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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Basic toxicokinetics

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Administrative data

Endpoint:
basic toxicokinetics in vitro / ex vivo
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable, well documented publication which meets basic scientific principles.

Data source

Reference
Reference Type:
publication
Title:
The reduction of hydroxylamine and some aryl hydroxomates by liver mitochondria from mammals and birds.
Author:
Bernheim, M.L.C.
Year:
1972
Bibliographic source:
Enzymologia, 43, 167-176

Materials and methods

Objective of study:
metabolism
Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
In-vitro test system with mitochondrial preparations from various liver sources, warm-blooded animals (mammals and birds) as well as from fish, reptiles, and amphibians. The enzymatic reduction of hydroxylamine and anthranilic hydroxamate with mitochondrial hydroxylamine reductase in the presence of NADH was considered.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Hydroxylammonium chloride
EC Number:
226-798-2
EC Name:
Hydroxylammonium chloride
Cas Number:
5470-11-1
Molecular formula:
ClH.H3NO
IUPAC Name:
hydroxyammonium chloride
Details on test material:
- Name of test material (as cited in study report): hydroxylamine, stored as the hydrochloride
- Stability under test conditions / Storage condition of test material: Hydroxylamine was stored as the hydrochloride at 4°C as a 0.1 M solution, and was stable for many months (it was diluted and neutralized just before use)
Radiolabelling:
no

Results and discussion

Applicant's summary and conclusion