Skip to Content
Merck
All Photos(2)

Documents

B25401

Sigma-Aldrich

Benzyl mercaptan

99%

Synonym(s):

α-Toluenethiol, α-Tolyl mercaptan, Benzenemethanethiol

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6H5CH2SH
CAS Number:
Molecular Weight:
124.20
Beilstein:
605864
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

>4 (vs air)

Assay

99%

form

liquid

refractive index

n20/D 1.575 (lit.)

bp

194-195 °C (lit.)

density

1.058 g/mL at 25 °C (lit.)

SMILES string

SCc1ccccc1

InChI

1S/C7H8S/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2

InChI key

UENWRTRMUIOCKN-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Benzyl mercaptan can be used as:
  • A nucleophilic reagent in the cleavage of proanthocyanidins into their constitutive subunits.
  • A reactant in the synthesis of dithiocarboxylic esters in the presence of phosphorus pentasulfide as a catalyst.
  • A modifier to functionalize the surface of CNT for enhanced interaction with Pt-nanoparticles.

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Phosphorus pentasulfide: A mild and versatile catalyst/reagent for the preparation of dithiocarboxylic esters.
Sudalai A, et al.
Organic Letters, 2(20), 3213-3216 (2000)
Analysis of proanthocyanidin cleavage products following acid-catalysis in the presence of excess phloroglucinol.
Kennedy JA and Jones GP
Journal of Agricultural and Food Chemistry, 49(4), 1740-1746 (2001)
Strongly enhanced interaction between evaporated Pt nanoparticles and functionalized multiwalled carbon nanotubes via plasma surface modifications: Effects of physical and chemical defects.
Yang DQ and Sacher E
The Journal of Physical Chemistry C, 112(11), 4075-4082 (2008)
Kenji Matsuno et al.
Bioorganic & medicinal chemistry letters, 20(17), 5126-5129 (2010-08-07)
S-benzylisothiourea 3a was discovered by its ability to inhibit indoleamine-2,3-dioxygenase (IDO) in our screening program. Subsequent optimization of the initial hit 3a lead to the identification of sub-muM inhibitors 3r and 10h, both of which suppressed kynurenine production in A431
Theresa K Tiefenbrunn et al.
Protein science : a publication of the Protein Society, 18(5), 970-979 (2009-04-23)
The type 1 repeat domain from thrombospondin has potent antiangiogenic activity and a structurally interesting fold, making it an attractive target for protein engineering. Chemical synthesis is an attractive approach for studying protein domains because it enables the use of

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service