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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: other routes
Type of information:
experimental study
Adequacy of study:
other information
Study period:
08. Mar 1966 - 21. Mar 1966
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable, well-documented study report which meets basic scientific principles.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1966
Report date:
1966

Materials and methods

Principles of method if other than guideline:
other: BASF-Test
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,1',1''-nitrilotripropan-2-ol
EC Number:
204-528-4
EC Name:
1,1',1''-nitrilotripropan-2-ol
Cas Number:
122-20-3
Molecular formula:
C9H21NO3
IUPAC Name:
1-[bis(2-hydroxypropyl)amino]propan-2-ol
Test material form:
solid
Specific details on test material used for the study:
- Analytical purity: ca. 92-95 %
- Impurities (identity and concentrations): ca. 3-6 % Diisopropanolamine; < 1 % Monoisopropanolamine

Test animals

Species:
mouse
Strain:
other: Kisslegg-mice
Sex:
male/female

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
water
Doses:
200, 400, 800, 1000, 1250, 1600 mg/kg
No. of animals per sex per dose:
5
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 1 400 mg/kg bw
Mortality:
1600 mg/kg: all animals died within the first 24 h.
1250 mg/kg: 1 female died within 24 h.
Clinical signs:
1600 mg/kg:
15 min post application: abdominal position, fluffed fur, intermittent respiration.
25 min post application: slight tremulous convulsions, abdominal position, accelerated respiration, mouth discharge, partly dyspnoea.

1250 and 1000 mg/kg:
15 min post application: staggering, accelerated respiration, abdominal position, flattened ears.
1 and 2 days post application: heavy ruffled fur, accelerated respiration, high stepping tremulous gait.
3 and 4 days post application: accelerated respiration, high stepping tremulous gait.

800 and 400 mg/kg:
10 min post application: high stepping, hoppling gait, accelerated respiration, gaunted sides, flattened ears, animals don´t continue in abominal position.
5 h and 1 day post application: abdominal position, heavy fluffed fur, gaunted sides, very calm attitude.

200 mg/kg: 5 h post application fluffed fur and accelerated respiration.
Gross pathology:
1250 mg/kg: 6x agglutination of intestinal loops.
800 mg/kg: 2x agglutination of intestinal loops.

Any other information on results incl. tables

Mortality:

Dose (mg/kg)  Conc. (%)  1 h  24 h  48 h  7 days  14 days
 1600  20  0/10  10/10  10/10  10/10  -
 1250  8  0/10  1/10  1/10  1/10  -
 1000  8  0/10  0/10  0/10  0/10  -
 800  8  0/10  0/10  0/10  0/10  -
 400  8  0/10  0/10  0/10  0/10  -
 200  2  0/10  0/10  0/10  0/10  -

Applicant's summary and conclusion