Chemical Safety Concerns of Sulfur Mustard Analog, 2-Chloroethyl Ethyl Sulfide, in Laboratory Study

: Sulfur mustard (SM), a classic chemical weapon in the vesicant category, can induce severe damage, for which the therapy is still limited even today. Laboratory work is essential in unveiling toxicological effects and developing medical countermeasures. Sulfur mustard analog 2-chloroethyl ethyl sulfide (CEES), is employed in the lab for less toxicity. However, due to its similar characteristics to SM (being oily, hydrophobic, and volatile), the manipulation of CEES still needs special attention to avoid personnel injury and laboratory pollution. Here, to clear the chemical safety concerns in the laboratory study of CEES, the working procedure and experimental data are summarized, which might help educate new researchers to be skilled and professional.

[1]  Tim Prescott Accidental sulfur mustard exposure from explosive ordnance in a UK military service person , 2020, BMJ Military Health.

[2]  L. Kenar,et al.  Recent sulfur mustard attacks in Middle East and experience of health professionals. , 2019, Toxicology letters.

[3]  M. Ortatatli,et al.  Victims of chemical terrorism, a family of four who were exposed to sulfur mustard. , 2019, Toxicology letters.

[4]  Jin Cheng,et al.  Phospholipid and Triglyceride keep vortex-dispersed sulfur mustard analog as undissolved droplets which induce necrosis from nearby cells via declining mitochondrial membrane potential , 2019, Fundamental Toxicological Sciences.

[5]  T. Sawyer,et al.  Comparative toxicity of mono- and bifunctional alkylating homologues of sulphur mustard in human skin keratinocytes. , 2017, Toxicology.

[6]  S. Younespour,et al.  Skin manifestations in sulfur mustard exposed victims with ophthalmologic complications: Association between early and late phase , 2016, Toxicology reports.

[7]  Bin Xu,et al.  A novel approach for high sensitive determination of sulfur mustard by derivatization and isotope-dilution LC-MS/MS analysis. , 2015, Talanta.

[8]  A. Khamesipour,et al.  Association of serum immunoglobulins levels and eye injuries in sulfur mustard exposed: Sardasht-Iran Cohort Study. , 2013, International immunopharmacology.

[9]  R. Rancourt,et al.  Tissue factor pathway inhibitor prevents airway obstruction, respiratory failure and death due to sulfur mustard analog inhalation. , 2013, Toxicology and applied pharmacology.

[10]  T. Ghazanfari,et al.  Conjunctival microbial florae in patients with seriously sulfur mustard induced eye injuries , 2013, Cutaneous and ocular toxicology.

[11]  R. Agarwal,et al.  Silibinin Attenuates Sulfur Mustard Analog-Induced Skin Injury by Targeting Multiple Pathways Connecting Oxidative Stress and Inflammation , 2012, PloS one.

[12]  P. Blain,et al.  DNA damage responses in cells exposed to sulphur mustard. , 2012, Toxicology letters.

[13]  R. Rancourt,et al.  Airway tissue factor-dependent coagulation activity in response to sulfur mustard analog 2-chloroethyl ethyl sulfide. , 2012, American journal of physiology. Lung cellular and molecular physiology.

[14]  R. Agarwal,et al.  Sulfur mustard analog, 2-chloroethyl ethyl sulfide-induced skin injury involves DNA damage and induction of inflammatory mediators, in part via oxidative stress, in SKH-1 hairless mouse skin. , 2011, Toxicology letters.

[15]  K. Anderson,et al.  Direct binding of sulfur mustard and chloroethyl ethyl sulphide to human cell membrane-associated proteins; implications for sulfur mustard pathology. , 2010, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[16]  A. Siraki,et al.  Free radical production from the interaction of 2-chloroethyl vesicants (mustard gas) with pyridine nucleotide-driven flavoprotein electron transport systems. , 2009, Toxicology and applied pharmacology.

[17]  D. Phillips,et al.  Effect of alkylating agents on initiation and elongation of the lac UV5 promoter. , 1993, Biochemistry.

[18]  S. Kent,et al.  Formation of O6-ethylthioethylguanine in DNA by reaction with the sulfur mustard, chloroethyl sulfide, and its apparent lack of repair by O6-alkylguanine-DNA alkyltransferase. , 1986, Carcinogenesis.