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Sesquimustard

HCID 19092
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Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
3563-36-8
Standard SMILES
ClCCSCCSCCCl
InChIKey
AMGNHZVUZWILSB-UHFFFAOYSA-N
Molecular formula
C6H12Cl2S2
Average molar mass
219.2 g/mol
Monoisotopic mass
217.9757481

Overview

This is a chemical weapon related to sulfur mustard (mustard gas) and is expected to react in a similar fashion. See the chemical datasheet for sulfur mustard for more information.

Names & identifiers

Preferred name
Sesquimustard
IUPAC
1,2-bis(2-chloroethylsulfanyl)ethane
English name
1,2-Bis(2-chloroethyl(thio)ethane
Molecular formula
C6H12Cl2S2
Molecular weight
219.2

Names & synonyms

SesquimustardSesquimustard QAgent QSesquisulfur Mustard3563-36-81,2-Bis(2-chloroethylthio)ethaneBis(2-chloroethylthio)ethaneHSM 1SM 11,8-Dichloro-3,6-dithiaoctane3,6-Dithia-1,8-octanedichlorideTL 86
Show more names
TL-86AMGNHZVUZWILSB-UHFFFAOYSA-N1,2-Bis(2-chloroethyl(thio)ethaneEthylenebis(2-chloroethyl sulfide)1,1'-(Ethylenebisthio)bis(2-chloroethane)
1,2-bis(2-chloroethylsulfanyl)ethaneSesqui-mustard QNSC 30025Ethane, 1,2-bis(2-chloro-ethylthio)-5Y1NV229POSsmNSC-30025Ethane, 1,2-bis[(2-chloroethyl)thio]-

Database identifiers

CAS
3563-36-8
PubChem CID
19092
DTXSID
DTXSID7074793
UNII
5Y1NV229PO
Nikkaji
J13.262D

Properties

Computed structural properties

XLogP
2.7
Topological polar surface area
50.6 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
2
Rotatable bonds
7
Heavy atoms
10
Formal charge
0
Complexity
53.7

Experimental & physicochemical properties

OdorGarlic-like odor
Density1.27 at 25 °C
Color/FormSolid
Solubility · 2 items

Although sulfur mustards have limited solubility in water at neutral pH, the small quantity that dissolves is reactive. /Sulfur mustards/

The sulfur mustards do not dissolve much in water, but dissolve easily in oils, fats, and other solvents. /Sulfur mustards/

Boiling PointDecomposes
DecompositionWhen heated to decomposition it emits very toxic fumes of SOx and Cl-.
Melting Point56 °C
Vapor Pressure3.5X10-6 mm Hg at 25 °C
Physical DescriptionThis is a chemical weapon related to sulfur mustard (mustard gas) and is expected to react in a similar fashion. See the chemical datasheet for sulfur mustard for more information.

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

Hazard information

Reactive GroupHalogenated Organic Compounds
Reactivity AlertsWater-Reactive
Air and Water ReactionsNo rapid reaction with air. No rapid reaction with water.
DHS Chemicals of Interest (COI) · 4 items

Sesquimustard

CUM 100g

CUM 100g

Chemical Weapons/Chemical Weapons Precursors chemical material that, if stolen or diverted, can be converted into weapons using simple chemistry, equipment, or techniques.

Safety & protection

Disposal Methods · 2 items

SRP: Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in air, soil or water; effects on animal, aquatic and plant life; and conformance with environmental and public health regulations. If it is possible or reasonable use an alternative chemical product with less inherent propensity for occupational harm/injury/toxicity or environmental contamination.

A simple and economical chemical neutralization method is developed against highly toxic chemical warfare agents viz. sulfur mustard (SM), sesquimustard, and their homologous/analogous. The method involves treatment of chemical warfare agents with sodium in inert solvents. This destruction method of sulfur mustards release innocuous products via desulfurization reactions. The products were characterized by GC-MS technique. The method is suitable in particular, for bulk destruction of heel of mustard stockpiles.

