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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Environmental fate & pathways

Additional information on environmental fate and behaviour

Administrative data

Endpoint:
additional information on environmental fate and behaviour
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment
Cross-reference
Reason / purpose for cross-reference:
reference to same study
Reference
Endpoint:
biotransformation and kinetics
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment
Qualifier:
no guideline available
Principles of method if other than guideline:
- Principle of test: Quantification of metabolites formed during degradation of 2-butoxyethanol
- Short description of test conditions: 3hrs exposure, then collection of metabolites by solvent extraction
- Parameters analysed / observed: Analysis of metabolites by GC-MS.
GLP compliance:
not specified
Type of medium:
aquatic
Transformation products:
yes
No.:
#1
No.:
#2
No.:
#3

As well as the transformation products, unchanged 2 -butoxyethanol was also detected.

This study was part of a larger study that examined the potential of 11 bacterial strains to degrade 2 -butoxyethanol. This particular species/strain grew the fastest and tolerated the highest substrate concentrations among the strains/species examined (and hence why it was used for this metabolite study). The maximum growth rate was 0.645 h-1 at a concentration of 5 mM (590mg/L), which was completely degraded within less than 6 h. A stable degradation of 2-BE could be achieved for concentrations of up to 30 mM (3540mg/L). Beyond that value, 2 -butoxyacetic acid

accumulated and the pH decreased to 6, inhibiting further growth.

.
Executive summary:

In a study that qualitatively measured the metabolites produced by bacterial degradation of 2 -butoxethanol, the bacterial strain Pseudomonas vancouverensis was found to produce the metabolites 2 -butoxyacetic acid, butanol and butanoic acid. These findings support the hypothesis that 2 -butoxyethanol degradation by bacteria in the environment proceeds by initial oxidation to 2 -butoxyacetic acid (as in mammals) followed by cleavage of the ether group to produce butanol and butanoic acid. The maximum growth rate was 0.645 h-1 at a concentration of 5 mM (590mg/L), which was completely degraded within less than 6 h. A stable degradation of 2-BE could be achieved for concentrations of up to 30 mM (3540mg/L).

Data source

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

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
- Principle of test: To identify bacterial strains that can utilise 2-butoxyethanol as a source of carbon
- Short description of test conditions: Samples used as sources of bacteria collected from a number of sources and grown in media with 2-butoxyethanol. These were then plated on solid growth medium, incubated then colonies harvested and DNA sequenced using PCR technique.
- Parameters analysed / observed: strains that had grown under the prescribed conditions using gene sequencing.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
2-butoxyethanol
EC Number:
203-905-0
EC Name:
2-butoxyethanol
Cas Number:
111-76-2
Molecular formula:
C6H14O2
IUPAC Name:
2-butoxyethanol

Results and discussion

Any other information on results incl. tables

The following strains were isolated and all found capable of utilising 2 -butoxyethanol as a carbon source:

Bacteria

Gram

Source (all in Germany)

Pseudomonas knackmussii

Gram-negative

Forest soil, Stuttgart

Pseudomonas putida

Gram-negative

Forest soil, Stuttgart

Hydrogenophaga pseudoflava

Gram-negative

Forest soil, Stuttgart

Pseudomonas umsongensis

Gram-negative

Forest soil, Stuttgart

Gordonia terrae

Gram-positive

Biotrickling filter, Stuttgart

Pseudomonas extremaustralis

Gram-negative

Biotrickling filter, Stuttgart

Pseudomonas plecoglossicida

Gram-negative

Activated sludge, Stuttgart

Pseudomonassp

Gram-negative

Activated sludge, Stuttgart

Pseudomonas putida

Gram-negative

Bioscrubber, Rastatt

Pseudomonas vancouverensis

Gram-negative

Bioscrubber, Rastatt

Cupriavidus oxalaticus

Gram-negative

Activated sludge, Stuttgart

Applicant's summary and conclusion

Executive summary:

In a study to examine how widely distributed are bacteria capable of utilising 2 -butoxyethanol as a source of carbon, all 11 bacterial strains sourced from four different bacterial colonies (two biofilter/bioscrubbers that can be considered adapted sources) and forest soil and activated sludge that can be considered non-adapted) were found capable of degrading the substance. It can be concluded that the bacteria capable of degrading 2 -butoxyethanol are widespread.