Basic information Safety Supplier Related

BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE

Basic information Safety Supplier Related

BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE Basic information

Product Name:
BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE
Synonyms:
  • TIMTEC-BB SBB001172
  • 2,2'-DIHYDROXY-5,5'-DICHLORODIPHENYL SULFIDE
  • 2,2'-THIOBIS(4-CHLOROPHENOL)
  • BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE
  • BIS(5-CHLORO-2-HYDROXYPHENYL) SULFIDE
  • FENTICHLOR
  • FENTICLOR
  • CHLORHYDROSULFIDE
CAS:
97-24-5
MF:
C12H8Cl2O2S
MW:
287.16
EINECS:
202-568-7
Product Categories:
  • Diphenyl Sulfides (for High-Performance Polymer Research)
  • Functional Materials
  • Reagent for High-Performance Polymer Research
Mol File:
97-24-5.mol
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BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE Chemical Properties

Melting point:
175°C
Boiling point:
416.7±45.0 °C(Predicted)
Density 
1.4186 (estimate)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
7.91±0.48(Predicted)
color 
White to Orange to Green
Merck 
14,4004
Stability:
Stable. Incompatible with strong oxidizing agents.
LogP
4.400 (est)
CAS DataBase Reference
97-24-5(CAS DataBase Reference)
EPA Substance Registry System
Fenticlor (97-24-5)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
RTECS 
SN0350000
HS Code 
2930.90.2900
HazardClass 
IRRITANT
Toxicity
LDLo intraperitoneal in mouse: 250mg/kg
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BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE Usage And Synthesis

Chemical Properties

white to pale yellow powder

Originator

Fenticlor,Shanghai Lansheng

Uses

Fungicide; especially used against Monosporium apiospermum: Reifferscheid, Seeliger, Dtsch. Med. Wochenschr. 80, 1841, 1850 (1955).

Uses

Fentichlor is a fungicide especially used against Monosporium apiospermum; topical antifungal and antibacterial agent in hairdressings, antifungal creams, and ointments; thermoplastic resin.

Definition

ChEBI: An aryl sulfide having two 5-chloro-2-hydroxyphenyl groups attached to sulfur; an antiinfective drug mostly used in veterinary medicine.

Preparation

Fenticlor is produced (1) by the reaction of 4-chlorophenol with sulfur dichloride in the presence of AlCl3 or (2) by chlorination of 2,2'-thiobisphenol with chlorine in glacial acetic acid or with SO2Cl2 in dichlorobenzene. It shows a tendency to discoloration. Fenticlor has a broad range of antimicrobial action; it is, e.g., effective against bacteria, fungi, yeasts, and algae. Fenticlor is therefore used as a preservative for aqueous functional fluids and to control algae and slime in process water circulation systems.

Manufacturing Process

1 mol bis(2-hydroxy-phenyl)-sulfide, prepared from sulfuryl chloride and phenol, in about 2500 ml glacial acetic acid was dissolved and heated for boiling. 2-3 mol gaseous chlorine was passed through that solution and on cooling bis(2-oxy-5-chlorphenyl)sulfide was fallen. It was recrystallized from acetic acid or light petroleum. MP: 175°C. A residue was dropped from filtrate with water as the white crystals, which melted at the same temperature.
Fenticlor may be also prepared by adding sulfuryl chloride to the solution of bis(2-hydroxy-phenyl)sulfide in dichlorobenzene

Therapeutic Function

Antifungal

General Description

White to cream-colored solid or pale yellow powder. White crystalline solid melting from 175.8-186.8°C. Odorless and insolbule in water.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE 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.

Hazard

Toxic by ingestion.

Fire Hazard

Flash point data are not available for BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE, but BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDE is probably combustible.

BIS(2-HYDROXY-5-CHLOROPHENYL) SULFIDESupplier

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