Protective Action Criteria (PAC) · 3 items

0.010 [ppm]

0.020 [ppm]

0.32 [ppm]

Chemistry & industry

Pharmacology

Metabolism/Metabolites · 1 item

Sesqui- and oxy-mustards pose a significant threat to military forces and civilians because they are potent vesicants. We have developed an isotope-dilution high-performance liquid chromatography-atmospheric pressure chemical ionization-tandem mass spectrometry method utilizing negative ion multiple reaction monitoring for the analysis of sesqui-mustard metabolites bis(2-hydroxyethylthio)alkanes (n = 1-5) and oxy-mustard metabolite bis(2-hydroxyethylthioethyl)ether in human urine. Relative standard deviations were < 10% and the reportable limits of detection were 1 ng/mL in 0.5 mL of urine. We applied this method to 100 samples collected from individuals with no known exposure to sesqui- or oxy-mustards, and no urines showed detectable levels of any of the analytes, suggesting that these metabolites may be used for monitoring exposure to sesqui- and oxy-mustards.

Uses & manufacturing

Uses · 3 items

Sesquimustard (Q) is 1,2-bis(2-chloroethylthio) ethane and is considered a more potent vesicant than /distilled mustard/ HD but its very low vapor pressure limits its effectiveness as a warfare agent, a condition remedied by combining it with HD to form agent HQ.

Vesicants include distilled mustard (HD), mustard gas (H), lewisite, mustard/lewisite, mustard/T, nitrogen mustard, phosgene oxime, sesqui mustard, and sulfur mustard.

Toxic chemical.

Methods of Manufacturing · 1 item

Synthesis: 1) 2-hydroxyethanethiol and vinyl chloride; 2) 1,2-bis(2-hydroxyethylthio)ethane and HCl gas; 3) 1,2-bis(2-hydroxyethylthio)ethane and thionyl chloride; 4) 1,2-ethanedithiol and vinyl chloride; 5) 2-hydroxyethanethiol and thiodiglycol with hydrochloric acid.

General Manufacturing Information · 4 items

Sesquimustard is listed in the CWC /Chemical Weapons Convention/ Annex on Chemicals under Schedule 1.

/The Chemical Weapons Convention (CWC) is an international treaty which bans the development, production, stockpiling, and transfer or use of chemical weapons. The Convention mandates the destruction and prohibition of chemical weapons and related facilities and provides for restrictions on international trade in toxic chemicals and precursors./ The Convention's monitoring and verification measures involve submission of declarations regarding ... /Schedule 1, 2, and 3 chemicals/ and inspections by the Organization for the Prohibition of Chemical Weapons of the facilities where these chemicals are produced. ... Schedule 1 lists chemicals considered to pose a high risk to the object and purpose of the Convention by virtue of their high potential for use in activities prohibited by the CWC. These chemicals have little or no use for peaceful purposes in commercial or industrial trade. ... Schedule 1 also lists precursor chemicals that may be used in the final single technological stage of production of any of the toxic chemicals listed in the schedule.

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Other Experimental Properties · 3 items

When heated to decomposition it emits very toxic fumes of SOx and Cl-.

No rapid reaction with air. No rapid reaction with water, but is water reactive.

Sesquimustard (Agent Q) has a much lower volatility than mustard gas and a lower vapor pressure than sulfur mustard which makes it inefficient as a respiratory agent by itself.

Physicochemical properties

Boiling point
57.8 °C · 57.8°C
Density
1.2151 · 1.2151 (estimate)
Henry's Law Constant
8.8 · 8.8×101 mol/(m3Pa) at 25℃, Ebert et al. (2023)
FDA UNII
5 Y1NV229PO · 5Y1NV229PO
EPA Substance Registry System
Sesquimustard (3563-36-8)
Hazardous Substances Data
3563 · 3563-36-8(Hazardous Substances Data)
Toxicity
50 inhalation · LC50 inhalation in dog: 90mg/m3/2M

Toxicology

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 1450(SRC), determined from a structure estimation method(2), indicates that sesquimustard is expected to have low mobility in soil(SRC). Volatilization of sesquimustard from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 4.7X10-9 atm-cu m/mole(SRC), developed using a fragment constant estimation method(2). The Sulfur Mustards do not dissolve much in water(3), but the small quantity that dissolves is reactive(4). The hydrolysis half-life of dissolved sesquimustard was determined to be 1.7 minutes at 25 °C(5). Sesquimustard is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 3.5X10-6 mm Hg at 25 °C(6). Biodegradation data in soil were not available(SRC, 2017).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 1450(SRC), determined from a structure estimation method(2), indicates that sesquimustard is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 4.7X10-9 atm-cu m/mole(SRC), developed using a fragment constant estimation method(2). The Sulfur Mustards do not dissolve much in water(4), but the small quantity that dissolves is reactive(5). The hydrolysis half-life of dissolved sesquimustard was determined to be 1.7 minutes at 25 °C(6). According to a classification scheme(7), an estimated BCF of 43(SRC), from an estimated log Kow of 2.99(2) and a regression-derived equation(2), suggests the potential for bioconcentration in aquatic organisms is moderate(SRC). Biodegradation data in water were not available(SRC, 2017).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), sesquimustard, which has a vapor pressure of 3.5X10-6 mm Hg at 25 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase sesquimustard is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 14 hours(SRC), calculated from its rate constant of 2.7X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase sesquimustard may be removed from the air by wet and dry deposition(SRC).

