dermal
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: Unsuitable test system

Data source

Reference
Reference Type:
publication
Title:
Effect of anti-flame treating agents on the skin
Author:
Aoyama M
Year:
1975
Bibliographic source:
Nagoya Med. J., vol 20, No. 1, 11-19

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Chemical was applied to the dorsal skin of rats every day during 20 days, and the changes were observed.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Tetrakis(hydroxymethyl)phosphonium chloride
EC Number:
204-707-7
EC Name:
Tetrakis(hydroxymethyl)phosphonium chloride
Cas Number:
124-64-1
Molecular formula:
C4H12O4P.Cl
IUPAC Name:
tetrakis(hydroxymethyl)phosphonium chloride
Details on test material:
- Name of test material (as cited in study report): tetrakis (hydroxymethyl) phosphonium chloride (THPC)
no other data

Test animals

Species:
rat
Strain:
other: white
Sex:
male

Administration / exposure

Type of coverage:
not specified
Vehicle:
not specified
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
20 days
Frequency of treatment:
daily
Doses / concentrations
Remarks:
Doses / Concentrations:
15, 20 and 30 %
Basis:

No. of animals per sex per dose:
4 males per dose
Control animals:
yes
Details on study design:
The test item was applied with a brush to cervico-dorsal region of the rats. A volume of 0.75 ml was applied to 3 x 3 cm unshaved area of the cervicodorsal skin once a day, for 20 days. It was observed wether the application of each agent would cause any skin reactions or not and how intense they would be.

Results and discussion

Results of examinations

Details on results:
Group A (15 %): The application of the test agent (THPC) caused redness on the 4th day, but because of marked loss in body weight of the animals, the application was discontinued on the 8th day, and the animals were sacrificed and necropsied on the 12th day of beginning of application. Inconsistency between text and table: the table in the publication provides observation results for this group also on days 12 to 20.

Group B (20 %): The animals of Group B showed similar responses to those of Group A.

Group C (30 %): The application of THPC caused slight redness to manifest on the second day, and this skin reaction was intensified on the 6th day; partial falling-off hair occured on the 7th day; the application of the test agent was discontinued on the 8th day, but all animals of this group showed marked losses of body weight and eventually died 9 days after the beginning of the application.

Control (distilled water): no skin reaction at all throughout the course of the experiment.

The histopathologic examinations showed that the THPC caused atrophy or enhanced keratinization of the epidermis and degenaration of hair roots to occurred in all of group A, B and C.

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion