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270865

Sigma-Aldrich

Benzene-1,2-dithiol

96%

Synonym(s):

1,2-Dimercaptobenzene

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About This Item

Linear Formula:
C6H4(SH)2
CAS Number:
17534-15-5
Molecular Weight:
142.24
Beilstein:
636154
EC Number:
241-530-4
MDL number:
MFCD00004835
UNSPSC Code:
12352100
PubChem Substance ID:
24856407
NACRES:
NA.22

Quality Level

200

Assay

96%
96%

form

liquid

bp

119-120 °C/17 mmHg (lit.)

mp

22-24 °C (lit.)

solubility

water: slightly soluble

density

1.236 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Sc1ccccc1S

InChI

1S/C6H6S2/c7-5-3-1-2-4-6(5)8/h1-4,7-8H

InChI key

JRNVQLOKVMWBFR-UHFFFAOYSA-N

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General description

The transition metal complexes with benzene-1,2-dithiol as ligand were studied by UV-vis, resonance Raman (rR) and infrared (IR) spectroscopies.

Application

Benzene-1,2-dithiol was used in the preparation of a new type of Schiff base that was required in the synthesis of a new series of copper(II) and zinc(II) complexes.

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

219.2 °F - closed cup

Flash Point(C)

104 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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N Raman et al.
European journal of medicinal chemistry, 45(11), 5438-5451 (2010-09-25)
A new series of copper(II) and zinc(II) complexes have been designed and synthesized using a new type of Schiff bases derived from the reaction of 3-(3-phenyl-allylidene)-pentane-2,4-dione with para substituted aniline and benzene-1,2-dithiol. Their structures have been established by analytical and
Valentina Straniero et al.
Antibiotics (Basel, Switzerland), 9(4) (2020-04-09)
Filamentous temperature-sensitive Z (FtsZ) is a prokaryotic protein with an essential role in the bacterial cell division process. It is widely conserved and expressed in both Gram-positive and Gram-negative strains. In the last decade, several research groups have pointed out
Y Zhang et al.
Analytical biochemistry, 239(2), 160-167 (1996-08-01)
A recently developed UV spectroscopic method for quantitating isothiocyanates (R-N=C=S) at the nanomole level is based on the observation that the highly electrophilic central carbon atom of the -N=C=S group can undergo successive nucleophilic additions with reagents containing two sulfhydryl
A dinuclear, triple-stranded helicate with a diamide-bridged catechol/benzenedithiol ligand.
F Ekkehardt Hahn et al.
Angewandte Chemie (International ed. in English), 43(36), 4807-4810 (2004-08-19)
Lingxiang Ye et al.
Clinica chimica acta; international journal of clinical chemistry, 316(1-2), 43-53 (2001-12-26)
Humans are exposed to substantial quantities of isothiocyanates and glucosinolates from vegetables. Since dietary isothiocyanates are widely regarded as potentially important chemoprotectors against cancer, reliable methods for measuring the plasma and tissue pharmacokinetics of isothiocyanates and their dithiocarbamate metabolites are
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