Toxicity Summary · 1 item

IDENTIFICATION AND USE: Sesquimustard (Q) is a vesicant/blister agent more potent than distilled mustard (HD). It is combined with HD to form agent HQ. It could also be formed in small amounts during storage of HD in ton containers. HUMAN STUDIES: Vesicants, also referred to as "blister agents," were the most commonly used chemical warfare agents during World War I. The most likely routes of exposure are inhalation, dermal contact, and ocular contact. Vesicants are highly reactive chemicals that combine with proteins, DNA, and other cellular components to result in cellular changes immediately after exposure. Clinical effects may be delayed for 2 to 24 hours. Following exposure, the most commonly encountered clinical effects include dermal (skin erythema and blistering), respiratory (pharyngitis, cough, dyspnea), ocular (conjunctivitis and burns), and gastrointestinal (nausea and vomiting). The amount and route of exposure to the vesicant, the type of vesicant, and the premorbid condition of the person exposed will contribute to the time of onset and the severity of illness. For example, ingestion of a vesicant leads to gastrointestinal symptoms more prominent than those that would result from inhalation exposure to the same dose and type of vesicant. ANIMAL STUDIES: Acute inhalation toxicity studies with sesquimustard have been made in mice, rats, guinea pigs, hamsters, pigeons, and dogs. Following exposure, animals show loss of body weight, coughing, dyspnea, ataxia, and diarrhea prior to death. Deaths occurred over a 14-day observation period with a primary peak between the third and sixth day. Tissue damage in most animals was limited to the upper respiratory tract and digestive tract.

Soil Adsorption/Mobility · 1 item

Using a structure estimation method based on molecular connectivity indices(1), the Koc of sesquimustard can be estimated to be 1450(SRC). According to a classification scheme(2), this estimated Koc value suggests that sesquimustard is expected to have low mobility in soil(SRC).

Human Toxicity Excerpts · 5 items

/SIGNS AND SYMPTOMS/ Vesicants, also referred to as "blister agents," were the most commonly used chemical warfare agents during World War I. The most likely routes of exposure are inhalation, dermal contact, and ocular contact. Vesicants are highly reactive chemicals that combine with proteins, DNA, and other cellular components to result in cellular changes immediately after exposure. Depending on the vesicant, clinical effects may occur immediately (as with phosgene oxime or lewisite) or may be delayed for 2 to 24 hours (as with mustards). Following exposure, the most commonly encountered clinical effects include dermal (skin erythema and blistering), respiratory (pharyngitis, cough, dyspnea), ocular (conjunctivitis and burns), and gastrointestinal (nausea and vomiting). The amount and route of exposure to the vesicant, the type of vesicant, and the premorbid condition of the person exposed will contribute to the time of onset and the severity of illness. For example, ingestion of a vesicant leads to gastrointestinal symptoms more prominent than those that would result from inhalation exposure to the same dose and type of vesicant. /Vesicants/

/SIGNS AND SYMPTOMS/ Respiratory signs and symptoms: chest tightness, clear rhinorrhea, cough Dyspnea (shortness of breath), hemoptysis, nasal irritation/pain, sore throat, tachypnea. /Vesicants/

/SIGNS AND SYMPTOMS/ Dermal signs and symptoms: blisters (within 1 hour with phosgene oxime, delayed for 2 to 12 hours with lewisite, delayed for 2 to 24 hours with mustards); erythema (immediate with lewisite and phosgene oxime, may be delayed for 2 to 24 hours with mustards); immediate blanching (phosgene oxime); itching; necrosis and eschar (over a period of 7 to 10 days). /Vesicants/

/SIGNS AND SYMPTOMS/ Ocular signs and symptoms: blindness, blurred vision, corneal ulceration, conjunctivitis, eyelid edema, eye pain/burning, lacrimation, photophobia. /Vesicants/

For more Human Toxicity Excerpts (Complete) data for Sesquimustard (10 total), please visit the HSDB record page.

