General Description
White or grayish white crystalline powder with a very faint aromatic or phenolic odor.
Reactivity Profile
2,2'-THIOBIS(4,6-DICHLOROPHENOL)(97-18-7) is incompatible with acids, diazo and azo compounds, halocarbons, isocyanates, aldehydes, alkali metals, nitrides, hydrides, and other strong reducing agents. Reactions with these materials may generate heat and toxic or flammable gases.
Air & Water Reactions
Insoluble in water.
Health Hazard
ACUTE/CHRONIC HAZARDS: This chemical is a skin irritant. When heated to decomposition or upon contact with acid or acid fumes, toxic fumes are evolved.
Potential Exposure
It is used as a surfactant-formulated
antimicrobial against bacteria, molds and yeast. It is proposed
as an agricultural fungicide. Other uses include deodorant,
germicide, fungistat, and in the manufacture of pharmaceuticals.
It is no longer allowed to be used in cosmetics. A food
additive in feed and drinking water of animals. Also a food
additive permitted in food for human consumption.
Fire Hazard
Flash point data is not available for this chemical, but 2,2'-THIOBIS(4,6-DICHLOROPHENOL) is probably combustible.
First aid
Move victim to fresh air. Call 911 or emergency
medical service. Give artificial respiration if victim is not
breathing. Do not use mouth-to-mouth method if victim
ingested or inhaled the substance; give artificial respiration
with the aid of a pocket mask equipped with a one-way
valve or other proper respiratory medical device.
Administer oxygen if breathing is difficult. Remove and isolate
contaminated clothing and shoes. In case of contact
with substance, immediately flush skin or eyes with running
water for at least 20 minutes. For minor skin contact, avoid
spreading material on unaffected skin. Keep victim warm
and quiet. Effects of exposure (inhalation, ingestion or skin
contact) to substance may be delayed. Ensure that medical
personnel are aware of the material(s) involved and take
precautions to protect themselves. Medical observation is
recommended for 24 to 48 hours after breathing overexposure,
as pulmonary edema may be delayed. As first aid for
pulmonary edema, a doctor or authorized paramedic may
consider administering a drug or other inhalation therapy.
Shipping
UN2811 Toxic solids, organic, n.o.s., Hazard
Class: 6.1; Labels: 6.1—Poisonous materials, Technical
Name Required.
Incompatibilities
Incompatible with oxidizers (chlorates,
nitrates, peroxides, permanganates, perchlorates, chlorine,
bromine, fluorine, etc.); contact may cause fires or explosions.
Keep away from alkaline materials, strong bases,
strong acids, oxoacids, epoxides.
Description
Bithionol (97-18-7) is an antihelmintic drug with bacteriostatic and fungicidal properties. Bithionol has also been found to be an inhibitor of glutamate dehydrogenase1,2?(IC50?= 4.8 μM bovine GDH1).
Chemical Properties
Bithionol is a white or grayish powder with a
slight phenolic odor.
Chemical Properties
off-white crystalline powder
Physical properties
Bithionol is virtually insoluble in water, readily soluble in ethanol, diethyl ether, acetone, glacial acetic acid, and dilute alkalis.
Uses
anthelmintic, antiseptic
Uses
bactericide; antihelmintic; algicide; proposed as agricultural fungicide; food additive in feed and drinking water for foodproducing
animals; permitted in food for human consumption; deodorant; in germicide pharmaceuticals, antibacterial agent in soaps,
cosmetics, veterinary antiseptic and antihelminthic products, industrial cleansers, etc.
Definition
ChEBI: An aryl sulfide that is diphenyl sulfide in which each phenyl group is substituted at position 2 by hydroxy and at positions 3 and 5 by chlorine. A fungicide and anthelmintic, it was used in various topical drug products for the treatment of liver flukes,
ut withdrawn after being shown to be a potent photosensitizer with the potential to cause serious skin disorders.
Production Methods
Bithionol is prepared by reaction of 2,4-dichlorophenol with sulfur dichloride and AlCl3 in carbon disulfide or tetrachloromethane. It is used as a microbicide to protect aqueous functional fluids from biodeterioration and to control algae and slime formation in process water systems.
Brand name
Lorothidol (Sterling Winthrop);Anafogene;Bacteriostat cs-1;Bidiphen;Lorothiodol;Neopellis;Nobacter;Prevenol;Tbp;Vancide bl.
World Health Organization (WHO)
Bithionol, which has bactericidal and anthelminthic activity, was
formerly available in soaps. By the late 1960s use of such preparations had been
associated with a risk of photosensitivity reactions and cross-sensitivity with other
halogenated disinfectants. This resulted in their withdrawal in the USA. Oral
preparations of bithionol remain available for the treatment of paragonimiasis and
fascioliasis.
Hazard
Toxic by ingestion.
Mechanism of action
Biothionol is bis-dichlorophenol, and it is structurally similar to hexachlorophene. It is the
antihelmintic drug of choice for treating humans infected with Fasciola hepatica. It is an
alternative drug to praziquantel that is used for treating pulmonary and cerebral paragonimiasis. The exact mechanism of action is not known, although it seems likely that it
inhibits oxidative phosphorylation in Paeagonumus westermani. Synonyms of this drug
are actamer, bitin, prevenol, and others.
Clinical Use
2,2’-Thiobis(4,6-dichlorophenol), or bis(2-hydroxy-3,5-dichlorophenyl)sulfide (Lorothidol, Bithin), a chlorinatedbisphenol, was formerly used in soaps and cosmetics for itsantimicrobial properties but was removed from the marketfor topical use because of reports of contact photodermatitis.Bithionol has useful anthelmintic properties and hasbeen used as a fasciolicide and taeniacide. It is still consideredthe agent of choice for the treatment of infestationscaused by the liver fluke Fasciola hepatica and the lungfluke Paragonimus westermani. Niclosamide is believed tobe superior to it for the treatment of tapeworm infestations.
Synthesis
Bithionol, 2,2-thiobis(4,6-dichlorophenol) (38.1.38), is made by reacting a
solution of 2,4-dichlorophenol in carbon tetrachloride with sulfur chloride in the presence
of aluminum chloride.
storage
Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Store in a refrigerator or a cooldry place.
