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540870

Sigma-Aldrich

3,5-Dichlorobenzenethiol

97%

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About This Item

Linear Formula:
Cl2C6H3SH
CAS Number:
Molecular Weight:
179.07
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

97%

mp

62-65 °C (lit.)

SMILES string

Sc1cc(Cl)cc(Cl)c1

InChI

1S/C6H4Cl2S/c7-4-1-5(8)3-6(9)2-4/h1-3,9H

InChI key

WRXIPCQPHZMXOO-UHFFFAOYSA-N

General description

3,5-Dichlorobenzenethiol (3,5-dichlorothiophenol) is a halogenated aromatic thiol.

Application

3,5-Dichlorobenzenethiol may be used to synthesize hyperbranched poly(phenylene sulfide) [HPPS] and bis-(3,5-dichlorophenyl) sulfide.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

540870-VAR:
540870-BULK:
540870-1G:
540870-5G:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Low-polydispersity Hyperbranched Polyphenylene Sulfide as a Protectant for Palladium Nanocomposites.
Meng Y, et al.
Chemistry Letters (Jpn), 44(4), 500-502 (2015)
Semimetallic transport in nanocomposites derived from grafting of linear and hyperbranched poly (phenylene sulfide) s onto the surface of functionalized multi-walled carbon nanotubes.
Jeon IY, et al.
Macromolecules, 41(20), 7423-7432 (2008)
Synthesis of dendritic oligo (aryl sulfone) s as supports for synthesis.
Taylor PC, et al.
Tetrahedron, 61(52), 12314-12322 (2005)
Homan Kang et al.
Scientific reports, 5, 10144-10144 (2015-05-29)
Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection, and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding, and optical encoding have been

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