This is a demo store. No orders will be fulfilled.

Diphenyl sulfide - analytical standard,>99%(GC), high purity , CAS No.139-66-2

In stock
Item Number
D107043
Grouped product items
SKU Size
Availability
Price Qty
D107043-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$69.90

Basic Description

Synonyms AKOS000119955 | B5P3Y93MNR | Diphenyl sulfide | MFCD00003064 | UNII-B5P3Y93MNR | DTXCID6024383 | InChI=1/C12H10S/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10 | Sulfide, diphenyl | Diphenylthiamethane | phenylsulfanylbenzene | Diphenylsulfide | Tox21_302182 |
Specifications & Purity analytical standard, ≥99%(GC)
Shipped In Normal
Grade analytical standard

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organosulfur compounds
Class Thioethers
Subclass Aryl thioethers
Intermediate Tree Nodes Not available
Direct Parent Diarylthioethers
Alternative Parents Polyphenyl thioethers  Thiophenol ethers  Sulfenyl compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents Diarylthioether - Polyphenyl thioether - Thiophenol ether - Benzenoid - Monocyclic benzene moiety - Sulfenyl compound - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as diarylthioethers. These are organosulfur compounds containing a thioether group that is substituted by two aryl groups.
External Descriptors aryl sulfide

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name phenylsulfanylbenzene
INCHI InChI=1S/C12H10S/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H
InChIKey LTYMSROWYAPPGB-UHFFFAOYSA-N
Smiles C1=CC=C(C=C1)SC2=CC=CC=C2
Isomeric SMILES C1=CC=C(C=C1)SC2=CC=CC=C2
WGK Germany 3
RTECS SX2275000
UN Number 2810
Molecular Weight 186.27
Beilstein 1907932
Reaxy-Rn 1907932
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1907932&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

2 results found

Lot Number Certificate Type Date Item
E1823154 Certificate of Analysis Jun 16, 2025 D107043
H1803082 Certificate of Analysis Apr 14, 2022 D107043

Chemical and Physical Properties

Refractive Index 1.633
Flash Point(°F) 126 °C
Flash Point(°C) 126°C
Boil Point(°C) 296°C
Melt Point(°C) -40°C
Molecular Weight 186.270 g/mol
XLogP3 4.500
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 1
Rotatable Bond Count 2
Exact Mass 186.05 Da
Monoisotopic Mass 186.05 Da
Topological Polar Surface Area 25.300 Ų
Heavy Atom Count 13
Formal Charge 0
Complexity 116.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Ying Chen, Ruili Pan, Liya Mei, Peijun Tian, Linlin Wang, Jianxin Zhao, Wei Chen, Gang Wang.  (2023)  Colon-Targeted Delivery of Indole Acetic Acid Helps Regulate Gut Motility by Activating the AHR Signaling Pathway.  Nutrients,  15  (19): (4282). 
2. Hongjian Gu, Cheng Liu, Qian Liu, Hang Jia, Yue Qiao, Wenqi Zhao, Yousi Chen, Xigao Jian.  (2023)  High- and low-temperature resistant and intrinsically flame retardant poly(bisphthalazinone thioether sulfone ketone)s: Synthesis, structures and properties.  CHEMICAL ENGINEERING JOURNAL,  471  (144480). 
3. Longwei Huang, Ke Zheng, Yuting Jin, Shaoqi Zhou.  (2023)  Chlorine-Resistant Loose Nanofiltration Membranes Fabricated via Interfacial Polymerization Using Sulfone Group-Containing Amine Monomer for Dye/Salt Separation.  Water,  15  (8): (1456). 
4. Li Fang, Qionghao Xu, Yanyan Qi, Xiaoxue Wu, Yanghe Fu, Qiang Xiao, Fumin Zhang, Weidong Zhu.  (2020)  Fe/Fe3C@N-doped porous carbon microspindles templated from a metal–organic framework as highly selective and stable catalysts for the catalytic oxidation of sulfides to sulfoxides.  Molecular Catalysis,  486  (110863). 

Solution Calculators

Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.