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Postion:Product Catalog >Chemical Reagents>Organic reagents>Tricyclic compound>Dibenzothiophene
Dibenzothiophene
  • Dibenzothiophene
  • Dibenzothiophene

Dibenzothiophene

Price $1
Package 1KG
Min. Order: 1G
Supply Ability: 1000KG
Update Time: 2019-07-06

Product Details

Product Name: Dibenzothiophene CAS No.: 132-65-0
EC-No.: 205-072-9 Min. Order: 1G
Purity: 98% Supply Ability: 1000KG
Release date: 2019/07/06

AD68

Dibenzothiophene Basic information
PAHs family General Description Uses
Product Name: Dibenzothiophene
Synonyms: Dibenzothiophe;Dibenzothiophene purified by sublimation, >=99%;[1,1'-Biphenyl]-2,2'-diyl sulfide;2,2’-biphenylylenesulfide;2,2'-Biphenylylene sulfide;9-Thiafluorene;alpha-Thiafluorene;dibenzo(b,d)thiophene
CAS: 132-65-0
MF: C12H8S
MW: 184.26
EINECS: 205-072-9
Product Categories: Heterocycle-oher series;Pharmaceutical Intermediates;Fluorene Derivatives;Organics;Thiophene&Benzothiophene;Benzothiophenes;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks
Mol File: 132-65-0.mol
Article illustration
 
Dibenzothiophene Chemical Properties
Melting point  97-100 °C(lit.)
Boiling point  332-333 °C(lit.)
Fp  170 °C
storage temp.  Store below +30°C.
solubility  0.0015g/l (Lit.)
form  Crystalline Powder and/or Chunks
color  white
PH 7 (50g/l, H2O, 20℃)(slurry)
Water Solubility  SOLUBLE
BRN  121101
CAS DataBase Reference 132-65-0(CAS DataBase Reference)
NIST Chemistry Reference Dibenzothiophene(132-65-0)
EPA Substance Registry System Dibenzothiophene(132-65-0)
 
Safety Information
Hazard Codes  Xn,N
Risk Statements  22-20/21/22-50/53
Safety Statements  36-61-60
RIDADR  2811
WGK Germany  3
RTECS  HQ3490550
TSCA  Yes
HazardClass  9
PackingGroup  III
HS Code  29349990
Hazardous Substances Data 132-65-0(Hazardous Substances Data)
 
 
Dibenzothiophene Usage And Synthesis
PAHs family Fluorene (FLU), dibenzofuran (DBF) and dibenzothiophene (DBT) are three ring PAHs largely derived from anthropogenic sources (e.g., petroleum products), although they can also form through natural processes (e.g., forest fires). These compounds share fluorene's basic molecular structure, only differing by one atom in the bridge of the furan ring: C in FLU, O in DBF, and S in DBT.
General Description Dibenzothiophene is an important representative of polycyclic aromatic hydrocarbons (PAHs) derivate consisting of 3 fused rings with keratolytic activity. DBT is a natural occurring compound found in petroleum. In industry, DBT is currently produced from biphenyl and hydrogen sulfide under catalytic oxidizing conditions.
Uses DBTs and DBT dioxides have been copolymerized with fluorenes to tune the chain arrangement and aggregation of fluorene-based organic light-emitting diodes (OLEDs).Unsubstituted DBT is a commercially available and inexpensive precursor, where both 3,7- and 2,8-positions can be substituted under different conditions. With the addition of DBT into the polymer, the fluorescence peak of the polymer witnessed a slight hypochromic shift. Dibenzothiophene was employed as heavy model sulfur compound to investigate the effect of heavy sulfur compounds on the percentage of sulfur in gasoline range during the Fluid Catalytic Cracking (FCC) process.
Chemical Properties White to light yellow crystal powder
Uses keratolytic
Definition ChEBI: A mancude organic heterotricyclic parent that consists of a thiophene ring flanked by two benzene rings ortho-fused across the 2,3- and 4,5-positions.

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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