1-Propanaminium, 3-amino-N-ethyl-N,N-dimethyl-, N-lanolin acyl derivs., Et sulfates

Endpoint summary

Description of key information

Based on the results of the read across study, the oral LD50 value of the test substance, 'iso and anteiso C10-40 AAP EDM-ES' was considered to be >2350 mg/kg bw, indicating low acute toxicity potential.

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records

Reference

Endpoint:

acute toxicity: oral

Type of information:

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

Adequacy of study:

key study

Study period:

January 1983

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

guideline study with acceptable restrictions

Justification for type of information:

Refer to section 13 of IUCLID for details on the read-across justification. The study with the read across substance is considered sufficient to fulfil the information requirements as further explained in the provided endpoint summary.

Reason / purpose for cross-reference:

read-across source

Qualifier:

equivalent or similar to guideline

Guideline:

OECD Guideline 401 (Acute Oral Toxicity)

Deviations:

not specified

GLP compliance:

not specified

Test type:

standard acute method

Limit test:

yes

Species:

rat

Strain:

Sprague-Dawley

Sex:

male/female

Details on test animals or test system and environmental conditions:

Test substance
- Age at study initiation: no data
- Weight at study initiation: m: 125 - 135g; f: 110 - 125g
- Fasting period before study: over night
- Housing: single caging, cage type: Macrolon type IlI./max. 5
- Diet: ad libitum; rat diet (R 4 Alleindiät für Ratten), Ssniff Spezialdiäten GmbH, 4770 Soest/Westfalen
- Water: ad libitum
- Acclimation period: 11 d

Environment conditions
- Temperature (°C): 20 - 23
- Humidity (%): 40 - 70
- Air changes (per hr): 10 per h
- Photoperiod (h dark / h light): 12 h daily

Route of administration:

oral: gavage

Vehicle:

water

Details on oral exposure:

Vehicle
- Concentration in vehicle: 500 mg/mL
- Amount of vehicle (if gavage): 10 mL/kg bw
The test substance was weighed out in a glass, then was filled with Aqua destillata up to the desired volume, was shaken well and afterwards labeled. The formulated test substance was a clear solution.

Doses:

5000 mg/kg bw

No. of animals per sex per dose:

5 males and 5 females

Control animals:

no

Details on study design:

The group of 5 female and 5 male rats were were given a single oral dose 5000 mg/kg of the test substance by gavage.

- Duration of observation period following administration: 14 d
- Body weights were recorded before treatment (Day 1), at the treatment day (Day 0), and on Days 7 and 14 after treatment
- Clinical observation: Animals were observed 1/4 h, 1/2 h, 1 h, 2 h, 4 h after dosing and thereafter once daily up to day 14.
- Necropsy of the survivors performed: yes

Statistics:

As none of the test animals died a calculation of the LD50 was not possible.

Key result

Sex:

male/female

Dose descriptor:

LD50

Effect level:

> 5 000 mg/kg bw

Based on:

test mat.

Remarks on result:

other: mortality 0/10

Key result

Sex:

male/female

Dose descriptor:

LD50

Effect level:

> 2 350 mg/kg bw

Based on:

act. ingr.

Remarks on result:

other: mortality 0/10

Mortality:

There were no mortalities.

Clinical signs:

other: Except of ruffled fur on the day of treatment, the animals were free of clinical-/toxicological symptoms during the entire observation period of 14 d.

Gross pathology:

Necropsies were performed on all animals at the end of the 14 d observation period. In one animal a slight thickening of the stomach mucosa could be observed. Necropsies of all other animals showed no test compound related macroscopic findings in the cranial, thoracic and abdominal cavity.

Interpretation of results:

other: Not classified based on EU CLP criteria

Conclusions:

Based on the results of read across study, the oral LD50 for the test substance was determined to > 2350 mg/kg bw.

Executive summary:

A study was conducted to determine the acute oral toxicity of the read across substance, 'C11-unstad. AAP TMA-MS (active: 47%)', according to the study similar to OECD Guideline 401.In the study, 5 male and 5 female Sprague-Dawley rats were given a single dose of the test substance at a dose of 5000 mg/kg bw (limit test). The test substance was formulated in water and applied in a volume of 10 mL/kg bw. Animals were subsequently observed for 14 consecutive days. There were no deaths following a single oral dose of the test substance. Except of ruffled fur on the day of treatment, the animals were free of clinical/ toxicological signs during the entire observation period of 14 d. Necropsies were performed on all animals at the end of the 14 d observation period. In one animal a slight thickening of the stomach mucosa could be observed. Necropsies of all other animals showed no test compound related macroscopic findings in the cranial, thoracic and abdominal cavity. Under the study conditions, the oral LD50 value of the test substance was determined to be >5000 mg/kg bw (i.e., equivalent to > 2350 mg a.i./kg bw) (Meisel, 1983). Based on the results of read across study, similar oral LD50 value is considered for the test substance, 'iso and anteiso C10-40 AAP EDM-ES'.

Endpoint conclusion

Endpoint conclusion:

no adverse effect observed

Dose descriptor:

LD50

Value:

2 350 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion

Endpoint conclusion:

no study available

Acute toxicity: via dermal route

Endpoint conclusion

Endpoint conclusion:

no study available

Additional information

A study was conducted to determine the acute oral toxicity of the read across substance, 'C11-unstad. AAP TMA-MS' (active: 47%), according to the study similar to OECD Guideline 401.In the study, 5 male and 5 female Sprague-Dawley rats were given a single dose of the test substance (a.i. 47 %) at a dose of 5000 mg/kg bw (limit test). The test substance was formulated in water and applied in a volume of 10 mL/kg bw. Animals were subsequently observed for 14 consecutive days. There were no deaths following a single oral dose of the test substance. Except of ruffled fur on the day of treatment, the animals were free of clinical/ toxicological signs during the entire observation period of 14 d. Necropsies were performed on all animals at the end of the 14 d observation period. In one animal a slight thickening of the stomach mucosa could be observed. Necropsies of all other animals showed no test compound related macroscopic findings in the cranial, thoracic and abdominal cavity. Under the study conditions, the oral LD50 value of the test substance was determined to be >5000 mg/kg bw (i.e., equivalent to > 2350 mg a.i./kg bw) (Meisel, 1983). Based on the results of read across study, similar oral LD50 value is considered for the test substance, 'iso and anteiso C10-40 AAP EDM-ES'.

Justification for classification or non-classification

Based on the results of an acute oral toxicity read across study, the test substance, 'iso and anteiso C10-40 AAP EDM-ES', does not warrant classification for acute oral toxicity, according to the EU CLP criteria (Regulation 1272/2008/EC).