Registration Dossier

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
calculation (if not (Q)SAR)
Adequacy of study:
key study
Study period:
July 2020
Reliability:
2 (reliable with restrictions)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2020
Report date:
2020

Materials and methods

Test guideline
Qualifier:
no guideline required
Principles of method if other than guideline:
FDA T.E.S.T Model: Predicted Oral rat LD50 for C14H29N2O3_1594816693124 for Nearest neighbor method
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
(carboxymethyl)dimethyl-3-[(1-oxooctyl)amino]propylammonium hydroxide
EC Number:
277-600-6
EC Name:
(carboxymethyl)dimethyl-3-[(1-oxooctyl)amino]propylammonium hydroxide
Cas Number:
73772-46-0
Molecular formula:
C14H30N2O3
IUPAC Name:
(carboxymethyl)dimethyl-3-[(1-oxooctyl)amino]propylammonium hydroxide
Test material form:
liquid

Test animals

Species:
rat

Results and discussion

Effect levels
Key result
Dose descriptor:
LD50
Effect level:
3 091.8 mg/kg bw
Based on:
test mat.

Applicant's summary and conclusion