1-Propanaminium, N-(carboxymethyl)-3-(formylamino)-N,N-dimethyl-, inner salt

Acute Toxicity: oral

Administrative data

Endpoint:

acute toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Study period:

06. Jun. 2005 - 22. Jun. 2005

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: GLP guideline study

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2005

Report date:

2005

Materials and methods

Test guideline

Test guideline 1

Qualifier:

according to guideline

Guideline:

OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)

Deviations:

no

Test guideline 2

Qualifier:

according to guideline

Guideline:

EU Method B.1 tris (Acute Oral Toxicity - Acute Toxic Class Method)

Deviations:

no

GLP compliance:

yes

Test type:

acute toxic class method

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

-

EC Number:

480-680-7

EC Name:

-

Cas Number:

120128-90-7

Molecular formula:

Hill formula: C8H16N2O3 CAS formula: C8H16N2O3

IUPAC Name:

480-680-7

Test animals

Species:

rat

Strain:

Wistar

Sex:

female

Details on test animals or test system and environmental conditions:

Species: rat
Breed: White Wistar
Breeder: Harlan Winkelmann, Borchen, Germany
Date of receipt: 2005-05-31
Number / Sex: 12 female
Body weights: 159.9 - 180.7 g at day of application
Age: about 8 weeks at day of application
Identification: dye marks and cage numbers
Diet: Altromin International, Lage, Germany, Type 1324 - 1188,
Water: Drinking water consisted of normal tap water from municipal sources (Stadtische Werke Krefeld AG, Krefeld, Germany). The water was monthly examined for pollutants which might interfere with the study. The data are retained in the archive.
Bedding material: Lignocel BK 10/20, Rettenmaier & Sohne GmbH & Co., Batch 02101 40915
Experimental animals:
Young healthy rats acclimatized for at least 5 days to laboratory conditions were used for this test. During the acclimatization period animals were observed for their health condition to assure that they were in best condition for this investigation. Only female rats were used.
Husbandry:
Three rats were housed in one Makrolon cage type VI each. A non-barrier system with air condition was used. The air conditioning had following nominal values: Temperature: 22°C ± 3°C, Humidity: 30 - 70 %. Climate control was run automatically. The lighting was in a 12-hour light/dark-cycle. Temperature and humidity were recorded continuously using a thermohygrometer, Lambrecht GmbH, Gottingen, Germany. The data were archived. There has been a deviation from nominal humidity values. On 2005-06-17 and 2005-06-18 the humidity was slightly higher (up to 75 %). However, this deviation is not supposed to have any effect on the experimental result.

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

water

Details on oral exposure:

The starting dose of 300 mg/kg body weight was applied to six female animals as 10 % (w/w) solution in tap water. Therefore 1.5 g of the test substance were added to 13.5 g tap water and mixed on a magnetic stirrer. The density of the 10 % solution was 1.025 g/ml and of the undiluted test substance 1.22 g/ml. The density of the undiluted test sUbstance was higher than 1.05 g/ml and therefore was considered in calculation of the application volume. The dose of 2000 mg/kg body weight was applied to six female animals with the undiluted test substance.
Dose volume: 300 mg/kg group: 0.48 - 0.51 mL; 2000 mg/kg: 0.27 - 0.30 mg/kg.

Doses:

300 mg/kg, 2000 mg/kg

No. of animals per sex per dose:

6 animals per dose (female only)

Control animals:

no

Details on study design:

- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Clinical examination was performed immediately, 0.5, 1.5 and 3.5 hours after test substance administration and thereafter daily; weighing at day 0, day 7, day 14
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight

Results and discussion

Effect levels

Effect levels 1

Sex:

female

Dose descriptor:

LD50

Effect level:

> 2 000 mg/kg bw

Based on:

test mat.

Effect levels 2

Sex:

female

Dose descriptor:

LD50

Effect level:

> 1 000 mg/kg bw

Based on:

other: solid matter (incl. NaCl)

Effect levels 3

Sex:

female

Dose descriptor:

LD50

Effect level:

> 830 mg/kg bw

Based on:

act. ingr.

Remarks on result:

other: test substance Formamidopropyldimethylbetain 50 %ig (50 %ig based on solid matter, active matter: 41.5 %)

Mortality:

No mortality occured.

Clinical signs:

No clinical signs observed

Body weight:

The body weight development of the animals was positive and within normal ranges.

Gross pathology:

The necropsy 14 days after application showed no substance related morphological visible pathologic organ findings.

Any other information on results incl. tables

Body weights

Animal ID	Sex	Dose [mg/kg]	Day 0 [g]	Mean±SD	Day 7 [g]	Mean±SD	Day 14 [g]	Mean±SD	Average weight gain [%]
425	F	300	168.4	165.6 ±3.8	190.7	186.0 ±9.6	197.6	198.0 ±7.6	+ 19.6
425 RV	F	300	166.8		183.8		197.7
425 RH	F	300	161.6		171.0		185.7
426	F	300	169.2		183.3		201.1
426 RV	F	300	159.9		187.2		196.8
426 RH	F	300	167.4		200.0		209.3
427	F	2000	173.7	171.2 ±5.8	196.0	191.7 ±8.6	208.7	204.7 ±6.1	+ 19.6
427 RV	F	2000	165.4		180.0		197.3
427 RH	F	2000	166.4		185.3		198.0
428	F	2000	180.7		204.3		212.9
428 RV	F	2000	167.9		189.8		205
428 RH	f	2000	173.0		194.7		205.9

Applicant's summary and conclusion

Interpretation of results:

practically nontoxic

Remarks:

Migrated information Criteria used for interpretation of results: expert judgment

Conclusions:

The LD50-value of the test substance Formamidopropyldimethylbetain 50 %ig is greater than 2000 mg/kg body weight.

Executive summary:

The test substance Formamidopropyldimethylbetain 50 %ig (50 %ig based on solid matter, active matter: 41.5 %) is a clear yellowish liquid. For labelling and classification purposes Formamidopropyldimethylbetain 50 %ig was tested regarding its acute toxic potential following oral application. Slight acute oral toxicity of Formamidopropyldimethylbetain 50 %ig was expected. Therefore the starting dose of 300 mg/kg body weight was chosen in the Acute-Toxic-Class-Method procedure, according to the OECD Guideline for the Testing of Chemicals No. 423 "Acute Oral Toxicity - Acute Toxic Class Method". A total of twelve female rats of the strain White Wistar were used in the study. The test substance Formamidopropyldimethylbetain 50 %ig was applied by gavage undiluted and as 10 % (w/w) solution in tap water. No toxic symptoms after administration of 300 mg/kg body weight were observed in six animals. In the next step the test substance Formamidopropyldimethylbetain 50 %ig was applied to six rats at a dose level of 2000 mg/kg body weight. No toxic symptoms were observed in this group, as well. No death occurred in all groups of the dose levels 300 mg/kg and 2000 mg/kg body weight. Body weight development of all animals was positive 7 days and 14 days post application. The necropsy 14 days after oral application showed no substance related morphological visible pathologic organ findings. Thus, the LD50-value for the test substance Formamidopropyldimethylbetain 50 %ig is higher than 2000 mg/kg. Therefore, the test substance Formamidopropyldimethylbetain 50 %ig has not to be classified according to the Globally Harmonised System. According to the guidance on classification as given in the Commission Directive 2004/73/EC the test substance Formamidopropyldimethylbetain 50 %ig has to be graded as not acute toxic by oral route.