Amines, C12-18-(even numbered) and C18-(unsaturated) alkyl

Acute Toxicity: oral

Administrative data

Endpoint:

acute toxicity: oral

Type of information:

experimental study

Adequacy of study:

key study

Study period:

13 Jun - 07 Jul 1983

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: Guideline study according to GLP

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

1983

Report date:

1983

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 401 (Acute Oral Toxicity)

GLP compliance:

yes

Test type:

standard acute method

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

Amines, coco alkyl

EC Number:

262-977-1

EC Name:

Amines, coco alkyl

Cas Number:

61788-46-3

IUPAC Name:

61788-46-3

Constituent 2

Reference substance name:

Coco Alkylamines

IUPAC Name:

Coco Alkylamines

Details on test material:

- Name of test material (as cited in study report): Armeen C

Test animals

Species:

rat

Strain:

other: BOR: WISW; SPF TNO

Sex:

male/female

Details on test animals or test system and environmental conditions:

TEST ANIMALS
- Source: Firma Winkelmann, Versuchstierzucht, 4791 Borchen 1, Gartenstraße 300, Germany
- Weight at study initiation: males: 170.1 - 190.8 g; females: 140.0 - 162.6 g
- Fasting period before study: The day before treatment, the animals were fasted for a period of 16 hours and received food 4 hours after treatment.
- Housing: in Makrolone cages (type III), max. 5 animals per cage
- Diet (e.g. ad libitum): pellets, Ssniff-R diet for rats (Ssniff Versuchstier-Diäten GmbH, 4770 Soest, Germany)
- Water (e.g. ad libitum): tap water; ad libitum; analytical controls were made periodically
- Acclimation period: approx. 7 days

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21 ± 2
- Humidity (%): 45-55
- Photoperiod (hrs dark / hrs light): 12/12

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

other: oleum arachidis

Details on oral exposure:

VEHICLE
- Concentration in vehicle: 20% dilution of the test substance in oleum arachidis; pH 8.1

Doses:

range finding study: 1000, 2500, 5000 mg/kg
main study: 500, 1000, 1500, 2000 mg/kg

No. of animals per sex per dose:

range finding study: 2 female animals per dose
main study: 5 animals per sex per dose

Control animals:

not specified

Details on study design:

- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: clinical signs: 20 min, 1 + 2 h, 3 + 6 h, 24 h, 48 h, 72 h and 7/14 d after treatment; weighing: at day 0 and at day 14
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight, macroscopic examination of the main organs

Statistics:

The LD50 was calculated according to a Probit Analysis, Finney´s method. (Probit Analysis, 3rd edition, Cambridge 1971)

Results and discussion

Preliminary study:

range finding study:
1000 mg/kg: 1/2 (3 days after application)
2500 mg/kg: 2/2 (4 days after application)
5000 mg/kg: 2/2 (4 days after application)

Effect levels

Effect levels 1

Sex:

male/female

Dose descriptor:

LD50

Effect level:

1 300 mg/kg bw

Effect levels 2

Sex:

male

Dose descriptor:

LD50

Effect level:

1 240 mg/kg bw

Effect levels 3

Sex:

female

Dose descriptor:

LD50

Effect level:

1 388 mg/kg bw

95% CL:

1 119 - 4 440

Mortality:

500 mg/kg: male: 1/5; female: 0/5 (48 hours after administration: one male animal died)
1000 mg/kg: male: 1/5; female: 1/5 (48 hours after administration: one male animal died; 5 days after administration: one female animal died)
1500 mg/kg: male: 2/5; female: 2/5 (48 hours after administration: one male and one female animal died; 5 days after administration: a further male and female animal died)
2000 mg/kg: male: 5/5; female: 5/5 (48 hours after application: 2 male animals and one female died; 5 days after application: all males were died; 7/14 days after application: all females were died)

Clinical signs:

other: at all doses: reduced consciousness with apathy, abnormal position and poor posture, loss of coordination (reduced excitability), cyanosis, limited but extreme salivation, piloerection, slightly reduced breathing rate, slight hypothermia The clinical sign

Gross pathology:

Macroscopic examinations of died animals (during the study period) showed slight redness and accumulation of fluid in the gastrointestinal tract.
Macroscopic examinations of sacrificed animals (at the end of the study) revealed no abnormalities of the main organs.

Applicant's summary and conclusion

Interpretation of results:

harmful

Remarks:

Migrated information Criteria used for interpretation of results: EU

Conclusions:

Based on the study results, the median lethal dose (LD 50) of Armen C is

Executive summary:

In an OECD TG 401 study, the test material Armeen C, a clear light-yellow, oily liquid, was orally applied to Wistar rats at doses of 500, 1000, 1500 and 2000 mg/kg bw. The substance was applied as a 20% solution in peanut oil (pH 8.1). At 500 mg/kg bw, two males died 5 and 7 days after treatment, respectively. At 1000 mg/kg bw, two males and two females died between days 5-14 (40%). At 1500 mg/kg bw, four males and four females and at 2000 mg/kg bw (80%), ten males and nine females died between days 5-14 (95%). An LD50 of 1300 mg/kg bw (1240 mg for male and 1390 mg for female rats) was calculated (probit analysis after Finney). Clinical signs, observed in all treatment groups, included apathia, slight to pronounced irregular postures, uncoordinated movements, reduced reflexes, cyanosis, salivation, piloerection, slightly reduced breathing rate and some cases of slight hypothermia. Symptoms started from 20 minutes after dosing on and were present until death or up to 7 days in survivors. After dissection of dead animals, slight reddening and liquid congregations were detected in the gastrointestinal tract. There were no pathological findings in the surviving animals.