Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Acute oral toxicity was determined according to OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2005
Report date:
2005

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
GLP compliance:
yes (incl. QA statement)
Test type:
acute toxic class method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
1-Amino-1-cyclopropanecarbonitrile hydrochloride
EC Number:
629-718-8
Cas Number:
127946-77-4
Molecular formula:
C4H7N2Cl
IUPAC Name:
1-Amino-1-cyclopropanecarbonitrile hydrochloride
Constituent 2
Reference substance name:
1-aminocyclopropane-1-carbonitrile hydrochloride
IUPAC Name:
1-aminocyclopropane-1-carbonitrile hydrochloride

Test animals

Species:
rat
Strain:
other: Albino Rats (Rattus norvegicus)
Sex:
female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
-Source: Harlan, Indianapolis, IN.
-Age: at least 49 daysold (adult)
-Weight: 202.3 - 224.2 grams
-Fasting period before study: food was withheld from the animals the night prior to dosing.
-Housing: single housing, cages: polycarbonate, bedding: hardwood chips.
-Diet: TEK 7012 Rodent diet, Harlan teklad, Madison, WI, ad libitum
-Water: tap water, ad libitum
-Acclimation period: minimum 5 days under the same conditions as for the test.

ENVIRONMENTAL CONDITIONS
-Temperature: 68°F
-Humidity: 30-70%
-Air changes: 10 to 15 per hr
-Photoperiod: 12 hrs dark/light cycle, full spectrum fluorescent lights.

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Details on oral exposure:
Albino rats were used in this study because they have historically been used for acute oral toxicity studies and the guidelines have no alternative (non-animal) methods. The number of animals used was recommended by the OECD guidelines. Oral administration corresponds to a likely route of human exposure. The test was based on a stepwise procedure with the use of a minimum number of animals per step, enabling sufficient information to be obtained on the acute toxicity of the test substance.
Doses:
The test substance was a powder and formulated as a suspension using water.
A limit test was carried out at 2000mg/Kg body weight.
All animals dosed at 2000 died before the end of the study. According to OECD, the subsequent dose was reduced to 300mg/Kg.
No. of animals per sex per dose:
3 animals for 2000mg/Kg (female)
6 animals for 300mg/Kg (female)
Control animals:
no
Details on study design:
-Duration of observation period following administration: 14 days.
-Frequency of observations and weighing: at day 0, day 7 and day 14.
-Necropsy of survivors performed: yes.
-Other examinations performed: clinical signs and body weight.

Results and discussion

Preliminary study:
All animals dosed at 2000 died before the end of the study. According to OECD, the subsequent dose was reduced to 300mg/Kg.
Effect levels
Sex:
female
Dose descriptor:
LDLo
Effect level:
> 300 mg/kg bw
Mortality:
At 300mg/Kg:
All animals survived the duration of the study (14 days).
Clinical signs:
other: At 300mg/Kg: No clinical manifestations of toxicity were observed in any of the animals at this dose for the duration of the in-life phase.
Gross pathology:
No unusual findings were found during necropsy in all animals dosed at 300mg/Kg.

Applicant's summary and conclusion

Interpretation of results:
harmful
Remarks:
Migrated information Criteria used for interpretation of results: OECD GHS
Conclusions:
The test substance as defined under the GHS for the classification of chemicals falls under Category 4, >300-2000.