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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
other: Letter of Access (See Section 13)
Adequacy of study:
key study

Data source

Reference
Reference Type:
other: Letter of Access (See Section 13)
Title:
Unnamed
Year:
1995
Report date:
1995

Materials and methods

Test guideline
Guideline:
EU Method B.1 (Acute Toxicity (Oral))
GLP compliance:
not specified
Remarks:
Letter of Access only
Test type:
acute toxic class method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
417-560-0
EC Name:
-
Cas Number:
67881-98-5
Molecular formula:
C11H22NO6P
IUPAC Name:
trimethyl[2-({2-[(2-methylprop-2-enoyl)oxy]ethyl phosphonato}oxy)ethyl]azanium

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
5 animals of each sex were tested during this study.

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
water
Doses:
Each test animan was dosed with 2000 mg/kg HEMA-PC
No. of animals per sex per dose:
5
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Remarks on result:
other: No 95% CL available due to results
Mortality:
No mortalities were observed during this study.
Clinical signs:
other: Pilo erection was observed in all rats within five minutes of dosing. This was accompanied at later intervals on day 1 by abnormal body carriage (hunched posture) Recovery of all animals was complete by day 2.
Gross pathology:
No abnormalities were recorded at the macroscopic examination on day 15.

Any other information on results incl. tables

Table 1. Results of Acute Toxicity: Oral Test

Sex

Dose (mg/kg)

Number of Animals

Number of Deaths

Male

2000

5

0

Female

2000

5

0

Applicant's summary and conclusion

Interpretation of results:
study cannot be used for classification
Remarks:
Migrated information
Conclusions:
The results of this study indicate that HEMA-PC is not classified as toxic, as the LD50 was determined to be >2000 mg/kg HEMA-PC.
Executive summary:

The oral acute toxicity of HEMA-PC was conducted using EU Method B.1 (Acute Toxicity - Oral).

The results of this study indicate that HEMA-PC is not classified as toxic, as the LD50 was determined to be >2000 mg/kg HEMA-PC.