Where It Comes From
1,3-Dichlorobenzene is produced by selective chlorination of benzene but in smaller quantities than the ortho and para isomers [1]. It is used as an industrial solvent, in the synthesis of other chlorinated aromatics, and as a component of mixed dichlorobenzene solvent blends [2]. Environmental contamination occurs at sites where mixed dichlorobenzene solvents were used or disposed of — it is found in soil and groundwater at various industrial Superfund sites [1]. Like other chlorinated aromatics, it is mobile in groundwater and resistant to natural biodegradation [2].
How You Are Exposed
Contaminated groundwater near former industrial solvent sites [1]. Occupational use of mixed dichlorobenzene solvents [2]. Some moth ball formulations historically contained mixed isomers [1].
Why It Matters
1,3-DCB is metabolized to 3,4-dichlorophenol and related catechol/quinone intermediates that cause oxidative stress [1]. Liver and kidney toxicity occur at occupational doses. EPA Group D (not classifiable as carcinogenic) based on current evidence [2]. CNS depression at high concentrations [1].
Who Is at Risk
Private well users near contaminated industrial sites [1]. Occupational solvent workers [2].
How to Lower Your Exposure
1. Test well water near industrial contamination sites [1]. 2. Activated carbon filtration [2].
References
- [1]ATSDR (2006). Toxicological Profile for Dichlorobenzenes. https://www.atsdr.cdc.gov/toxprofiles/tp10.pdf
- [2]EPA IRIS: 1,3-Dichlorobenzene. https://iris.epa.gov/
Recovery & Clinical Information
Body Half-Life
Blood half-life approximately 1-3 days [1].
Testing & Biomarkers
Urine 3,4-dichlorophenol [1].
Interventions
Remove from contaminated water; carbon filtration [1].
Recovery Timeline
Blood levels decline over days [1].
Recovery References
- [1]ATSDR (2006). Toxicological Profile. https://www.atsdr.cdc.gov/toxprofiles/tp10.pdf
- [2]EPA IRIS. https://iris.epa.gov/