Artificial Pollution Sources · 1 item

Sesquimustard's production may result in its release to the environment through various waste streams; its use as a chemical warfare agent(1) will result in its direct release to the environment(SRC). Destruction of US stockpiles of chemical agents, including sulfur mustards, was mandated by the Chemical Weapons Convention to take place before April 2007(2).

Sediment/Soil Concentrations · 1 item

SOIL: In August 1988, chemical weapons were reported used against Kurdish populations in the mountainous region of northern Iraq close to the borders of Turkey and Iran(1). In November of that year, soil samples (and other samples) were collected from a hillside site of an impacted bomb(1). Analysis of the soil samples identified degradation products of sulfur mustard and sesquimustard(1).

Environmental Bioconcentration · 1 item

An estimated BCF of 43 was calculated in fish for sesquimustard(SRC), using an estimated log Kow of 2.99(1) and a regression-derived equation(1). According to a classification scheme(2), this BCF suggests the potential for bioconcentration in aquatic organisms is moderate(SRC).

Volatilization from Water/Soil · 1 item

The Henry's Law constant for sesquimustard is estimated as 4.7X10-9 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that sesquimustard is expected to be essentially nonvolatile from water surfaces(2). In addition, any sesquimustard that dissolves into water will be reactive with the water(3). Sesquimustard's Henry's Law constant indicates that volatilization from moist soil surfaces is not expected to occur(SRC). Sesquimustard is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 3.5X10-6 mm Hg at 25 °C(4).

Non-Human Toxicity Excerpts · 1 item

/LABORATORY ANIMALS: Acute Exposure/ Acute inhalation toxicity studies with 1,2-bis(2-chloroethylthio)ethane have been made in mice, rats, guinea pigs, hamsters, pigeons, and dogs. Following exposure, animals show loss of body weight, coughing, dyspnea, ataxia, and diarrhea prior to death. Deaths occurred over a 14-day observation period with a primary peak between the third and sixth day. Pigeons were the least sensitive of the species tested. Tissue damage in most animals was limited to the upper respiratory tract and digestive tract.

Environmental Abiotic Degradation · 1 item

The rate constant for the vapor-phase reaction of sesquimustard with photochemically-produced hydroxyl radicals has been estimated as 2.7X10-11 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1). This corresponds to an atmospheric half-life of about 14 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1). The apparent hydrolysis half-life of sesquimustard at 28 °C was determined to be 8.1 minutes in an aqueous solution containing 32% dioxane(1); the hydrolysis half-life extrapolated to pure water at 25 °C is 1.7 minutes(2).

Probable Routes of Human ExposureOccupational exposure to sesquimustard may occur through inhalation and dermal contact with this compound at workplaces where sesquimustard is produced or used. (SRC)
Other Environmental Concentrations · 1 item

Sesquimustard decontamination derivatives were detected in decontamination waste from chemical weapons (CW) agents stored in containers on Johnston Atoll (US territory located in the Pacific Ocean) since 1971(1). Sesquimustard occurs as an impurity in sulfur mustard used as a chemical warfare agent(2).

Regulatory information

DHS Chemicals of Interest (COI) · 4 items

Sesquimustard

CUM 100g

CUM 100g

Chemical Weapons/Chemical Weapons Precursors chemical material that, if stolen or diverted, can be converted into weapons using simple chemistry, equipment, or techniques.

Safety data

Toxicity
LC50 inhalation in dog: 90mg/m3/2M
Hazardous Substances Data
3563-36-8(Hazardous Substances Data)

...HD /sulfur mustard/ stored for approximately 40 years in ton containers was 89.2% pure. The main impurity (4.7%) was 1,2-bis-(2-chloroethylthioethane), also know as compound Q or sesquimustard.

In the period following World War I and during World War II, a wide variety of sulfur analogues of mustard were investigated and many potent vesicants were discovered. Each had two 2-chloroethyl groups attached to a sulfur atom. Examples of such compounds are 1,2-bis(2-chloroethylthio)ethane (Chemical Agent Symbol Q), ... and bis(2-chloroethylthioethyl) ether (T), ... . It is noteworthy that each 2-chloroethyl group is associated with a separate sulfur atom, not with the same one as for mustard. Both Q and T are more vesicant than mustard, but neither is as volatile. For that reason, neither is as effective by the vapor route.