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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Physical & Chemical properties

Oxidising properties

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Administrative data

Endpoint:
oxidising properties
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable, well documented publication which meets basic scientific principles

Data source

Referenceopen allclose all

Reference Type:
other: EU Risk Assessment
Title:
European Union Risk Assessment Report 1,3-BUTADIENE, CAS No: 106-99-0, EINECS No:203-450-8
Author:
[ECB] European Chemicals Bureau
Year:
2002
Bibliographic source:
published; It can be accessed through the Europa Server (http://europa.eu.int).
Reference Type:
publication
Title:
Explosions in butadiene systems
Author:
Alexander DS
Year:
1959
Bibliographic source:
Ind Eng Chem 51: 733-738

Materials and methods

Principles of method if other than guideline:
EU Risk Assessment on the major component of C4 Hydrocarbons: 1,3-Butadiene
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Buta-1,3-diene
EC Number:
203-450-8
EC Name:
Buta-1,3-diene
Cas Number:
106-99-0
Molecular formula:
C4H6
IUPAC Name:
buta-1,3-diene
Details on test material:
- Name of test material (as cited in study report): 1,3-butadiene
- CAS number: 106-99-0
- EINECS number: 203-450-8

Results and discussion

Any other information on results incl. tables

EU Risk Assessment on the major component of C4 Hydrocarbons: 1,3-Butadiene:

Testing of oxidising properties of 1,3-butadiene is not applicable because it does not contain functional groups capable of producing an oxidising effect. However olefins with allylic hydrocarbons are prone to peroxide formation and 1,3-butadiene will readily form butadiene polyperoxide, (C4H6O2)x, in the presence of oxygen. At lower temperatures this is an alternating copolymer of butadiene and oxygen, although at elevated temperatures (>50°C) the proportion of oxygen decreases. Butadiene polyperoxide is nearly insoluble in liquefied butadiene and separates out to form ¿globules¿ which settle to form a viscous residue. Butadiene polyperoxide is prone to self-heating and above a critical radius will result in explosive decomposition (Alexander, 1959).

Applicant's summary and conclusion

Executive summary:

According to EU Risk Assessment Report (2002) the major component of C4 Hydrocarbons: 1,3 ¿butadiene does not have oxidising properties (it does not contain functional groups capable of producing an oxidising effect).