Home Other Building Blocks Dibutyl sulfide

Dibutyl sulfide

CAS No.:
544-40-1
Catalog Number:
AG003SUY
Molecular Formula:
C8H18S
Molecular Weight:
146.2935
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
10g
95%
1 week
United States
$59
- +
25g
95%
1 week
United States
$66
- +
100g
95%
1 week
United States
$107
- +
Product Description
Catalog Number:
AG003SUY
Chemical Name:
Dibutyl sulfide
CAS Number:
544-40-1
Molecular Formula:
C8H18S
Molecular Weight:
146.2935
MDL Number:
MFCD00009468
IUPAC Name:
1-butylsulfanylbutane
InChI:
InChI=1S/C8H18S/c1-3-5-7-9-8-6-4-2/h3-8H2,1-2H3
InChI Key:
HTIRHQRTDBPHNZ-UHFFFAOYSA-N
SMILES:
CCCCSCCCC
EC Number:
208-870-5
UNII:
3E3H471GA3
NSC Number:
8460
FEMA Number:
2215
Properties
Complexity:
37.8  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
146.113g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
146.292g/mol
Monoisotopic Mass:
146.113g/mol
Rotatable Bond Count:
6  
Topological Polar Surface Area:
25.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
3.4  
Literature
Title Journal
Electrons, photons, and force: quantitative single-molecule measurements from physics to biology. ACS nano 20110222
Gold and gold-iron modified zeolites--towards the adsorptive deodourisation. Journal of hazardous materials 20100715
Experimental and theoretical studies of the reaction of the OH radical with alkyl sulfides: 3. Kinetics and mechanism of the OH initiated oxidation of dimethyl, dipropyl, and dibutyl sulfides: reactivity trends in the alkyl sulfides and development of a predictive expression for the reaction of OH with DMS. The journal of physical chemistry. A 20090618
Rate of dibutylsulfide decomposition by ozonation and the O3/H2O2 advanced oxidation process. Journal of hazardous materials 20090530
A quantitative single-molecule study of thioether molecular rotors. ACS nano 20081125
Effect of temperature and initial dibutyl sulfide concentration in chloroform on its oxidation rate by ozone. Journal of hazardous materials 20080915
Dimethyl sulfide on Cu{111}: molecular self-assembly and submolecular resolution imaging. ACS nano 20071201
Adsorption, interaction, and manipulation of dibutyl sulfide on cu{111}. ACS nano 20070801
Identification of the reactive intermediates produced upon photolysis of p-azidoacetophenone and its tetrafluoro analogue in aqueous and organic solvents: implications for photoaffinity labeling. Biochemistry 20070220
Aquasonolysis of thioethers. Ultrasonics sonochemistry 20060501
Photochemical relationships in Sacoglossan polypropionates. Journal of natural products 20050401
Photo-oxidation of di-n-butylsulfide by various electron transfer sensitizers in oxygenated acetonitrile. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20050201
Electron transfer and singlet oxygen mechanisms in the photooxygenation of dibutyl sulfide and thioanisole in MeCN sensitized by N-methylquinolinium tetrafluoborate and 9,10-dicyanoanthracene. The probable involvement of a thiadioxirane intermediate in electron transfer photooxygenations. Journal of the American Chemical Society 20031231
Volatile metabolites of higher plant crops as a photosynthesizing life support system component under temperature stress at different light intensities. Advances in space research : the official journal of the Committee on Space Research (COSPAR) 20030101
Oxidation of sulfides and disulfides under electron transfer or singlet oxygen photosensitization using soluble or grafted sensitizers. Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20020501
Stand-off tissue-based biosensors for the detection of chemical warfare agents using photosynthetic fluorescence induction. Biosensors & bioelectronics 20010901
Induction of histone acetylation in mouse erythroleukemia cells by some organosulfur compounds including allyl isothiocyanate. International journal of cancer 20010615
Properties