← All chemicals

CAS 108-38-3

m-Xylene (1,3-Dimethylbenzene)

aromatic solventHAPVOC

m-Xylene is the meta isomer of xylene, occurring in petroleum and used as a solvent and chemical intermediate — toxicologically similar to the other xylene isomers with CNS effects at occupational concentrations, and representing a major component of the BTEX (benzene, toluene, ethylbenzene, xylene) contamination mixture found at petroleum-contaminated sites.

Where It Comes From

m-Xylene is the most abundant xylene isomer in mixed xylenes from petroleum, typically comprising 40-70% of commercial mixed xylenes [1]. It is produced during catalytic reforming of naphtha in petroleum refining and is also found in coal tar [2]. m-Xylene is used primarily in isophthalic acid production (a phthalate resin precursor for PET bottles and coatings), as a solvent in paints and coatings, and as a component of aviation fuel [1]. It is a major component of the BTEX mixture that leaches from gasoline into groundwater at underground storage tank spill sites — one of the most ubiquitous groundwater contamination problems in the United States [2].

How You Are Exposed

Gasoline exposure (refueling, underground storage tank leaks) is a major source for the general population [1]. Occupational exposure in petroleum refining, solvent manufacturing, and coating/paint applications [2]. Contaminated groundwater from UST spill sites [1].

Why It Matters

m-Xylene is metabolized to 3-methylhippuric acid by oxidation to m-methylbenzoic acid and conjugation with glycine [1]. At occupational concentrations, it causes CNS effects (dizziness, headache, impaired coordination) and potentially vestibular toxicity [2]. EPA classifies xylenes as Group D (not classifiable as carcinogenic) — CNS and liver toxicity rather than cancer are the primary health concerns [1].

Who Is at Risk

Petroleum and chemical workers, painters, and people in BTEX-contaminated water communities [1].

How to Lower Your Exposure

1. Water-based coatings instead of solvent-based products [1]. 2. Test wells near gas stations and underground storage tanks [2]. 3. Ventilate painting and coating operations [1].

References

  1. [1]ATSDR (2007). Toxicological Profile for Xylenes. https://www.atsdr.cdc.gov/toxprofiles/tp71.pdf
  2. [2]EPA IRIS: Xylenes. https://iris.epa.gov/

Recovery & Clinical Information

Body Half-Life

Blood half-life approximately 1-3 hours [1]. Urinary 3-methylhippuric acid (3-MHA) is the biomarker [2].

Testing & Biomarkers

Urine 3-MHA end-of-shift for m-xylene exposure [1].

Interventions

Remove from exposure; improve ventilation [1].

Recovery Timeline

Blood xylene clears within hours [1].

Recovery References

  1. [1]ATSDR (2007). Toxicological Profile for Xylenes. https://www.atsdr.cdc.gov/toxprofiles/tp71.pdf
  2. [2]ACGIH (2023). BEI for Xylenes. https://www.acgih.org/

Track your exposure to m-Xylene (1,3-Dimethylbenzene)

Pollution Profile maps your lifetime exposure history to EPA-tracked chemicals.

Get early access

We use cookies and analytics to understand how people use Pollution Profile and improve the experience. We never sell your data. Learn more.