Skip to Content
Merck
All Photos(3)

Documents

247545

Sigma-Aldrich

Di-tert-butyl disulfide

97%

Synonym(s):

tert-Butyl disulfide

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
(CH3)3CSSC(CH3)3
CAS Number:
110-06-5
Molecular Weight:
178.36
Beilstein:
1698170
EC Number:
203-734-1
MDL number:
MFCD00008838
UNSPSC Code:
12352100
PubChem Substance ID:
24854874
NACRES:
NA.22

vapor density

5 (vs air)

vapor pressure

51.7 mmHg ( 37.7 °C)

Assay

97%

form

liquid

refractive index

n20/D 1.490 (lit.)

bp

200-201 °C (lit.)

density

0.923 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)SSC(C)(C)C

InChI

1S/C8H18S2/c1-7(2,3)9-10-8(4,5)6/h1-6H3

InChI key

BKCNDTDWDGQHSD-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Mechanism of the oxidation of di-tert-butyl disulfide in the presence of H2O2 catalyzed by bis(acetylacetonato)oxovanadium and a chiral Schiff-base ligand has been investigated.

Application

Di-tert-butyl disulfide has been used in the preparation of gold-supported thin film from symmetrical and mixed disulphide adsorbates.

Pictograms

Environment
GHS09

Hazard Statements

H411

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Chronic 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

143.6 °F - closed cup

Flash Point(C)

62 °C - closed cup

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

Suzanne A Blum et al.
The Journal of organic chemistry, 68(1), 150-155 (2003-01-08)
The mechanism of the oxidation of di-tert-butyl disulfide (1) to the chiral thiosulfinate (2) by H(2)O(2) catalyzed by bis(acetylacetonato)oxovanadium and a chiral Schiff-base ligand (3) has been investigated. Techniques included (51)V NMR spectroscopy, solvent effects on reaction enantioselectivity, and the
Yoonsu Park et al.
Nanomaterials (Basel, Switzerland), 11(1) (2021-01-13)
Colloidal nanoparticles (NPs) have been recently spotlighted as building blocks for various nanostructured devices. Their collective properties have been exhibited by arranging them on a substrate to form assembled NPs. In particular, electrophoretic deposition (EPD) is an emerging fabrication method
Contact angle goniometry, ellipsometry, XPS, and TOF-SIMS analysis of gold-supported, mixed self-assembled monolayers formed from mixed dialkyl disulfides.
Offord DA, et al.
Langmuir, 10(3), 761-766 (1994)
Yang Liu et al.
ACS nano, 12(8), 7803-7811 (2018-07-10)
Heterogeneous copper sulfide based nanostructures have attracted intense attention based on their potential to combine the plasmonic properties of copper-deficient copper sulfides with properties of other semiconductors and metals. In general, copper sulfides are versatile platforms for production of other

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