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B101796

Sigma-Aldrich

Dibutyl sulfide

96%

Synonym(s):

1,1′-Thiobisbutane, Butyl sulfide, NSC 8460

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About This Item

Linear Formula:
CH3(CH2)3S(CH2)3CH3
CAS Number:
544-40-1
Molecular Weight:
146.29
Beilstein:
1732829
EC Number:
208-870-5
MDL number:
MFCD00009468
UNSPSC Code:
12352100
PubChem Substance ID:
24891540
NACRES:
NA.22

vapor density

5.07 (vs air)

Quality Level

200

vapor pressure

5.17 mmHg ( 37.7 °C)

Assay

96%

form

liquid

refractive index

n20/D 1.452 (lit.)

bp

188-189 °C (lit.)

mp

−76 °C (lit.)

density

0.838 g/mL at 25 °C (lit.)

SMILES string

CCCCSCCCC

InChI

1S/C8H18S/c1-3-5-7-9-8-6-4-2/h3-8H2,1-2H3

InChI key

HTIRHQRTDBPHNZ-UHFFFAOYSA-N

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

170.6 °F - closed cup

Flash Point(C)

77 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Izabela Sobczak et al.
Journal of hazardous materials, 179(1-3), 444-452 (2010-04-07)
Zeolites exhibiting different structures (Y, Beta, and ZSM-5) were modified with gold and iron and applied for odour adsorption from the air containing dibutyl sulphide (Bu(2)S) used as a representative odour producing compound. The structure of the zeolites used determines
Ashleigh E Baber et al.
ACS nano, 2(11), 2385-2391 (2009-02-12)
This paper describes a fundamental, single-molecule study of the motion of a set of thioethers supported on Au surfaces. Thioethers constitute a simple, robust system with which molecular rotation can be actuated both thermally and mechanically. Low-temperature scanning tunneling microscopy
The effect of dibutyl sulphide on hepatocytes studied by means of the isolated rat liver perfusion after preceding exposure to tetrachloromethane and phenobarbital in vivo.
O Nováková et al.
Acta Universitatis Carolinae. Medica, 27(1-2), 139-145 (1981-01-01)
Stanisław Popiel et al.
Journal of hazardous materials, 157(2-3), 319-327 (2008-02-23)
A scheme of dibutyl sulfide (DBS) oxidation with ozone and generation of transitional products was determined in this study. The main identified intermediate product was dibutyl sulfoxide (DBSO), and the main end product of DBS oxidation was dibutyl sulfone (DBSO2).
C A Sanders et al.
Biosensors & bioelectronics, 16(7-8), 439-446 (2001-09-07)
Tissue biosensors made from immobilized whole-cell photosynthetic microorganisms have been developed for the detection of airborne chemical warfare agents and simulants. The sensor read-out is based on well-known principles of fluorescence induction by living photosynthetic tissue. Like the cyanobacteria and
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